Trimethylaminuria: causes and diagnosis of a socially distressing condition - Wikidata - wikimedia - TriplyDB

Trimethylaminuria: causes and diagnosis of a socially distressing condition

Trimethylaminuria: causes and diagnosis of a socially distressing condition

http://www.wikidata.org/entity/Q24604974

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Association of FMO3 Variants and Trimethylamine N-Oxide Concentration, Disease Progression, and Mortality in CKD Patients Archaebiotics: proposed therapeutic use of archaea to prevent trimethylaminuria and cardiovascular disease.Archaea and the human gut: new beginning of an old story.Betaine and Trimethylamine-N-Oxide as Predictors of Cardiovascular Outcomes Show Different Patterns in Diabetes Mellitus: An Observational Study Comparative genomics highlights the unique biology of Methanomassiliicoccales, a Thermoplasmatales-related seventh order of methanogenic archaea that encodes pyrrolysine.Fish Malodour syndrome in a child Clinical utility gene card for: trimethylaminuria.Clinical utility gene card for: Trimethylaminuria - update 2014 Halitosis: the multidisciplinary approach.Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing Microbial conversion of choline to trimethylamine requires a glycyl radical enzyme A review of trimethylaminuria: (fish odor syndrome).Idiosyncratic Drug-Induced Liver Injury (IDILI): Potential Mechanisms and Predictive Assays.Relationships between flavin-containing mono-oxygenase 3 (FMO3) genotype and trimethylaminuria phenotype in a Japanese population.Metagenomic data-mining reveals contrasting microbial populations responsible for trimethylamine formation in human gut and marine ecosystems.Genomics and metagenomics of trimethylamine-utilizing Archaea in the human gut microbiome.Intestinal microbial metabolism of phosphatidylcholine: a novel insight in the cardiovascular risk scenario.Transient massive trimethylaminuria associated with food protein-induced enterocolitis syndrome.Immunogenic properties of the human gut-associated archaeon Methanomassiliicoccus luminyensis and its susceptibility to antimicrobial peptides.Growth Characteristics of Methanomassiliicoccus luminyensis and Expression of Methyltransferase Encoding Genes.Faecal microbiota transplantation in patients with Clostridium difficile and significant comorbidities as well as in patients with new indications: A case series.Trimethylaminuria.

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P2860

Trimethylaminuria: causes and diagnosis of a socially distressing condition

http://www.wikidata.org/entity/Q24604974

description

2011 nî lūn-bûn

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2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2011 թվականի փետրվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Trimethylaminuria: causes and diagnosis of a socially distressing condition

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Trimethylaminuria: causes and diagnosis of a socially distressing condition

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Trimethylaminuria: causes and diagnosis of a socially distressing condition

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Trimethylaminuria: causes and diagnosis of a socially distressing condition

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Trimethylaminuria: causes and diagnosis of a socially distressing condition

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Trimethylaminuria: causes and diagnosis of a socially distressing condition

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Trimethylaminuria: causes and diagnosis of a socially distressing condition

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Trimethylaminuria: causes and diagnosis of a socially distressing condition

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Clinical Biochemist Reviews

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Trimethylaminuria: causes and diagnosis of a socially distressing condition

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Caroline Henderson

http://www.w3.org/2001/XMLSchema#string

Christopher J McEntyre

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Michael Lever

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Peter M George

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Richard J Mackay

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P2860

Trimethylaminuria: the fish-odour syndrome

Mild trimethylaminuria caused by common variants in FMO3 gene

Two novel mutations of the FMO3 gene in a proband with trimethylaminuria

Identification of novel variants of the flavin-containing monooxygenase gene family in African Americans

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

Trimethylamine N-oxide synthesis: a human variant

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

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

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

Quantitative analysis of FMO gene mRNA levels in human tissues

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