Search Results - "ATPases Associated with Diverse Cellular Activities/genetics"
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1
Authors: et al.
Source: Molecular microbiology, vol. 121, no. 1, pp. 98-115
Henriksen, C, Bæk, K T, Wacnik, K, Gallay, C, Veening, J W, Foster, S J & Frees, D 2024, ' The ClpX chaperone and a hypermorphic FtsA variant with impaired self-interaction are mutually compensatory for coordinating Staphylococcus aureus cell division ', Molecular Microbiology, vol. 121, no. 1, pp. 98-115 . https://doi.org/10.1111/mmi.15200Subject Terms: cell division, Staphylococcus aureus, Escherichia coli Proteins, Humans, Bacterial Proteins/metabolism, Endopeptidase Clp/genetics, Endopeptidase Clp/metabolism, Staphylococcus aureus/metabolism, Cell Division/genetics, Escherichia coli Proteins/metabolism, Escherichia coli/metabolism, Staphylococcal Infections, ATPases Associated with Diverse Cellular Activities/genetics, Molecular Chaperones/genetics, Molecular Chaperones/metabolism, AAA+ ATPases, ClpX, FtsA, peptidoglycan, Endopeptidase Clp, 3. Good health, Bacterial Proteins, 13. Climate action, Escherichia coli, ATPases Associated with Diverse Cellular Activities, Cell Division, Molecular Chaperones
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/38041395
https://serval.unil.ch/notice/serval:BIB_1CBBE39ACD1F
https://serval.unil.ch/resource/serval:BIB_1CBBE39ACD1F.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_1CBBE39ACD1F5
https://curis.ku.dk/ws/files/381511667/The_ClpX_chaperone_and_a_hypermorphic_FtsA_variant_with_impaired.pdf -
2
Authors: et al.
Contributors: et al.
Source: American Journal of Medical Genetics Part A. 191:582-585
Subject Terms: Male, 0301 basic medicine, Adolescent, Optic Atrophy* / pathology, Hereditary* / genetics, Metalloendopeptidases / genetics, Hereditary* / diagnosis, SPG7, 03 medical and health sciences, 0302 clinical medicine, Optic Atrophy* / diagnosis, Optic Atrophy* / genetics, Optic Atrophy, Autosomal Dominant, autosomal dominant optic atrophy, Spastic Paraplegia, Humans, Hereditary* / complications, Paraplegia, Spastic Paraplegia, Hereditary, Paraplegia / genetics, Metalloendopeptidases, Autosomal Dominant, ATPases Associated with Diverse Cellular Activities / genetics, Optic Atrophy, Phenotype, infantile nystagmus syndrome, Mutation, ATPases Associated with Diverse Cellular Activities
Access URL: https://pubmed.ncbi.nlm.nih.gov/36367250
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3
Authors: et al.
Source: Molecular microbiology, vol. 121, no. 1, pp. 98-115
Subject Terms: Humans, Bacterial Proteins/metabolism, Endopeptidase Clp/genetics, Endopeptidase Clp/metabolism, Staphylococcus aureus/metabolism, Cell Division/genetics, Escherichia coli Proteins/metabolism, Escherichia coli/metabolism, Staphylococcal Infections, ATPases Associated with Diverse Cellular Activities/genetics, Molecular Chaperones/genetics, Molecular Chaperones/metabolism, Staphylococcus aureus, AAA+ ATPases, ClpX, FtsA, cell division, peptidoglycan
File Description: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/pmid/38041395; info:eu-repo/semantics/altIdentifier/eissn/1365-2958; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_1CBBE39ACD1F5; https://serval.unil.ch/notice/serval:BIB_1CBBE39ACD1F; https://serval.unil.ch/resource/serval:BIB_1CBBE39ACD1F.P001/REF.pdf
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4
Authors: et al.
