Suchergebnisse - "Enzyme Inhibitors pharmacology"
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1
Autoren:
Quelle: J Med Chem
Schlagwörter: Antimicrobial resistance, MEP pathway, IspD, anti-infectives, Enzyme Inhibitors/chemistry [MeSH], Herbicides/metabolism [MeSH], Enzyme Inhibitors/pharmacology [MeSH], Herbicides/chemical synthesis [MeSH], Perspective, Anti-Infective Agents/pharmacology [MeSH], Humans [MeSH], Herbicides/chemistry [MeSH], Anti-Infective Agents/chemistry [MeSH], Herbicides/pharmacology [MeSH], Anti-Infective Agents, Herbicides, Humans, Drug Resistance, Microbial, Enzyme Inhibitors
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2
Autoren: et al.
Quelle: Sci Adv
Schlagwörter: Pyrazoles/pharmacology, Small Molecule Libraries/chemistry, Antineoplastic Agents, Pyrazoles/chemistry, OPA1 protein, human, GTP Phosphohydrolases/antagonists & inhibitors, Drug Resistance, Neoplasm/drug effects, Biochimie, biophysique & biologie moléculaire, GTP Phosphohydrolases, Small Molecule Libraries, Cytochromes c/metabolism, Enzyme Inhibitors/chemistry, Structure-Activity Relationship, Cell Line, Tumor, Mitochondria/metabolism, Antineoplastic Agents/chemistry, Small Molecule Libraries/pharmacology, Humans, Enzyme Inhibitors, Proto-Oncogene Proteins c-bcl-2/antagonists & inhibitors, Enzyme Inhibitors/pharmacology, Apoptosis/drug effects, Cytochromes c, GTP Phosphohydrolases/chemistry, Life sciences, Mitochondria/drug effects, Proto-Oncogene Proteins c-bcl-2, Sciences du vivant, Pyrazoles, Proto-Oncogene Proteins c-bcl-2/metabolism, Biomedicine and Life Sciences, GTP Phosphohydrolases/metabolism, Antineoplastic Agents/pharmacology, Biochemistry, biophysics & molecular biology
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3
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Leukemia
Schlagwörter: 0301 basic medicine, DNA Damage / drug effects, Article, Mice, 03 medical and health sciences, Leukemia, Myeloid, Acute / pathology, [SDV.CAN] Life Sciences [q-bio]/Cancer, Cell Line, Tumor, Humans, Animals, Enzyme Inhibitors, Fatty Acids / biosynthesis, 0303 health sciences, Stearoyl-CoA Desaturase / metabolism, Fatty Acids, Enzyme Inhibitors / pharmacology, Prognosis, Xenograft Model Antitumor Assays, 3. Good health, Leukemia, Myeloid, Acute, Fatty Acids / metabolism, Leukemia, Myeloid, Acute / metabolism, Stearoyl-CoA Desaturase / genetics, Leukemia, Myeloid, Acute / drug therapy, Stearoyl-CoA Desaturase, Stearoyl-CoA Desaturase / antagonists & inhibitors, DNA Damage
Dateibeschreibung: application/pdf
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4
Autoren: et al.
Quelle: J Enzyme Inhib Med Chem
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 40, Iss 1 (2025)
Wróbel, T M, Grudzińska, A, Yakubu, J, du Toit, T, Sharma, K, Harrington, J C, Björkling, F, Jørgensen, F S & Pandey, A V 2025, ' Pyridine indole hybrids as novel potent CYP17A1 inhibitors ', Journal of Enzyme Inhibition and Medicinal Chemistry, vol. 40, no. 1, 2463014 . https://doi.org/10.1080/14756366.2025.2463014Schlagwörter: Pyridines/pharmacology, Enzyme Inhibitors/pharmacology, Indoles, Molecular Structure, Dose-Response Relationship, Drug, Pyridines, Steroid 17-alpha-Hydroxylase, RM1-950, Steroid 17-alpha-Hydroxylase/antagonists & inhibitors, prostate cancer, Dose-Response Relationship, Indoles/chemistry, Molecular Docking Simulation, Structure-Activity Relationship, CYP17A1, inhibitors, Humans, Therapeutics. Pharmacology, Drug, Enzyme Inhibitors, enzyme inhibition, Research Article
Dateibeschreibung: application/pdf
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5
Autoren: et al.
