These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
270 related articles for article (PubMed ID: 22279577)
1. The origin and evolution of variable number tandem repeat of CLEC4M gene in the global human population. Li H; Wang JX; Wu DD; Wang HW; Tang NL; Zhang YP PLoS One; 2012; 7(1):e30268. PubMed ID: 22279577 [TBL] [Abstract][Full Text] [Related]
2. The VNTR polymorphism of the CLEC4M gene and susceptibility to HIV-1 infection in Han Chinese population. Li H; Fu WP; Hong ZH Infect Genet Evol; 2013 Jul; 17():137-41. PubMed ID: 23602836 [TBL] [Abstract][Full Text] [Related]
3. Distribution of the 3' VNTR polymorphism in the human dopamine transporter gene in world populations. Mitchell RJ; Howlett S; Earl L; White NG; McComb J; Schanfield MS; Briceno I; Papiha SS; Osipova L; Livshits G; Leonard WR; Crawford MH Hum Biol; 2000 Apr; 72(2):295-304. PubMed ID: 10803661 [TBL] [Abstract][Full Text] [Related]
4. The neck-region polymorphism of DC-SIGNR in peri-centenarian from Han Chinese population. Li H; Wang CY; Wang JX; Tang NL; Xie L; Gong YY; Yang Z; Xu LY; Kong QP; Zhang YP BMC Med Genet; 2009 Dec; 10():134. PubMed ID: 20003397 [TBL] [Abstract][Full Text] [Related]
5. Polymorphisms in the C-type lectin genes cluster in chromosome 19 and predisposition to severe acute respiratory syndrome coronavirus (SARS-CoV) infection. Li H; Tang NL; Chan PK; Wang CY; Hui DS; Luk C; Kwok R; Huang W; Sung JJ; Kong QP; Zhang YP J Med Genet; 2008 Nov; 45(11):752-8. PubMed ID: 18697825 [TBL] [Abstract][Full Text] [Related]
6. Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. Manderstedt E; Lind-Halldén C; Lethagen S; Halldén C PLoS One; 2018; 13(2):e0192024. PubMed ID: 29389944 [TBL] [Abstract][Full Text] [Related]
7. Inferring microevolutionary patterns from allele-size frequency distributions of minisatellite loci: a worldwide study of the APOB 3' hypervariable region polymorphism. Destro-Bisol G; Capelli C; Belledi M Hum Biol; 2000 Oct; 72(5):733-51. PubMed ID: 11126722 [TBL] [Abstract][Full Text] [Related]
8. Evolution of a VNTR located within the promoter region of the thiopurine methyltransferase gene: inferences from population and sequence data. Alves S; Amorim A; Prata MJ Hum Genet; 2002 Aug; 111(2):172-8. PubMed ID: 12189491 [TBL] [Abstract][Full Text] [Related]
9. The VNTR polymorphism of the DC-SIGNR gene and susceptibility to HIV-1 infection: a meta-analysis. Li H; Yu XM; Wang JX; Hong ZH; Tang NL PLoS One; 2012; 7(9):e42972. PubMed ID: 22957026 [TBL] [Abstract][Full Text] [Related]
10. The C-type lectin receptor CLEC4M binds, internalizes, and clears von Willebrand factor and contributes to the variation in plasma von Willebrand factor levels. Rydz N; Swystun LL; Notley C; Paterson AD; Riches JJ; Sponagle K; Boonyawat B; Montgomery RR; James PD; Lillicrap D Blood; 2013 Jun; 121(26):5228-37. PubMed ID: 23529928 [TBL] [Abstract][Full Text] [Related]
11. A novel isoform of platelet glycoprotein Ib alpha is prevalent in African Americans. Aramaki KM; Reiner AP Am J Hematol; 1999 Jan; 60(1):77-9. PubMed ID: 9883812 [TBL] [Abstract][Full Text] [Related]
12. Polymorphism at VNTR locus 3 to the apolipoprotein B gene in a Tunisian population: difference from other ethnic groups. Buresi C; Desmarais E; Vigneron S; Ben Rayana C; Chaabouni H; Roizes G Genet Epidemiol; 1995; 12(4):381-9. PubMed ID: 8536955 [TBL] [Abstract][Full Text] [Related]
13. Distribution of 42-bp variable tandem repeat polymorphism of the cold-induced autoinflammatory syndrome 1 (CIAS1) gene in eight human populations. Omi T; Koda Y; Soejima M; Munkhtulga L; Iwamoto S Leg Med (Tokyo); 2011 Jan; 13(1):44-6. PubMed ID: 21035374 [TBL] [Abstract][Full Text] [Related]
14. Genetic relationship between the 3'-VNTR and diallelic apolipoprotein B gene polymorphisms: haplotype analysis in individuals of European and south Asian origin. Renges HH; Peacock R; Dunning AM; Talmud P; Humphries SE Ann Hum Genet; 1992 Jan; 56(1):11-33. PubMed ID: 1586131 [TBL] [Abstract][Full Text] [Related]
15. Study on VNTR polymorphism of gene IL-1RA in 19 Chinese populations. Jiang J; Zhang X; Sun D; Jin Y; Bai J; Chen F; Fu S Int J Immunogenet; 2010 Apr; 37(2):73-7. PubMed ID: 20002810 [TBL] [Abstract][Full Text] [Related]
16. Interpopulational and intrapopulational genetic diversity of Amerindians as revealed by six variable number of tandem repeats. Zago MA; Silva Júnior WA; Tavella MH; Santos SE; Guerreiro JF; Figueiredo MS Hum Hered; 1996; 46(5):274-89. PubMed ID: 8854143 [TBL] [Abstract][Full Text] [Related]
17. Specificity of genetic diversity in D1S80 revealed by SNP-VNTR haplotyping. Limborska SA; Khrunin AV; Flegontova OV; Tasitz VA; Verbenko DA Ann Hum Biol; 2011 Sep; 38(5):564-9. PubMed ID: 21834750 [TBL] [Abstract][Full Text] [Related]
18. Novel alleles of 31-bp VNTR polymorphism in the human cystathionine β-synthase (CBS) gene were detected in healthy Asians. Gan YY; Chen CF J Genet; 2010 Dec; 89(4):449-55. PubMed ID: 21273695 [TBL] [Abstract][Full Text] [Related]
19. Structural analysis of insulin minisatellite alleles reveals unusually large differences in diversity between Africans and non-Africans. Stead JD; Jeffreys AJ Am J Hum Genet; 2002 Dec; 71(6):1273-84. PubMed ID: 12404181 [TBL] [Abstract][Full Text] [Related]
20. Worldwide distribution of the MYH9 kidney disease susceptibility alleles and haplotypes: evidence of historical selection in Africa. Oleksyk TK; Nelson GW; An P; Kopp JB; Winkler CA PLoS One; 2010 Jul; 5(7):e11474. PubMed ID: 20634883 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]