(Q28367534)

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Frequencies of thiopurine S-methyltransferase mutant alleles (TPMT2, 3A, 3B and 3C) in 151 healthy Japanese subjects and the inheritance of TPMT*3C in the family of a propositus

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scholarly article

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Frequencies of thiopurine S-methyltransferase mutant alleles (TPMT*2, *3A, *3B and *3C) in 151 healthy Japanese subjects and the inheritance of TPMT*3C in the family of a propositus (English)

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author name string

T Kubota

1

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K Chiba

2

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language of work or name

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publication date

May 2001

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British Journal of Clinical Pharmacology

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51

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5

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475-7

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Detection of known and new mutations in the thiopurine S-methyltransferase gene by single-strand conformation polymorphism analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014472

20 March 2017

Human thiopurine methyltransferase pharmacogenetics: gene sequence polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014472

20 March 2017

Enhanced proteolysis of thiopurine S-methyltransferase (TPMT) encoded by mutant alleles in humans (TPMT*3A, TPMT*2): mechanisms for the genetic polymorphism of TPMT activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014472

20 March 2017

Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014472

20 March 2017

Genetic polymorphism of thiopurine S-methyltransferase: clinical importance and molecular mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014472

20 March 2017

Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014472

20 March 2017

Human thiopurine methyltransferase pharmacogenetics. Kindred with a terminal exon splice junction mutation that results in loss of activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2014472

29 September 2017

Genotypic and phenotypic analysis of the polymorphic thiopurine S-methyltransferase gene (TPMT) in a European population.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2001.01371.X

21 January 2018

Thiopurine methyltransferase alleles in British and Ghanaian populations

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2125.2001.01371.X

21 January 2018

Thiopurine methyltransferase genotype and the toxicity of azathioprine in Japanese

1 reference

https://pubmed.ncbi.nlm.nih.gov/11422006

12 December 2020

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Detection assay of rare variants of the thiopurine methyltransferase gene by PCR-RFLP using a mismatch primer in a Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/11422006

12 December 2020

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Azathioprine-induced myelosuppression in thiopurine methyltransferase deficient heart transplant recipient

1 reference

https://pubmed.ncbi.nlm.nih.gov/11422006

12 December 2020

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Thiopurine methyltransferase activity in American white subjects and black subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/11422006

12 December 2020

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Polymorphism of the thiopurine S-methyltransferase gene in African-Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/11422006

12 December 2020

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The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/11422006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of thiopurine methyltransferase polymorphism in a Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/11422006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1046/J.1365-2125.2001.01371.X

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