Identification of annotated bioactive molecules that impair motility of the blood fluke Schistosoma mansoni

Neglected tropical diseases are of growing worldwide concern and schistosomiasis, caused by parasitic flatworms, continues to be a major threat with more than 200 million people requiring preventive treatment. As praziquantel (PZQ) remains the treatment of choice, an urgent need for alternative trea...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:International journal for parasitology -- drugs and drug resistance Ročník 13; s. 73 - 88
Hlavní autoři: Duguet, Thomas B., Glebov, Anastasia, Hussain, Asimah, Kulkarni, Shashank, Mochalkin, Igor, Geary, Timothy G., Rashid, Mohammed, Spangenberg, Thomas, Ribeiro, Paula
Médium: Journal Article
Jazyk:angličtina
Vydáno: England Elsevier Ltd 01.08.2020
Elsevier
Témata:
ISSN:2211-3207, 2211-3207
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Abstract Neglected tropical diseases are of growing worldwide concern and schistosomiasis, caused by parasitic flatworms, continues to be a major threat with more than 200 million people requiring preventive treatment. As praziquantel (PZQ) remains the treatment of choice, an urgent need for alternative treatments motivates research to identify new lead compounds that would complement PZQ by filling the therapeutic gaps associated with this treatment. Because impairing parasite neurotransmission remains a core strategy for control of parasitic helminths, we screened a library of 708 compounds with validated biological activity in humans on the blood fluke Schistosoma mansoni, measuring their effect on the motility on schistosomulae and adult worms. The primary phenotypic screen performed on schistosomulae identified 70 compounds that induced changes in viability and/or motility. Screening different concentrations and incubation times identified molecules with fast onset of activity on both life stages at low concentration (1 μM). To complement this study, similar assays were performed with chemical analogs of the cholinomimetic drug arecoline and the calcilytic molecule NPS-2143, two compounds that rapidly inhibited schistosome motility; 17 arecoline and 302 NPS-2143 analogs were tested to enlarge the pool of schistosomicidal molecules. Finally, validated hit compounds were tested on three functionally-validated neuroregulatory S. mansoni G-protein coupled receptors (GPCRs): Sm5HTR (serotonin-sensitive), SmGPR2 (histamine) and SmD2 (dopamine), revealing NPS-2143 and analogs as potent inhibitors of dopamine/epinine responses on both human and S. mansoni GPCRs. This study highlights the potential for repurposing known human therapeutic agents for potential schistosomicidal effects and expands the list of hits for further progression. [Display omitted] •Screening annotated bioactive molecules to ease new treatment search.•Coupling motility recording of treated parasite and molecular target search.•Exploiting chemical analogs to expand bioactive compound search.•The larvicidal NPS-2143 acts on dopaminergic GPCRs.
AbstractList Neglected tropical diseases are of growing worldwide concern and schistosomiasis, caused by parasitic flatworms, continues to be a major threat with more than 200 million people requiring preventive treatment. As praziquantel (PZQ) remains the treatment of choice, an urgent need for alternative treatments motivates research to identify new lead compounds that would complement PZQ by filling the therapeutic gaps associated with this treatment. Because impairing parasite neurotransmission remains a core strategy for control of parasitic helminths, we screened a library of 708 compounds with validated biological activity in humans on the blood fluke Schistosoma mansoni, measuring their effect on the motility on schistosomulae and adult worms. The primary phenotypic screen performed on schistosomulae identified 70 compounds that induced changes in viability and/or motility. Screening different concentrations and incubation times identified molecules with fast onset of activity on both life stages at low concentration (1 μM). To complement this study, similar assays were performed with chemical analogs of the cholinomimetic drug arecoline and the calcilytic molecule NPS-2143, two compounds that rapidly inhibited schistosome motility; 17 arecoline and 302 NPS-2143 analogs were tested to enlarge the pool of schistosomicidal molecules. Finally, validated hit compounds were tested on three functionally-validated neuroregulatory S. mansoni G-protein coupled receptors (GPCRs): Sm5HTR (serotonin-sensitive), SmGPR2 (histamine) and SmD2 (dopamine), revealing NPS-2143 and analogs as potent inhibitors of dopamine/epinine responses on both human and S. mansoni GPCRs. This study highlights the potential for repurposing known human therapeutic agents for potential schistosomicidal effects and expands the list of hits for further progression. Image 1 • Screening annotated bioactive molecules to ease new treatment search. • Coupling motility recording of treated parasite and molecular target search. • Exploiting chemical analogs to expand bioactive compound search. • The larvicidal NPS-2143 acts on dopaminergic GPCRs.
Neglected tropical diseases are of growing worldwide concern and schistosomiasis, caused by parasitic flatworms, continues to be a major threat with more than 200 million people requiring preventive treatment. As praziquantel (PZQ) remains the treatment of choice, an urgent need for alternative treatments motivates research to identify new lead compounds that would complement PZQ by filling the therapeutic gaps associated with this treatment. Because impairing parasite neurotransmission remains a core strategy for control of parasitic helminths, we screened a library of 708 compounds with validated biological activity in humans on the blood fluke Schistosoma mansoni, measuring their effect on the motility on schistosomulae and adult worms. The primary phenotypic screen performed on schistosomulae identified 70 compounds that induced changes in viability and/or motility. Screening different concentrations and incubation times identified molecules with fast onset of activity on both life stages at low concentration (1 μM). To complement this study, similar assays were performed with chemical analogs of the cholinomimetic drug arecoline and the calcilytic molecule NPS-2143, two compounds that rapidly inhibited schistosome motility; 17 arecoline and 302 NPS-2143 analogs were tested to enlarge the pool of schistosomicidal molecules. Finally, validated hit compounds were tested on three functionally-validated neuroregulatory S. mansoni G-protein coupled receptors (GPCRs): Sm5HTR (serotonin-sensitive), SmGPR2 (histamine) and SmD2 (dopamine), revealing NPS-2143 and analogs as potent inhibitors of dopamine/epinine responses on both human and S. mansoni GPCRs. This study highlights the potential for repurposing known human therapeutic agents for potential schistosomicidal effects and expands the list of hits for further progression.
Neglected tropical diseases are of growing worldwide concern and schistosomiasis, caused by parasitic flatworms, continues to be a major threat with more than 200 million people requiring preventive treatment. As praziquantel (PZQ) remains the treatment of choice, an urgent need for alternative treatments motivates research to identify new lead compounds that would complement PZQ by filling the therapeutic gaps associated with this treatment. Because impairing parasite neurotransmission remains a core strategy for control of parasitic helminths, we screened a library of 708 compounds with validated biological activity in humans on the blood fluke Schistosoma mansoni, measuring their effect on the motility on schistosomulae and adult worms. The primary phenotypic screen performed on schistosomulae identified 70 compounds that induced changes in viability and/or motility. Screening different concentrations and incubation times identified molecules with fast onset of activity on both life stages at low concentration (1 μM). To complement this study, similar assays were performed with chemical analogs of the cholinomimetic drug arecoline and the calcilytic molecule NPS-2143, two compounds that rapidly inhibited schistosome motility; 17 arecoline and 302 NPS-2143 analogs were tested to enlarge the pool of schistosomicidal molecules. Finally, validated hit compounds were tested on three functionally-validated neuroregulatory S. mansoni G-protein coupled receptors (GPCRs): Sm5HTR (serotonin-sensitive), SmGPR2 (histamine) and SmD2 (dopamine), revealing NPS-2143 and analogs as potent inhibitors of dopamine/epinine responses on both human and S. mansoni GPCRs. This study highlights the potential for repurposing known human therapeutic agents for potential schistosomicidal effects and expands the list of hits for further progression. [Display omitted] •Screening annotated bioactive molecules to ease new treatment search.•Coupling motility recording of treated parasite and molecular target search.•Exploiting chemical analogs to expand bioactive compound search.•The larvicidal NPS-2143 acts on dopaminergic GPCRs.
Neglected tropical diseases are of growing worldwide concern and schistosomiasis, caused by parasitic flatworms, continues to be a major threat with more than 200 million people requiring preventive treatment. As praziquantel (PZQ) remains the treatment of choice, an urgent need for alternative treatments motivates research to identify new lead compounds that would complement PZQ by filling the therapeutic gaps associated with this treatment. Because impairing parasite neurotransmission remains a core strategy for control of parasitic helminths, we screened a library of 708 compounds with validated biological activity in humans on the blood fluke Schistosoma mansoni, measuring their effect on the motility on schistosomulae and adult worms. The primary phenotypic screen performed on schistosomulae identified 70 compounds that induced changes in viability and/or motility. Screening different concentrations and incubation times identified molecules with fast onset of activity on both life stages at low concentration (1 μM). To complement this study, similar assays were performed with chemical analogs of the cholinomimetic drug arecoline and the calcilytic molecule NPS-2143, two compounds that rapidly inhibited schistosome motility; 17 arecoline and 302 NPS-2143 analogs were tested to enlarge the pool of schistosomicidal molecules. Finally, validated hit compounds were tested on three functionally-validated neuroregulatory S. mansoni G-protein coupled receptors (GPCRs): Sm5HTR (serotonin-sensitive), SmGPR2 (histamine) and SmD2 (dopamine), revealing NPS-2143 and analogs as potent inhibitors of dopamine/epinine responses on both human and S. mansoni GPCRs. This study highlights the potential for repurposing known human therapeutic agents for potential schistosomicidal effects and expands the list of hits for further progression.Neglected tropical diseases are of growing worldwide concern and schistosomiasis, caused by parasitic flatworms, continues to be a major threat with more than 200 million people requiring preventive treatment. As praziquantel (PZQ) remains the treatment of choice, an urgent need for alternative treatments motivates research to identify new lead compounds that would complement PZQ by filling the therapeutic gaps associated with this treatment. Because impairing parasite neurotransmission remains a core strategy for control of parasitic helminths, we screened a library of 708 compounds with validated biological activity in humans on the blood fluke Schistosoma mansoni, measuring their effect on the motility on schistosomulae and adult worms. The primary phenotypic screen performed on schistosomulae identified 70 compounds that induced changes in viability and/or motility. Screening different concentrations and incubation times identified molecules with fast onset of activity on both life stages at low concentration (1 μM). To complement this study, similar assays were performed with chemical analogs of the cholinomimetic drug arecoline and the calcilytic molecule NPS-2143, two compounds that rapidly inhibited schistosome motility; 17 arecoline and 302 NPS-2143 analogs were tested to enlarge the pool of schistosomicidal molecules. Finally, validated hit compounds were tested on three functionally-validated neuroregulatory S. mansoni G-protein coupled receptors (GPCRs): Sm5HTR (serotonin-sensitive), SmGPR2 (histamine) and SmD2 (dopamine), revealing NPS-2143 and analogs as potent inhibitors of dopamine/epinine responses on both human and S. mansoni GPCRs. This study highlights the potential for repurposing known human therapeutic agents for potential schistosomicidal effects and expands the list of hits for further progression.