Quelle: Photochemistry and Photobiology. 100:1894-1901
Schlagwörter: Keratinocytes, 0301 basic medicine, Extracellular Vesicles* / metabolism, Imipramine, Skin* / radiation effects, Ultraviolet Rays, Dermatology, Skin* / drug effects, Extracellular Vesicles, 03 medical and health sciences, Keratinocytes* / drug effects, Skin* / cytology, Humans, Enzyme Inhibitors, Keratinocytes* / metabolism, Skin*metabolism, Skin, Keratinocytes* / radiation effects, Ultravioet Rays, 0303 health sciences, Enzyme Inhibitors / pharmacology, Sphingomyelin Phosphodiesterase* / antagonists & inhibitors, Dna, DNA, 3. Good health, Sphingomyelin Phosphodiesterase, Imipramine* / pharmacology, Sphingomyelin Phospodiesterase* / metabolism, DNA Damage
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/38433456
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6
Autoren: et al.
Quelle: Br J Cancer
Schlagwörter: 0301 basic medicine, 0303 health sciences, Lung Neoplasms, Medizin, Adenocarcinoma of Lung, Adenocarcinoma, Article, 3. Good health, Adenocarcinoma of Lung [MeSH], Pancreatic Neoplasms/genetics [MeSH], Mutation [MeSH], Humans [MeSH], Lung Neoplasms/genetics [MeSH], Colorectal Neoplasms/drug therapy [MeSH], Animals [MeSH], Pancreatic Neoplasms/drug therapy [MeSH], 631/67/1612, Proto-Oncogene Proteins p21(ras)/genetics [MeSH], Enzyme Inhibitors/pharmacology [MeSH], Adenocarcinoma/drug therapy [MeSH], Adenocarcinoma/genetics [MeSH], Transferases [MeSH], 631/67/1504, Colorectal Neoplasms/genetics [MeSH], 631/67/1059, Lung Neoplasms/drug therapy [MeSH], Disease Models, Animal [MeSH], article, Pancreatic Neoplasms, Proto-Oncogene Proteins p21(ras), Disease Models, Animal, 03 medical and health sciences, Transferases, Mutation, Humans, Animals, Enzyme Inhibitors, Colorectal Neoplasms
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7
Autoren: et al.
Weitere Verfasser: et al.
Quelle: ISSN: 1568-7864.
Schlagwörter: Base excision repair, Cancer, Inflammation, OGG1 modulators, Oxidative DNA damage, Small molecules, Transcriptional regulation, MESH: Animals, DNA Damage, DNA Glycosylases* / antagonists & inhibitors, DNA Glycosylases* / metabolism, DNA Repair* / drug effects, Enzyme Inhibitors* / pharmacology, Humans, Neoplasms / drug therapy, Neoplasms / genetics, Oxidative Stress, Small Molecule Libraries* / pharmacology, [SDV]Life Sciences [q-bio]
Relation: info:eu-repo/semantics/altIdentifier/pmid/40120404; PUBMED: 40120404
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8
Autoren: Kaschina, Elena
Quelle: Hypertens Res
Schlagwörter: Renin-Angiotensin System, Comment, Hypertension, RAAS, Renin-Angiotensin System/drug effects [MeSH], Humans [MeSH], Hypertension/physiopathology [MeSH], Losartan, Angiotensin-Converting Enzyme Inhibitors/therapeutic use [MeSH], Exercise/physiology [MeSH], Exercise, Hypertension/drug therapy [MeSH], SHR, Angiotensin-Converting Enzyme Inhibitors/pharmacology [MeSH], Renin-Angiotensin System/physiology [MeSH], Antihypertensive Agents/therapeutic use [MeSH], comment, Humans, Angiotensin-Converting Enzyme Inhibitors, Antihypertensive Agents
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9
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Hypertension Research. 45:2008-2017
Schlagwörter: Losartan / therapeutic use, Albuminuria / etiology, Renal endpoint, Antihypertensive Agents / therapeutic use, Angiotensin-Converting Enzyme Inhibitors, Blood Pressure, Diabetic nephropathy, Losartan, Proteinuria / etiology, Angiotensin Receptor Antagonists, 03 medical and health sciences, Hypertension, 0302 clinical medicine, Double-Blind Method, Angiotensin Receptor Antagonists / pharmacology, Diabetes Mellitus, Humans, Albuminuria, Diabetic Nephropathies, Renal Insufficiency, Mortality, Renal Insufficiency, Chronic, Antihypertensive Agents, Angiotensin-Converting Enzyme Inhibitors / pharmacology, Chronic* / complications, Diabetic Nephropathies* / drug therapy, 3. Good health, Losartan / pharmacology, Proteinuria, Chronic* / drug therapy, Albuminuria / chemically induced, Proteinuria / drug therapy
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/36123398
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10
Autoren: et al.