Source: J Neurol
Subject Terms: 2. Zero hunger, 03 medical and health sciences, Original Communication, 0302 clinical medicine, Spastic Paraplegia, Hereditary, Amyotrophic Lateral Sclerosis, Mutation, ATPases Associated with Diverse Cellular Activities, Humans, Metalloendopeptidases, Metalloendopeptidases/genetics [MeSH], Mutation/genetics [MeSH], Spastic Paraplegia, Hereditary/diagnostic imaging [MeSH], Amyotrophic lateral sclerosis, SPG7, Humans [MeSH], Spastic Paraplegia, Hereditary/genetics [MeSH], Amyotrophic Lateral Sclerosis/diagnostic imaging [MeSH], ATPases Associated with Diverse Cellular Activities/genetics [MeSH], Motor neuron disease, Hereditary spastic paraplegia, Amyotrophic Lateral Sclerosis/genetics [MeSH], Whole-exome sequencing, 3. Good health
Access URL: https://link.springer.com/content/pdf/10.1007/s00415-020-09861-w.pdf
https://pubmed.ncbi.nlm.nih.gov/32447552
https://pubmed.ncbi.nlm.nih.gov/32447552/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419373
https://link.springer.com/content/pdf/10.1007/s00415-020-09861-w.pdf
https://link.springer.com/article/10.1007/s00415-020-09861-w
https://www.ncbi.nlm.nih.gov/pubmed/32447552
https://repository.publisso.de/resource/frl:6469692 -
5
Authors: et al.
Contributors: et al.
Source: Hum Mol Genet
Human Molecular Genetics, 27, 3, pp. 529-545Subject Terms: Male, 0301 basic medicine, Carrier Proteins/genetics, relationship - sibling, Whole Exome Sequencing/methods, Cilia/metabolism, zebrafish arm cilia, Genetics(clinical), Zebrafish, triphosphatases, 0303 health sciences, Articles, Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences, congenital heart disease, Pedigree, 3. Good health, homozygote, Phenotype, name=Genetics(clinical), adenosine, cytoplasm, Female, Microtubule-Associated Proteins, inversu mutation, Genotype, phenotype, name=Genetics, dynein atpase, Mutation, Missense, embryo, Radboud University Medical Center, Missense/genetics, heart, cell motility, Tumor Suppressor Proteins/genetics, ATPases Associated with Diverse Cellular Activities/genetics, handedness, 03 medical and health sciences, Zebrafish Proteins/genetics, Exome Sequencing, Genetics, Animals, Humans, Cilia, Molecular Biology, carrier proteins, mice vesicle pathogenicity heart looping gene complementation cardiac development, DNA Helicases/genetics, missense mutation, Tumor Suppressor Proteins, situs, DNA Helicases, name=Molecular Biology, Microtubule-Associated Proteins/genetics, Zebrafish Proteins, HEK293 Cells, Mutation, ATPases Associated with Diverse Cellular Activities, Human Genetics - Radboud University Medical Center, Carrier Proteins
File Description: application/pdf; image/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/29228333
https://eprints.whiterose.ac.uk/124772/8/ddx422.pdf
https://academic.oup.com/hmg/article-abstract/27/3/529/4708237
http://dspace.library.uu.nl/handle/1874/363979
https://discovery.dundee.ac.uk/ws/files/19840888/ddx422.pdf
https://www.narcis.nl/publication/RecordID/oai%3Arepository.ubn.ru.nl%3A2066%2F183867
http://eprints.whiterose.ac.uk/124772/
https://www.rug.nl/research/portal/files/78292890/ddx422.pdf
https://dspace.library.uu.nl/handle/1874/363979
https://repository.ubn.ru.nl//bitstream/handle/2066/183867/183867.pdf
https://hdl.handle.net/2066/183867
https://discovery-pp.ucl.ac.uk/id/eprint/10040807/ -
6
Authors: et al.
Source: Redox Biol
Redox Biology, Vol 17, Iss, Pp 1-15 (2018)Subject Terms: Leptin, 0301 basic medicine, Medicine (General), Kidney, MicroRNAs (genetics), Mice, Mesangial cells, Non-alcoholic Fatty Liver Disease, Mesangial Cells (metabolism, Oxidative Stress (genetics), Biology (General), Non-alcoholic Fatty Liver Disease (genetics, Mice, Knockout, 0303 health sciences, Signal Transduction (genetics), STAT Transcription Factors (genetics), STAT Transcription Factors, Mesangial Cells, NADPH Oxidase 2, Peroxynitrous Acid (metabolism), Leptin (genetics), Environmental Health, Research Paper, Signal Transduction, QH301-705.5, Knockout, Diet, High-Fat, Janus Kinases (genetics), NADPH Oxidase 2 (genetics), 03 medical and health sciences, Inflammation (genetics, R5-920, miR21, NAFLD, Peroxynitrous Acid, NADPH, pathology), Animals, Humans, Janus Kinases, Inflammation, DNA Helicases, JAK/STAT, NOX-2, Diet, Kidney (metabolism, High-Fat, MicroRNAs, Oxidative Stress, Oxidative stress, siRNA, ATPases Associated with Diverse Cellular Activities (genetics), DNA Helicases (genetics), ATPases Associated with Diverse Cellular Activities, metabolism
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/29660503
https://doaj.org/article/74b238fabfc549c98d1cd9024c69439c
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006523
http://europepmc.org/articles/PMC6006523
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006523
https://www.sciencedirect.com/science/article/pii/S2213231718302337
https://core.ac.uk/display/158393144
https://pubmed.ncbi.nlm.nih.gov/29660503/ -
7
Authors: et al.