Author Mochalkin, Igor
Kulkarni, Shashank
Rashid, Mohammed
Ribeiro, Paula
Geary, Timothy G.
Glebov, Anastasia
Hussain, Asimah
Spangenberg, Thomas
Duguet, Thomas B.
Author_xml – sequence: 1
  givenname: Thomas B.
  surname: Duguet
  fullname: Duguet, Thomas B.
  email: thomas.duguet@mail.mcgill.ca
  organization: Institute of Parasitology, McGill University, Sainte-Anne-de-Bellevue, Quebec, Canada
– sequence: 2
  givenname: Anastasia
  surname: Glebov
  fullname: Glebov, Anastasia
  organization: Institute of Parasitology, McGill University, Sainte-Anne-de-Bellevue, Quebec, Canada
– sequence: 3
  givenname: Asimah
  surname: Hussain
  fullname: Hussain, Asimah
  organization: Institute of Parasitology, McGill University, Sainte-Anne-de-Bellevue, Quebec, Canada
– sequence: 4
  givenname: Shashank
  surname: Kulkarni
  fullname: Kulkarni, Shashank
  organization: EMD Serono Research and Development Institute, Billerica, MA, USA
– sequence: 5
  givenname: Igor
  surname: Mochalkin
  fullname: Mochalkin, Igor
  organization: EMD Serono Research and Development Institute, Billerica, MA, USA
– sequence: 6
  givenname: Timothy G.
  surname: Geary
  fullname: Geary, Timothy G.
  organization: Institute of Parasitology, McGill University, Sainte-Anne-de-Bellevue, Quebec, Canada
– sequence: 7
  givenname: Mohammed
  surname: Rashid
  fullname: Rashid, Mohammed
  organization: Institute of Parasitology, McGill University, Sainte-Anne-de-Bellevue, Quebec, Canada
– sequence: 8
  givenname: Thomas
  orcidid: 0000-0002-5654-8919
  surname: Spangenberg
  fullname: Spangenberg, Thomas
  email: thomas.spangenberg@merckgroup.com
  organization: Global Health Institute of Merck, Ares Trading S.A., a subsidiary of Merck KGaA (Darmstadt, Germany), Eysins, Switzerland
– sequence: 9
  givenname: Paula
  surname: Ribeiro
  fullname: Ribeiro, Paula
  organization: Institute of Parasitology, McGill University, Sainte-Anne-de-Bellevue, Quebec, Canada
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32531750$$D View this record in MEDLINE/PubMed
BookMark eNqFUk1vEzEQtVARLaH_AKE9ckmwvev94ICEKj4iVeIAnC1_zDaz9drBdiL13-M0oWo5gC8ejd97Y715L8mZDx4Iec3oilHWvptWOG2tjStOOV1RsaKUPyMXnDO2rDntzh7V5-QypYmW01LWM_qCnNdc1KwT9ILcri34jCMalTH4KoyV8j5klcFWGoMyGfdQzcGB2TlIVd6oXOG8VRhLN6PDfHdg5Q1U2oVgq9HtbqH6bjaYckhhVtWsfAoeX5Hno3IJLk_3gvz8_OnH1dfl9bcv66uP10sj-JCXumuN0lSNuh9rOraNqseOKwUD5dbSVhvDBz42THBq637oYRBa8Fb3tBRa1wuyPuraoCa5jTireCeDQnnfCPFGqpjROJAKRKc7Ubdd0zZlhra94D10FLqurZkqWh-OWtudnsGaYlZU7ono0xePG3kT9rLjfcOKzQvy9iQQw68dpCxnTAacUx7CLkleUMPQsKYv0DePZz0M-bOtAmiOABNDShHGBwij8pALOcljLuQhF5IKWXJRaO__ohnM9-suP0b3P_LJACgb2yNEmQyCN2AxgsnFUvy3wG-2ndgO
CitedBy_id crossref_primary_10_1038_s42003_023_05675_4
crossref_primary_10_1371_journal_pntd_0009432
crossref_primary_10_1080_14656566_2024_2333372
crossref_primary_10_1016_j_drudis_2022_04_004
crossref_primary_10_3389_fphar_2022_872212
crossref_primary_10_1016_j_pt_2021_05_004
crossref_primary_10_3389_fimmu_2021_642383
Cites_doi 10.1007/BF00389899
10.1186/s40249-015-0071-z
10.1126/science.1243106
10.1111/febs.14029
10.1007/s004360050227
10.1016/j.ijpara.2010.04.006
10.2174/1568026618666180427145308
10.1371/journal.pntd.0001494
10.2174/0929867325666180926145537
10.1242/dmm.033563
10.1007/s00436-001-0585-0
10.1002/wmts.19
10.1371/journal.pntd.0000478
10.1007/s00436-002-0751-z
10.1038/s41598-018-26532-z
10.1016/0035-9203(73)90039-4
10.1039/C5MD00596E
10.1371/journal.ppat.1003878
10.1016/j.exppara.2007.08.002
10.1371/journal.pntd.0001523
10.1016/S0140-6736(13)61949-2
10.1371/journal.pntd.0003962
10.1139/Z09-126
10.1371/journal.pntd.0002610
10.1371/journal.pntd.0004063
10.1016/j.molbiopara.2008.11.007
10.1371/journal.pntd.0001762
10.1128/AAC.02582-16
10.1371/journal.pntd.0007693
10.1016/0035-9203(87)90282-3
10.4155/fmc.15.26
10.1021/acsinfecdis.9b00237
10.1016/j.exppara.2005.01.002
10.1016/j.molbiopara.2009.06.003
10.7554/eLife.41337
10.1016/j.ijpddr.2018.09.001
10.1074/jbc.AC119.011093
10.1093/jac/dkt491
10.1186/1471-2164-12-14
10.1021/ml3003814
10.1186/s40364-016-0075-2
10.1371/journal.ppat.1005651
10.1074/jbc.C100273200
10.1186/1476-4598-13-42
10.1172/JCI17416
10.1016/j.bmc.2010.09.041
10.1111/j.1476-5381.2011.01511.x
10.1186/s13071-019-3747-6
10.1371/journal.ppat.1004181
10.1016/j.molbiopara.2010.12.001
10.1016/j.molbiopara.2014.06.002
10.7554/eLife.35755
10.1017/S0031182000066270
10.1371/journal.pntd.0000504
10.1038/s41598-017-18457-w
10.1371/journal.ppat.1003942
10.1038/s41596-018-0101-y
10.1155/2016/9521349
10.1186/s13071-017-2293-3
10.1021/acs.jafc.5b03749
10.1111/j.1527-3458.2001.tb00189.x
10.1016/j.molbiopara.2018.09.004
10.1093/bioinformatics/btu831
10.1016/S1473-3099(15)00066-3
10.1016/j.tmaid.2008.06.006
10.1016/S0022-3565(24)29333-2
10.1371/journal.pone.0184192
10.1371/journal.pntd.0004659
10.1002/cmdc.201800572
10.4269/ajtmh.1983.32.83
10.1677/joe.1.06924
10.1016/S0166-6851(01)00400-5
10.4137/EBO.S9405
10.1186/s13071-015-1233-3
10.1016/j.molbiopara.2015.09.001
10.1074/jbc.R112.406280
10.1371/journal.ppat.1003254
10.1016/j.molbiopara.2007.03.010
10.1007/s10158-012-0132-y
10.1111/j.1476-5381.1966.tb01845.x
ContentType Journal Article
Copyright 2020 The Authors
Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.
2020 The Authors 2020
Copyright_xml – notice: 2020 The Authors
– notice: Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.
– notice: 2020 The Authors 2020
DBID 6I.
AAFTH
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
DOA
DOI 10.1016/j.ijpddr.2020.05.002
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList
MEDLINE


MEDLINE - Academic
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2211-3207
EndPage 88
ExternalDocumentID oai_doaj_org_article_ae57b753674642aabd8528e70e77631a
PMC7284125
32531750
10_1016_j_ijpddr_2020_05_002
S2211320720300129
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
--K
0R~
0SF
1~5
457
4G.
5VS
6I.
7-5
AACTN
AAEDT
AAEDW
AAFTH
AAIKJ
AALRI
AAXUO
ABMAC
ACGFS
ADBBV
ADEZE
AEXQZ
AFTJW
AGHFR
AITUG
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
AOIJS
BAWUL
BCNDV
DIK
EBS
EJD
FDB
GROUPED_DOAJ
HYE
HZ~
IPNFZ
IXB
KQ8
M41
M48
NCXOZ
O-L
O9-
OK1
RIG
ROL
RPM
SSZ
XH2
AAYWO
AAYXX
ADVLN
AFJKZ
APXCP
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
ID FETCH-LOGICAL-c529t-b76cab0afb8f30f64a3f72aae902dd06bcc292f41520d3898e95b526b8095bbb3
IEDL.DBID DOA
ISICitedReferencesCount 11
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000556674900009&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 2211-3207
IngestDate Fri Oct 03 12:41:31 EDT 2025
Tue Sep 30 16:53:08 EDT 2025
Fri Jul 11 07:05:52 EDT 2025
Thu Apr 03 07:08:26 EDT 2025
Wed Nov 05 20:54:49 EST 2025
Tue Nov 18 21:50:52 EST 2025
Wed May 17 01:22:43 EDT 2023
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords NPS-2143
Schistosomiasis
Screening
GPCR
Anthelmintic
Motility
Language English
License This is an open access article under the CC BY license.
Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.
This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c529t-b76cab0afb8f30f64a3f72aae902dd06bcc292f41520d3898e95b526b8095bbb3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Current address: Vertex Pharmaceuticals, San Diego, CA, USA.
Deceased March 4, 2017.