Quelle: J Enzyme Inhib Med Chem
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 37, Iss 1, Pp 1773-1811 (2022)
Journal of enzyme inhibition and medicinal chemistry, vol. 37, no. 1, pp. 1773-1811Schlagwörter: 0301 basic medicine, Cancer immunotherapy, RM1-950, Heme, Triazoles, 01 natural sciences, 0104 chemical sciences, 3. Good health, 03 medical and health sciences, Enzyme Inhibitors/chemistry, Enzyme Inhibitors/pharmacology, Indoleamine-Pyrrole 2,3,-Dioxygenase, Triazoles/chemistry, Triazoles/pharmacology, X-ray crystallography, structure-based drug design, tryptophan metabolism, Therapeutics. Pharmacology, Enzyme Inhibitors, Research Paper
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/35758198
https://doaj.org/article/cf28d46a56e84bc6b249d5272612f6f4
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_EF494F840FDA2
https://serval.unil.ch/resource/serval:BIB_EF494F840FDA.P001/REF.pdf
https://serval.unil.ch/notice/serval:BIB_EF494F840FDA -
11
Autoren:
Quelle: Oncotarget
Franciosa, G & Olsen, J V 2023, ' Impact of SHP2 tyrosine phosphorylation on the development of acquired resistance to allosteric SHP2 inhibitors ', OncoTarget, vol. 14, pp. 281-283 . https://doi.org/10.18632/oncotarget.28392Schlagwörter: Enzyme Inhibitors/pharmacology, Protein Tyrosine Phosphatase, Non-Receptor Type 11/genetics, Tumor, Protein Tyrosine Phosphatase, Non-Receptor Type 11, Cell Line, Non-Receptor Type 11/genetics, Editorial, Protein Kinase Inhibitors/pharmacology, Cell Line, Tumor, Humans, Tyrosine, Protein Tyrosine Phosphatase, Phosphorylation, Enzyme Inhibitors, Protein Kinase Inhibitors
Dateibeschreibung: application/pdf
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12
Autoren: et al.
Weitere Verfasser: et al.
Quelle: ISSN: 1999-4915 ; Viruses ; https://anses.hal.science/anses-04549222 ; Viruses, 2024, 16 (3), pp.388. ⟨10.3390/v16030388⟩ ; https://www.mdpi.com/1999-4915/16/3/388.
