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Journal Abstract Search

146 related items for PubMed ID: 16321988

  • 21. 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 01; 10(25):2907-16. PubMed ID: 11741834
    [Abstract] [Full Text] [Related]

  • 22. Analysis of HLA DR2&DQ6 (DRB1*1501, DQA1*0102, DQB1*0602) haplotypes in Iranian patients with multiple sclerosis.
    Ghabaee M, Bayati A, Amri Saroukolaei S, Sahraian MA, Sanaati MH, Karimi P, Houshmand M, Sadeghian H, Hashemi Chelavi L.
    Cell Mol Neurobiol; 2009 Feb 01; 29(1):109-14. PubMed ID: 18726686
    [Abstract] [Full Text] [Related]

  • 23. Genetic and functional studies in multiple sclerosis patients from Martinique attest for a specific and direct role of the HLA-DR locus in the syndrome.
    Quelvennec E, Bera O, Cabre P, Alizadeh M, Smadja D, Jugde F, Edan G, Semana G.
    Tissue Antigens; 2003 Feb 01; 61(2):166-71. PubMed ID: 12694585
    [Abstract] [Full Text] [Related]

  • 24. Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome.
    Sinisalo J, Vlachopoulou E, Marchesani M, Nokelainen J, Mäyränpää MI, Lappalainen J, Paakkanen R, Wennerström A, Salli K, Niemi HJ, Männistö S, Salo P, Junttila J, Eskola M, Nikus K, Arstila TP, Perola M, Huikuri H, Karhunen PJ, Kovanen PT, Palotie A, Havulinna AS, Lluis-Ganella C, Marrugat J, Elosua R, Salomaa V, Nieminen MS, Lokki ML.
    Circ Cardiovasc Genet; 2016 Feb 01; 9(1):55-63. PubMed ID: 26679868
    [Abstract] [Full Text] [Related]

  • 25. Confirmation of the novel association at the BTNL2 locus with ulcerative colitis.
    Pathan S, Gowdy RE, Cooney R, Beckly JB, Hancock L, Guo C, Barrett JC, Morris A, Jewell DP.
    Tissue Antigens; 2009 Oct 01; 74(4):322-9. PubMed ID: 19659809
    [Abstract] [Full Text] [Related]

  • 26. HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility.
    Chao MJ, Barnardo MC, Lincoln MR, Ramagopalan SV, Herrera BM, Dyment DA, Montpetit A, Sadovnick AD, Knight JC, Ebers GC.
    Proc Natl Acad Sci U S A; 2008 Sep 02; 105(35):13069-74. PubMed ID: 18765817
    [Abstract] [Full Text] [Related]

  • 27. Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations.
    Alcina A, Abad-Grau Mdel M, Fedetz M, Izquierdo G, Lucas M, Fernández O, Ndagire D, Catalá-Rabasa A, Ruiz A, Gayán J, Delgado C, Arnal C, Matesanz F.
    PLoS One; 2012 Sep 02; 7(1):e29819. PubMed ID: 22253788
    [Abstract] [Full Text] [Related]

  • 28. TAP2 polymorphisms in Australian multiple sclerosis patients.
    Bennetts BH, Teutsch SM, Heard RN, Dunckley H, Stewart GJ.
    J Neuroimmunol; 1995 Jun 02; 59(1-2):113-21. PubMed ID: 7797612
    [Abstract] [Full Text] [Related]

  • 29. Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.
    Barcellos LF, Sawcer S, Ramsay PP, Baranzini SE, Thomson G, Briggs F, Cree BC, Begovich AB, Villoslada P, Montalban X, Uccelli A, Savettieri G, Lincoln RR, DeLoa C, Haines JL, Pericak-Vance MA, Compston A, Hauser SL, Oksenberg JR.
    Hum Mol Genet; 2006 Sep 15; 15(18):2813-24. PubMed ID: 16905561
    [Abstract] [Full Text] [Related]

  • 30. DQB1*0602 rather than DRB1*1501 confers susceptibility to multiple sclerosis-like disease induced by proteolipid protein (PLP).
    Kaushansky N, Altmann DM, David CS, Lassmann H, Ben-Nun A.
    J Neuroinflammation; 2012 Feb 08; 9():29. PubMed ID: 22316121
    [Abstract] [Full Text] [Related]

  • 31. An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 gene.
    Ramagopalan SV, McMahon R, Dyment DA, Sadovnick AD, Ebers GC, Wittkowski KM.
    BMC Med Genet; 2009 Feb 04; 10():10. PubMed ID: 19193207
    [Abstract] [Full Text] [Related]

  • 32. Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2.
    Mitsunaga S, Hosomichi K, Okudaira Y, Nakaoka H, Kunii N, Suzuki Y, Kuwana M, Sato S, Kaneko Y, Homma Y, Kashiwase K, Azuma F, Kulski JK, Inoue I, Inoko H.
    J Hum Genet; 2013 Apr 04; 58(4):210-5. PubMed ID: 23364395
    [Abstract] [Full Text] [Related]

  • 33. HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course.
    Barcellos LF, Oksenberg JR, Begovich AB, Martin ER, Schmidt S, Vittinghoff E, Goodin DS, Pelletier D, Lincoln RR, Bucher P, Swerdlin A, Pericak-Vance MA, Haines JL, Hauser SL, Multiple Sclerosis Genetics Group.
    Am J Hum Genet; 2003 Mar 04; 72(3):710-6. PubMed ID: 12557126
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  • 36. DQB1*0602 allele shows a strong association with multiple sclerosis in patients in Malaga, Spain.
    Fernández O, Fernández V, Alonso A, Caballero A, Luque G, Bravo M, León A, Mayorga C, Leyva L, de Ramón E.
    J Neurol; 2004 Apr 04; 251(4):440-4. PubMed ID: 15083289
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  • 38. Association of susceptibility to multiple sclerosis in Southern Han Chinese with HLA-DRB1, -DPB1 alleles and DRB1-DPB1 haplotypes: distinct from other populations.
    Wu XM, Wang C, Zhang KN, Lin AY, Kira J, Hu GZ, Qu XH, Xiong YQ, Cao WF, Gong LY.
    Mult Scler; 2009 Dec 04; 15(12):1422-30. PubMed ID: 19965521
    [Abstract] [Full Text] [Related]

  • 39. The DRB1 Val86/Val86 genotype associates with multiple sclerosis in Australian patients.
    Teutsch SM, Bennetts BH, Buhler MM, Heard RN, Stewart GJ.
    Hum Immunol; 1999 Aug 04; 60(8):715-22. PubMed ID: 10439317
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