ORCID 0000-0002-5654-8919
OpenAccessLink https://doaj.org/article/ae57b753674642aabd8528e70e77631a
PMID 32531750
PQID 2412994148
PQPubID 23479
PageCount 16
ParticipantIDs doaj_primary_oai_doaj_org_article_ae57b753674642aabd8528e70e77631a
pubmedcentral_primary_oai_pubmedcentral_nih_gov_7284125
proquest_miscellaneous_2412994148
pubmed_primary_32531750
crossref_primary_10_1016_j_ijpddr_2020_05_002
crossref_citationtrail_10_1016_j_ijpddr_2020_05_002
elsevier_sciencedirect_doi_10_1016_j_ijpddr_2020_05_002
PublicationCentury 2000
PublicationDate 2020-08-01
PublicationDateYYYYMMDD 2020-08-01
PublicationDate_xml – month: 08
  year: 2020
  text: 2020-08-01
  day: 01
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle International journal for parasitology -- drugs and drug resistance
PublicationTitleAlternate Int J Parasitol Drugs Drug Resist
PublicationYear 2020
Publisher Elsevier Ltd
Elsevier
Publisher_xml – name: Elsevier Ltd
– name: Elsevier
References Holden-Dye, Walker (bib32) 2007
Bibo-Verdugo, Wang, Almaliti, Ta, Jiang, Wong, Lietz, Suzuki, El-Sakkary, Hook, Salvesen, Gerwick, Caffrey, O'Donoghue (bib7) 2019; 5
Gold (bib26) 1997; 83
Maccesi, Aguiar, Pasche, Padilla, Suzuki, Montefusco, Abagyan, Keiser, Mourao, Caffrey (bib44) 2019; 12
Chan, Agbedanu, Grab, Zamanian, Dosa, Day, Marchant (bib9) 2015; 9
Nemeth, Delmar, Heaton, Miller, Lambert, Conklin, Gowen, Gleason, Bhatnagar, Fox (bib57) 2001; 299
Van Nassauw, Toovey, Van Op den Bosch, Timmermans, Vercruysse (bib79) 2008; 6
El-Sakkary, Chen, Arkin, Caffrey, Ribeiro (bib19) 2018; 11
Kohn, Anderson, Roberts-Misterly, Greenberg (bib36) 2001; 276
Day, Chen, Miller, Tian, Bennett, Pax (bib16) 1996; 113
Mine, Zhang (bib53) 2015; 63
Li, Ziniel, He, Kommer, Crowther, He, Liu, Van Voorhis, Williams, Wang (bib42) 2015; 4
Kos, Karaplis, Peng, Hediger, Goltzman, Mohammad, Guise, Pollak (bib37) 2003; 111
Ingram-Sieber, Cowan, Panic, Vargas, Mansour, Bickle, Wells, Spangenberg, Keiser (bib33) 2014; 8
Cioli, Pica-Mattoccia, Basso, Guidi (bib14) 2014; 195
Atwood, Lopez, Wager-Miller, Mackie, Straiker (bib4) 2011; 12
Chan, McCorvy, Acharya, Johns, Day, Roth, Marchant (bib12) 2016; 12
Ward, Riccardi (bib80) 2012; 165
Gupta, Aggarwal, Singh, Yadav, Khan (bib29) 2018; 8
El-Shehabi, Taman, Moali, El-Sakkary, Ribeiro (bib21) 2012; 6
El-Shehabi, Ribeiro (bib20) 2010; 40
Kovac, Vargas, Keiser (bib38) 2017; 10
Kuhn, Kellenberger, Said-Hassane, Villa, Rognan, Lobstein, Haiech, Hibert, Schuber, Muller-Steffner (bib39) 2010; 18
Wolstenholme (bib85) 2012; 287
Joeckel, Haber, Prawitt, Junker, Hampel, Thuroff, Roos, Brenner (bib35) 2014; 13
Ribeiro, Geary (bib69) 2009; 88
Taman, Ribeiro (bib73) 2009; 168
Weth, Haeberlein, Haimann, Zhang, Grevelding (bib82) 2019
Gonnert, Andrews (bib27) 1977; 52
Lai, Biedermann, Ekpo, Garba, Mathieu, Midzi, Mwinzi, N'Goran, Raso, Assare, Sacko, Schur, Talla, Tchuente, Toure, Winkler, Utzinger, Vounatsou (bib40) 2015; 15
Barker, Bueding, Timms (bib5) 1966; 26
Colley, Bustinduy, Secor, King (bib15) 2014; 383
Lewis (bib41) 2001
Ittiprasert, Mann, Karinshak, Coghlan, Rinaldi, Sankaranarayanan, Chaidee, Tanno, Kumkhaek, Prangtaworn, Mentink-Kane, Cochran, Driguez, Holroyd, Tracey, Rodpai, Everts, Hokke, Hoffmann, Berriman, Brindley (bib34) 2019; 8
Morais, Oliveira, Paula, Ornelas, Moreira, Badoco, Magalhaes, Verjovski-Almeida, Rodrigues (bib54) 2017; 12
Patocka, Sharma, Rashid, Ribeiro (bib64) 2014; 10
Guerra-Sa, Castro-Borges, Evangelista, Kettelhut, Rodrigues (bib28) 2005; 109
Dosa, Ward, Walters, Kim (bib18) 2013; 4
Bibo-Verdugo, Jiang, Caffrey, O'Donoghue (bib6) 2017; 284
Ribeiro, Gupta, El-Sakkary (bib70) 2012; 12
MacDonald, Buxton, Kimber, Day, Robertson, Ribeiro (bib45) 2014; 10
Park, Gunaratne, Chulkov, Moehring, McCusker, Dosa, Chan, Stucky, Marchant (bib62) 2019; 294
Gemmell (bib25) 1973; 48
Mansour, Paveley, Gardner, Bell, Parkinson, Bickle (bib48) 2016; 10
Tekwu, Anyan, Boamah, Baffour-Awuah, Keyetat Tekwu, Penlap Beng, Nyarko, Bosompem (bib75) 2016; 4
Valentim, Cioli, Chevalier, Cao, Taylor, Holloway, Pica-Mattoccia, Guidi, Basso, Tsai, Berriman, Carvalho-Queiroz, Almeida, Aguilar, Frantz, Hart, LoVerde, Anderson (bib78) 2013; 342
Bourin, Chue, Guillon (bib8) 2001; 7
Neves, Dantas, Senger, Valente, Rezende-Neto, Chaves, Kamentsky, Carpenter, Silva-Junior, Andrade (bib58) 2016; 7
Panic, Vargas, Scandale, Keiser (bib61) 2015; 9
Chan, Agbedanu, Zamanian, Gruba, Haynes, Day, Marchant (bib10) 2014; 10
Eweas, Allam (bib22) 2018; 225
Mellin, Busch, Wang, Kath (bib51) 1983; 32
Whatley, Padalino, Whiteland, Geyer, Hulme, Chalmers, Forde-Thomas, Ferla, Brancale, Hoffmann (bib83) 2019; 13
Foster (bib23) 1987; 81
Rybczynska, Lehmann, Jurska-Jasko, Boblewski, Orlewska, Foks, Drewnowska (bib71) 2006; 191
Hamdan, Mousa, Ribeiro (bib31) 2002; 88
Salvador-Recatala, Greenberg (bib72) 2012; 1
Patocka, Ribeiro (bib63) 2007; 154
Chan, Day, Marchant (bib11) 2018; 7
Hamdan, Abramovitz, Mousa, Xie, Durocher, Ribeiro (bib30) 2002; 119
Lombardo, Pasche, Panic, Endriss, Keiser (bib43) 2019; 14
Nabhan, El-Shehabi, Patocka, Ribeiro (bib55) 2007; 117
Weeks, Roberts, Leasure, Suzuki, Robinson, Currey, Wangchuk, Eichenberger, Saxton, Bird, Kraemer, Loukas, Hawdon, Caffrey, Liachko (bib81) 2018; 8
Foster, Cheetham, King (bib24) 1973; 67
Abdulla, Ruelas, Wolff, Snedecor, Lim, Xu, Renslo, Williams, McKerrow, Caffrey (bib1) 2009; 3
Thomas, Timson (bib76) 2020; 27
Vale, Gouveia, Rinaldi, Brindley, Gartner, Correia da Costa (bib77) 2017; 61
Aragon, Imani, Blackburn, Cupit, Melman, Goronga, Webb, Loker, Cunningham (bib2) 2009; 164
Asarnow, Rojo-Arreola, Suzuki, Caffrey, Singh (bib3) 2015; 31
Ramamoorthi, Graef, Dent (bib67) 2015; 7
Cioli, Pica-Mattoccia (bib13) 2003; 1
Mader, Rennar, Ventura, Grevelding, Schlitzer (bib47) 2018; 13
Marcellino, Gut, Lim, Singh, McKerrow, Sakanari (bib49) 2012; 6
Olliaro, Delgado-Romero, Keiser (bib59) 2014; 69
You, McManus, Hu, Smout, Brindley, Gobert (bib84) 2013; 9
Marchant, Harding, Chan (bib50) 2018; 8
Rashid, MacDonald, Ribeiro (bib68) 2015
Paveley, Mansour, Hallyburton, Bleicher, Benn, Mikic, Guidi, Gilbert, Hopkins, Bickle (bib65) 2012; 6
Nagarathnam, Kalaimathy, Balakrishnan, Sowdhamini (bib56) 2012; 8
MacDonald, Kimber, Day, Ribeiro (bib46) 2015; 202
Taman, Ribeiro (bib74) 2011; 176
Pereira, Curra, Garcia (bib66) 2018; 18
de Almeida, de Carvalho, Gazolla, Silva Pinto, da Silva, de Moraes, Da Silva Filho (bib17) 2016; 2016
Holden-dye, Walker (bib86) 2014
Melman, Steinauer, Cunningham, Kubatko, Mwangi, Wynn, Mutuku, Karanja, Colley, Black, Secor, Mkoji, Loker (bib52) 2009; 3
Panic, Flores, Ingram-Sieber, Keiser (bib60) 2015; 8
El-Shehabi (10.1016/j.ijpddr.2020.05.002_bib21) 2012; 6
Rashid (10.1016/j.ijpddr.2020.05.002_bib68) 2015
Lai (10.1016/j.ijpddr.2020.05.002_bib40) 2015; 15
Lewis (10.1016/j.ijpddr.2020.05.002_bib41) 2001
Melman (10.1016/j.ijpddr.2020.05.002_bib52) 2009; 3
MacDonald (10.1016/j.ijpddr.2020.05.002_bib46) 2015; 202
Kos (10.1016/j.ijpddr.2020.05.002_bib37) 2003; 111
Asarnow (10.1016/j.ijpddr.2020.05.002_bib3) 2015; 31
Holden-dye (10.1016/j.ijpddr.2020.05.002_bib86) 2014
Holden-Dye (10.1016/j.ijpddr.2020.05.002_bib32) 2007
Li (10.1016/j.ijpddr.2020.05.002_bib42) 2015; 4
Ribeiro (10.1016/j.ijpddr.2020.05.002_bib69) 2009; 88
Gemmell (10.1016/j.ijpddr.2020.05.002_bib25) 1973; 48
You (10.1016/j.ijpddr.2020.05.002_bib84) 2013; 9
Vale (10.1016/j.ijpddr.2020.05.002_bib77) 2017; 61
Mader (10.1016/j.ijpddr.2020.05.002_bib47) 2018; 13
Thomas (10.1016/j.ijpddr.2020.05.002_bib76) 2020; 27
de Almeida (10.1016/j.ijpddr.2020.05.002_bib17) 2016; 2016
