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Items: 1 to 20 of 79

1.

Genetic polymorphisms of glycine N-acyltransferase (GLYAT) in a French Caucasian population.

Lino Cardenas CL, Bourgine J, Cauffiez C, Allorge D, Lo-Guidice JM, Broly F, Chevalier D.

Xenobiotica. 2010 Dec;40(12):853-61. doi: 10.3109/00498254.2010.519407. Epub 2010 Oct 7.

PMID:
20925583
2.

Genetic polymorphisms of glycine N-acyltransferase in Japanese individuals.

Yamamoto A, Nonen S, Fukuda T, Yamazaki H, Azuma J.

Drug Metab Pharmacokinet. 2009;24(1):114-7.

3.

Enzymatic characterization and elucidation of the catalytic mechanism of a recombinant bovine glycine N-acyltransferase.

Badenhorst CP, Jooste M, van Dijk AA.

Drug Metab Dispos. 2012 Feb;40(2):346-52. doi: 10.1124/dmd.111.041657. Epub 2011 Nov 9.

PMID:
22071172
4.

Conservation of the coding regions of the glycine N-acyltransferase gene further suggests that glycine conjugation is an essential detoxification pathway.

van der Sluis R, Badenhorst CP, Erasmus E, van Dyk E, van der Westhuizen FH, van Dijk AA.

Gene. 2015 Oct 15;571(1):126-34. doi: 10.1016/j.gene.2015.06.081. Epub 2015 Jul 3.

PMID:
26149650
5.

Genetic polymorphism of bile acid CoA: amino acid N-acyltransferase in Japanese individuals.

Tougou K, Fukuda T, Ito T, Yamazaki H, Fujio Y, Azuma J.

Drug Metab Pharmacokinet. 2007 Apr;22(2):125-8.

6.

Characterisation of novel defective thiopurine S-methyltransferase allelic variants.

Garat A, Cauffiez C, Renault N, Lo-Guidice JM, Allorge D, Chevalier D, Houdret N, Chavatte P, Loriot MA, Gala JL, Broly F.

Biochem Pharmacol. 2008 Aug 1;76(3):404-15. doi: 10.1016/j.bcp.2008.05.009. Epub 2008 May 18.

PMID:
18602085
7.

[The association between polymorphism of the serotonin 2A, 2C receptor genes and obstructive sleep apnea-hypopnea syndrome in Han population].

Zhu JY, Hu K, Ma ZS, Liu D.

Zhonghua Jie He He Hu Xi Za Zhi. 2007 Dec;30(12):912-7. Chinese.

PMID:
18336767
8.

Ethnic differences in the distribution of CYP3A5 gene polymorphisms.

Quaranta S, Chevalier D, Allorge D, Lo-Guidice JM, Migot-Nabias F, Kenani A, Imbenotte M, Broly F, Lacarelle B, Lhermitte M.

Xenobiotica. 2006 Dec;36(12):1191-200.

PMID:
17162466
9.

Characterisation of the influence of genetic variations on the enzyme activity of a recombinant human glycine N-acyltransferase.

van der Sluis R, Badenhorst CP, van der Westhuizen FH, van Dijk AA.

Gene. 2013 Feb 25;515(2):447-53. doi: 10.1016/j.gene.2012.12.003. Epub 2012 Dec 10.

PMID:
23237781
10.

DNA sequence variants of the platelet-derived growth factor A-chain gene.

Baron R, Silverman ES, Grasemann H, Collins T, Drazen JM.

Clin Exp Allergy. 2001 Oct;31(10):1501-8.

PMID:
11678848
11.

Identification of genetic polymorphisms of CYP2S1 in a Finnish Caucasian population.

Saarikoski ST, Suitiala T, Holmila R, Impivaara O, Järvisalo J, Hirvonen A, Husgafvel-Pursiainen K.

Mutat Res. 2004 Oct 4;554(1-2):267-77.

PMID:
15450424
12.

The interferon-gamma receptor gene polymorphisms (Val14Met and Gln64Arg) are not associated with systemic lupus erythematosus in Chinese patients.

Yao X, Chen ZQ, Gong JQ, Chen M, Li AS, Liu J.

Arch Dermatol Res. 2007 Oct;299(8):367-71. Epub 2007 Jul 6.

PMID:
17618444
13.

Histamine N-methyltransferase gene polymorphisms in Chinese and their relationship with enzyme activity in erythrocytes.

Chen GL, Wang H, Wang W, Xu ZH, Zhou G, He F, Zhou HH.

Pharmacogenetics. 2003 Jul;13(7):389-97.

PMID:
12835614
14.
15.

The human FE65 gene: genomic structure and an intronic biallelic polymorphism associated with sporadic dementia of the Alzheimer type.

Hu Q, Kukull WA, Bressler SL, Gray MD, Cam JA, Larson EB, Martin GM, Deeb SS.

Hum Genet. 1998 Sep;103(3):295-303.

PMID:
9799084
16.

Identification of novel polymorphisms in the 5' flanking region of CYP1A2, characterization of interethnic variability, and investigation of their functional significance.

Aitchison KJ, Gonzalez FJ, Quattrochi LC, Sapone A, Zhao JH, Zaher H, Elizondo G, Bryant C, Munro J, Collier DA, Makoffa AI, Kerwin RW.

Pharmacogenetics. 2000 Nov;10(8):695-704.

PMID:
11186132
17.

Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South Africa.

Pang H, Liu Y, Koda Y, Soejima M, Jia J, Schlaphoff T, Du Toit ED, Kimura H.

Hum Genet. 1998 Jun;102(6):675-80.

PMID:
9703429
18.

Analysis of CYP1A1 exon 7 polymorphisms by PCR-SSCP in a Brazilian population and description of two novel gene variations.

Amorim LM, Lotsch PF, Simão Td Tde A, Gallo CV, Pinto LF.

Mutat Res. 2004 Mar 22;547(1-2):35-40.

PMID:
15013696
19.

Interleukin-4 gene polymorphisms in Japanese and Caucasian patients with aggressive periodontitis.

Gonzales JR, Kobayashi T, Michel J, Mann M, Yoshie H, Meyle J.

J Clin Periodontol. 2004 May;31(5):384-9.

PMID:
15086621
20.

Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.

Hutcheson KA, Paluru PC, Bernstein SL, Koh J, Rappaport EF, Leach RA, Young TL.

Mol Vis. 2005 Jul 14;11:501-8.

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