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Trimethylaminuria has an autosomal recessive pattern of inheritance. Most cases of trimethylaminuria appear to be inherited in an autosomal recessive pattern, which means two copies of the gene in each cell are altered. The parents of an individual with an autosomal recessive disorder are both carriers of one copy of the altered gene.
Trimethylaminuria is a rare defect in the production of the enzyme flavin-containing monooxygenase 3 (FMO3). [19] [20] Those suffering from trimethylaminuria are unable to convert choline-derived trimethylamine into trimethylamine oxide. Trimethylamine then accumulates and is released in the person's sweat, urine, and breath, giving off a ...
2328 14262 Ensembl ENSG00000007933 ENSMUSG00000026691 UniProt P31513 P97501 RefSeq (mRNA) NM_001002294 NM_006894 NM_001319173 NM_001319174 NM_008030 RefSeq (protein) NP_001002294 NP_001306102 NP_001306103 NP_008825 NP_032056 Location (UCSC) Chr 1: 171.09 – 171.12 Mb Chr 1: 162.78 – 162.81 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Flavin-containing monooxygenase 3 (FMO3 ...
Knowing—and manipulating—your "biological age"is certainly en vogue right, with longevity bros and our surging wellness era taking center stage in the public consciousness.But while it may be ...
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Trimethylamine (TMA) is an organic compound with the formula N(CH 3) 3.It is a trimethylated derivative of ammonia.TMA is widely used in industry. [5] [6] At higher concentrations it has an ammonia-like odor, and can cause necrosis of mucous membranes on contact. [7]
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