Weth (10.1016/j.ijpddr.2020.05.002_bib82) 2019
Van Nassauw (10.1016/j.ijpddr.2020.05.002_bib79) 2008; 6
Mine (10.1016/j.ijpddr.2020.05.002_bib53) 2015; 63
Foster (10.1016/j.ijpddr.2020.05.002_bib23) 1987; 81
Mellin (10.1016/j.ijpddr.2020.05.002_bib51) 1983; 32
Ingram-Sieber (10.1016/j.ijpddr.2020.05.002_bib33) 2014; 8
Abdulla (10.1016/j.ijpddr.2020.05.002_bib1) 2009; 3
Gonnert (10.1016/j.ijpddr.2020.05.002_bib27) 1977; 52
Valentim (10.1016/j.ijpddr.2020.05.002_bib78) 2013; 342
Cioli (10.1016/j.ijpddr.2020.05.002_bib13) 2003; 1
Taman (10.1016/j.ijpddr.2020.05.002_bib73) 2009; 168
Gupta (10.1016/j.ijpddr.2020.05.002_bib29) 2018; 8
Marchant (10.1016/j.ijpddr.2020.05.002_bib50) 2018; 8
Hamdan (10.1016/j.ijpddr.2020.05.002_bib30) 2002; 119
Hamdan (10.1016/j.ijpddr.2020.05.002_bib31) 2002; 88
Kohn (10.1016/j.ijpddr.2020.05.002_bib36) 2001; 276
Pereira (10.1016/j.ijpddr.2020.05.002_bib66) 2018; 18
Chan (10.1016/j.ijpddr.2020.05.002_bib12) 2016; 12
El-Shehabi (10.1016/j.ijpddr.2020.05.002_bib20) 2010; 40
Aragon (10.1016/j.ijpddr.2020.05.002_bib2) 2009; 164
Day (10.1016/j.ijpddr.2020.05.002_bib16) 1996; 113
Morais (10.1016/j.ijpddr.2020.05.002_bib54) 2017; 12
Dosa (10.1016/j.ijpddr.2020.05.002_bib18) 2013; 4
Wolstenholme (10.1016/j.ijpddr.2020.05.002_bib85) 2012; 287
Tekwu (10.1016/j.ijpddr.2020.05.002_bib75) 2016; 4
Foster (10.1016/j.ijpddr.2020.05.002_bib24) 1973; 67
Nagarathnam (10.1016/j.ijpddr.2020.05.002_bib56) 2012; 8
Bibo-Verdugo (10.1016/j.ijpddr.2020.05.002_bib6) 2017; 284
Ramamoorthi (10.1016/j.ijpddr.2020.05.002_bib67) 2015; 7
Paveley (10.1016/j.ijpddr.2020.05.002_bib65) 2012; 6
Chan (10.1016/j.ijpddr.2020.05.002_bib10) 2014; 10
Kovac (10.1016/j.ijpddr.2020.05.002_bib38) 2017; 10
MacDonald (10.1016/j.ijpddr.2020.05.002_bib45) 2014; 10
Mansour (10.1016/j.ijpddr.2020.05.002_bib48) 2016; 10
Patocka (10.1016/j.ijpddr.2020.05.002_bib64) 2014; 10
Barker (10.1016/j.ijpddr.2020.05.002_bib5) 1966; 26
Chan (10.1016/j.ijpddr.2020.05.002_bib11) 2018; 7
Panic (10.1016/j.ijpddr.2020.05.002_bib60) 2015; 8
Ribeiro (10.1016/j.ijpddr.2020.05.002_bib70) 2012; 12
Marcellino (10.1016/j.ijpddr.2020.05.002_bib49) 2012; 6
Bibo-Verdugo (10.1016/j.ijpddr.2020.05.002_bib7) 2019; 5
Maccesi (10.1016/j.ijpddr.2020.05.002_bib44) 2019; 12
Guerra-Sa (10.1016/j.ijpddr.2020.05.002_bib28) 2005; 109
Eweas (10.1016/j.ijpddr.2020.05.002_bib22) 2018; 225
Panic (10.1016/j.ijpddr.2020.05.002_bib61) 2015; 9
El-Sakkary (10.1016/j.ijpddr.2020.05.002_bib19) 2018; 11
Cioli (10.1016/j.ijpddr.2020.05.002_bib14) 2014; 195
Salvador-Recatala (10.1016/j.ijpddr.2020.05.002_bib72) 2012; 1
Atwood (10.1016/j.ijpddr.2020.05.002_bib4) 2011; 12
Ittiprasert (10.1016/j.ijpddr.2020.05.002_bib34) 2019; 8
Bourin (10.1016/j.ijpddr.2020.05.002_bib8) 2001; 7
Chan (10.1016/j.ijpddr.2020.05.002_bib9) 2015; 9
Ward (10.1016/j.ijpddr.2020.05.002_bib80) 2012; 165
Nabhan (10.1016/j.ijpddr.2020.05.002_bib55) 2007; 117
Gold (10.1016/j.ijpddr.2020.05.002_bib26) 1997; 83
Olliaro (10.1016/j.ijpddr.2020.05.002_bib59) 2014; 69
Colley (10.1016/j.ijpddr.2020.05.002_bib15) 2014; 383
Kuhn (10.1016/j.ijpddr.2020.05.002_bib39) 2010; 18
Taman (10.1016/j.ijpddr.2020.05.002_bib74) 2011; 176
Nemeth (10.1016/j.ijpddr.2020.05.002_bib57) 2001; 299
Joeckel (10.1016/j.ijpddr.2020.05.002_bib35) 2014; 13
Patocka (10.1016/j.ijpddr.2020.05.002_bib63) 2007; 154
Whatley (10.1016/j.ijpddr.2020.05.002_bib83) 2019; 13
Neves (10.1016/j.ijpddr.2020.05.002_bib58) 2016; 7
Rybczynska (10.1016/j.ijpddr.2020.05.002_bib71) 2006; 191
Lombardo (10.1016/j.ijpddr.2020.05.002_bib43) 2019; 14
Weeks (10.1016/j.ijpddr.2020.05.002_bib81) 2018; 8
Park (10.1016/j.ijpddr.2020.05.002_bib62) 2019; 294
References_xml – volume: 176
  start-page: 42
  year: 2011
  end-page: 50
  ident: bib74
  article-title: Glutamate-mediated signaling in
  publication-title: Mol. Biochem. Parasitol.
– volume: 52
  start-page: 129
  year: 1977
  end-page: 150
  ident: bib27
  article-title: Praziquantel, a new broad-spectrum antischistosomal agent
  publication-title: Zeitschrift fur Parasitenkunde (Berlin, Germany)
– volume: 113
  start-page: 55
  year: 1996
  end-page: 61
  ident: bib16
  article-title: Cholinergic inhibition of muscle fibres isolated from
  publication-title: Parasitology
– volume: 109
  start-page: 228
  year: 2005
  end-page: 236
  ident: bib28
  article-title: : functional proteasomes are required for development in the vertebrate host
  publication-title: Exp. Parasitol.
– volume: 342
  start-page: 1385
  year: 2013
  end-page: 1389
  ident: bib78
  article-title: Genetic and molecular basis of drug resistance and species-specific drug action in schistosome parasites
  publication-title: Science
– volume: 1
  start-page: 85
  year: 2012
  end-page: 93
  ident: bib72
  article-title: Calcium channels of schistosomes: unresolved questions and unexpected answers
  publication-title: Wiley Interdiscipl. Rev. Membr. Transp. Signal.
– volume: 202
  start-page: 29
  year: 2015
  end-page: 37
  ident: bib46
  article-title: A constitutively active G protein-coupled acetylcholine receptor regulates motility of larval
  publication-title: Mol. Biochem. Parasitol.
– volume: 12
  start-page: 493
  year: 2019
  ident: bib44
  article-title: Multi-center screening of the Pathogen Box collection for schistosomiasis drug discovery
  publication-title: Parasites Vectors
– volume: 5
  start-page: 1802
  year: 2019
  end-page: 1812
  ident: bib7
  article-title: The proteasome as a drug target in the metazoan pathogen,
  publication-title: ACS Infect. Dis.
– volume: 4
  start-page: 40
  year: 2015
  ident: bib42
  article-title: High-throughput screening against thioredoxin glutathione reductase identifies novel inhibitors with potential therapeutic value for schistosomiasis
  publication-title: Infect Dis Poverty
– volume: 26
  start-page: 656
  year: 1966
  end-page: 665
  ident: bib5
  article-title: The possible role of acetylcholine in
  publication-title: Br. J. Pharmacol. Chemother.
– volume: 164
  start-page: 57
  year: 2009
  end-page: 65
  ident: bib2
  article-title: Towards an understanding of the mechanism of action of praziquantel
  publication-title: Mol. Biochem. Parasitol.
– volume: 88
  start-page: 583
  year: 2002
  end-page: 586
  ident: bib31
  article-title: Codon optimization improves heterologous expression of a
  publication-title: Parasitol. Res.
– volume: 12
  year: 2017
  ident: bib54
  article-title: Effects of proteasome inhibitor MG-132 on the parasite
  publication-title: PloS One
– volume: 191
  start-page: 189
  year: 2006
  end-page: 195
  ident: bib71
  article-title: Hypertensive effect of calcilytic NPS 2143 administration in rats
  publication-title: J. Endocrinol.
– volume: 225
  start-page: 94
  year: 2018
  end-page: 102
  ident: bib22
  article-title: Targeting thioredoxin glutathione reductase as a potential antischistosomal drug target
  publication-title: Mol. Biochem. Parasitol.
– volume: 6
  start-page: 253
  year: 2008
  end-page: 258
  ident: bib79
  article-title: Schistosomicidal activity of the antimalarial drug, mefloquine, in
  publication-title: Trav. Med. Infect. Dis.
– volume: 7
  start-page: 1176
  year: 2016
  end-page: 1182
  ident: bib58
  article-title: The antidepressant drug paroxetine as a new lead candidate in schistosome drug discovery
  publication-title: MedChemComm
– volume: 165
  start-page: 35
  year: 2012
  end-page: 48
  ident: bib80
  article-title: New concepts in calcium-sensing receptor pharmacology and signalling
  publication-title: Br. J. Pharmacol.