Schlagwörter: oseltamivir resistance, group-1 neuraminidases, influenzaAviruses, H274Y-NA substitution, H275Y-NA substitution, MESH: Amino Acid Substitution Antiviral Agents / pharmacology Drug Resistance, Viral / genetics Enzyme Inhibitors / pharmacology Humans Influenza A Virus, H1N1 Subtype* / genetics Influenza A virus* / genetics Influenza, Human* Neuraminidase / genetics Neuraminidase / metabolism Oseltamivir / pharmacology Reverse Genetics, [SDV]Life Sciences [q-bio]
Relation: info:eu-repo/semantics/altIdentifier/pmid/38543754; PUBMED: 38543754; PUBMEDCENTRAL: PMC10975200
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13
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Anticancer Research. 42:589-598
Schlagwörter: 0301 basic medicine, Apoptosis, Endoplasmic Reticulum, Colorectal Neoplasms / genetics, Mice, Protein Serine-Threonine Kinases / antagonists & inhibitors, Autophagic Cell Death / drug effects, Enzyme Inhibitors, 0303 health sciences, Tumor, Fluorouracil / pharmacology, Protein Serine-Threonine Kinases / genetics, Protein-Tyrosine Kinases / antagonists & inhibitors, Protein-Tyrosine Kinases, Cellular Reprogramming, Endoplasmic Reticulum Stress, Colorectal Neoplasms / drug therapy, 3. Good health, DYRK1A protein, endoplasmic reticulum stress, Fluorouracil, Colorectal Neoplasms, Glycolysis, Metabolic Networks and Pathways, autophagy, Autophagic Cell Death, colorectal cancer, Protein Serine-Threonine Kinases, Apoptosis / drug effects, Cellular Reprogramming / genetics, Colorectal Neoplasms / pathology, Cell Line, 03 medical and health sciences, Cell Line, Tumor, Autophagy / drug effects, Autophagy, Endoplasmic Reticulum / drug effects, Animals, Humans, Metabolic Networks and Pathways / drug effects, Glycolysis / drug effects, Cell Proliferation, Enzyme Inhibitors / pharmacology, protein kinases, Endoplasmic Reticulum Stress / drug effects, Protein-Tyrosine Kinases / genetics, Reactive Oxygen Species / metabolism, Endoplasmic Reticulum / genetics, Xenograft Model Antitumor Assays, DYRK1B protein, Cell Proliferation / drug effects, Reactive Oxygen Species
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/34969768
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14
Autoren: et al.
Weitere Verfasser: et al.
Quelle: J Med Chem
Schlagwörter: 0301 basic medicine, Fluorine Radioisotopes, Cytochrome P-450 Enzyme Inhibitors/chemistry, Cytochrome P-450 CYP11B2/metabolism, Physique, chimie, mathématiques & sciences de la terre, Sciences de la santé humaine, Hyperaldosteronism/diagnostic imaging, Mice, Structure-Activity Relationship, 03 medical and health sciences, Hyperaldosteronism/drug therapy, Physical, chemical, mathematical & earth Sciences, Endocrinology, metabolism & nutrition, Drug Development, Drug Discovery, Hyperaldosteronism, Chimie, Animals, Cytochrome P-450 CYP11B2, Cytochrome P-450 Enzyme Inhibitors, Humans, Cytochrome P-450 CYP11B2/antagonists & inhibitors, Cytochrome P-450 CYP11B2/analysis, Human health sciences, Cytochrome P-450 Enzyme Inhibitors/pharmacology, Mice, Inbred BALB C, 0303 health sciences, Radiochemistry, Dose-Response Relationship, Drug, Molecular Structure, Cytochrome P-450 Enzyme Inhibitors/chemical synthesis, Hyperaldosteronism/metabolism, Radiologie, médecine & imagerie nucléaire, Fluorine-18, 3. Good health, Chemistry, Positron-Emission Tomography, Molecular Medicine, Female, Radiology, nuclear medicine & imaging, Endocrinologie, métabolisme & nutrition
Zugangs-URL: https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.1c00539
https://pubmed.ncbi.nlm.nih.gov/34137616
https://discovery.ucl.ac.uk/id/eprint/10130438/
https://europepmc.org/article/MED/34137616
https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.1c00539
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273890/
https://pubmed.ncbi.nlm.nih.gov/34137616/ -
15
Autoren: et al.
Weitere Verfasser: et al.
