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Items: 1 to 20 of 97

1.

Non-synonymous single nucleotide polymorphisms in genes for immunoregulatory galectins: association of galectin-8 (F19Y) occurrence with autoimmune diseases in a Caucasian population.

Pál Z, Antal P, Srivastava SK, Hullám G, Semsei AF, Gál J, Svébis M, Soós G, Szalai C, André S, Gordeeva E, Nagy G, Kaltner H, Bovin NV, Molnár MJ, Falus A, Gabius HJ, Buzás EI.

Biochim Biophys Acta. 2012 Oct;1820(10):1512-8. doi: 10.1016/j.bbagen.2012.05.015. Epub 2012 Jun 7.

PMID:
22683700
2.

Natural single amino acid polymorphism (F19Y) in human galectin-8: detection of structural alterations and increased growth-regulatory activity on tumor cells.

Ruiz FM, Scholz BA, Buzamet E, Kopitz J, André S, Menéndez M, Romero A, Solís D, Gabius HJ.

FEBS J. 2014 Mar;281(5):1446-64. doi: 10.1111/febs.12716. Epub 2014 Feb 3.

3.

Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population.

Pál Z, Varga Z, Semsei Á, Reményi V, Rózsa C, Falus A, Illes Z, Buzás EI, Molnar MJ.

Hum Immunol. 2012 Feb;73(2):193-5. doi: 10.1016/j.humimm.2011.11.001. Epub 2011 Nov 12.

PMID:
22119518
4.

A novel galectin-1 and interleukin 2 receptor β haplotype is associated with autoimmune myasthenia gravis.

Pál Z, Antal P, Millinghoffer A, Hullám G, Pálóczi K, Tóth S, Gabius HJ, Molnár MJ, Falus A, Buzás EI.

J Neuroimmunol. 2010 Dec 15;229(1-2):107-11. doi: 10.1016/j.jneuroim.2010.07.015. Epub 2010 Aug 21.

PMID:
20728947
5.

Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women.

Pal Z, Gal A, Remenyi V, Tordai A, Molnar MJ.

Neuromuscul Disord. 2009 Dec;19(12):822-4. doi: 10.1016/j.nmd.2009.09.002. Epub 2009 Sep 29.

PMID:
19793653
6.

Association between the PTPN22 gene and rheumatoid arthritis and juvenile idiopathic arthritis in a UK population: further support that PTPN22 is an autoimmunity gene.

Hinks A, Barton A, John S, Bruce I, Hawkins C, Griffiths CE, Donn R, Thomson W, Silman A, Worthington J.

Arthritis Rheum. 2005 Jun;52(6):1694-9.

7.

Tapasin gene polymorphism in systemic onset juvenile rheumatoid arthritis: a family-based case-control study.

Bukulmez H, Fife M, Tsoras M, Thompson SD, Twine NA, Woo P, Olson JM, Elston RC, Glass DN, Colbert RA.

Arthritis Res Ther. 2005;7(2):R285-90. Epub 2005 Jan 11.

8.

No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations.

Cinek O, Hradsky O, Ahmedov G, Slavcev A, Kolouskova S, Kulich M, Sumnik Z.

Diabetes Res Clin Pract. 2007 May;76(2):297-303. Epub 2006 Sep 26.

PMID:
17000021
9.

The PTPN22gain-of-function+1858T(+) genotypes correlate with low IL-2 expression in thymomas and predispose to myasthenia gravis.

Chuang WY, Ströbel P, Belharazem D, Rieckmann P, Toyka KV, Nix W, Schalke B, Gold R, Kiefer R, Klinker E, Opitz A, Inoue M, Kuo TT, Müller-Hermelink HK, Marx A.

Genes Immun. 2009 Dec;10(8):667-72. doi: 10.1038/gene.2009.64. Epub 2009 Aug 20.

PMID:
19693092
10.

Why is PTPN22 a good candidate susceptibility gene for autoimmune disease?

Burn GL, Svensson L, Sanchez-Blanco C, Saini M, Cope AP.

