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Items: 1 to 20 of 353

1.

Genetic variation of FUT3 in Ghanaians, Caucasians, and Mongolians.

Soejima M, Munkhtulga L, Iwamoto S, Koda Y.

Transfusion. 2009 May;49(5):959-66. doi: 10.1111/j.1537-2995.2008.02069.x. Epub 2009 Jan 21.

PMID:
19175549
2.

Genetic variation of FUT2 in Ovambos, Turks, and Mongolians.

Soejima M, Nakajima T, Fujihara J, Takeshita H, Koda Y.

Transfusion. 2008 Jul;48(7):1423-31. doi: 10.1111/j.1537-2995.2008.01710.x. Epub 2008 Apr 18.

PMID:
18422843
3.

Distribution of Lewis (FUT3)genotype and allele: frequencies in a biethnic United States population.

Cakir B, Pankow JS, Salomaa V, Couper D, Morris TL, Brantley KR, Hiller KM, Heiss G, Weston BW.

Ann Hematol. 2002 Oct;81(10):558-65. Epub 2002 Oct 11.

PMID:
12424536
4.

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
6.

Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene.

Koda Y, Tachida H, Soejima M, Takenaka O, Kimura H.

Ann Hum Genet. 2004 Mar;68(Pt 2):110-9.

PMID:
15008790
7.

Evaluation of genetic variation and association in the matrix metalloproteinase 9 (MMP9) gene in ESRD patients.

Hirakawa S, Lange EM, Colicigno CJ, Freedman BI, Rich SS, Bowden DW.

Am J Kidney Dis. 2003 Jul;42(1):133-42.

PMID:
12830465
8.

Haplotype variation and linkage disequilibrium in 313 human genes.

Stephens JC, Schneider JA, Tanguay DA, Choi J, Acharya T, Stanley SE, Jiang R, Messer CJ, Chew A, Han JH, Duan J, Carr JL, Lee MS, Koshy B, Kumar AM, Zhang G, Newell WR, Windemuth A, Xu C, Kalbfleisch TS, Shaner SL, Arnold K, Schulz V, Drysdale CM, Nandabalan K, Judson RS, Ruano G, Vovis GF.

Science. 2001 Jul 20;293(5529):489-93. Epub 2001 Jul 12. Erratum in: Science 2001 Aug 10;293(5532):1048.

9.

Sequence variation and linkage disequilibrium in the GABA transporter-1 gene (SLC6A1) in five populations: implications for pharmacogenetic research.

Hirunsatit R, Ilomäki R, Malison R, Räsänen P, Ilomäki E, Kranzler HR, Kosten T, Sughondhabirom A, Thavichachart N, Tangwongchai S, Listman J, Mutirangura A, Gelernter J, Lappalainen J.

BMC Genet. 2007 Oct 17;8:71.

10.

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
11.

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.

12.

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.

13.
14.

Lewis (FUT3) genotypes in two different Chinese populations.

Liu YH, Koda Y, Soejima M, Pang H, Wang B, Kimura H.

J Forensic Sci. 1999 Jan;44(1):82-6.

PMID:
9987874
15.

Knops blood group haplotypes among distinct Brazilian populations.

Covas DT, de Oliveira FS, Rodrigues ES, Abe-Sandes K, Silva WA Jr, Fontes AM.

Transfusion. 2007 Jan;47(1):147-53.

PMID:
17207243
16.

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
17.
18.

Lewis enzyme (alpha1-3/4 fucosyltransferase) polymorphisms do not explain the Lewis phenotype in the gastric mucosa of a Portuguese population.

Serpa J, Almeida R, Oliveira C, Silva FS, Silva E, Reis C, Le Pendu J, Oliveira G, Ribeiro LM, David L.

J Hum Genet. 2003;48(4):183-9. Epub 2003 Mar 20.

PMID:
12730721
19.

TRAF1 polymorphisms associated with rheumatoid arthritis susceptibility in Asians and in Caucasians.

Han TU, Bang SY, Kang C, Bae SC.

Arthritis Rheum. 2009 Sep;60(9):2577-84. doi: 10.1002/art.24759.

20.

Single nucleotide polymorphisms and haplotype frequencies of UGT2B4 and UGT2B7 in a Japanese population.

Saeki M, Saito Y, Jinno H, Tanaka-Kagawa T, Ohno A, Ozawa S, Ueno K, Kamakura S, Kamatani N, Komamura K, Kitakaze M, Sawada J.

Drug Metab Dispos. 2004 Sep;32(9):1048-54.

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