Quelle: idUS. Depósito de Investigación de la Universidad de Sevilla
Universidad de Sevilla (US)Schlagwörter: Models, Molecular, Molecular Stereoisomerism, Glycoside Hydrolases, Stereoisomerism, Chemistry Techniques, Synthetic, MESH: Carbohydrate Conformation Chemistry Techniques, 01 natural sciences, Imino Sugars, 3. Good health, 0104 chemical sciences, Synthetic Enzyme Inhibitors / chemical synthesis* Enzyme Inhibitors / chemistry Enzyme Inhibitors / pharmacology* Glycoside Hydrolases / antagonists & inhibitors* Glycosides / chemical synthesis* Glycosides / chemistry Glycosides / pharmacology* Imino Sugars / chemistry* Models, C-glycoside, 13. Climate action, Carbohydrate Conformation, [CHIM]Chemical Sciences, Glycosides, Enzyme Inhibitors
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/33427829
https://hdl.handle.net/11441/141423
https://hal.archives-ouvertes.fr/hal-03376475
http://pubs.rsc.org/en/content/articlelanding/2021/ob/d0ob02249g
http://www.ncbi.nlm.nih.gov/pubmed/33427829
https://crystallography.net/cod/7157828.html
https://pubs.rsc.org/en/content/articlelanding/2021/ob/d0ob02249g
https://www.ncbi.nlm.nih.gov/pubmed/33427829
https://idus.us.es/handle//11441/141423 -
16
Autoren: et al.
Quelle: Acta Physiologica. 239
Schlagwörter: cystathionine-gamma lyase, soluble guanylate cyclase, Enzyme Inhibitors/pharmacology, Arterioles/drug effects, Hydrogen Sulfide/metabolism, hydrogen sulfide, Cystathionine gamma-Lyase, Pharmacology and Toxicology, Farmakologi och toxikologi, Inbred C57BL, contractility, Mice, Inbred C57BL, Mice, Arterioles, Vasoconstriction, Cystathionine gamma-Lyase/antagonists & inhibitors, endothelial NO synthase, Animals, Humans, Hydrogen Sulfide, Enzyme Inhibitors, intracerebral arterioles
Dateibeschreibung: application/pdf
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17
Autoren: et al.
Schlagwörter: Adult, Angiotensin I/administration & dosage, Angiotensin II/administration & dosage, Angiotensin-Converting Enzyme Inhibitors/pharmacokinetics, Angiotensin-Converting Enzyme Inhibitors/pharmacology, Antihypertensive Agents/pharmacokinetics, Antihypertensive Agents/pharmacology, Area Under Curve, Benzazepines/pharmacokinetics, Benzazepines/pharmacology, Blood Pressure/drug effects, Double-Blind Method, Enzyme Inhibitors/pharmacokinetics, Enzyme Inhibitors/pharmacology, Humans, Male, Neprilysin/antagonists & inhibitors, Placebos, Pyridines/pharmacokinetics, Pyridines/pharmacology, Reference Values
Relation: Journal of Cardiovascular Pharmacology; https://iris.unil.ch/handle/iris/98446; serval:BIB_3E9FAC34D6E6; 000072247800012; 9514186
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18
Autoren: et al.
Weitere Verfasser: et al.
Quelle: J Clin Oncol
Digital.CSIC. Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
instname
JOURNAL OF CLINICAL ONCOLOGY
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
RISalud-ANDALUCIA. Repositorio Institucional de Salud de Andalucía
Instituto de Investigación Sanitaria La Fe (IIS La Fe)
Scientia
Scientia. Dipòsit d'Informació Digital del Departament de Salut
Salamero, O, Montesinos, P, Willekens, C, Pérez-Simón, J A, Pigneux, A, Récher, C, Popat, R, Carpio, C, Molinero, C, Mascaró, C, Vila, J, Arévalo, M I, Maes, T, Buesa, C, Bosch, F & Somervaille, T C P 2020, 'First-in-Human Phase I Study of Iadademstat (ORY-1001) : A First-in-Class Lysine-Specific Histone Demethylase 1A Inhibitor, in Relapsed or Refractory Acute Myeloid Leukemia', Journal of Clinical Oncology, vol. 38, no. 36, pp. 4260-4273. https://doi.org/10.1200/JCO.19.03250Schlagwörter: Myeloid, Mucositis, Adult, Male, 0301 basic medicine, Other subheadings::Other subheadings::/therapeutic use, Leukemia, Myeloid, Acute/drug therapy, Otros calificadores::Otros calificadores::/uso terapéutico, Histone Demethylases/antagonists & inhibitors, 03 medical and health sciences, Recurrence, COMPUESTOS QUÍMICOS Y DROGAS::acciones y usos químicos::acciones