– volume: 8
  start-page: 975
  year: 2018
  ident: bib81
  article-title: Sertraline, paroxetine, and chlorpromazine are rapidly acting anthelmintic drugs capable of clinical repurposing
  publication-title: Sci. Rep.
– volume: 12
  start-page: 13
  year: 2012
  end-page: 28
  ident: bib70
  article-title: Biogenic amines and the control of neuromuscular signaling in schistosomes
  publication-title: Invertebr. Neurosci.
– volume: 12
  start-page: 14
  year: 2011
  ident: bib4
  article-title: Expression of G protein-coupled receptors and related proteins in HEK293, AtT20, BV2, and N18 cell lines as revealed by microarray analysis
  publication-title: BMC Genom.
– volume: 67
  start-page: 685
  year: 1973
  end-page: 693
  ident: bib24
  article-title: Studies with the schistosomicide oxamniquine (UK-4271). II. Activity in primates
  publication-title: Trans. R. Soc. Trop. Med. Hyg.
– volume: 2016
  start-page: 9521349
  year: 2016
  ident: bib17
  article-title: Flavonoids and sesquiterpene lactones from
  publication-title: Evid Based Complement Alternat Med
– volume: 154
  start-page: 125
  year: 2007
  end-page: 133
  ident: bib63
  article-title: Characterization of a serotonin transporter in the parasitic flatworm,
  publication-title: Mol. Biochem. Parasitol.
– volume: 31
  start-page: 1515
  year: 2015
  end-page: 1518
  ident: bib3
  article-title: The QDREC web server: determining dose-response characteristics of complex macroparasites in phenotypic drug screens
  publication-title: Bioinformatics
– volume: 8
  start-page: 550
  year: 2018
  end-page: 558
  ident: bib50
  article-title: Structure-activity profiling of alkaloid natural product pharmacophores against a
  publication-title: Int J Parasitol Drugs Drug Resist
– volume: 13
  year: 2019
  ident: bib83
  article-title: The repositioning of epigenetic probes/inhibitors identifies new anti-schistosomal lead compounds and chemotherapeutic targets
  publication-title: PLoS Neglected Trop. Dis.
– volume: 168
  start-page: 24
  year: 2009
  end-page: 33
  ident: bib73
  article-title: Investigation of a dopamine receptor in
  publication-title: Mol. Biochem. Parasitol.
– volume: 276
  start-page: 36873
  year: 2001
  end-page: 36876
  ident: bib36
  article-title: Schistosome calcium channel beta subunits. Unusual modulatory effects and potential role in the action of the antischistosomal drug praziquantel
  publication-title: J. Biol. Chem.
– volume: 195
  start-page: 23
  year: 2014
  end-page: 29
  ident: bib14
  article-title: Schistosomiasis control: praziquantel forever?
  publication-title: Mol. Biochem. Parasitol.
– volume: 3
  start-page: e478
  year: 2009
  ident: bib1
  article-title: Drug discovery for schistosomiasis: hit and lead compounds identified in a library of known drugs by medium-throughput phenotypic screening
  publication-title: PLoS Neglected Trop. Dis.
– volume: 1
  start-page: S3
  year: 2003
  end-page: 9
  ident: bib13
  article-title: Praziquantel
  publication-title: Parasitol Res 90 Supp
– volume: 48
  start-page: 649
  year: 1973
  end-page: 652
  ident: bib25
  article-title: Surveillance of
  publication-title: Bull. World Health Organ.
– volume: 13
  start-page: 42
  year: 2014
  ident: bib35
  article-title: High calcium concentration in bones promotes bone metastasis in renal cell carcinomas expressing calcium-sensing receptor
  publication-title: Mol. Canc.
– volume: 7
  year: 2018
  ident: bib11
  article-title: Coalescing beneficial host and deleterious antiparasitic actions as an antischistosomal strategy
  publication-title: Elife
– volume: 8
  start-page: 8399
  year: 2018
  ident: bib29
  article-title: Ubiquitin proteasome pathway proteins as potential drug targets in parasite
  publication-title: Sci. Rep.
– volume: 6
  year: 2012
  ident: bib49
  article-title: WormAssay: a novel computer application for whole-plate motion-based screening of macroscopic parasites
  publication-title: PLoS Neglected Trop. Dis.
– volume: 10
  year: 2016
  ident: bib48
  article-title: High throughput screening identifies novel lead compounds with activity against larval, juvenile and adult
  publication-title: PLoS Neglected Trop. Dis.
– volume: 117
  start-page: 337
  year: 2007
  end-page: 347
  ident: bib55
  article-title: The 26S proteasome in
  publication-title: Exp. Parasitol.
– volume: 8
  start-page: 624
  year: 2015
  ident: bib60
  article-title: Fluorescence/luminescence-based markers for the assessment of
  publication-title: Parasites Vectors
– volume: 81
  start-page: 55
  year: 1987
  end-page: 59
  ident: bib23
  article-title: A review of clinical experience with oxamniquine
  publication-title: Trans. R. Soc. Trop. Med. Hyg.
– volume: 111
  start-page: 1021
  year: 2003
  end-page: 1028
  ident: bib37
  article-title: The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormone
  publication-title: J. Clin. Invest.
– volume: 299
  start-page: 323
  year: 2001
  end-page: 331
  ident: bib57
  article-title: Calcilytic compounds: potent and selective Ca
  publication-title: J. Pharmacol. Exp. Therapeut.
– volume: 61
  year: 2017
  ident: bib77
  article-title: Praziquantel for schistosomiasis: single-drug metabolism revisited, mode of action, and resistance
  publication-title: Antimicrob. Agents Chemother.
– volume: 383
  start-page: 2253
  year: 2014
  end-page: 2264
  ident: bib15
  article-title: Human schistosomiasis
  publication-title: Lancet
– volume: 11
  year: 2018
  ident: bib19
  article-title: Octopamine signaling in the metazoan pathogen
  publication-title: Dis Model Mech
– volume: 8
  year: 2014
  ident: bib33
  article-title: Orally active antischistosomal early leads identified from the open access malaria box
  publication-title: PLoS Neglected Trop. Dis.
– volume: 6
  start-page: e1523
  year: 2012
  ident: bib21
  article-title: A novel G protein-coupled receptor of
  publication-title: PLoS Neglected Trop. Dis.
– volume: 10
  start-page: 365
  year: 2017
  ident: bib38
  article-title: and
  publication-title: Parasites Vectors
– volume: 4
  start-page: 21
  year: 2016
  ident: bib75
  article-title: Mechanically produced schistosomula as a higher-throughput tools for phenotypic pre-screening in drug sensitivity assays: current research and future trends
  publication-title: Biomark Res.
– volume: 287
  start-page: 40232
  year: 2012
  end-page: 40238
  ident: bib85
  article-title: Glutamate-gated chloride channels
  publication-title: J. Biol. Chem.
– volume: 40
  start-page: 1395
  year: 2010
  end-page: 1406
  ident: bib20
  article-title: Histamine signalling in
  publication-title: Int. J. Parasitol.
– volume: 15
  start-page: 927
  year: 2015
  end-page: 940
  ident: bib40
  article-title: Spatial distribution of schistosomiasis and treatment needs in sub-Saharan Africa: a systematic review and geostatistical analysis
  publication-title: Lancet Infect. Dis.
– volume: 83
  start-page: 163
  year: 1997
  end-page: 169
  ident: bib26
  article-title: Assessment of the viability of
  publication-title: Parasitol. Res.
– volume: 9
  year: 2013
  ident: bib84
  article-title: Transcriptional responses of in vivo praziquantel exposure in schistosomes identifies a functional role for calcium signalling pathway member CamKII
  publication-title: PLoS Pathog.
– volume: 88
  start-page: 1
  year: 2009
  end-page: 22
  ident: bib69
  article-title: Neuronal signaling in schistosomes: current status and prospects for postgenomics
  publication-title: Can. J. Zool.
– volume: 7
  start-page: 727
  year: 2015
  end-page: 735
  ident: bib67
  article-title: Repurposing pharma assets: an accelerated mechanism for strengthening the schistosomiasis drug development pipeline
  publication-title: Future Med. Chem.
– year: 2001
  ident: bib41
  article-title: Schistosomiasis
  publication-title: Curr. Protoc. Im.
– volume: 4
  start-page: 254
  year: 2013
  end-page: 258
  ident: bib18
  article-title: Synthesis of novel analogs of cabergoline: improving cardiovascular safety by removing 5-HT2B receptor agonism
  publication-title: ACS Med. Chem. Lett.
– volume: 6
  year: 2012
  ident: bib65
  article-title: Whole organism high-content screening by label-free, image-based Bayesian classification for parasitic diseases
  publication-title: PLoS Neglected Trop. Dis.
– volume: 10
  year: 2014
  ident: bib64
  article-title: Serotonin signaling in
  publication-title: PLoS Pathog.
– volume: 18
  start-page: 315
  year: 2018
  end-page: 320
  ident: bib66
  article-title: Ubiquitin proteasome system as a potential drug target for malaria
  publication-title: Curr. Top. Med. Chem.
– volume: 14
  start-page: 461
  year: 2019
  end-page: 481
  ident: bib43
  article-title: Life cycle maintenance and drug-sensitivity assays for early drug discovery in
  publication-title: Nat. Protoc.
– volume: 7
  start-page: 25
  year: 2001
  end-page: 47
  ident: bib8
  article-title: Paroxetine: a review
  publication-title: CNS Drug Rev.
– start-page: 1
  year: 2019
  end-page: 8
  ident: bib82
  article-title: Towards deorphanizing G protein-coupled receptors of
  publication-title: Parasitology
– volume: 10
  year: 2014
  ident: bib45
  article-title: Functional characterization of a novel family of acetylcholine-gated chloride channels in
  publication-title: PLoS Pathog.
– start-page: 1
  year: 2014
  end-page: 29
  ident: bib86
  article-title: Anthelmintic drugs and nematicides: studies in
  publication-title: WormBook. pp.
– start-page: 1
  year: 2007
  end-page: 13
  ident: bib32
  article-title: Anthelmintic Drugs. WormBook
– volume: 3
  start-page: e504
  year: 2009
  ident: bib52
  article-title: Reduced susceptibility to praziquantel among naturally occurring Kenyan isolates of
  publication-title: PLoS Neglected Trop. Dis.
– volume: 69
  start-page: 863
  year: 2014
  end-page: 870
  ident: bib59
  article-title: The little we know about the pharmacokinetics and pharmacodynamics of praziquantel (racemate and
  publication-title: J. Antimicrob. Chemother.
