About: Patrick Dansette

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	Forscher (de) forskare (sv) researcher (en) 연구원 (ko) investigador (es) chercheur (fr) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy)
rdfs:label	Patrick Dansette (en) Patrick Dansette (es) Patrick Dansette (nl) Patrick Dansette (ast)
skos:prefLabel	Patrick Dansette (en) Patrick Dansette (es) Patrick Dansette (nl) Patrick Dansette (ast)
name	Patrick Dansette (en) Patrick Dansette (es) Patrick Dansette (nl) Patrick Dansette (ast)
given name	wds:Q57419431-7B7A66C8-0C22-43EB-98E6-731FDAB6E925
given name	Patrick
instance of	wds:Q57419431-76B0C5AC-21BB-4966-823D-24794EAE8D76
instance of	Homo sapiens
skos:altLabel	Patrick M. Dansette (en) Philip Dansette ( an error in one paper with Bresnick) (en)
occupation	wds:Q57419431-7B3554DB-0A11-460B-BB4B-4C539B20DBB2
employer	wds:Q57419431-0F496E44-F949-4052-A90E-FD33AEB500EC wds:Q57419431-1329A64C-4DE8-44E1-9B13-529C6E8174C7 wds:Q57419431-2FE513E9-9D40-4B76-AA9C-963F910258A9 wds:Q57419431-4ADA40AF-0794-4CEC-A736-C10CEEF433F5 wds:Q57419431-5782A3DE-AF46-4090-9D9F-8837B7D4BD0D wds:Q57419431-9F9C1538-8F4E-4C21-8512-441BFBD228E3
sex or gender	wds:Q57419431-7FEFCE8C-0136-400E-BC22-93D8F55A67FB
ISNI	wds:Q57419431-561FFE54-7D6E-4FB2-B0B5-5056370A4319
VIAF ID	wds:Q57419431-D425F36C-110F-4EE9-9952-F8F72D5E9CF9
IdRef ID	wds:Q57419431-D2FAEB13-1DE9-4ECD-84AD-D53912C5B09F
Persée author ID	wds:Q57419431-2C0588E3-0D26-4E54-A3CF-CCA80A81548D
date of birth	wds:Q57419431-18CF107E-E60A-406E-8492-28F5C80338B0
National Library of Israel J9U ID	wds:Q57419431-93F2F49C-0BD9-49FD-BB7F-771B05235C9B
VIAF ID	http://viaf.org/viaf/43805079
IdRef ID	http://www.idref.fr/059548274/id
Persée author ID	http://data.persee.fr/person/277916
occupation	researcher
employer	National Institutes of Health Délégation Paris B Délégation Ile-de-France Sud Laboratoire Albert Fert
sex or gender	male
ISNI	0000000038433558
VIAF ID	43805079
IdRef ID	059548274
Persée author ID	277916
date of birth	1927-01-01 00:00:00Z (xsd:dateTime)
National Library of Israel J9U ID	987007354762005171
ORCID iD	wds:Q57419431-1889F388-F5C3-4DCC-AEFB-9A1906F518ED
ORCID iD	https://orcid.org/0000-0002-3694-3348
ORCID iD	0000-0002-3694-3348
ResearcherID	wds:Q57419431-FE1BDAB1-5109-4C11-8458-41CCE3A08E0B
Publons author ID	wds:Q57419431-03e12d40-a29b-4c22-8b2b-e4072dd49e24
ResearcherID	B-8384-2014
Publons author ID	1739510
Mendeley person ID	wds:Q57419431-53FC0856-26DA-40DC-BB57-95E4F3248429
Mendeley person ID	patrick-dansette2
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57419431
is author of	Unusual regioselectivity and active site topology of human cytochrome P450 2J2 A new intermediate in naphthoquinone and menaquinone biosynthesis The Substrate Binding Site of Human Liver Cytochrome P450 2C9: An Approach Using Designed Tienilic Acid Derivatives and Molecular Modeling Cytochromes P450 catalyze both steps of the major pathway of clopidogrel bioactivation, whereas paraoxonase catalyzes the formation of a minor thiol metabolite isomer. Sulfaphenazole derivatives as tools for comparing cytochrome P450 2C5 and human cytochromes P450 2Cs: identification of a new high affinity substrate common to those enzymes. Continuous fluorometric assay of epoxide hydrase activity Dehydrogenation of the indoline-containing drug 4-chloro-N-(2-methyl-1-indolinyl)-3-sulfamoylbenzamide (indapamide) by CYP3A4: correlation with in silico predictions Mutagenic and cytotoxic activity of benzol[a]pyrene 4,5-, 7,8-, and 9,10-oxides and the six corresponding phenols Effects of Inducers and Epoxide Hydrase on the Metabolism of Benzo[ a ]pyrene by Liver Microsomes and a Reconstituted System: Analysis by High Pressure Liquid Chromatography Ferrocenyl quinone methides as strong antiproliferative agents: formation by metabolic and chemical oxidation of ferrocenyl phenols. Comparison of the Substrate Specificities of Human Liver Cytochrome P450s 2C9 and 2C18: Application to the Design of a Specific Substrate of CYP 2C18 The Substrate Binding Site of Human Liver Cytochrome P450 2C9: An NMR Study† Determinants of Cytochrome P450 2C8 Substrate Binding: STRUCTURES OF COMPLEXES WITH MONTELUKAST, TROGLITAZONE, FELODIPINE, AND 9-CIS-RETINOIC ACID Epoxide hydrase and glutathione S-transferase activities with selected alkene and arene oxides in several marine species Indirect cytotoxicity of flucloxacillin toward human biliary epithelium via metabolite formation in hepatocytes. Human anti-endoplasmic reticulum autoantibodies appearing in a drug-induced hepatitis are directed against a human liver cytochrome P-450 that hydroxylates the drug Induction of drug metabolizing enzymes in the liver of diabetic mice. Carcinogenicity of benzo[a]pyrene 4,5-, 7,8-, and 9,10-oxides on mouse skin UPD-glucuronosyltransferase, epoxide hydrolase and gultathione S-transferase Synthesis of sulfaphenazole derivatives and their use as inhibitors and tools for comparing the active sites of human liver cytochromes P450 of the 2C subfamily. Diclofenac and Its Derivatives As Tools for Studying Human Cytochromes P450 Active Sites: Particular Efficiency and Regioselectivity of P450 2Cs Partial purification of human liver cytochrome P 450 Opposite Behaviors of Reactive Metabolites of Tienilic Acid and Its Isomer toward Liver Proteins: Use of Specific Anti-Tienilic Acid−Protein Adduct Antibodies and the Possible Relationship with Different Hepatotoxic Effects of the Two Compounds Selective, competitive and mechanism-based inhibitors of human cytochrome P450 2J2. Assay and partial purification of epoxide hydrase from rat liver microsomes Facile synthesis of arene oxides at the K regions of polycyclic hydrocarbons Mechanism of catalysis for the hydration of substituted styrene oxides by hepatic epoxide hydrase Oxidative metabolism of ferrocene analogues of tamoxifen: characterization and antiproliferative activities of the metabolites. Oxidative activation of the thiophene ring by hepatic enzymes. Hydroxylation and formation of electrophilic metabolites during metabolism of tienilic acid and its isomer by rat liver microsomes. Hydroxylation of the thiophene ring by hepatic monooxygenases Metabolic Activation of Prasugrel: Nature of the Two Competitive Pathways Resulting in the Opening of Its Thiophene Ring

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