farmacológicas::mecanismos moleculares de acción farmacológica::inhibidores enzimáticos, 80 and over, Acute/drug therapy, Humans, Diferenciación celular, Enzyme Inhibitors, Aged, Enzyme Inhibitors/pharmacology, Aged, 80 and over, Histone Demethylases, Leukemia, Infecciones, Leucèmia mieloide aguda, Sangre, ORIGINAL REPORTS, Middle Aged, CHEMICALS AND DRUGS::Chemical Actions and Uses::Pharmacologic Actions::Molecular Mechanisms of Pharmacological Action::Enzyme Inhibitors, 3. Good health, Leukemia, Myeloid, Acute, ENFERMEDADES::neoplasias::neoplasias por tipo histológico::leucemia::leucemia mieloide::leucemia mieloide aguda, Azacitidina, Farmacocinética, Female, DISEASES::Neoplasms::Neoplasms by Histologic Type::Leukemia::Leukemia, Myeloid::Leukemia, Myeloid, Acute, Diarrea, Inhibidors enzimàtics - Ús terapèutic
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/33052756
http://hdl.handle.net/10261/237089
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=13287
https://hdl.handle.net/10668/27814
https://hdl.handle.net/11351/6309
https://pubmed.ncbi.nlm.nih.gov/33052756/
https://digital.csic.es/bitstream/10261/237089/1/Myeloid_Leukemia.pdf
http://www.ncbi.nlm.nih.gov/pubmed/33052756
https://ascopubs.org/doi/10.1200/JCO.19.03250
https://digital.csic.es/handle/10261/237089
https://christie.openrepository.com/handle/10541/623429 -
19
Autoren: et al.
Quelle: Eur Heart J
Jiang, X, Eales, J M, Scannali, D, Nazgiewicz, A, Prestes, P, Maier, M, Denniff, M, Xu, X, Saluja, S, Cano-Gamez, E, Wystrychowski, W, Szulinska, M, Antczak, A, Byars, S, Skrypnik, D, Glyda, M, Król, R, Zywiec, J, Zukowska-Szczechowska, E, Burrell, L M, Woolf, A S, Greenstein, A, Bogdanski, P, Keavney, B, Morris, A P, Heagerty, A, Williams, B, Harrap, S B, Trynka, G, Samani, N J, Guzik, T J, Charchar, F J & Tomaszewski, M 2020, 'Hypertension and renin-angiotensin system blockers are not associated with expression of angiotensin-converting enzyme 2 (ACE2) in the kidney', European Heart Journal, vol. 41, no. 48, pp. 4580-4588. https://doi.org/10.1093/eurheartj/ehaa794
European Heart JournalSchlagwörter: Male, 0301 basic medicine, estimated glomerular filtration rate, ACE2, renin-angiotensin system, Angiotensin-Converting Enzyme Inhibitors, Lung/metabolism, Kidney, Diuretics/pharmacology, 0302 clinical medicine, Antihypertensive treatment, Rats, Inbred SHR, Estimated glomerular filtration rate, Diuretics, Lung, Hypertension/drug therapy, Age Factors, Antihypertensive Agents/pharmacology, Middle Aged, 3. Good health, Angiotensin-Converting Enzyme 2/genetics, Kidney Tubules, Transcriptome/drug effects, Hypertension, COVID-19/complications, Female, Angiotensin-Converting Enzyme 2, Renin-angiotensin system, Cardiology and Cardiovascular Medicine, Sequence Analysis, Glomerular Filtration Rate, Adult, kidney, hypertension, Inbred SHR, Adrenergic beta-Antagonists, Angiotensin Receptor Antagonists/pharmacology, Angiotensin-Converting Enzyme Inhibitors/pharmacology, antihypertensive treatment, Angiotensin Receptor Antagonists, 03 medical and health sciences, Sex Factors, Clinical Research, Animals, Humans, Antihypertensive Agents, Aged, Sequence Analysis, RNA, SARS-CoV-2, Gene Expression Profiling, Kidney Tubules/metabolism, COVID-19, Rats, Renin-Angiotensin System/drug effects, RNA, Adrenergic beta-Antagonists/pharmacology, Transcriptome, transcriptome
Zugangs-URL: https://academic.oup.com/eurheartj/article-pdf/41/48/4580/35329302/ehaa794.pdf
https://pubmed.ncbi.nlm.nih.gov/33206176
https://research.manchester.ac.uk/en/publications/409c0f50-6f4f-4ad0-abf5-a2c8875974e1
https://doi.org/10.1093/eurheartj/ehaa794
https://ruj.uj.edu.pl/xmlui/handle/item/278850
http://www.scopus.com/inward/record.url?scp=85099324025&partnerID=8YFLogxK
https://research.manchester.ac.uk/en/publications/409c0f50-6f4f-4ad0-abf5-a2c8875974e1
https://doi.org/10.1093/eurheartj/ehaa794
https://discovery-pp.ucl.ac.uk/id/eprint/10116179/ -
20
Autoren: et al.
