Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 56

Cited In for PubMed (Select 20159113)

1.

Seeking balance: Potentiation and inhibition of multiple sclerosis autoimmune responses by IL-6 and IL-10.

Ireland SJ, Monson NL, Davis LS.

Cytokine. 2015 Jun;73(2):236-44. doi: 10.1016/j.cyto.2015.01.009. Epub 2015 Mar 17. Review.

PMID:
25794663
2.

Genetic determinants of risk and progression in multiple sclerosis.

Didonna A, Oksenberg JR.

Clin Chim Acta. 2015 Feb 4. pii: S0009-8981(15)00056-X. doi: 10.1016/j.cca.2015.01.034. [Epub ahead of print]

PMID:
25661088
3.

Genetic Epidemiology of Psoriasis.

Gupta R, Debbaneh MG, Liao W.

Curr Dermatol Rep. 2014 Mar;3(1):61-78.

4.

Genome-wide association studies in neurology.

Tan MS, Jiang T, Tan L, Yu JT.

Ann Transl Med. 2014 Dec;2(12):124. doi: 10.3978/j.issn.2305-5839.2014.11.12. Review.

5.

Genetic association of rs1520333 G/A polymorphism in the IL7 gene with multiple sclerosis susceptibility in Isfahan population.

Ghavimi R, Pourhossein M, Ghaedi K, Alesahebfosoul F, Honardoost MA, Maracy MR.

Adv Biomed Res. 2014 Nov 29;3:238. doi: 10.4103/2277-9175.145742. eCollection 2014.

6.

Increasing Incidence in Relapsing-Remitting MS and High Rates among Young Women in Finland: A Thirty-Year Follow-Up.

Sumelahti ML, Holmberg MH, Murtonen A, Huhtala H, Elovaara I.

Mult Scler Int. 2014;2014:186950. doi: 10.1155/2014/186950. Epub 2014 Nov 9.

7.

Mouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and Perspectives.

Caignard G, Eva MM, van Bruggen R, Eveleigh R, Bourque G, Malo D, Gros P, Vidal SM.

Genes (Basel). 2014 Sep 29;5(4):887-925. doi: 10.3390/genes5040887. Review.

8.
9.

Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease.

Flanagan SE, Haapaniemi E, Russell MA, Caswell R, Lango Allen H, De Franco E, McDonald TJ, Rajala H, Ramelius A, Barton J, Heiskanen K, Heiskanen-Kosma T, Kajosaari M, Murphy NP, Milenkovic T, Seppänen M, Lernmark Å, Mustjoki S, Otonkoski T, Kere J, Morgan NG, Ellard S, Hattersley AT.

Nat Genet. 2014 Aug;46(8):812-4. doi: 10.1038/ng.3040. Epub 2014 Jul 20.

10.

A prostate cancer model build by a novel SVM-ID3 hybrid feature selection method using both genotyping and phenotype data from dbGaP.

Yücebaş SC, Aydın Son Y.

PLoS One. 2014 Mar 20;9(3):e91404. doi: 10.1371/journal.pone.0091404. eCollection 2014. Erratum in: PLoS One. 2014;9(12):e114956.

11.

Inflammatory bowel disease: an increased risk factor for neurologic complications.

Morís G.

World J Gastroenterol. 2014 Feb 7;20(5):1228-37. doi: 10.3748/wjg.v20.i5.1228. Review.

12.

Association between Tumor Necrosis Factor- α-308 G/A Polymorphism and Multiple Sclerosis: A Systematic Review and Meta-Analysis.

Tolide-Ie H, Tabatabaee HR, Kamali-Sarvestani E.

Iran J Med Sci. 2014 Jan;39(1):2-10. Review.

13.

Therapeutic efficacy of suppressing the Jak/STAT pathway in multiple models of experimental autoimmune encephalomyelitis.

Liu Y, Holdbrooks AT, De Sarno P, Rowse AL, Yanagisawa LL, McFarland BC, Harrington LE, Raman C, Sabbaj S, Benveniste EN, Qin H.

J Immunol. 2014 Jan 1;192(1):59-72. doi: 10.4049/jimmunol.1301513. Epub 2013 Dec 9.

14.

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.

Lencz T, Guha S, Liu C, Rosenfeld J, Mukherjee S, DeRosse P, John M, Cheng L, Zhang C, Badner JA, Ikeda M, Iwata N, Cichon S, Rietschel M, Nöthen MM, Cheng AT, Hodgkinson C, Yuan Q, Kane JM, Lee AT, Pisanté A, Gregersen PK, Pe'er I, Malhotra AK, Goldman D, Darvasi A.

Nat Commun. 2013;4:2739. doi: 10.1038/ncomms3739.

15.

Association of single-nucleotide polymorphisms in the STAT3 gene with autoimmune thyroid disease in Chinese individuals.

Xiao L, Muhali FS, Cai TT, Song RH, Hu R, Shi XH, Jiang WJ, Li DF, He ST, Xu J, Zhang JA.

Funct Integr Genomics. 2013 Nov;13(4):455-61. doi: 10.1007/s10142-013-0337-0. Epub 2013 Oct 1.

16.

Therapeutic targeting of STAT pathways in CNS autoimmune diseases.

Egwuagu CE, Larkin Iii J.

JAKSTAT. 2013 Jan 1;2(1):e24134. doi: 10.4161/jkst.24134. Review.

17.

The genetics of multiple sclerosis: review of current and emerging candidates.

Muñoz-Culla M, Irizar H, Otaegui D.

Appl Clin Genet. 2013 Aug 8;6:63-73. doi: 10.2147/TACG.S29107. eCollection 2013. Review.

18.

A non-stop S-antigen gene mutation is associated with late onset hereditary retinal degeneration in dogs.

Goldstein O, Jordan JA, Aguirre GD, Acland GM.

Mol Vis. 2013 Aug 27;19:1871-84. eCollection 2013.

19.

Contribution of genome-wide association studies to scientific research: a pragmatic approach to evaluate their impact.

Ricigliano VA, Umeton R, Germinario L, Alma E, Briani M, Di Segni N, Montesanti D, Pierelli G, Cancrini F, Lomonaco C, Grassi F, Palmieri G, Salvetti M.

PLoS One. 2013 Aug 14;8(8):e71198. doi: 10.1371/journal.pone.0071198. eCollection 2013.

20.

Genetic burden in multiple sclerosis families.

Isobe N, Damotte V, Lo Re V, Ban M, Pappas D, Guillot-Noel L, Rebeix I, Compston A, Mack T, Cozen W, Fontaine B, Hauser SL, Oksenberg JR, Sawcer S, Gourraud PA.

Genes Immun. 2013 Oct;14(7):434-40. doi: 10.1038/gene.2013.37. Epub 2013 Aug 1.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk