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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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Absence of ethnic differences in the pharmacokinetics of moxifloxacin, simvastatin, and meloxicam among three East Asian populations and Caucasians

British journal of clinical pharmacology, 2016-06, Vol.81 (6), p.1078-1090

2016

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Irinotecan pharmacokinetics/pharmacodynamics and UGT1A genetic polymorphisms in Japanese: roles of UGT1A16 and 28

Pharmacogenetics and genomics, 2007-07, Vol.17 (7), p.497-504

2007

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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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Pharmacokinetics of Gemcitabine in Japanese Cancer Patients: The Impact of a Cytidine Deaminase Polymorphism

Journal of clinical oncology, 2007-01, Vol.25 (1), p.32-42

2007

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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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Identification of a candidate single-nucleotide polymorphism related to chemotherapeutic response through a combination of knowledge-based algorithm and hypothesis-free genomic data

Journal of bioscience and bioengineering, 2013-12, Vol.116 (6), p.768-773

2013

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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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Construction of possible integrated predictive index based on EGFR and ANXA3 polymorphisms for chemotherapy response in fluoropyrimidine-treated Japanese gastric cancer patients using a bioinformatic method

BMC cancer, 2015-10, Vol.15 (1), p.718-718, Article 718

2015

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Identification of a Predictive Biomarker for Hematologic Toxicities of Gemcitabine

Journal of clinical oncology, 2009-05, Vol.27 (13), p.2261-2268

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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Survival Prediction for Pancreatic Cancer Patients Receiving Gemcitabine Treatment

Molecular & cellular proteomics, 2010-04, Vol.9 (4), p.695-704

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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Development of a simple genotyping method for the HLA-A31:01-tagging SNP in Japanese

Pharmacogenomics, 2015-10, Vol.16 (15), p.1689-1699

2015

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Genetic variations and haplotype structures of the DPYD gene encoding dihydropyrimidine dehydrogenase in Japanese and their ethnic differences

Journal of human genetics, 2007-10, Vol.52 (10), p.804-819

2007

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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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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

Absence of ethnic differences in the pharmacokinetics of moxifloxacin, simvastatin, and meloxicam among three East Asian populations and Caucasians

Irinotecan pharmacokinetics/pharmacodynamics and UGT1A genetic polymorphisms in Japanese: roles of UGT1A16 and 28

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

Pharmacokinetics of Gemcitabine in Japanese Cancer Patients: The Impact of a Cytidine Deaminase Polymorphism

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

Identification of a candidate single-nucleotide polymorphism related to chemotherapeutic response through a combination of knowledge-based algorithm and hypothesis-free genomic data

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

Construction of possible integrated predictive index based on EGFR and ANXA3 polymorphisms for chemotherapy response in fluoropyrimidine-treated Japanese gastric cancer patients using a bioinformatic method

Identification of a Predictive Biomarker for Hematologic Toxicities of Gemcitabine

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

Application of a combination of a knowledge-based algorithm and 2-stage screening to hypothesis-free genomic data on irinotecan-treated patients for identification of a candidate single nucleotide polymorphism related to an adverse effect

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

Survival Prediction for Pancreatic Cancer Patients Receiving Gemcitabine Treatment

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

Development of a simple genotyping method for the HLA-A31:01-tagging SNP in Japanese

Genetic variations and haplotype structures of the DPYD gene encoding dihydropyrimidine dehydrogenase in Japanese and their ethnic differences

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

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