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Journal Abstract Search

235 related items for PubMed ID: 15496200

  • 1. Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA-DR3.
    Price P, Santoso L, Mastaglia F, Garlepp M, Kok CC, Allcock R, Laing N.
    Tissue Antigens; 2004 Nov; 64(5):575-80. PubMed ID: 15496200
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  • 6. Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype.
    Mastaglia FL, Needham M, Scott A, James I, Zilko P, Day T, Kiers L, Corbett A, Witt CS, Allcock R, Laing N, Garlepp M, Christiansen FT.
    Neuromuscul Disord; 2009 Nov; 19(11):763-5. PubMed ID: 19720533
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  • 7. Common HLA-B8-DR3 haplotype in Northern India is different from that found in Europe.
    Witt CS, Price P, Kaur G, Cheong K, Kanga U, Sayer D, Christiansen F, Mehra NK.
    Tissue Antigens; 2002 Dec; 60(6):474-80. PubMed ID: 12542740
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  • 8. Multi-SNP analysis of MHC region: remarkable conservation of HLA-A1-B8-DR3 haplotype.
    Aly TA, Eller E, Ide A, Gowan K, Babu SR, Erlich HA, Rewers MJ, Eisenbarth GS, Fain PR.
    Diabetes; 2006 May; 55(5):1265-9. PubMed ID: 16644681
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  • 9. Familial inclusion body myositis in a mother and son with different ancestral MHC haplotypes.
    Mastaglia F, Price P, Walters S, Fabian V, Miller J, Zilko P.
    Neuromuscul Disord; 2006 Nov; 16(11):754-8. PubMed ID: 16934978
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  • 10. Sporadic inclusion body myositis: phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases.
    Needham M, James I, Corbett A, Day T, Christiansen F, Phillips B, Mastaglia FL.
    J Neurol Neurosurg Psychiatry; 2008 Sep; 79(9):1056-60. PubMed ID: 18258695
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  • 11. A high frequency of the A30, B18, DR3, DRw52, DQw2 extended haplotype in Sardinian celiac disease patients: further evidence that disease susceptibility is conferred by DQ A1*0501, B1*0201.
    Congia M, Frau F, Lampis R, Frau R, Mele R, Cucca F, Muntoni F, Porcu S, Boi F, Contu L.
    Tissue Antigens; 1992 Feb; 39(2):78-83. PubMed ID: 1349446
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  • 12. Type 1 diabetes in the Spanish population: additional factors to class II HLA-DR3 and -DR4.
    Urcelay E, Santiago JL, de la Calle H, Martínez A, Méndez J, Ibarra JM, Maluenda C, Fernández-Arquero M, de la Concha EG.
    BMC Genomics; 2005 Apr 20; 6():56. PubMed ID: 15842729
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  • 13. Contribution of MHC class I chain-related A (MICA) gene polymorphism to genetic susceptibility for systemic lupus erythematosus.
    Gambelunghe G, Gerli R, Bocci EB, Del Sindaco P, Ghaderi M, Sanjeevi CB, Bistoni O, Bini V, Falorni A.
    Rheumatology (Oxford); 2005 Mar 20; 44(3):287-92. PubMed ID: 15522921
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  • 14. A Gambian TNF haplotype matches the European HLA-A1,B8,DR3 and Chinese HLA-A33,B58,DR3 haplotypes.
    Price P, Bolitho P, Jaye A, Glasson M, Yindom LM, Sirugo G, Chase D, McDermid J, Whittle H.
    Tissue Antigens; 2003 Jul 20; 62(1):72-5. PubMed ID: 12859597
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  • 15. The genetic basis for the association of the 8.1 ancestral haplotype (A1, B8, DR3) with multiple immunopathological diseases.
    Price P, Witt C, Allcock R, Sayer D, Garlepp M, Kok CC, French M, Mallal S, Christiansen F.
    Immunol Rev; 1999 Feb 20; 167():257-74. PubMed ID: 10319267
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  • 16. Central MHC genes affect IgA levels in the human: reciprocal effects in IgA deficiency and IgA nephropathy.
    Matthews VB, Witt CS, French MA, Machulla HK, De la Concha EG, Cheong KY, Vigil P, Hollingsworth PN, Warr KJ, Christiansen FT, Price P.
    Hum Immunol; 2002 May 20; 63(5):424-33. PubMed ID: 11975987
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  • 17. Susceptibility locus for IgA deficiency and common variable immunodeficiency in the HLA-DR3, -B8, -A1 haplotypes.
    Schroeder HW, Zhu ZB, March RE, Campbell RD, Berney SM, Nedospasov SA, Turetskaya RL, Atkinson TP, Go RC, Cooper MD, Volanakis JE.
    Mol Med; 1998 Feb 20; 4(2):72-86. PubMed ID: 9508785
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  • 18. Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversification in the class III region.
    Vorechovsky I, Kralovicova J, Laycock MD, Webster AD, Marsh SG, Madrigal A, Hammarström L.
    Eur J Hum Genet; 2001 Aug 20; 9(8):590-8. PubMed ID: 11528504
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  • 19. Evaluation of IgA deficiency in Sardinians indicates a susceptibility gene is encoded within the HLA class III region.
    Cucca F, Zhu ZB, Khanna A, Cossu F, Congia M, Badiali M, Lampis R, Frau F, De Virgiliis S, Cao A, Arnone M, Piras P, Campbell RD, Cooper MD, Volanakis JE, Powis SH.
    Clin Exp Immunol; 1998 Jan 20; 111(1):76-80. PubMed ID: 9472664
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  • 20. Sporadic inclusion body myositis: variability in prevalence and phenotype and influence of the MHC.
    Mastaglia FL.
    Acta Myol; 2009 Oct 20; 28(2):66-71. PubMed ID: 20128139
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