Quelle: Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Dipòsit Digital de la UB
instnameSchlagwörter: Male, 0301 basic medicine, Cardiac & Cardiovascular Systems, p38 Mitogen-Activated Protein Kinases/metabolism, Oncologia, B55/PP2A-phosphatase, tumor progression, Angiogenesis Inhibitors, Apoptosis, Human Umbilical Vein Endothelial Cells/drug effects, Inbred C57BL, p38 Mitogen-Activated Protein Kinases, ANGIOGENESIS, ACTIVATION, Mice, Carcinoma, Lewis Lung, Protein Phosphatase 2/antagonists & inhibitors, Protein Phosphatase 2, Enzyme Inhibitors, Phosphorylation, 1102 Cardiorespiratory Medicine and Haematology, Endothelial Cells/drug effects, Enzyme Inhibitors/pharmacology, Mice, Knockout, Hypoxia-Inducible Factor-Proline Dioxygenases/genetics, 0303 health sciences, Tumor, vascular endothelial growth factor, Neovascularization, Pathologic, apoptosis, P38, PROTEIN PHOSPHATASE 2A, Hematology, VEGF, endothelial cells, PP2A, 3. Good health, Oncology, oncology, Female, Biologia del desenvolupament, 3201 Cardiovascular medicine and haematology, Life Sciences & Biomedicine, Signal Transduction, Lewis Lung/drug therapy, Knockout, INHIBITION, Breast Neoplasms, Vascular Remodeling, perfusion, Cell Line, MECHANISMS, Hypoxia-Inducible Factor-Proline Dioxygenases, Angiogenesis Inhibitors/pharmacology, blood vessels, developmental biology, 03 medical and health sciences, Breast Neoplasms/drug therapy, Cell Line, Tumor, Developmental biology, KINASE, Human Umbilical Vein Endothelial Cells, Animals, Humans, Neovascularization, Pathologic, Science & Technology, Carcinoma, 3202 Clinical sciences, Endothelial Cells, 1103 Clinical Sciences, Mice, Inbred C57BL, Peripheral Vascular Disease, Cardiovascular System & Hematology, METASTASIS, Cardiovascular System & Cardiology
Dateibeschreibung: application/pdf
Zugangs-URL: https://www.ahajournals.org/doi/pdf/10.1161/CIRCRESAHA.119.316071
https://pubmed.ncbi.nlm.nih.gov/32527198
https://hdl.handle.net/2445/199448
https://cris.maastrichtuniversity.nl/en/publications/d96637ad-1fdd-4778-a8d9-ff88a0197f22
https://doi.org/10.1161/CIRCRESAHA.119.316071
https://pubmed.ncbi.nlm.nih.gov/32527198/
https://iris.unito.it/handle/2318/1782133
https://www.ahajournals.org/doi/10.1161/CIRCRESAHA.119.316071
https://www.ncbi.nlm.nih.gov/pubmed/32527198
https://www.narcis.nl/publication/RecordID/oai%3Acris.maastrichtuniversity.nl%3Apublications%2Fd96637ad-1fdd-4778-a8d9-ff88a0197f22
https://www.scilit.net/article/90dc76a9603b09c6a249ba2b51c4ae9b
http://hdl.handle.net/2445/199448
https://hdl.handle.net/2318/1782133
https://doi.org/10.1161/CIRCRESAHA.119.316071
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