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1.	Hiratsuka, M, et al. (author) GENETIC POLYMORPHISMS AND HAPLOTYPE STRUCTURES OF THE CYP2W1 GENE IN A JAPANESE POPULATION 2007 In: DRUG METABOLISM REVIEWS. - 0360-2532. ; 39, s. 159-160 Conference paper (other academic/artistic)
2.	Santos, M, et al. (author) NOVEL COPY NUMBER VARIANTS IN PHARMACOGENES CONTRIBUTE TO INTERINDIVIDUAL DIFFERENCES IN DRUG PHARMACOKINETICS 2018 In: BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY. - 1742-7835. ; 123, s. 89-89 Conference paper (other academic/artistic)
3.	Santos, M, et al. (author) Novel copy-number variations in pharmacogenes contribute to interindividual differences in drug pharmacokinetics 2018 In: Genetics in medicine : official journal of the American College of Medical Genetics. - : Elsevier BV. - 1530-0366. ; 20:6, s. 622-629 Journal article (peer-reviewed)
4.	Santos, M, et al. (author) Novel copy-number variations in pharmacogenes contribute to interindividual differences in drug pharmacokinetics 2019 In: EUROPEAN JOURNAL OF HUMAN GENETICS. - 1018-4813. ; 27, s. 545-546 Conference paper (other academic/artistic)
5.	Lofgren, S, et al. (author) Generation of mice transgenic for human CYP2C18 and CYP2C19: characterization of the sexually dimorphic gene and enzyme expression 2008 In: Drug metabolism and disposition: the biological fate of chemicals. - : American Society for Pharmacology & Experimental Therapeutics (ASPET). - 1521-009X. ; 36:5, s. 955-962 Journal article (peer-reviewed)
6.	Jukic, MM, et al. (author) Functional characterization of CYP2D7 gene variants 2018 In: Pharmacogenomics. - : Future Medicine Ltd. - 1744-8042 .- 1462-2416. ; 19:12, s. 931-936 Journal article (peer-reviewed)abstract The ultrarapid CYP2D6 metabolizer (UM) phenotype is caused by CYP2D6 gene duplications in some, but not all, UM individuals. CYP2D6 and the adjacent pseudogene CYP2D7 are highly homologous; however, CYP2D7 harbors a premature stop codon, which is absent in carriers of the rare CYP2D7 variant rs530303678. We addressed whether rs530303678 could generate a functionally active protein, causing the UM phenotype. However, unlike CYP2D6 variants, two CYP2D7 rs530303678 variant isoforms, previously described in liver, showed neither significant protein expression nor catalytic activity toward the CYP2D6 substrates bufuralol or dextromethorphan. We conclude that loss of the stop codon in CYP2D7 does not result in the generation of enzymatically active protein in human liver and thus, cannot cause the UM phenotype.
7.	Musyoka, K, et al. (author) CYP3A4 gene variants in residents of Lake Victoria region, Kenya, 2013 2023 In: TROPICAL MEDICINE & INTERNATIONAL HEALTH. - 1360-2276. ; 28, s. 136-136 Conference paper (other academic/artistic)
8.	Rico, EMG, et al. (author) CYP2D6 genotyping analysis and functional characterization of novel allelic variants in a Ni-Vanuatu and Kenyan population by assessing dextromethorphan O-demethylation activity 2020 In: Drug metabolism and pharmacokinetics. - : Elsevier BV. - 1880-0920 .- 1347-4367. ; 35:1, s. 89-101 Journal article (peer-reviewed)
9.	Siamoglou, S, et al. (author) Identification and functional validation of novel pharmacogenomic variants using a next-generation sequencing-based approach for clinical pharmacogenomics 2022 In: Pharmacological research. - 1096-1186. ; 176, s. 106087- Journal article (peer-reviewed)
10.	Siamoglou, S, et al. (author) Identification and functional validation of novel pharmacogenomic variants using a next-generation sequencing-based approach for clinical pharmacogenomics 2022 In: Pharmacological research. - : Elsevier BV. - 1096-1186 .- 1043-6618. ; 176, s. 106087- Journal article (peer-reviewed)
11.	Zhou, YT, et al. (author) An optimized prediction framework to assess the functional impact of pharmacogenetic variants 2019 In: The pharmacogenomics journal. - : Springer Science and Business Media LLC. - 1473-1150 .- 1470-269X. ; 19:2, s. 115-126 Journal article (peer-reviewed)
12.	Zhou, Y, et al. (author) AN OPTIMIZED PREDICTION FRAMEWORK TO ASSESS THE FUNCTIONAL IMPACT OF PHARMACOGENETIC VARIANTS 2018 In: BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY. - 1742-7835. ; 123, s. 5-5 Conference paper (other academic/artistic)
13.	Hiratsuka, M, et al. (author) Editorial: Population Pharmacogenomics (PGx): From Variant Identification to Clinical Implementation 2021 In: Frontiers in genetics. - : Frontiers Media SA. - 1664-8021. ; 12, s. 736626- Journal article (other academic/artistic)

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Result 1-13 of 13

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Type of publication: journal article (8); conference paper (5)

Type of content: peer-reviewed (7); other academic/artistic (6)

Author/Editor: Hiratsuka, M (13); Lauschke, VM (8); Ingelman-Sundberg, M (6); Kumondai, M (6); Zhou, YT (4); Rodriguez-Antona, C (3); show more...; Niemi, M (3); Santos, M (3); Zhou, Y. (2); Saito, T (2); Mkrtchian, S (2); Kaneko, A (2); Fukunaga, K (2); Mushiroda, T. (2); Patrinos, GP (2); YAMAZAKI, S (2); Gitaka, J (2); Koromina, M (2); Kordou, Z (2); Tsermpini, EE (2); Sasaki, T. (1); Saito, S. (1); Ishikawa, M (1); Gomez, A. (1); Terelius, Y (1); Karlgren, M (1); Lindqvist, A (1); Ngara, M (1); Lofgren, S (1); Lauschke, V (1); Baldwin, RM (1); Chan, C (1); Chan, CW (1); Jukic, MM (1); Sim, SC (1); Tachibana, M (1); Kongere, J (1); Fransson-Steen, R (1); Hanzawa, Y (1); Sakuyama, K (1); Mizugaki, M (1); Kikuchi, A. (1); Kagaya, W (1); Omondi, P (1); Carlberg, A (1); Schulke, M (1); Snait, M (1); Edenro, A (1); Musyoka, K (1); Kijogi, C (1); show less...

University: Karolinska Institutet (13)

Language: English (13)

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