– volume: 18
  start-page: 7900
  year: 2010
  end-page: 7910
  ident: bib39
  article-title: Identification by high-throughput screening of inhibitors of
  publication-title: Bioorg. Med. Chem.
– volume: 294
  start-page: 18873
  year: 2019
  end-page: 18880
  ident: bib62
  article-title: The anthelmintic drug praziquantel activates a schistosome transient receptor potential channel
  publication-title: J. Biol. Chem.
– volume: 32
  start-page: 83
  year: 1983
  end-page: 93
  ident: bib51
  article-title: Neuropharmacology of the parasitic trematode,
  publication-title: Am. J. Trop. Med. Hyg.
– volume: 10
  year: 2014
  ident: bib10
  article-title: Death and axes": unexpected Ca
  publication-title: PLoS Pathog.
– volume: 9
  year: 2015
  ident: bib61
  article-title: Activity profile of an FDA-approved compound library against
  publication-title: PLoS Neglected Trop. Dis.
– volume: 8
  start-page: 229
  year: 2012
  end-page: 259
  ident: bib56
  article-title: Cross-genome clustering of human and
  publication-title: Evol Bioinform Online
– volume: 27
  start-page: 676
  year: 2020
  end-page: 696
  ident: bib76
  article-title: The mechanism of action of praziquantel: can new drugs exploit similar mechanisms?
  publication-title: Curr. Med. Chem.
– volume: 9
  year: 2015
  ident: bib9
  article-title: Ergot alkaloids (re)generate new leads as antiparasitics
  publication-title: PLoS Neglected Trop. Dis.
– volume: 12
  year: 2016
  ident: bib12
  article-title: A miniaturized screen of a
  publication-title: PLoS Pathog.
– volume: 63
  start-page: 9987
  year: 2015
  end-page: 9995
  ident: bib53
  article-title: Calcium-sensing receptor (CaSR)-mediated anti-inflammatory effects of L-amino acids in intestinal epithelial cells
  publication-title: J. Agric. Food Chem.
– volume: 284
  start-page: 1503
  year: 2017
  end-page: 1517
  ident: bib6
  article-title: Targeting proteasomes in infectious organisms to combat disease
  publication-title: FEBS J.
– volume: 13
  start-page: 2374
  year: 2018
  end-page: 2389
  ident: bib47
  article-title: Chemotherapy for fighting schistosomiasis: past, present and future
  publication-title: ChemMedChem
– start-page: 171
  year: 2015
  end-page: 189
  ident: bib68
  article-title: Functional genomics of serotonin receptors in helminth parasites: elucidation of receptor function through RNA interference (RNAi)
  publication-title: Serotonin Receptor Technologies
– volume: 119
  start-page: 75
  year: 2002
  end-page: 86
  ident: bib30
  article-title: A novel
  publication-title: Mol. Biochem. Parasitol.
– volume: 8
  year: 2019
  ident: bib34
  article-title: Programmed genome editing of the omega-1 ribonuclease of the blood fluke,
  publication-title: eLife
– volume: 52
  start-page: 129
  year: 1977
  ident: 10.1016/j.ijpddr.2020.05.002_bib27
  article-title: Praziquantel, a new broad-spectrum antischistosomal agent
  publication-title: Zeitschrift fur Parasitenkunde (Berlin, Germany)
  doi: 10.1007/BF00389899
– volume: 4
  start-page: 40
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib42
  article-title: High-throughput screening against thioredoxin glutathione reductase identifies novel inhibitors with potential therapeutic value for schistosomiasis
  publication-title: Infect Dis Poverty
  doi: 10.1186/s40249-015-0071-z
– volume: 342
  start-page: 1385
  year: 2013
  ident: 10.1016/j.ijpddr.2020.05.002_bib78
  article-title: Genetic and molecular basis of drug resistance and species-specific drug action in schistosome parasites
  publication-title: Science
  doi: 10.1126/science.1243106
– volume: 284
  start-page: 1503
  year: 2017
  ident: 10.1016/j.ijpddr.2020.05.002_bib6
  article-title: Targeting proteasomes in infectious organisms to combat disease
  publication-title: FEBS J.
  doi: 10.1111/febs.14029
– volume: 83
  start-page: 163
  year: 1997
  ident: 10.1016/j.ijpddr.2020.05.002_bib26
  article-title: Assessment of the viability of Schistosoma mansoni schistosomula by comparative uptake of various vital dyes
  publication-title: Parasitol. Res.
  doi: 10.1007/s004360050227
– volume: 40
  start-page: 1395
  year: 2010
  ident: 10.1016/j.ijpddr.2020.05.002_bib20
  article-title: Histamine signalling in Schistosoma mansoni: immunolocalisation and characterisation of a new histamine-responsive receptor (SmGPR-2)
  publication-title: Int. J. Parasitol.
  doi: 10.1016/j.ijpara.2010.04.006
– volume: 18
  start-page: 315
  year: 2018
  ident: 10.1016/j.ijpddr.2020.05.002_bib66
  article-title: Ubiquitin proteasome system as a potential drug target for malaria
  publication-title: Curr. Top. Med. Chem.
  doi: 10.2174/1568026618666180427145308
– volume: 6
  year: 2012
  ident: 10.1016/j.ijpddr.2020.05.002_bib49
  article-title: WormAssay: a novel computer application for whole-plate motion-based screening of macroscopic parasites
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0001494
– volume: 27
  start-page: 676
  year: 2020
  ident: 10.1016/j.ijpddr.2020.05.002_bib76
  article-title: The mechanism of action of praziquantel: can new drugs exploit similar mechanisms?
  publication-title: Curr. Med. Chem.
  doi: 10.2174/0929867325666180926145537
– volume: 11
  year: 2018
  ident: 10.1016/j.ijpddr.2020.05.002_bib19
  article-title: Octopamine signaling in the metazoan pathogen Schistosoma mansoni: localization, small-molecule screening and opportunities for drug development
  publication-title: Dis Model Mech
  doi: 10.1242/dmm.033563
– volume: 88
  start-page: 583
  year: 2002
  ident: 10.1016/j.ijpddr.2020.05.002_bib31
  article-title: Codon optimization improves heterologous expression of a Schistosoma mansoni cDNA in HEK293 cells
  publication-title: Parasitol. Res.
  doi: 10.1007/s00436-001-0585-0
– volume: 1
  start-page: 85
  year: 2012
  ident: 10.1016/j.ijpddr.2020.05.002_bib72
  article-title: Calcium channels of schistosomes: unresolved questions and unexpected answers
  publication-title: Wiley Interdiscipl. Rev. Membr. Transp. Signal.
  doi: 10.1002/wmts.19
– volume: 3
  start-page: e478
  year: 2009
  ident: 10.1016/j.ijpddr.2020.05.002_bib1
  article-title: Drug discovery for schistosomiasis: hit and lead compounds identified in a library of known drugs by medium-throughput phenotypic screening
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0000478
– volume: 1
  start-page: S3
  year: 2003
  ident: 10.1016/j.ijpddr.2020.05.002_bib13
  article-title: Praziquantel
  publication-title: Parasitol Res 90 Supp
  doi: 10.1007/s00436-002-0751-z
– volume: 8
  start-page: 8399
  year: 2018
  ident: 10.1016/j.ijpddr.2020.05.002_bib29
  article-title: Ubiquitin proteasome pathway proteins as potential drug targets in parasite Trypanosoma cruzi
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-018-26532-z
– volume: 67
  start-page: 685
  year: 1973
  ident: 10.1016/j.ijpddr.2020.05.002_bib24
  article-title: Studies with the schistosomicide oxamniquine (UK-4271). II. Activity in primates
  publication-title: Trans. R. Soc. Trop. Med. Hyg.
  doi: 10.1016/0035-9203(73)90039-4
– volume: 7
  start-page: 1176
  year: 2016
  ident: 10.1016/j.ijpddr.2020.05.002_bib58
  article-title: The antidepressant drug paroxetine as a new lead candidate in schistosome drug discovery
  publication-title: MedChemComm
  doi: 10.1039/C5MD00596E
– volume: 10
  year: 2014
  ident: 10.1016/j.ijpddr.2020.05.002_bib64
  article-title: Serotonin signaling in Schistosoma mansoni: a serotonin-activated G protein-coupled receptor controls parasite movement
  publication-title: PLoS Pathog.
  doi: 10.1371/journal.ppat.1003878
– start-page: 1
  year: 2014
  ident: 10.1016/j.ijpddr.2020.05.002_bib86
  article-title: Anthelmintic drugs and nematicides: studies in Caenorhabditis elegans
  publication-title: WormBook. pp.
– volume: 117
  start-page: 337
  year: 2007
  ident: 10.1016/j.ijpddr.2020.05.002_bib55
  article-title: The 26S proteasome in Schistosoma mansoni: bioinformatics analysis, developmental expression, and RNA interference (RNAi) studies
  publication-title: Exp. Parasitol.
  doi: 10.1016/j.exppara.2007.08.002
– volume: 6
  start-page: e1523
  year: 2012
  ident: 10.1016/j.ijpddr.2020.05.002_bib21
  article-title: A novel G protein-coupled receptor of Schistosoma mansoni (SmGPR-3) is activated by dopamine and is widely expressed in the nervous system
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0001523
– volume: 383
  start-page: 2253
  year: 2014
  ident: 10.1016/j.ijpddr.2020.05.002_bib15
  article-title: Human schistosomiasis
  publication-title: Lancet
  doi: 10.1016/S0140-6736(13)61949-2
– volume: 9
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib61
  article-title: Activity profile of an FDA-approved compound library against Schistosoma mansoni
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0003962
– volume: 88
  start-page: 1
  year: 2009
  ident: 10.1016/j.ijpddr.2020.05.002_bib69
  article-title: Neuronal signaling in schistosomes: current status and prospects for postgenomics
  publication-title: Can. J. Zool.
  doi: 10.1139/Z09-126
– volume: 8
  year: 2014
  ident: 10.1016/j.ijpddr.2020.05.002_bib33
  article-title: Orally active antischistosomal early leads identified from the open access malaria box
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0002610
– volume: 9
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib9
  article-title: Ergot alkaloids (re)generate new leads as antiparasitics
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0004063
– volume: 164
  start-page: 57
  year: 2009
  ident: 10.1016/j.ijpddr.2020.05.002_bib2
  article-title: Towards an understanding of the mechanism of action of praziquantel
  publication-title: Mol. Biochem. Parasitol.
