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Items: 1 to 20 of 150

1.

Genetics of Behçet's disease: lessons learned from genomewide association studies.

Gül A.

Curr Opin Rheumatol. 2014 Jan;26(1):56-63. doi: 10.1097/BOR.0000000000000003. Review.

PMID:
24257369
2.

Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.

Kirino Y, Bertsias G, Ishigatsubo Y, Mizuki N, Tugal-Tutkun I, Seyahi E, Ozyazgan Y, Sacli FS, Erer B, Inoko H, Emrence Z, Cakar A, Abaci N, Ustek D, Satorius C, Ueda A, Takeno M, Kim Y, Wood GM, Ombrello MJ, Meguro A, Gül A, Remmers EF, Kastner DL.

Nat Genet. 2013 Feb;45(2):202-7. doi: 10.1038/ng.2520. Epub 2013 Jan 6.

3.

Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians.

Sousa I, Shahram F, Francisco D, Davatchi F, Abdollahi BS, Ghaderibarmi F, Nadji A, Mojarad Shafiee N, Xavier JM, Oliveira SA.

Arthritis Rheumatol. 2015 Oct;67(10):2742-8. doi: 10.1002/art.39240.

4.

The immunogenetics of Behçet's disease: A comprehensive review.

Takeuchi M, Kastner DL, Remmers EF.

J Autoimmun. 2015 Nov;64:137-48. doi: 10.1016/j.jaut.2015.08.013. Epub 2015 Sep 5. Review.

5.

HLA and non-HLA genes in Behçet's disease: a multicentric study in the Spanish population.

Montes-Cano MA, Conde-Jaldón M, García-Lozano JR, Ortiz-Fernández L, Ortego-Centeno N, Castillo-Palma MJ, Espinosa G, Graña-Gil G, González-Gay MA, Barnosi-Marín AC, Solans R, Fanlo P, Camps T, Castañeda S, Sánchez-Bursón J, Núñez-Roldán A, Martín J, González-Escribano MF.

Arthritis Res Ther. 2013 Oct 4;15(5):R145. doi: 10.1186/ar4328.

6.

Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease.

Hughes T, Coit P, Adler A, Yilmaz V, Aksu K, Düzgün N, Keser G, Cefle A, Yazici A, Ergen A, Alpsoy E, Salvarani C, Casali B, Kötter I, Gutierrez-Achury J, Wijmenga C, Direskeneli H, Saruhan-Direskeneli G, Sawalha AH.

Nat Genet. 2013 Mar;45(3):319-24. doi: 10.1038/ng.2551. Epub 2013 Feb 10.

PMID:
23396137
7.

Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.

Remmers EF, Cosan F, Kirino Y, Ombrello MJ, Abaci N, Satorius C, Le JM, Yang B, Korman BD, Cakiris A, Aglar O, Emrence Z, Azakli H, Ustek D, Tugal-Tutkun I, Akman-Demir G, Chen W, Amos CI, Dizon MB, Kose AA, Azizlerli G, Erer B, Brand OJ, Kaklamani VG, Kaklamanis P, Ben-Chetrit E, Stanford M, Fortune F, Ghabra M, Ollier WE, Cho YH, Bang D, O'Shea J, Wallace GR, Gadina M, Kastner DL, Gül A.

Nat Genet. 2010 Aug;42(8):698-702. doi: 10.1038/ng.625. Epub 2010 Jul 11.

8.

Significant associations of HLA-B*5101 and B*5108, and lack of association of class II alleles with Behçet's disease in Italian patients.

Kera J, Mizuki N, Ota M, Katsuyama Y, Pivetti-Pezzi P, Ohno S, Inoko H.

Tissue Antigens. 1999 Dec;54(6):565-71.

PMID:
10674970
9.

Pathogenesis of Behçet's disease: autoinflammatory features and beyond.

Gül A.

Semin Immunopathol. 2015 Jul;37(4):413-8. doi: 10.1007/s00281-015-0502-8. Epub 2015 Jun 12. Review.

PMID:
26068404
10.

Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility.

Hou S, Xiao X, Li F, Jiang Z, Kijlstra A, Yang P.

Hum Genet. 2012 Dec;131(12):1841-50. doi: 10.1007/s00439-012-1200-4. Epub 2012 Jul 25.

PMID:
22829007
11.

[Behçet's disease from the aspect of autoinflammatory disease].

Ishigatsubo Y, Samukawa S.

Nihon Rinsho Meneki Gakkai Kaishi. 2011;34(5):408-19. Review. Japanese.

12.

Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease.

Kirino Y, Zhou Q, Ishigatsubo Y, Mizuki N, Tugal-Tutkun I, Seyahi E, Özyazgan Y, Ugurlu S, Erer B, Abaci N, Ustek D, Meguro A, Ueda A, Takeno M, Inoko H, Ombrello MJ, Satorius CL, Maskeri B, Mullikin JC, Sun HW, Gutierrez-Cruz G, Kim Y, Wilson AF, Kastner DL, Gül A, Remmers EF.

Proc Natl Acad Sci U S A. 2013 May 14;110(20):8134-9. doi: 10.1073/pnas.1306352110. Epub 2013 Apr 30.

13.

The genetics of Behçet's disease in a Chinese population.

Hou S, Kijlstra A, Yang P.

Front Med. 2012 Dec;6(4):354-9. doi: 10.1007/s11684-012-0234-2. Epub 2012 Nov 15. Review.

PMID:
23161479
14.

Behçet's disease: an update on the pathogenesis.

Gül A.

Clin Exp Rheumatol. 2001 Sep-Oct;19(5 Suppl 24):S6-12.

PMID:
11760403
15.

Tumour necrosis factor-alpha gene promoter region -308 and -376 G-->A polymorphisms in Behçet's disease.

Duymaz-Tozkir J, Gül A, Uyar FA, Ozbek U, Saruhan-Direskeneli G.

Clin Exp Rheumatol. 2003 Jul-Aug;21(4 Suppl 30):S15-8.

PMID:
14727453
16.

Class I and class II MHC polymorphisms in Mexican patients with Behçet's disease.

Soto-Vega E, García-Muñoz R, Richaud-Patin Y, Zúñiga-Ramos J, Crispín JC, Díaz-Jouanen E, Flores-Suárez LF, Llorente L, Granados J.

Immunol Lett. 2004 May 15;93(2-3):211-5.

PMID:
15158619
17.

A strong association between HLA-B*5101 and Behçet's disease in Greek patients.

Mizuki N, Ohno S, Ando H, Chen L, Palimeris GD, Stavropoulos-Ghiokas E, Ishihara M, Goto K, Nakamura S, Shindo Y, Isobe K, Ito N, Inoko H.

Tissue Antigens. 1997 Jul;50(1):57-60.

PMID:
9243757
18.

Behçet's disease associated with one of the HLA-B51 subantigens, HLA-B* 5101.

Mizuki N, Inoko H, Ando H, Nakamura S, Kashiwase K, Akaza T, Fujino Y, Masuda K, Takiguchi M, Ohno S.

Am J Ophthalmol. 1993 Oct 15;116(4):406-9.

PMID:
8213969
19.

Close association of HLA-Bw51 with Behçet's disease.

Ohno S, Ohguchi M, Hirose S, Matsuda H, Wakisaka A, Aizawa M.

Arch Ophthalmol. 1982 Sep;100(9):1455-8.

PMID:
6956266
20.

The absence of disease-specific polymorphisms within the HLA-B51 gene that is the susceptible locus for Behçet's disease.

Sano K, Yabuki K, Imagawa Y, Shiina T, Mizuki N, Ohno S, Kulski JK, Inoko H.

Tissue Antigens. 2001 Aug;58(2):77-82.

PMID:
11696219

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