Source: Lepelley, A, Mina, E D, Nieuwenhove, E V, Waumans, L, Fraitag, S, Rice, G I, Dhir, A, Frémond, M-L, Rodero, M P, Seabra, L, Carter, E, Bodemer, C, Buhas, D, Callewaert, B, Lonlay, P D, Somer, L D, Dyment, D A, Faes, F, Grove, L, Holden, S, Hully, M, Kurian, M A, McMillan, H J, Suetens, K, Tyynismaa, H, Chhun, S, Wai, T, Wouters, C, Bader-Meunier, B & Crow, Y J 2021, 'Enhanced cGAS-STING–dependent interferon signaling associated with mutations in ATAD3A', Journal of Experimental Medicine, vol. 218, no. 10, e20201560. https://doi.org/10.1084/jem.20201560
Subject Terms: ATPases Associated with Diverse Cellular Activities/genetics, Child, Preschool, DNA, Mitochondrial/genetics, Female, Genes, Dominant, Humans, Interferons/genetics, Male, Membrane Proteins/genetics, Mitochondrial Proteins/genetics, Mutation, Nucleotidyltransferases/genetics, Scleroderma, Systemic/genetics, Signal Transduction, THP-1 Cells, Young Adult
File Description: application/pdf
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8
Authors: et al.
Source: Biochimica et Biophysica Acta - Molecular Basis of Disease, 1866 (11), 165900 (2020-11)
Subject Terms: Intra-hepatic cholestasis, Oxysterol, PEX1 c.2528G>A, PEX1 p.Gly843Asp, Peroxisome biogenesis disorder, Very long-chain fatty acid, Bile Acids and Salts, Membrane Proteins, Oxysterols, Glucose-6-Phosphatase, ATPases Associated with Diverse Cellular Activities, Pex1 protein, mouse, ATPases Associated with Diverse Cellular Activities/genetics, ATPases Associated with Diverse Cellular Activities/metabolism, Alleles, Animals, Bile Acids and Salts/metabolism, Cell Membrane/metabolism, Female, Glucose-6-Phosphatase/metabolism, Hepatocytes/metabolism, Longitudinal Studies, Male, Membrane Proteins/metabolism, Mice, Inbred C57BL, Oxysterols/metabolism, RNA-Seq, Zellweger Syndrome/genetics
Relation: https://api.elsevier.com/content/article/PII:S0925443920302489?httpAccept=text/xml; urn:issn:0925-4439; https://orbi.uliege.be/handle/2268/291349; info:hdl:2268/291349; info:pmid:32693164
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9
Authors: et al.
Subject Terms: ATPases Associated with Diverse Cellular Activities/genetics, Adolescent, Adult, Alleles, Animals, Cerebral Palsy/etiology/metabolism/*pathology, Child, Preschool, Epilepsy/etiology/metabolism/*pathology, Female, Genetic Predisposition to Disease, Genetic Variation, Hearing Loss/etiology/metabolism/*pathology, Humans, Infant, Newborn, Intellectual Disability/etiology/metabolism/*pathology, Male, Muscle Spasticity/etiology/metabolism/*pathology, Rats, Young Adult, AAA+ superfamily, ATPase, spata5l1, cerebral palsy, epilepsy, intellectual disability, movement disorder, neurodevelopmental disorder, sensorineural hearing loss
Relation: https://linkinghub.elsevier.com/retrieve/pii/S0002-9297(21)00302-5; American journal of human genetics; PMC8546233; https://hdl.handle.net/11287/622267
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10
Authors: et al.
Contributors: et al.