  doi: 10.1016/j.molbiopara.2008.11.007
– volume: 6
  year: 2012
  ident: 10.1016/j.ijpddr.2020.05.002_bib65
  article-title: Whole organism high-content screening by label-free, image-based Bayesian classification for parasitic diseases
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0001762
– volume: 61
  year: 2017
  ident: 10.1016/j.ijpddr.2020.05.002_bib77
  article-title: Praziquantel for schistosomiasis: single-drug metabolism revisited, mode of action, and resistance
  publication-title: Antimicrob. Agents Chemother.
  doi: 10.1128/AAC.02582-16
– volume: 13
  year: 2019
  ident: 10.1016/j.ijpddr.2020.05.002_bib83
  article-title: The repositioning of epigenetic probes/inhibitors identifies new anti-schistosomal lead compounds and chemotherapeutic targets
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0007693
– volume: 81
  start-page: 55
  year: 1987
  ident: 10.1016/j.ijpddr.2020.05.002_bib23
  article-title: A review of clinical experience with oxamniquine
  publication-title: Trans. R. Soc. Trop. Med. Hyg.
  doi: 10.1016/0035-9203(87)90282-3
– volume: 7
  start-page: 727
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib67
  article-title: Repurposing pharma assets: an accelerated mechanism for strengthening the schistosomiasis drug development pipeline
  publication-title: Future Med. Chem.
  doi: 10.4155/fmc.15.26
– volume: 5
  start-page: 1802
  year: 2019
  ident: 10.1016/j.ijpddr.2020.05.002_bib7
  article-title: The proteasome as a drug target in the metazoan pathogen, Schistosoma mansoni
  publication-title: ACS Infect. Dis.
  doi: 10.1021/acsinfecdis.9b00237
– volume: 109
  start-page: 228
  year: 2005
  ident: 10.1016/j.ijpddr.2020.05.002_bib28
  article-title: Schistosoma mansoni: functional proteasomes are required for development in the vertebrate host
  publication-title: Exp. Parasitol.
  doi: 10.1016/j.exppara.2005.01.002
– volume: 168
  start-page: 24
  year: 2009
  ident: 10.1016/j.ijpddr.2020.05.002_bib73
  article-title: Investigation of a dopamine receptor in Schistosoma mansoni: functional studies and immunolocalization
  publication-title: Mol. Biochem. Parasitol.
  doi: 10.1016/j.molbiopara.2009.06.003
– volume: 8
  year: 2019
  ident: 10.1016/j.ijpddr.2020.05.002_bib34
  article-title: Programmed genome editing of the omega-1 ribonuclease of the blood fluke, Schistosoma mansoni
  publication-title: eLife
  doi: 10.7554/eLife.41337
– volume: 8
  start-page: 550
  year: 2018
  ident: 10.1016/j.ijpddr.2020.05.002_bib50
  article-title: Structure-activity profiling of alkaloid natural product pharmacophores against a Schistosoma serotonin receptor
  publication-title: Int J Parasitol Drugs Drug Resist
  doi: 10.1016/j.ijpddr.2018.09.001
– volume: 294
  start-page: 18873
  year: 2019
  ident: 10.1016/j.ijpddr.2020.05.002_bib62
  article-title: The anthelmintic drug praziquantel activates a schistosome transient receptor potential channel
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.AC119.011093
– start-page: 1
  year: 2007
  ident: 10.1016/j.ijpddr.2020.05.002_bib32
– volume: 69
  start-page: 863
  year: 2014
  ident: 10.1016/j.ijpddr.2020.05.002_bib59
  article-title: The little we know about the pharmacokinetics and pharmacodynamics of praziquantel (racemate and R-enantiomer)
  publication-title: J. Antimicrob. Chemother.
  doi: 10.1093/jac/dkt491
– year: 2001
  ident: 10.1016/j.ijpddr.2020.05.002_bib41
  article-title: Schistosomiasis
  publication-title: Curr. Protoc. Im.
– volume: 12
  start-page: 14
  year: 2011
  ident: 10.1016/j.ijpddr.2020.05.002_bib4
  article-title: Expression of G protein-coupled receptors and related proteins in HEK293, AtT20, BV2, and N18 cell lines as revealed by microarray analysis
  publication-title: BMC Genom.
  doi: 10.1186/1471-2164-12-14
– volume: 4
  start-page: 254
  year: 2013
  ident: 10.1016/j.ijpddr.2020.05.002_bib18
  article-title: Synthesis of novel analogs of cabergoline: improving cardiovascular safety by removing 5-HT2B receptor agonism
  publication-title: ACS Med. Chem. Lett.
  doi: 10.1021/ml3003814
– volume: 4
  start-page: 21
  year: 2016
  ident: 10.1016/j.ijpddr.2020.05.002_bib75
  article-title: Mechanically produced schistosomula as a higher-throughput tools for phenotypic pre-screening in drug sensitivity assays: current research and future trends
  publication-title: Biomark Res.
  doi: 10.1186/s40364-016-0075-2
– volume: 12
  year: 2016
  ident: 10.1016/j.ijpddr.2020.05.002_bib12
  article-title: A miniaturized screen of a Schistosoma mansoni serotonergic G protein-coupled receptor identifies novel classes of parasite-selective inhibitors
  publication-title: PLoS Pathog.
  doi: 10.1371/journal.ppat.1005651
– volume: 276
  start-page: 36873
  year: 2001
  ident: 10.1016/j.ijpddr.2020.05.002_bib36
  article-title: Schistosome calcium channel beta subunits. Unusual modulatory effects and potential role in the action of the antischistosomal drug praziquantel
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.C100273200
– volume: 13
  start-page: 42
  year: 2014
  ident: 10.1016/j.ijpddr.2020.05.002_bib35
  article-title: High calcium concentration in bones promotes bone metastasis in renal cell carcinomas expressing calcium-sensing receptor
  publication-title: Mol. Canc.
  doi: 10.1186/1476-4598-13-42
– volume: 111
  start-page: 1021
  year: 2003
  ident: 10.1016/j.ijpddr.2020.05.002_bib37
  article-title: The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormone
  publication-title: J. Clin. Invest.
  doi: 10.1172/JCI17416
– start-page: 171
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib68
  article-title: Functional genomics of serotonin receptors in helminth parasites: elucidation of receptor function through RNA interference (RNAi)
– volume: 18
  start-page: 7900
  year: 2010
  ident: 10.1016/j.ijpddr.2020.05.002_bib39
  article-title: Identification by high-throughput screening of inhibitors of Schistosoma mansoni NAD(+) catabolizing enzyme
  publication-title: Bioorg. Med. Chem.
  doi: 10.1016/j.bmc.2010.09.041
– volume: 165
  start-page: 35
  year: 2012
  ident: 10.1016/j.ijpddr.2020.05.002_bib80
  article-title: New concepts in calcium-sensing receptor pharmacology and signalling
  publication-title: Br. J. Pharmacol.
  doi: 10.1111/j.1476-5381.2011.01511.x
– volume: 12
  start-page: 493
  year: 2019
  ident: 10.1016/j.ijpddr.2020.05.002_bib44
  article-title: Multi-center screening of the Pathogen Box collection for schistosomiasis drug discovery
  publication-title: Parasites Vectors
  doi: 10.1186/s13071-019-3747-6
– volume: 10
  year: 2014
  ident: 10.1016/j.ijpddr.2020.05.002_bib45
  article-title: Functional characterization of a novel family of acetylcholine-gated chloride channels in Schistosoma mansoni
  publication-title: PLoS Pathog.
  doi: 10.1371/journal.ppat.1004181
– volume: 176
  start-page: 42
  year: 2011
  ident: 10.1016/j.ijpddr.2020.05.002_bib74
  article-title: Glutamate-mediated signaling in Schistosoma mansoni: a novel glutamate receptor is expressed in neurons and the female reproductive tract
  publication-title: Mol. Biochem. Parasitol.
  doi: 10.1016/j.molbiopara.2010.12.001
– volume: 195
  start-page: 23
  year: 2014
  ident: 10.1016/j.ijpddr.2020.05.002_bib14
  article-title: Schistosomiasis control: praziquantel forever?
  publication-title: Mol. Biochem. Parasitol.
  doi: 10.1016/j.molbiopara.2014.06.002
– volume: 7
  year: 2018
  ident: 10.1016/j.ijpddr.2020.05.002_bib11
  article-title: Coalescing beneficial host and deleterious antiparasitic actions as an antischistosomal strategy
  publication-title: Elife
  doi: 10.7554/eLife.35755
– volume: 113
  start-page: 55
  year: 1996
  ident: 10.1016/j.ijpddr.2020.05.002_bib16
  article-title: Cholinergic inhibition of muscle fibres isolated from Schistosoma mansoni (Trematoda:Digenea)
  publication-title: Parasitology
  doi: 10.1017/S0031182000066270
– volume: 3
  start-page: e504
  year: 2009
  ident: 10.1016/j.ijpddr.2020.05.002_bib52
  article-title: Reduced susceptibility to praziquantel among naturally occurring Kenyan isolates of Schistosoma mansoni
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0000504
– volume: 8
  start-page: 975
  year: 2018
  ident: 10.1016/j.ijpddr.2020.05.002_bib81
  article-title: Sertraline, paroxetine, and chlorpromazine are rapidly acting anthelmintic drugs capable of clinical repurposing
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-017-18457-w
– volume: 10
  year: 2014
  ident: 10.1016/j.ijpddr.2020.05.002_bib10
  article-title: Death and axes": unexpected Ca2+ entry phenologs predict new anti-schistosomal agents
  publication-title: PLoS Pathog.
  doi: 10.1371/journal.ppat.1003942
– volume: 14
  start-page: 461
  year: 2019
  ident: 10.1016/j.ijpddr.2020.05.002_bib43
  article-title: Life cycle maintenance and drug-sensitivity assays for early drug discovery in Schistosoma mansoni
  publication-title: Nat. Protoc.
  doi: 10.1038/s41596-018-0101-y
– volume: 2016
  start-page: 9521349
  year: 2016
  ident: 10.1016/j.ijpddr.2020.05.002_bib17
  article-title: Flavonoids and sesquiterpene lactones from Artemisia absinthium and Tanacetum parthenium against Schistosoma mansoni worms
  publication-title: Evid Based Complement Alternat Med
  doi: 10.1155/2016/9521349
– volume: 10
  start-page: 365
  year: 2017
  ident: 10.1016/j.ijpddr.2020.05.002_bib38
  article-title: In vitro and in vivo activity of R- and S- praziquantel enantiomers and the main human metabolite trans-4-hydroxy-praziquantel against Schistosoma haematobium
  publication-title: Parasites Vectors
  doi: 10.1186/s13071-017-2293-3
– volume: 63
  start-page: 9987
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib53
  article-title: Calcium-sensing receptor (CaSR)-mediated anti-inflammatory effects of L-amino acids in intestinal epithelial cells
  publication-title: J. Agric. Food Chem.