FEBS Lett. 2011 Dec 1;585(23):3689-98. doi: 10.1016/j.febslet.2011.04.032. Epub 2011 Apr 20. Review.

11.

Association study of 3 rheumatoid arthritis risk loci in systemic sclerosis in European Caucasian population.

Coustet B, Dieude P, Wipft J, Avouac J, Hachulla E, Diot E, Cracowski JL, Tiev KP, Sibilia J, Mouthon L, Frances C, Amoura Z, Carpentier P, Meyer O, Kahan A, Boileau C, Allanore Y.

Clin Exp Rheumatol. 2011 Mar-Apr;29(2 Suppl 65):S6-9. Epub 2011 May 12.

PMID:
21586211
12.

PTPN22 1858T is not a risk factor for North American pemphigus vulgaris.

Sachdev A, Bhanusali DG, Patterson KC, Zamora MB, Ghuman A, Gerlach JA, Sinha AA.

Exp Dermatol. 2011 Jun;20(6):514-9. doi: 10.1111/j.1600-0625.2011.01272.x.

PMID:
21585555
13.

The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysis.

Dieudé P, Guedj M, Wipff J, Avouac J, Hachulla E, Diot E, Granel B, Sibilia J, Cabane J, Meyer O, Mouthon L, Kahan A, Boileau C, Allanore Y.

Arthritis Rheum. 2008 Jul;58(7):2183-8. doi: 10.1002/art.23601.

14.

FOXP3 -3279 and IVS9+459 polymorphisms are associated with genetic susceptibility to myasthenia gravis.

Zhang J, Chen Y, Jia G, Chen X, Lu J, Yang H, Zhou W, Xiao B, Zhang N, Li J.

Neurosci Lett. 2013 Feb 8;534:274-8. doi: 10.1016/j.neulet.2012.11.048. Epub 2012 Dec 7.

PMID:
23228687
15.

The +1858C/T PTPN22 gene polymorphism confers genetic susceptibility to rheumatoid arthritis in Mexican population from the Western Mexico.

Torres-Carrillo NM, Ruiz-Noa Y, Martínez-Bonilla GE, Leyva-Torres SD, Torres-Carrillo N, Palafox-Sánchez CA, Navarro-Hernández RE, Rangel-Villalobos H, Oregón-Romero E, Muñoz-Valle JF.

Immunol Lett. 2012 Sep;147(1-2):41-6. doi: 10.1016/j.imlet.2012.05.007. Epub 2012 Jun 26.

PMID:
22743847
17.

Association of common polymorphisms in known susceptibility genes with rheumatoid arthritis in a Slovak population using osteoarthritis patients as controls.

Stark K, Rovenský J, Blazicková S, Grosse-Wilde H, Ferencik S, Hengstenberg C, Straub RH.

Arthritis Res Ther. 2009;11(3):R70. doi: 10.1186/ar2699. Epub 2009 May 15.

18.

Association of PTPN22 single nucleotide polymorphism with rheumatoid arthritis but not with allergic asthma.

Majorczyk E, Jasek M, Płoski R, Wagner M, Kosior A, Pawlik A, Obojski A, Luszczek W, Nowak I, Wiśniewski A, Kuśnierczyk P.

Eur J Hum Genet. 2007 Oct;15(10):1043-8. Epub 2007 Jun 20.

19.

Immunogenetic heterogeneity and associated autoimmune disorders in myasthenia gravis: a population-based survey in the province of Ferrara, northern Italy.

Tola MR, Caniatti LM, Casetta I, Granieri E, Conighi C, Quatrale R, Monetti VC, Paolino E, Govoni V, Pascarella R, et al.

Acta Neurol Scand. 1994 Nov;90(5):318-23.

PMID:
7887131
20.

Ethnic differences in allele frequency of autoimmune-disease-associated SNPs.

Mori M, Yamada R, Kobayashi K, Kawaida R, Yamamoto K.

J Hum Genet. 2005;50(5):264-6. Epub 2005 May 10.

PMID:
15883854
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