Source: Sci Rep
Subject Terms: Cytosol / chemistry, 0301 basic medicine, Peroxisomes / genetics, Peroxisome-Targeting Signal 1 Receptor / chemistry, Ubiquitination / genetics, Peroxisome-Targeting Signal 1 Receptor, ATPases Associated with Diverse Cellular Activities / chemistry, Cytosol / metabolism, Peroxisomal Targeting Signal 2 Receptor / genetics, Article, Peroxisomal Targeting Signals, Membrane Proteins / chemistry, Ubiquitin / chemistry, Mice, 03 medical and health sciences, Cytosol, Ubiquitin / metabolism, Peroxisomes, Animals, Humans, Peroxisomes / chemistry, Amino Acid Sequence, Protein Interaction Maps, Peroxisomal Targeting Signals / genetics, Peroxisomal Targeting Signal 2 Receptor, Membrane Proteins / genetics, 0303 health sciences, Peroxisomal Targeting Signal 2 Receptor / chemistry, Fibroblasts / chemistry, Ubiquitin, Amino Acid Sequence / genetics, Ubiquitination, Membrane Proteins, Protein Interaction Maps / genetics, Fibroblasts, ATPases Associated with Diverse Cellular Activities / genetics, Molecular Docking Simulation, Protein Transport, Mutation, Peroxisome-Targeting Signal 1 Receptor / genetics, Protein Transport / genetics, ATPases Associated with Diverse Cellular Activities, Click Chemistry
File Description: application/pdf
Access URL: https://www.nature.com/articles/s41598-018-34200-5.pdf
https://pubmed.ncbi.nlm.nih.gov/30375424
https://pubmed.ncbi.nlm.nih.gov/30375424/
http://ui.adsabs.harvard.edu/abs/2018NatSR...816014H/abstract
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207756
https://www.nature.com/articles/s41598-018-34200-5.pdf
https://www.nature.com/articles/s41598-018-34200-5
https://repositorio-aberto.up.pt/bitstream/10216/127420/1/10.1038-s41598-018-34200-5.pdf
https://hdl.handle.net/10216/127420 -
11
Authors: et al.
Source: The American journal of human genetics 110(7), 1098 - 1109 (2023). doi:10.1016/j.ajhg.2023.05.009
Subject Terms: info:eu-repo/classification/ddc/570, Humans, Spinocerebellar Ataxias: genetics, Spinocerebellar Ataxias: diagnosis, Cerebellar Ataxia: genetics, Phenotype, Ataxia: genetics, Genetic Testing, ATPases Associated with Diverse Cellular Activities: genetics, ATP-Dependent Proteases: genetics, Ubiquitin-Protein Ligases: genetics, Spinocerebellar Ataxia, SCA, CACNA1A, PRKCG, AFG3L2, ITPR1, STUB1, SPTBN2, KCNC3, onset, AFG3L2 protein, human, ATPases Associated with Diverse Cellular Activities, ATP-Dependent Proteases, STUB1 protein, Ubiquitin-Protein Ligases
Subject Geographic: DE
Relation: info:eu-repo/semantics/altIdentifier/pmid/pmid:37301203; info:eu-repo/semantics/altIdentifier/issn/1537-6605; info:eu-repo/semantics/altIdentifier/issn/0002-9297; https://pub.dzne.de/record/258998
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12
Authors: et al.
Source: Annals of neurology 88(1), 18 - 32 (2020). doi:10.1002/ana.25723
Subject Terms: info:eu-repo/classification/ddc/610, ATP-Dependent Proteases: genetics, ATPases Associated with Diverse Cellular Activities: genetics, Adolescent, Adult, Aged, Child, Female, GTP Phosphohydrolases: genetics, Genetic Testing, High-Throughput Nucleotide Sequencing, Humans, Male, Middle Aged, Mutation, Optic Atrophy: genetics, Optic Nerve Diseases: genetics, Pedigree, Exome Sequencing, Young Adult
Subject Geographic: DE
Relation: info:eu-repo/semantics/altIdentifier/pmid/pmid:32219868; info:eu-repo/semantics/altIdentifier/issn/0364-5134; info:eu-repo/semantics/altIdentifier/issn/1531-8249; https://pub.dzne.de/record/151660
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13
Authors: et al.
