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212 related items for PubMed ID: 11093438
1. A study of C4AQ0 and MHC haplotypes in Icelandic multicase families with systemic lupus erythematosus. Kristjánsdóttir H, Bjarnadóttir K, Hjálmarsdóttir IB, Gröndal G, Arnason A, Steinsson K. J Rheumatol; 2000 Nov; 27(11):2590-6. PubMed ID: 11093438 [Abstract] [Full Text] [Related]
2. Association of three systemic lupus erythematosus susceptibility factors, PD-1.3A, C4AQ0, and low levels of mannan-binding lectin, with autoimmune manifestations in Icelandic multicase systemic lupus erythematosus families. Kristjansdottir H, Saevarsdottir S, Gröndal G, Alarcón-Riquelme ME, Erlendsson K, