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Journal Abstract Search

822 related items for PubMed ID: 19515430

  • 21. Genetic association analysis of the interleukin 7 gene (IL7) in multiple sclerosis.
    Lundmark F, Duvefelt K, Hillert J.
    J Neuroimmunol; 2007 Dec; 192(1-2):171-3. PubMed ID: 17913246
    [Abstract] [Full Text] [Related]

  • 22. Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.
    Qiu XS, Tang NL, Yeung HY, Lee KM, Hung VW, Ng BK, Ma SL, Kwok RH, Qin L, Qiu Y, Cheng JC.
    Spine (Phila Pa 1976); 2007 Jul 15; 32(16):1748-53. PubMed ID: 17632395
    [Abstract] [Full Text] [Related]

  • 23. 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. PubMed ID: 20471697
    [Abstract] [Full Text] [Related]

  • 24. Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?
    Ghezzi S, Del Bo R, Scarlato M, Nardini M, Carlesi C, Prelle A, Corti S, Mancuso M, Briani C, Siciliano G, Murri L, Bresolin N, Comi GP.
    Neurobiol Aging; 2009 May 25; 30(5):842-4. PubMed ID: 17888545
    [Abstract] [Full Text] [Related]

  • 25. 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 25; 192(1-2):215-8. PubMed ID: 17967488
    [Abstract] [Full Text] [Related]

  • 26. The high producer variant of the Fc-receptor like-3 (FCRL3) gene is involved in protection against multiple sclerosis.
    Matesanz F, Fernández O, Milne RL, Fedetz M, Leyva L, Guerrero M, Delgado C, Lucas M, Izquierdo G, Alcina A.
    J Neuroimmunol; 2008 Mar 25; 195(1-2):146-50. PubMed ID: 18313765
    [Abstract] [Full Text] [Related]

  • 27. Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.
    Perera D, Stankovich J, Butzkueven H, Taylor BV, Foote SJ, Kilpatrick TJ, Rubio JP.
    J Neuroimmunol; 2009 Jun 25; 211(1-2):105-9. PubMed ID: 19375175
    [Abstract] [Full Text] [Related]

  • 28. The interleukin 23 receptor gene in multiple sclerosis: a case-control study.
    Roos IM, Kockum I, Hillert J.
    J Neuroimmunol; 2008 Feb 25; 194(1-2):173-80. PubMed ID: 18164077
    [Abstract] [Full Text] [Related]

  • 29. Association of the PPARgamma gene polymorphism Pro12Ala with delayed onset of multiple sclerosis.
    Klotz L, Schmidt S, Heun R, Klockgether T, Kölsch H.
    Neurosci Lett; 2009 Jan 02; 449(1):81-3. PubMed ID: 18977277
    [Abstract] [Full Text] [Related]

  • 30. Association of Fcgamma receptor polymorphisms with adult onset Still's disease in Korea.
    Woo JH, Sung YK, Lee JS, Chung WT, Choe JY, Song GG, Yoo DH.
    J Rheumatol; 2009 Feb 02; 36(2):347-50. PubMed ID: 19040302
    [Abstract] [Full Text] [Related]

  • 31. Gender-associated differences of perforin polymorphisms in the susceptibility to multiple sclerosis.
    Camiña-Tato M, Morcillo-Suárez C, Bustamante MF, Ortega I, Navarro A, Muntasell A, López-Botet M, Sánchez A, Carmona P, Julià E, Tortola MT, Audí L, Oksenberg JR, Martin R, Montalban X, Comabella M.
    J Immunol; 2010 Nov 01; 185(9):5392-404. PubMed ID: 20921521
    [Abstract] [Full Text] [Related]

  • 32. Search for genetic factors associated with susceptibility to multiple sclerosis.
    Forte GI, Ragonese P, Salemi G, Scola L, Candore G, D'Amelio M, Crivello A, Di Benedetto N, Nuzzo D, Giacalone A, Lio D, Caruso C.
    Ann N Y Acad Sci; 2006 May 01; 1067():264-9. PubMed ID: 16803996
    [Abstract] [Full Text] [Related]

  • 33. Gene variations in GSTM3 are a risk factor for Alzheimer's disease.
    Hong GS, Heun R, Jessen F, Popp J, Hentschel F, Kelemen P, Schulz A, Maier W, Kölsch H.
    Neurobiol Aging; 2009 May 01; 30(5):691-6. PubMed ID: 17904251
    [Abstract] [Full Text] [Related]

  • 34. CTLA4 exon 1 and promoter polymorphisms in patients with multiple sclerosis.
    Yousefipour G, Erfani N, Momtahan M, Moghaddasi H, Ghaderi A.
    Acta Neurol Scand; 2009 Dec 01; 120(6):424-9. PubMed ID: 19737153
    [Abstract] [Full Text] [Related]

  • 35. 3'UTR C2370A allele of the IL-23 receptor gene is associated with relapsing-remitting multiple sclerosis.
    Illes Z, Safrany E, Peterfalvi A, Magyari L, Farago B, Pozsonyi E, Rozsa C, Komoly S, Melegh B.
    Neurosci Lett; 2008 Jan 24; 431(1):36-8. PubMed ID: 18180107
    [Abstract] [Full Text] [Related]

  • 36. Association of common T cell activation gene polymorphisms with multiple sclerosis in Australian patients.
    Teutsch SM, Booth DR, Bennetts BH, Heard RN, Stewart GJ.
    J Neuroimmunol; 2004 Mar 24; 148(1-2):218-30. PubMed ID: 14975605
    [Abstract] [Full Text] [Related]

  • 37. Single-nucleotide polymorphisms in CCL2 gene are not associated with susceptibility to systemic sclerosis.
    Carulli MT, Spagnolo P, Fonseca C, Welsh KI, duBois RM, Black CM, Denton CP.
    J Rheumatol; 2008 May 24; 35(5):839-44. PubMed ID: 18381789
    [Abstract] [Full Text] [Related]

  • 38. Lack of association between TNF-alpha polymorphisms and Alzheimer's disease in an Italian cohort.
    Tedde A, Putignano AL, Nacmias B, Bagnoli S, Cellini E, Sorbi S.
    Neurosci Lett; 2008 Dec 03; 446(2-3):139-42. PubMed ID: 18834925
    [Abstract] [Full Text] [Related]

  • 39. Lack of association between Interleukin-18 gene promoter polymorphisms and onset of Alzheimer's disease.
    Segat L, Milanese M, Arosio B, Vergani C, Crovella S.
    Neurobiol Aging; 2010 Jan 03; 31(1):162-4. PubMed ID: 18433937
    [Abstract] [Full Text] [Related]

  • 40. The interferon gene cluster: a candidate region for MS predisposition? Multiple Sclerosis Study Group.
    Miterski B, Jaeckel S, Epplen JT, Pöhlau D, Hardt C.
    Genes Immun; 1999 Sep 03; 1(1):37-44. PubMed ID: 11197304
    [Abstract] [Full Text] [Related]

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