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Items: 1 to 20 of 87

1.

No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosis.

Guerini FR, Clerici M, Cagliani R, Malhotra S, Montalban X, Forni D, Agliardi C, Riva S, Caputo D, Galimberti D, Asselta R, Fenoglio C, Scarpini E, Comi GP, Bresolin N, Comabella M, Sironi M.

J Neuroimmunol. 2014 Jun 15;271(1-2):49-52. doi: 10.1016/j.jneuroim.2014.04.006. Epub 2014 Apr 16.

PMID:
24794504
2.

Variants of the IFI16 gene affecting the levels of expression of mRNA are associated with susceptibility to Behçet disease.

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

J Rheumatol. 2015 Apr;42(4):695-701. doi: 10.3899/jrheum.140949. Epub 2015 Feb 1.

PMID:
25641891
4.

Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations.

Kristjansdottir G, Sandling JK, Bonetti A, Roos IM, Milani L, Wang C, Gustafsdottir SM, Sigurdsson S, Lundmark A, Tienari PJ, Koivisto K, Elovaara I, Pirttilä T, Reunanen M, Peltonen L, Saarela J, Hillert J, Olsson T, Landegren U, Alcina A, Fernández O, Leyva L, Guerrero M, Lucas M, Izquierdo G, Matesanz F, Syvänen AC.

J Med Genet. 2008 Jun;45(6):362-9. doi: 10.1136/jmg.2007.055012. Epub 2008 Feb 19.

5.

Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study.

La Russa A, Cittadella R, De Marco EV, Valentino P, Andreoli V, Trecroci F, Latorre V, Gambardella A, Quattrone A.

J Neuroimmunol. 2010 Aug 25;225(1-2):175-9. doi: 10.1016/j.jneuroim.2010.04.016. Epub 2010 May 14.

PMID:
20471697
6.

Interferon gamma allelic variants: sex-biased multiple sclerosis susceptibility and gene expression.

Kantarci OH, Hebrink DD, Schaefer-Klein J, Sun Y, Achenbach S, Atkinson EJ, Heggarty S, Cotleur AC, de Andrade M, Vandenbroeck K, Pelfrey CM, Weinshenker BG.

Arch Neurol. 2008 Mar;65(3):349-57. doi: 10.1001/archneurol.2007.66.

PMID:
18332247
7.

Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis.

Alcina A, Fernández O, Gonzalez JR, Catalá-Rabasa A, Fedetz M, Ndagire D, Leyva L, Guerrero M, Arnal C, Delgado C, Lucas M, Izquierdo G, Matesanz F.

Eur J Hum Genet. 2010 Jul;18(7):827-31. doi: 10.1038/ejhg.2009.240. Epub 2010 Jan 20.

8.

Polymorphism in IFI16 affects CD4(+) T-cell counts in HIV-1 infection.

Booiman T, Kootstra NA.

Int J Immunogenet. 2014 Dec;41(6):518-20. doi: 10.1111/iji.12157. Epub 2014 Nov 3.

PMID:
25363454
9.

Autosome-wide copy number variation association analysis for rheumatoid arthritis using the WTCCC high-density SNP genotype data.

Uddin M, Sturge M, Rahman P, Woods MO.

J Rheumatol. 2011 May;38(5):797-801. doi: 10.3899/jrheum.100758. Epub 2011 Mar 1.

PMID:
21362769
10.

No evidence of association of the rare nsSNP rs35667974 in IFIH1 with multiple sclerosis.

Bergamaschi L, Ban M, Leone MA, Sawcer SJ, D'Alfonso S.

J Neuroimmunol. 2010 Apr 15;221(1-2):112-4. doi: 10.1016/j.jneuroim.2010.01.005. Epub 2010 Feb 1.

11.

Toll-like receptor-9 in Spanish multiple sclerosis patients: an association with the gender.

Dominguez-Mozo MI, Garcia-Montojo M, López-Cavanillas M, De Las Heras V, Garcia-Martinez A, Arias-Leal AM, Casanova I, Urcelay E, Arroyo R, Alvarez-Lafuente R.

Eur J Neurol. 2014 Mar;21(3):537-40. doi: 10.1111/ene.12209. Epub 2013 Jun 4.

PMID:
23731219
12.

Lack of association between the interferon regulatory factor-1 (IRF1) locus at 5q31.1 and multiple sclerosis in Germany, northern Italy, Sardinia and Sweden.

Vandenbroeck K, Hardt C, Louage J, Fiten P, Jäckel S, Ronsse I, Epplen JT, Grimaldi LM, Olsson T, Marrosu MG, Billiau A, Opdenakker G.

Genes Immun. 2000;1(4):290-2.

13.

The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis.

Alcina A, Vandenbroeck K, Otaegui D, Saiz A, Gonzalez JR, Fernandez O, Cavanillas ML, Cénit MC, Arroyo R, Alloza I, García-Barcina M, Antigüedad A, Leyva L, Izquierdo G, Lucas M, Fedetz M, Pinto-Medel MJ, Olascoaga J, Blanco Y, Comabella M, Montalban X, Urcelay E, Matesanz F.

Genes Immun. 2010 Jul;11(5):439-45. doi: 10.1038/gene.2010.30. Epub 2010 May 27.

PMID:
20508602
14.

TLR4 haplotypes in multiple sclerosis: a case-control study in the Spanish population.

Urcelay E, Blanco-Kelly F, de Las Heras V, de la Concha EG, Arroyo R, Martínez A.

J Neuroimmunol. 2007 Dec;192(1-2):215-8. Epub 2007 Oct 29.

PMID:
17967488
15.

Brief report: candidate gene study in systemic sclerosis identifies a rare and functional variant of the TNFAIP3 locus as a risk factor for polyautoimmunity.

Koumakis E, Giraud M, Dieudé P, Cohignac V, Cuomo G, Airò P, Hachulla E, Matucci-Cerinic M, Diot E, Caramaschi P, Mouthon L, Riccieri V, Cracowski JL, Tiev KP, Francès C, Amoura Z, Sibilia J, Cosnes A, Carpentier P, Valentini G, Manetti M, Guiducci S, Meyer O, Kahan A, Boileau C, Chiocchia G, Allanore Y.

Arthritis Rheum. 2012 Aug;64(8):2746-52. doi: 10.1002/art.34490.

16.

Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis.

Cagliani R, Fumagalli M, Guerini FR, Riva S, Galimberti D, Comi GP, Agliardi C, Scarpini E, Pozzoli U, Forni D, Caputo D, Asselta R, Biasin M, Paraboschi EM, Bresolin N, Clerici M, Sironi M.

Hum Genet. 2012 Jan;131(1):87-97. doi: 10.1007/s00439-011-1053-2. Epub 2011 Jul 7.

PMID:
21735172
17.

Role of the MHC2TA gene in autoimmune diseases.

Martínez A, Sánchez-Lopez M, Varadé J, Mas A, Martín MC, de Las Heras V, Arroyo R, Mendoza JL, Díaz-Rubio M, Fernández-Gutiérrez B, de la Concha EG, Urcelay E.

Ann Rheum Dis. 2007 Mar;66(3):325-9. Epub 2006 Sep 29.

18.

Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis.

Alcina A, Ramagopalan SV, Fernández O, Catalá-Rabasa A, Fedetz M, Ndagire D, Leyva L, Arnal C, Delgado C, Lucas M, Izquierdo G, Ebers GC, Matesanz F.

Eur J Hum Genet. 2010 May;18(5):618-20. doi: 10.1038/ejhg.2009.213. Epub 2009 Nov 25.

19.

Overexpression of the DNA sensor proteins, absent in melanoma 2 and interferon-inducible 16, contributes to tumorigenesis of oral squamous cell carcinoma with p53 inactivation.

Kondo Y, Nagai K, Nakahata S, Saito Y, Ichikawa T, Suekane A, Taki T, Iwakawa R, Enari M, Taniwaki M, Yokota J, Sakoda S, Morishita K.

Cancer Sci. 2012 Apr;103(4):782-90. doi: 10.1111/j.1349-7006.2012.02211.x. Epub 2012 Feb 23.

20.

A polymorphic variant in the MHC2TA gene is not associated with systemic lupus erythematosus.

Linga-Reddy MV, Gunnarsson I, Svenungsson E, Sturfelt G, Jönsen A, Truedsson L, Nordmark G, Rönnblom L, Alarcón-Riquelme ME.

Tissue Antigens. 2007 Nov;70(5):412-4. Epub 2007 Aug 17.

PMID:
17711409
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