  doi: 10.1021/acs.jafc.5b03749
– volume: 7
  start-page: 25
  year: 2001
  ident: 10.1016/j.ijpddr.2020.05.002_bib8
  article-title: Paroxetine: a review
  publication-title: CNS Drug Rev.
  doi: 10.1111/j.1527-3458.2001.tb00189.x
– volume: 225
  start-page: 94
  year: 2018
  ident: 10.1016/j.ijpddr.2020.05.002_bib22
  article-title: Targeting thioredoxin glutathione reductase as a potential antischistosomal drug target
  publication-title: Mol. Biochem. Parasitol.
  doi: 10.1016/j.molbiopara.2018.09.004
– volume: 31
  start-page: 1515
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib3
  article-title: The QDREC web server: determining dose-response characteristics of complex macroparasites in phenotypic drug screens
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btu831
– volume: 15
  start-page: 927
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib40
  article-title: Spatial distribution of schistosomiasis and treatment needs in sub-Saharan Africa: a systematic review and geostatistical analysis
  publication-title: Lancet Infect. Dis.
  doi: 10.1016/S1473-3099(15)00066-3
– volume: 6
  start-page: 253
  year: 2008
  ident: 10.1016/j.ijpddr.2020.05.002_bib79
  article-title: Schistosomicidal activity of the antimalarial drug, mefloquine, in Schistosoma mansoni-infected mice
  publication-title: Trav. Med. Infect. Dis.
  doi: 10.1016/j.tmaid.2008.06.006
– volume: 299
  start-page: 323
  year: 2001
  ident: 10.1016/j.ijpddr.2020.05.002_bib57
  article-title: Calcilytic compounds: potent and selective Ca2+ receptor antagonists that stimulate secretion of parathyroid hormone
  publication-title: J. Pharmacol. Exp. Therapeut.
  doi: 10.1016/S0022-3565(24)29333-2
– volume: 12
  year: 2017
  ident: 10.1016/j.ijpddr.2020.05.002_bib54
  article-title: Effects of proteasome inhibitor MG-132 on the parasite Schistosoma mansoni
  publication-title: PloS One
  doi: 10.1371/journal.pone.0184192
– volume: 10
  year: 2016
  ident: 10.1016/j.ijpddr.2020.05.002_bib48
  article-title: High throughput screening identifies novel lead compounds with activity against larval, juvenile and adult Schistosoma mansoni
  publication-title: PLoS Neglected Trop. Dis.
  doi: 10.1371/journal.pntd.0004659
– volume: 13
  start-page: 2374
  year: 2018
  ident: 10.1016/j.ijpddr.2020.05.002_bib47
  article-title: Chemotherapy for fighting schistosomiasis: past, present and future
  publication-title: ChemMedChem
  doi: 10.1002/cmdc.201800572
– volume: 32
  start-page: 83
  year: 1983
  ident: 10.1016/j.ijpddr.2020.05.002_bib51
  article-title: Neuropharmacology of the parasitic trematode, Schistosoma mansoni
  publication-title: Am. J. Trop. Med. Hyg.
  doi: 10.4269/ajtmh.1983.32.83
– volume: 191
  start-page: 189
  year: 2006
  ident: 10.1016/j.ijpddr.2020.05.002_bib71
  article-title: Hypertensive effect of calcilytic NPS 2143 administration in rats
  publication-title: J. Endocrinol.
  doi: 10.1677/joe.1.06924
– volume: 119
  start-page: 75
  year: 2002
  ident: 10.1016/j.ijpddr.2020.05.002_bib30
  article-title: A novel Schistosoma mansoni G protein-coupled receptor is responsive to histamine
  publication-title: Mol. Biochem. Parasitol.
  doi: 10.1016/S0166-6851(01)00400-5
– volume: 8
  start-page: 229
  year: 2012
  ident: 10.1016/j.ijpddr.2020.05.002_bib56
  article-title: Cross-genome clustering of human and C. elegans G-protein coupled receptors
  publication-title: Evol Bioinform Online
  doi: 10.4137/EBO.S9405
– volume: 8
  start-page: 624
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib60
  article-title: Fluorescence/luminescence-based markers for the assessment of Schistosoma mansoni schistosomula drug assays
  publication-title: Parasites Vectors
  doi: 10.1186/s13071-015-1233-3
– volume: 202
  start-page: 29
  year: 2015
  ident: 10.1016/j.ijpddr.2020.05.002_bib46
  article-title: A constitutively active G protein-coupled acetylcholine receptor regulates motility of larval Schistosoma mansoni
  publication-title: Mol. Biochem. Parasitol.
  doi: 10.1016/j.molbiopara.2015.09.001
– start-page: 1
  year: 2019
  ident: 10.1016/j.ijpddr.2020.05.002_bib82
  article-title: Towards deorphanizing G protein-coupled receptors of Schistosoma mansoni using the MALAR yeast two-hybrid system
  publication-title: Parasitology
– volume: 287
  start-page: 40232
  issue: 48
  year: 2012
  ident: 10.1016/j.ijpddr.2020.05.002_bib85
  article-title: Glutamate-gated chloride channels
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.R112.406280
– volume: 9
  year: 2013
  ident: 10.1016/j.ijpddr.2020.05.002_bib84
  article-title: Transcriptional responses of in vivo praziquantel exposure in schistosomes identifies a functional role for calcium signalling pathway member CamKII
  publication-title: PLoS Pathog.
  doi: 10.1371/journal.ppat.1003254
– volume: 154
  start-page: 125
  year: 2007
  ident: 10.1016/j.ijpddr.2020.05.002_bib63
  article-title: Characterization of a serotonin transporter in the parasitic flatworm, Schistosoma mansoni: cloning, expression and functional analysis
  publication-title: Mol. Biochem. Parasitol.
  doi: 10.1016/j.molbiopara.2007.03.010
– volume: 12
  start-page: 13
  year: 2012
  ident: 10.1016/j.ijpddr.2020.05.002_bib70
  article-title: Biogenic amines and the control of neuromuscular signaling in schistosomes
  publication-title: Invertebr. Neurosci.
  doi: 10.1007/s10158-012-0132-y
– volume: 26
  start-page: 656
  year: 1966
  ident: 10.1016/j.ijpddr.2020.05.002_bib5
  article-title: The possible role of acetylcholine in Schistosoma mansoni
  publication-title: Br. J. Pharmacol. Chemother.
  doi: 10.1111/j.1476-5381.1966.tb01845.x
– volume: 48
  start-page: 649
  year: 1973
  ident: 10.1016/j.ijpddr.2020.05.002_bib25
  article-title: Surveillance of Echinococcus granulosus in dogs with arecoline hydrobromide
  publication-title: Bull. World Health Organ.
SSID ssj0000601810
Score 2.2470057
Snippet Neglected tropical diseases are of growing worldwide concern and schistosomiasis, caused by parasitic flatworms, continues to be a major threat with more than...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
elsevier
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 73
SubjectTerms Animals
Anthelmintic
Drug Evaluation, Preclinical
Drug Repositioning
GPCR
Humans
Motility
NPS-2143
Receptors, G-Protein-Coupled - drug effects
Schistosoma mansoni - drug effects
Schistosomiasis
Schistosomiasis mansoni - drug therapy
Schistosomicides - chemistry
Schistosomicides - pharmacology
Screening
Title Identification of annotated bioactive molecules that impair motility of the blood fluke Schistosoma mansoni
URI https://dx.doi.org/10.1016/j.ijpddr.2020.05.002
https://www.ncbi.nlm.nih.gov/pubmed/32531750
https://www.proquest.com/docview/2412994148
https://pubmed.ncbi.nlm.nih.gov/PMC7284125
https://doaj.org/article/ae57b753674642aabd8528e70e77631a
Volume 13
WOSCitedRecordID wos000556674900009&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVAON
  databaseName: DOAJ Directory of Open Access Journals
  customDbUrl:
  eissn: 2211-3207
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0000601810
  issn: 2211-3207
  databaseCode: DOA
  dateStart: 20110101
  isFulltext: true
  titleUrlDefault: https://www.doaj.org/
  providerName: Directory of Open Access Journals
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrZ3LT9wwEIctilDVC-qDx_aBXKnXgHFw7BzbqqiXokpQaW-WnyLAJmg327-fGTtZ7ZbDXnrNOpvYM7Y_O-PfEPLFytLFKrhCOethgcJUYYADCiUiCr6Z0jqTkk3Iqys1nda_11J9YUxYlgfODXdmgpAWmLqSF4DKxlivBFdBsiCha5wnNGKyXltM5TEYhahwg4Vz1OmDIuO5uRTc1dw9eo9yoJydru2qjPNSku_fmJ6e4-e_UZRr09Lla7I_8CT9muvxhuyE9i15-Wv4Yv6O3OeTuHHYmqNdpKZtO0RMT23TmTTe0VnOkhsWtL81PcWzk82cYqAeYjreBaBIU5Q7jQ_L-0CvXZIqXnQzQ2cGj5A1B-TP5Y-b7z-LIcFC4QSv-8LKyhnLTLQqlixWYJoooY1Dzbj3rLLO8ZpHnOOZB7JRoRZW8MoqADNrbXlIdtuuDceEeujn3FtYYF7A2AuFwdbOVQpwU9SWnU9IOTavdoP6OCbBeNBjmNmdzkbRaBTNhAajTEixuusxq29sKf8NLbcqi9rZ6QJ4lB48Sm_zqAmRo931gCEZL-Cvmi2P_zy6iYZeip9eTBu65UIDJ8G8D02jJuQou83qJUsuEOIYPHfDoTZqsflL29wmJXAJcAGE-v5_VPsDeYVVycGNH8luP1-GT2TP_e2bxfyEvJBTdZI62RNi4SsO
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Identification+of+annotated+bioactive+molecules+that+impair+motility+of+the+blood+fluke+Schistosoma+mansoni&rft.jtitle=International+journal+for+parasitology+--+drugs+and+drug+resistance&rft.au=Duguet%2C+Thomas+B&rft.au=Glebov%2C+Anastasia&rft.au=Hussain%2C+Asimah&rft.au=Kulkarni%2C+Shashank&rft.date=2020-08-01&rft.eissn=2211-3207&rft.volume=13&rft.spage=73&rft_id=info:doi/10.1016%2Fj.ijpddr.2020.05.002&rft_id=info%3Apmid%2F32531750&rft.externalDocID=32531750
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2211-3207&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2211-3207&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2211-3207&client=summon