These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 18612409)

  • 1. Variants of ST8SIA1 are associated with risk of developing multiple sclerosis.
    Husain S; Yildirim-Toruner C; Rubio JP; Field J; ; Schwalb M; Cook S; Devoto M; Vitale E
    PLoS One; 2008 Jul; 3(7):e2653. PubMed ID: 18612409
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Variants in ST8SIA1 do not play a major role in susceptibility to multiple sclerosis in Canadian families.
    Ramagopalan SV; Morrison KM; Para A; Handel A; Disanto G; Handunnetthi L; Orton SM; Sadovnick AD; Ebers GC
    J Neuroimmunol; 2009 Jul; 212(1-2):142-4. PubMed ID: 19428123
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12.
    Vitale E; Cook S; Sun R; Specchia C; Subramanian K; Rocchi M; Nathanson D; Schwalb M; Devoto M; Rohowsky-Kochan C
    Hum Mol Genet; 2002 Feb; 11(3):295-300. PubMed ID: 11823448
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A NOTCH4 association with multiple sclerosis is secondary to HLA-DR*1501.
    Duvefelt K; Anderson M; Fogdell-Hahn A; Hillert J
    Tissue Antigens; 2004 Jan; 63(1):13-20. PubMed ID: 14651518
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Risk alleles for multiple sclerosis identified by a genomewide study.
    ; Hafler DA; Compston A; Sawcer S; Lander ES; Daly MJ; De Jager PL; de Bakker PI; Gabriel SB; Mirel DB; Ivinson AJ; Pericak-Vance MA; Gregory SG; Rioux JD; McCauley JL; Haines JL; Barcellos LF; Cree B; Oksenberg JR; Hauser SL
    N Engl J Med; 2007 Aug; 357(9):851-62. PubMed ID: 17660530
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The association of -330 interleukin-2 gene polymorphism and HLA-DR15 allele in Iranian patients with multiple sclerosis.
    Sayad A
    Int J Immunogenet; 2014 Aug; 41(4):330-4. PubMed ID: 24919928
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The genetics of multiple sclerosis. A review.
    Kalman B; Lublin FD
    Biomed Pharmacother; 1999 Sep; 53(8):358-70. PubMed ID: 10554670
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy.
    D'Alfonso S; Bolognesi E; Guerini FR; Barizzone N; Bocca S; Ferrante D; Castelli L; Bergamaschi L; Agliardi C; Ferrante P; Naldi P; Leone M; Caputo D; Ballerini C; Salvetti M; Galimberti D; Massacesi L; Trojano M; Momigliano-Richiardi P
    Genes Immun; 2008 Jan; 9(1):7-15. PubMed ID: 17928868
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An investigation of NOS2A promoter polymorphisms in Australian multiple sclerosis patients.
    Bugeja MJ; Booth DR; Bennetts BH; Heard RN; Burgner D; Stewart GJ
    Eur J Hum Genet; 2005 Jul; 13(7):815-22. PubMed ID: 15856071
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic contribution to multiple sclerosis risk among Ashkenazi Jews.
    Khankhanian P; Matsushita T; Madireddy L; Lizée A; Din L; Moré JM; Gourraud PA; Hauser SL; Baranzini SE; Oksenberg JR
    BMC Med Genet; 2015 Jul; 16():55. PubMed ID: 26212423
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage disequilibrium analyses within chromosome 19p in multiple sclerosis.
    Vyshkina T; Kalman B
    Mult Scler; 2008 May; 14(4):433-9. PubMed ID: 18208878
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multiple sclerosis is associated with genes within or close to the HLA-DR-DQ subregion on a normal DR15,DQ6,Dw2 haplotype.
    Hillert J; Olerup O
    Neurology; 1993 Jan; 43(1):163-8. PubMed ID: 8093808
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association to the Glypican-5 gene in multiple sclerosis.
    Lorentzen AR; Melum E; Ellinghaus E; Smestad C; Mero IL; Aarseth JH; Myhr KM; Celius EG; Lie BA; Karlsen TH; Franke A; Harbo HF
    J Neuroimmunol; 2010 Sep; 226(1-2):194-7. PubMed ID: 20692050
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Highly conserved extended haplotypes of the major histocompatibility complex and their relationship to multiple sclerosis susceptibility.
    Goodin DS; Khankhanian P; Gourraud PA; Vince N
    PLoS One; 2018; 13(2):e0190043. PubMed ID: 29438392
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia.
    Marrosu MG; Murru R; Murru MR; Costa G; Zavattari P; Whalen M; Cocco E; Mancosu C; Schirru L; Solla E; Fadda E; Melis C; Porru I; Rolesu M; Cucca F
    Hum Mol Genet; 2001 Dec; 10(25):2907-16. PubMed ID: 11741834
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Susceptibility variants in the CD58 gene locus point to a role of microRNA-548ac in the pathogenesis of multiple sclerosis.
    Hecker M; Fitzner B; Blaschke J; Blaschke P; Zettl UK
    Mutat Res Rev Mutat Res; 2015; 763():161-7. PubMed ID: 25795118
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Estimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs.
    Watson CT; Disanto G; Breden F; Giovannoni G; Ramagopalan SV
    Sci Rep; 2012; 2():770. PubMed ID: 23105968
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients.
    Jensen CJ; Stankovich J; Van der Walt A; Bahlo M; Taylor BV; van der Mei IA; Foote SJ; Kilpatrick TJ; Johnson LJ; Wilkins E; Field J; Danoy P; Brown MA; ; Rubio JP; Butzkueven H
    PLoS One; 2010 Apr; 5(4):e10003. PubMed ID: 20368992
    [TBL] [Abstract][Full Text] [Related]  

  • 19. HLA-A confers an HLA-DRB1 independent influence on the risk of multiple sclerosis.
    Brynedal B; Duvefelt K; Jonasdottir G; Roos IM; Akesson E; Palmgren J; Hillert J
    PLoS One; 2007 Jul; 2(7):e664. PubMed ID: 17653284
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CTLA-4 and multiple sclerosis: the A49G single nucleotide polymorphism shows no association with multiple sclerosis in a Southern Australian population.
    Wray BN; Stankovich J; Whittock L; Dwyer T; Ponsonby AL; van der Mei IA; Taylor B; Dickinson J; Foote S; McMorran BJ
    J Neuroimmunol; 2008 May; 196(1-2):139-42. PubMed ID: 18378005
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.