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Items: 1 to 20 of 172

1.
2.

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

Dolphin CT, Janmohamed A, Smith RL, Shephard EA, Phillips IR.

Nat Genet. 1997 Dec;17(4):491-4.

PMID:
9398858
3.

Human flavin-containing monooxygenase form 3: cDNA expression of the enzymes containing amino acid substitutions observed in individuals with trimethylaminuria.

Cashman JR, Bi YA, Lin J, Youil R, Knight M, Forrest S, Treacy E.

Chem Res Toxicol. 1997 Aug;10(8):837-41.

PMID:
9282831
4.

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

Zhang J, Tran Q, Lattard V, Cashman JR.

Pharmacogenetics. 2003 Aug;13(8):495-500.

PMID:
12893987
5.

A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuria.

Forrest SM, Knight M, Akerman BR, Cashman JR, Treacy EP.

Pharmacogenetics. 2001 Mar;11(2):169-74.

PMID:
11266081
6.

Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FM03) gene in patients with fish-odour syndrome.

Dolphin CT, Janmohamed A, Smith RL, Shephard EA, Phillips IR.

Pharmacogenetics. 2000 Dec;10(9):799-807.

PMID:
11191884
7.

A novel mutation in the flavin-containing monooxygenase 3 gene, FM03, that causes fish-odour syndrome: activity of the mutant enzyme assessed by proton NMR spectroscopy.

Murphy HC, Dolphin CT, Janmohamed A, Holmes HC, Michelakakis H, Shephard EA, Chalmers RA, Phillips IR, Iles RA.

Pharmacogenetics. 2000 Jul;10(5):439-51.

PMID:
10898113
8.

A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene.

Teresa E, Lonardo F, Fiumara A, Lombardi C, Russo P, Zuppi C, Scarano G, Musumeci S, Gianfrancesco F.

Mol Genet Metab. 2006 Jun;88(2):192-5. Epub 2006 Apr 4.

PMID:
16600650
9.

Mutation, polymorphism and perspectives for the future of human flavin-containing monooxygenase 3.

Zhou J, Shephard EA.

Mutat Res. 2006 Jun;612(3):165-71. Epub 2006 Feb 14. Review.

PMID:
16481213
10.

Trimethylaminuria (fish odor syndrome): genotype characterization among Portuguese patients.

Ferreira F, Esteves S, Almeida LS, Gaspar A, da Costa CD, Janeiro P, Bandeira A, Martins E, Teles EL, Garcia P, Azevedo L, Vilarinho L.

Gene. 2013 Sep 15;527(1):366-70. doi: 10.1016/j.gene.2013.05.025. Epub 2013 Jun 17.

PMID:
23791655
11.

Sequence variations in the flavin-containing mono-oxygenase 3 gene (FMO3) in fish odour syndrome.

Basarab T, Ashton GH, Menagé HP, McGrath JA.

Br J Dermatol. 1999 Jan;140(1):164-7.

PMID:
10215790
12.

Phenotyping of flavin-containing monooxygenase using caffeine metabolism and genotyping of FMO3 gene in a Korean population.

Park CS, Chung WG, Kang JH, Roh HK, Lee KH, Cha YN.

Pharmacogenetics. 1999 Apr;9(2):155-64.

PMID:
10376762
14.

A nonsense mutation in the FMO3 gene underlies fishy off-flavor in cow's milk.

Lundén A, Marklund S, Gustafsson V, Andersson L.

Genome Res. 2002 Dec;12(12):1885-8.

15.

FMO3 allelic variants in Sicilian and Sardinian populations: trimethylaminuria and absence of fish-like body odor.

D'Angelo R, Esposito T, Calabrò M, Rinaldi C, Robledo R, Varriale B, Sidoti A.

Gene. 2013 Feb 25;515(2):410-5. doi: 10.1016/j.gene.2012.12.047. Epub 2012 Dec 21.

PMID:
23266626
16.

Trimethylaminuria and a human FMO3 mutation database.

Hernandez D, Addou S, Lee D, Orengo C, Shephard EA, Phillips IR.

Hum Mutat. 2003 Sep;22(3):209-13. Review.

PMID:
12938085
17.

Molecular cloning, sequencing, and expression in Escherichia coli of mouse flavin-containing monooxygenase 3 (FMO3): comparison with the human isoform.

Falls JG, Cherrington NJ, Clements KM, Philpot RM, Levi PE, Rose RL, Hodgson E.

Arch Biochem Biophys. 1997 Nov 1;347(1):9-18.

PMID:
9344459
18.

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

Yamazaki H, Fujita H, Gunji T, Zhang J, Kamataki T, Cashman JR, Shimizu M.

Mol Genet Metab. 2007 Jan;90(1):58-63. Epub 2006 Sep 25.

PMID:
16996766
19.
20.

Population-specific polymorphisms of the human FMO3 gene: significance for detoxication.

Cashman JR, Akerman BR, Forrest SM, Treacy EP.

Drug Metab Dispos. 2000 Feb;28(2):169-73.

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