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Results: 1 to 20 of 215

Similar articles for PubMed (Select 11191884)

1.

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
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.

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
4.

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
5.

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
6.

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
7.

Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children.

Chalmers RA, Bain MD, Michelakakis H, Zschocke J, Iles RA.

J Inherit Metab Dis. 2006 Feb;29(1):162-72.

PMID:
16601883
8.

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
9.

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.

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
12.
13.

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
14.

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
15.

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
16.

Functional characterization of genetic variants of human FMO3 associated with trimethylaminuria.

Yeung CK, Adman ET, Rettie AE.

Arch Biochem Biophys. 2007 Aug 15;464(2):251-9. Epub 2007 May 2.

17.

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

Akerman BR, Forrest S, Chow L, Youil R, Knight M, Treacy EP.

Hum Mutat. 1999;13(5):376-9.

PMID:
10338091
18.

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

Shimizu M, Kobayashi Y, Hayashi S, Aoki Y, Yamazaki H.

Mol Genet Metab. 2012 Nov;107(3):330-4. doi: 10.1016/j.ymgme.2012.06.014. Epub 2012 Jul 1.

PMID:
22819296
19.

[Fish odour--could be a sign of trimethylaminuria].

Haugaard LK, Lund AM, Patursson P, Christensen E.

Ugeskr Laeger. 2010 Nov 22;172(47):3268-9. Danish.

PMID:
21092725
20.

In vivo variability of TMA oxidation is partially mediated by polymorphisms of the FMO3 gene.

Lambert DM, Mamer OA, Akerman BR, Choinière L, Gaudet D, Hamet P, Treacy EP.

Mol Genet Metab. 2001 Jul;73(3):224-9.

PMID:
11461189
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