(Q54455137)

30 May 2018

title

Stop codon mutations in the flavin-containing monooxygenase 3 (FMO3) gene responsible for trimethylaminuria in a Japanese population. (English)

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30 May 2018

author

Hiroshi Yamazaki

1

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30 May 2018

author name string

Haruka Fujita

2

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30 May 2018

Takaaki Gunji

3

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30 May 2018

Jun Zhang

4

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30 May 2018

Tetsuya Kamataki

5

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30 May 2018

John R Cashman

6

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30 May 2018

Makiko Shimizu

7

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30 May 2018

publication date

25 September 2006

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30 May 2018

Molecular Genetics and Metabolism

published in

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30 May 2018

volume

90

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30 May 2018

issue

1

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30 May 2018

page(s)

58-63

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30 May 2018

An overview of the mechanism, substrate specificities, and structure of FMOs

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Organization and evolution of the flavin-containing monooxygenase genes of human and mouse: identification of novel gene and pseudogene clusters.

7 January 2021

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Molecular cloning of the flavin-containing monooxygenase (form II) cDNA from adult human liver

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Quantitative analysis of FMO gene mRNA levels in human tissues

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Quantitation and kinetic properties of hepatic microsomal and recombinant flavin-containing monooxygenases 3 and 5 from humans

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Human hepatic flavin-containing monooxygenases 1 (FMO1) and 3 (FMO3) developmental expression

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Trimethylaminuria and a human FMO3 mutation database

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Deleterious mutations in the flavin-containing monooxygenase 3 (FMO3) gene causing trimethylaminuria

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Flavin-containing monooxygenase genetic polymorphism: impact on chemical metabolism and drug development.

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Interindividual differences of human flavin-containing monooxygenase 3: genetic polymorphisms and functional variation

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Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication

7 January 2021

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Biochemical and clinical aspects of the human flavin-containing monooxygenase form 3 (FMO3) related to trimethylaminuria.

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Trimethylaminuria: susceptibility of heterozygotes

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Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome

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The implications of polymorphisms in mammalian flavin-containing monooxygenases in drug discovery and development

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Two novel single nucleotide polymorphisms (SNPs) of the FMO3 gene in Japanese.

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Effects of the dietary supplements, activated charcoal and copper chlorophyllin, on urinary excretion of trimethylamine in Japanese trimethylaminuria patients

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A mutation in the flavin-containing monooxygenase 3 gene and its effects on catalytic activity for N-oxidation of trimethylamine in vitro

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Two new polymorphisms of the FMO3 gene in Caucasian and African-American populations: comparative genetic and functional studies

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Three Novel Single Nucleotide Polymorphisms of the FMO3 Gene in a Japanese Population

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Structural organization of the human flavin-containing monooxygenase 3 gene (FMO3), the favored candidate for fish-odor syndrome, determined directly from genomic DNA

7 January 2021

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Mechanism of action of a flavin-containing monooxygenase

7 January 2021

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Mild trimethylaminuria observed in a Japanese cohort with liver damage

7 January 2021

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Discovery of novel flavin-containing monooxygenase 3 (FMO3) single nucleotide polymorphisms and functional analysis of upstream haplotype variants

7 January 2021

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Alternative processing events in human FMO genes

7 January 2021

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10.1016/J.YMGME.2006.08.008

7 January 2021

Identifiers

DOI

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30 May 2018

PubMed ID

16996766

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30 May 2018