Source: EBioMedicine 54, 102730 (2020). doi:10.1016/j.ebiom.2020.102730
Subject Terms: info:eu-repo/classification/ddc/610, ATPases Associated with Diverse Cellular Activities: genetics, Acyl-CoA Dehydrogenase: genetics, DNA Polymerase gamma: genetics, Databases, Genetic: statistics & numerical data, Genes, Recessive, Genetic Predisposition to Disease, Humans, Metalloendopeptidases: genetics, Mitochondrial Diseases: epidemiology, Mitochondrial Diseases: genetics, Solute Carrier Family 22 Member 5: genetics
Subject Geographic: DE
Relation: info:eu-repo/semantics/altIdentifier/pmid/pmid:32305867; info:eu-repo/semantics/altIdentifier/issn/2352-3964; https://pub.dzne.de/record/151525
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14
Authors: et al.
Contributors: et al.
Source: Life Sci Alliance
Subject Terms: RNA, Messenger/genetics, 0301 basic medicine, OPA1, GTP Phosphohydrolases, Mitochondrial Ribosomes, Mice, Mitochondrial Proteins/biosynthesis, ATP-Dependent Proteases, RNA, Small Interfering, SPASTIC PARAPLEGIA, Research Articles, Fibroblasts/metabolism, RNA, Small Interfering/genetics, 0303 health sciences, M-AAA PROTEASE, Metalloendopeptidases, Mitochondrial Membranes/metabolism, READ ALIGNMENT, Mitochondria, 3. Good health, Phenotype, ATP-Dependent Proteases/genetics, Gene Knockdown Techniques, Mitochondrial Membranes, TURNOVER, Metalloendopeptidases/metabolism, mice, COMPUTATIONAL PLATFORM, ATAXIA, Transfection, mitochondria, AFG3L2, protein synthesis, inner mitochondrial membrane, chloramphenicol, ATPases Associated with Diverse Cellular Activities/genetics, Mitochondrial Proteins, 03 medical and health sciences, Mitochondria/metabolism, DNA DELETIONS, Animals, Humans, RNA, Messenger, Biochemistry, cell and molecular biology, MUTATIONS, Mitochondrial Ribosomes/metabolism, Fibroblasts, Biomedicine, HEK293 Cells, Protein Biosynthesis, Mutation, ATPases Associated with Diverse Cellular Activities, GTP Phosphohydrolases/metabolism, mutation, MEMBRANE
File Description: application/pdf
Access URL: https://www.life-science-alliance.org/content/lsa/2/1/e201800219.full.pdf
https://pubmed.ncbi.nlm.nih.gov/30683687
https://www.life-science-alliance.org/content/2/1/e201800219
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348486
https://researchportal.vub.be/en/publications/mitochondrial-stress-response-triggered-by-defects-in-protein-syn
https://pubmed.ncbi.nlm.nih.gov/30683687/
https://researchportal.helsinki.fi/en/publications/mitochondrial-stress-response-triggered-by-defects-in-protein-syn
https://www.life-science-alliance.org/content/lsa/2/1/e201800219.full.pdf
http://hdl.handle.net/10852/74240
https://doi.org/10.26508/lsa.201800219
http://hdl.handle.net/10138/307109
http://hdl.handle.net/21.11116/0000-000B-3F6D-6
https://biblio.vub.ac.be/vubir/mitochondrial-stress-response-triggered-by-defects-in-protein-synthesis-quality-control(beda7a9c-abd7-4e20-a570-c27a4ff7d0b8).html -
15
Authors: et al.
Source: Neurology 92(23), e2679-e2690 (2019). doi:10.1212/WNL.0000000000007606
Subject Terms: info:eu-repo/classification/ddc/610, White People: genetics, ATPases Associated with Diverse Cellular Activities: genetics, Adult, Cerebellar Ataxia: genetics, Cerebellar Ataxia: physiopathology, Cohort Studies, Electromyography, European Continental Ancestry Group: genetics, Female, Humans, Loss of Function Mutation, Magnetic Resonance Imaging, Male, Metalloendopeptidases: genetics, Middle Aged, Paraplegia: genetics, Paraplegia: physiopathology, Phenotype, Polymorphism, Single Nucleotide, Spastic Paraplegia, Hereditary: genetics, Hereditary: physiopathology, Young Adult, Metalloendopeptidases, SPG7 protein, human, ATPases Associated with Diverse Cellular Activities
Subject Geographic: DE
Relation: info:eu-repo/semantics/altIdentifier/issn/1526-632X; info:eu-repo/semantics/altIdentifier/pmid/pmid:31068484; info:eu-repo/semantics/altIdentifier/issn/0028-3878; https://pub.dzne.de/record/140892
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