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Items: 1 to 20 of 1708

1.

Patterns of genetic variation in the hypertension candidate gene GRK4: ethnic variation and haplotype structure.

Lohmueller KE, Wong LJ, Mauney MM, Jiang L, Felder RA, Jose PA, Williams SM.

Ann Hum Genet. 2006 Jan;70(Pt 1):27-41.

2.
4.

Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype.

Kim KS, Kim GS, Hwang JY, Lee HJ, Park MH, Kim KJ, Jung J, Cha HS, Shin HD, Kang JH, Park EK, Kim TH, Hong JM, Koh JM, Oh B, Kimm K, Kim SY, Lee JY.

BMC Med Genet. 2007 Nov 26;8:70.

5.

Sequence variation of bradykinin receptors B1 and B2 and association with hypertension.

Cui J, Melista E, Chazaro I, Zhang Y, Zhou X, Manolis AJ, Baldwin CT, Destefano AL, Gavras H.

J Hypertens. 2005 Jan;23(1):55-62.

PMID:
15643125
6.

Haplotype structure and evidence for positive selection at the human IL13 locus.

Zhou G, Zhai Y, Dong X, Zhang X, He F, Zhou K, Zhu Y, Wei H, Yao Z, Zhong S, Shen Y, Qiang B, He F.

Mol Biol Evol. 2004 Jan;21(1):29-35. Epub 2003 Aug 29.

PMID:
12949127
7.

Single-nucleotide polymorphisms in the interleukin-10 gene: differences in frequencies, linkage disequilibrium patterns, and haplotypes in three United States ethnic groups.

Lazarus R, Klimecki WT, Palmer LJ, Kwiatkowski DJ, Silverman EK, Brown A, Martinez F, Weiss ST.

Genomics. 2002 Aug;80(2):223-8.

PMID:
12160736
8.

Association of specific haplotypes of D2 dopamine receptor gene with vulnerability to heroin dependence in 2 distinct populations.

Xu K, Lichtermann D, Lipsky RH, Franke P, Liu X, Hu Y, Cao L, Schwab SG, Wildenauer DB, Bau CH, Ferro E, Astor W, Finch T, Terry J, Taubman J, Maier W, Goldman D.

Arch Gen Psychiatry. 2004 Jun;61(6):597-606.

PMID:
15184239
9.

Sequence polymorphism at the human apolipoprotein AII gene ( APOA2): unexpected deficit of variation in an African-American sample.

Fullerton SM, Clark AG, Weiss KM, Taylor SL, Stengård JH, Salomaa V, Boerwinkle E, Nickerson DA.

Hum Genet. 2002 Jul;111(1):75-87. Epub 2002 Jun 14. Erratum in: Hum Genet 2002 Dec;111(6):577-8.

PMID:
12136239
10.

Haplotype frequency distribution and linkage disequilibrium analysis of single nucleotide polymorphisms at the human FMO3 gene locus.

Hao DC, Sun J, Furnes B, Schlenk D, Hou ZF, Zhang YP, Yang SL, Yang L.

Biochem Genet. 2006 Oct;44(7-8):391-407. Epub 2006 Nov 10.

PMID:
17096187
12.

Analysis of allele and haplotype diversity across 25 genomic regions in three Eastern European populations.

Khrunin A, Mihailov E, Nikopensius T, Krjutskov K, Limborska S, Metspalu A.

Hum Hered. 2009;68(1):35-44. doi: 10.1159/000210447. Epub 2009 Apr 1.

PMID:
19339784
13.

Redefinition of the human kappa opioid receptor gene (OPRK1) structure and association of haplotypes with opiate addiction.

Yuferov V, Fussell D, LaForge KS, Nielsen DA, Gordon D, Ho A, Leal SM, Ott J, Kreek MJ.

Pharmacogenetics. 2004 Dec;14(12):793-804.

PMID:
15608558
14.

Haplotype architecture of the norepinephrine transporter gene SLC6A2 in four populations.

Belfer I, Phillips G, Taubman J, Hipp H, Lipsky RH, Enoch MA, Max MB, Goldman D.

J Hum Genet. 2004;49(5):232-45.

PMID:
15362567
15.

Association of the growth hormone receptor gene polymorphisms with mandibular height in a Korean population.

Kang EH, Yamaguchi T, Tajima A, Nakajima T, Tomoyasu Y, Watanabe M, Yamaguchi M, Park SB, Maki K, Inoue I.

Arch Oral Biol. 2009 Jun;54(6):556-62. doi: 10.1016/j.archoralbio.2009.03.002. Epub 2009 Apr 2.

PMID:
19344888
16.

The G protein-coupled receptor kinase 4 gene affects blood pressure in young normotensive twins.

Zhu H, Lu Y, Wang X, Treiber FA, Harshfield GA, Snieder H, Dong Y.

Am J Hypertens. 2006 Jan;19(1):61-6.

PMID:
16461192
17.

Genetic signature consistent with selection against the CYP3A4*1B allele in non-African populations.

Schirmer M, Toliat MR, Haberl M, Suk A, Kamdem LK, Klein K, Brockmöller J, Nürnberg P, Zanger UM, Wojnowski L.

Pharmacogenet Genomics. 2006 Jan;16(1):59-71.

PMID:
16344723
18.

Whole-genome patterns of common DNA variation in three human populations.

Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR.

Science. 2005 Feb 18;307(5712):1072-9.

19.

SNP identification, linkage disequilibrium, and haplotype analysis for a 200-kb genomic region in a Korean population.

Kim KJ, Lee HJ, Park MH, Cha SH, Kim KS, Kim HT, Kimm K, Oh B, Lee JY.

Genomics. 2006 Nov;88(5):535-40. Epub 2006 Aug 17.

20.

Haplotype-based linkage of tryptophan hydroxylase 2 to suicide attempt, major depression, and cerebrospinal fluid 5-hydroxyindoleacetic acid in 4 populations.

Zhou Z, Roy A, Lipsky R, Kuchipudi K, Zhu G, Taubman J, Enoch MA, Virkkunen M, Goldman D.

Arch Gen Psychiatry. 2005 Oct;62(10):1109-18.

PMID:
16203956

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