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Pharmacogenomics of severe cutaneous adverse reactions and drug-induced liver injury

Journal of human genetics, 2013-06, Vol.58 (6), p.317-326

2013

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Clinical Profiles of Japanese Patients with Stevens–Johnson Syndrome/Toxic Epidermal Necrolysis Collected by a Nationwide System from 2006 to 2023

Biological and Pharmaceutical Bulletin, 2024/01/01, Vol.47(1), pp.88-97

2024

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The risk of cutaneous adverse reactions among patients with the HLA-A 31:01 allele who are given carbamazepine, oxcarbazepine or eslicarbazepine: a perspective review

Therapeutic Advances in Drug Safety, 2013-12, Vol.4 (6), p.246-253

2013

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Development of a Rapid and Inexpensive Assay for Detecting a Surrogate Genetic Polymorphism of HLA-B58:01: A Partially Predictive but Useful Biomarker for Allopurinol-related Stevens-Johnson Syndrome/toxic Epidermal Necrolysis in Japanese

DRUG METABOLISM AND PHARMACOKINETICS, 2012, Vol.27 (4), p.447-450

2012

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Drugs causing severe ocular surface involvements in Japanese patients with Stevens–Johnson syndrome/toxic epidermal necrolysis

Allergology international, 2015-10, Vol.64 (4), p.379-381

2015

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Racial variability in haplotype frequencies of UGT1A1 and glucuronidation activity of a novel single nucleotide polymorphism 686C> T (P229L) found in an African-American

Drug metabolism and disposition, 2005-03, Vol.33 (3), p.458

2005

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Prediction of Severe Adverse Drug Reactions Using Pharmacogenetic Biomarkers

DRUG METABOLISM AND PHARMACOKINETICS, 2010-01, Vol.25 (2), p.122-133

2010

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Substrate-dependent functional alterations of seven CYP2C9 variants found in Japanese subjects

Drug metabolism and disposition, 2009-09, Vol.37 (9), p.1895

2009

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Genetic Polymorphisms and Haplotypes of POR, Encoding Cytochrome P450 Oxidoreductase, in a Japanese Population

DRUG METABOLISM AND PHARMACOKINETICS, 2011-01, Vol.26 (1), p.107-116

2011

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Additive effects of drug transporter genetic polymorphisms on irinotecan pharmacokinetics/pharmacodynamics in Japanese cancer patients

Cancer chemotherapy and pharmacology, 2010-05, Vol.66 (1), p.95-105

2010

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Ethnic Differences of two Non-synonymous Single Nucleotide Polymorphisms in CDA Gene

DRUG METABOLISM AND PHARMACOKINETICS, 2009-01, Vol.24 (6), p.553-556

2009

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Utilization of Genomic Biomarkers for Post-marketing Safety of Drugs

YAKUGAKU ZASSHI, 2015/05/01, Vol.135(5), pp.671-679

Kaniwa, Nahoko

2015

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Close association of UGT1A9 IVS1+399C>T with UGT1A128, 6, or 60 haplotype and its apparent influence on 7-ethyl-10-hydroxycamptothecin (SN-38) glucuronidation in Japanese

Drug metabolism and disposition, 2009-02, Vol.37 (2), p.272

2009

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Functional characterization of human UDP-glucuronosyltransferase 1A9 variant, D256N, found in Japanese cancer patients

The Journal of pharmacology and experimental therapeutics, 2003-08, Vol.306 (2), p.688

2003

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Genetic Variation and Haplotype Structure of the ABC Transporter Gene ABCG2 in a Japanese Population

DRUG METABOLISM AND PHARMACOKINETICS, 2006-01, Vol.21 (2), p.109-121

2006

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Twenty Novel Genetic Variations and Haplotype Structures of the DCK Gene Encoding Human Deoxycytidine Kinase (dCK)

DRUG METABOLISM AND PHARMACOKINETICS, 2008-01, Vol.23 (5), p.379-384

2008

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Genetic Variations and Haplotypes of UGT1A4 in a Japanese Population

DRUG METABOLISM AND PHARMACOKINETICS, 2005, Vol.20 (2), p.144-151

2005

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Thirty Novel Genetic Variations in the SLC29A1 Gene Encoding Human Equilibrative Nucleoside Transporter 1 (hENT1)

DRUG METABOLISM AND PHARMACOKINETICS, 2006-01, Vol.21 (3), p.248-256

2006

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Genetic Variations and Frequencies of Major Haplotypes in SLCO1B1 Encoding the Transporter OATP1B1 in Japanese Subjects: SLCO1B117 is More Prevalent Than 15

DRUG METABOLISM AND PHARMACOKINETICS, 2007, Vol.22 (6), p.456-461

2007

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Haplotypes and a novel defective allele of CES2 found in a Japanese population

Drug metabolism and disposition, 2007-10, Vol.35 (10), p.1865

2007

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Genetic Variation and Haplotype Structures of the Glutathione S-transferase Genes GSTA1 and GSTA2 in Japanese Colorectal Cancer Patients

Drug metabolism and pharmacokinetics, 2011-01, Vol.26 (6), p.646-658

2011

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Genetic Polymorphisms of UGT1A6 in a Japanese Population

DRUG METABOLISM AND PHARMACOKINETICS, 2005, Vol.20 (1), p.85-90

2005

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Genetic Variations and Haplotypes of ABCC2 Encoding MRP2 in a Japanese Population

DRUG METABOLISM AND PHARMACOKINETICS, 2008-01, Vol.23 (2), p.139-147

2008

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Pharmacogenomics of severe cutaneous adverse reactions

Pharmacogenomics, 2013-04, Vol.14 (6), p.595-598

2013

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A combinatorial haplotype of the UDP-glucuronosyltransferase 1A1 gene (#60-#IB) increases total bilirubin concentrations in Japanese volunteers

Clinical chemistry (Baltimore, Md.), 2007-02, Vol.53 (2), p.356-358

2007

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Pharmacogenomics of severe cutaneous adverse reactions and drug-induced liver injury

Clinical Profiles of Japanese Patients with Stevens–Johnson Syndrome/Toxic Epidermal Necrolysis Collected by a Nationwide System from 2006 to 2023

The risk of cutaneous adverse reactions among patients with the HLA-A 31:01 allele who are given carbamazepine, oxcarbazepine or eslicarbazepine: a perspective review

Development of a Rapid and Inexpensive Assay for Detecting a Surrogate Genetic Polymorphism of HLA-B58:01: A Partially Predictive but Useful Biomarker for Allopurinol-related Stevens-Johnson Syndrome/toxic Epidermal Necrolysis in Japanese

Drugs causing severe ocular surface involvements in Japanese patients with Stevens–Johnson syndrome/toxic epidermal necrolysis

Racial variability in haplotype frequencies of UGT1A1 and glucuronidation activity of a novel single nucleotide polymorphism 686C> T (P229L) found in an African-American

Prediction of Severe Adverse Drug Reactions Using Pharmacogenetic Biomarkers

Substrate-dependent functional alterations of seven CYP2C9 variants found in Japanese subjects

Genetic Polymorphisms and Haplotypes of POR, Encoding Cytochrome P450 Oxidoreductase, in a Japanese Population

Additive effects of drug transporter genetic polymorphisms on irinotecan pharmacokinetics/pharmacodynamics in Japanese cancer patients

Ethnic Differences of two Non-synonymous Single Nucleotide Polymorphisms in CDA Gene

Utilization of Genomic Biomarkers for Post-marketing Safety of Drugs

Close association of UGT1A9 IVS1+399C>T with UGT1A128, 6, or 60 haplotype and its apparent influence on 7-ethyl-10-hydroxycamptothecin (SN-38) glucuronidation in Japanese

Functional characterization of human UDP-glucuronosyltransferase 1A9 variant, D256N, found in Japanese cancer patients

Genetic Variation and Haplotype Structure of the ABC Transporter Gene ABCG2 in a Japanese Population

Twenty Novel Genetic Variations and Haplotype Structures of the DCK Gene Encoding Human Deoxycytidine Kinase (dCK)

Genetic Variations and Haplotypes of UGT1A4 in a Japanese Population

Thirty Novel Genetic Variations in the SLC29A1 Gene Encoding Human Equilibrative Nucleoside Transporter 1 (hENT1)

Genetic Variations and Frequencies of Major Haplotypes in SLCO1B1 Encoding the Transporter OATP1B1 in Japanese Subjects: SLCO1B117 is More Prevalent Than 15

Haplotypes and a novel defective allele of CES2 found in a Japanese population

Genetic Variation and Haplotype Structures of the Glutathione S-transferase Genes GSTA1 and GSTA2 in Japanese Colorectal Cancer Patients

Genetic Polymorphisms of UGT1A6 in a Japanese Population

Genetic Variations and Haplotypes of ABCC2 Encoding MRP2 in a Japanese Population

Pharmacogenomics of severe cutaneous adverse reactions

A combinatorial haplotype of the UDP-glucuronosyltransferase 1A1 gene (#60-#IB) increases total bilirubin concentrations in Japanese volunteers

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