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Results: 1 to 20 of 193

1.

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
[PubMed - indexed for MEDLINE]
2.

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
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
5.

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
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

A novel mutation in the flavin-containing monooxygenase 3 gene (FMO3) of a Norwegian family causes trimethylaminuria.

Allerston CK, Vetti HH, Houge G, Phillips IR, Shephard EA.

Mol Genet Metab. 2009 Sep-Oct;98(1-2):198-202. doi: 10.1016/j.ymgme.2009.06.002. Epub 2009 Jun 6.

PMID:
19577495
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

Fishy taint in chicken eggs is associated with a substitution within a conserved motif of the FMO3 gene.

Honkatukia M, Reese K, Preisinger R, Tuiskula-Haavisto M, Weigend S, Roito J, Mäki-Tanila A, Vilkki J.

Genomics. 2005 Aug;86(2):225-32.

PMID:
15916878
[PubMed - indexed for MEDLINE]
10.

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
[PubMed - indexed for MEDLINE]
11.

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

Dolphin CT, Riley JH, Smith RL, Shephard EA, Phillips IR.

Genomics. 1997 Dec 1;46(2):260-7.

PMID:
9417913
[PubMed - indexed for MEDLINE]
12.

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
[PubMed - indexed for MEDLINE]
13.

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
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
16.
17.

Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohort.

Akerman BR, Lemass H, Chow LM, Lambert DM, Greenberg C, Bibeau C, Mamer OA, Treacy EP.

Mol Genet Metab. 1999 Sep;68(1):24-31.

PMID:
10479479
[PubMed - indexed for MEDLINE]
18.

Phenotypes of flavin-containing monooxygenase activity determined by ranitidine N-oxidation are positively correlated with genotypes of linked FM03 gene mutations in a Korean population.

Kang JH, Chung WG, Lee KH, Park CS, Kang JS, Shin IC, Roh HK, Dong MS, Baek HM, Cha YN.

Pharmacogenetics. 2000 Feb;10(1):67-78.

PMID:
10739174
[PubMed - indexed for MEDLINE]
19.

Novel variants of the human flavin-containing monooxygenase 3 (FMO3) gene associated with trimethylaminuria.

Motika MS, Zhang J, Zheng X, Riedler K, Cashman JR.

Mol Genet Metab. 2009 Jun;97(2):128-35. doi: 10.1016/j.ymgme.2009.02.006. Epub 2009 Feb 27.

PMID:
19321370
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

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
[PubMed - indexed for MEDLINE]
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