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Functional analysis of CYP2D6.31 variant: Homology modeling suggests possible disruption of redox partner interaction by Arg440His substitution.
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- Proteins, 2005, v. 59, n. 2, p. 339, doi. 10.1002/prot.20399
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- Article
Characterization of new mutations in the coding sequence and 5'-untranslated region of the human prostacyclin synthase gene (CYP8A1).
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- Human Genetics, 2001, v. 108, n. 2, p. 148, doi. 10.1007/s004390000444
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- Article
Arachidonic acid ω-hydroxylase CYP4A11: inter-ethnic variations in the 8590T>C loss-of-function variant.
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- Molecular Biology Reports, 2012, v. 39, n. 2, p. 1503, doi. 10.1007/s11033-011-0888-x
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- Article
Identification of a novel splice-site mutation in the CYP1A2 gene.
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- British Journal of Clinical Pharmacology, 2003, v. 56, n. 3, p. 341, doi. 10.1046/j.1365-2125.2003.01858.x
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First report of a genetic polymorphism of the cytochrome P450 3A43 (CYP3A43) gene: Identification of a loss-of-function variant (Communicated by Richard G.H. Cotton) Online Citation: Human Mutation, Mutation in Brief #682 (2003) Online http://www.interscience.wiley.com/homepages/38515/pdf/mutation/682.pdf)
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- Human Mutation, 2004, v. 23, n. 1, p. 101, doi. 10.1002/humu.9211
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- Article
Detection of known and new mutations in the thiopurine S-methyltransferase gene by single-strand conformation polymorphism analysis.
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- Human Mutation, 1998, v. 12, n. 3, p. 177, doi. 10.1002/(SICI)1098-1004(1998)12:3<177::AID-HUMU5>3.0.CO;2-E
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- Article
Tungsten Carbide-Cobalt as a Nanoparticulate Reference Positive Control in In Vitro Genotoxicity Assays.
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- Toxicological Sciences, 2014, v. 137, n. 1, p. 125, doi. 10.1093/toxsci/kft222
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- Article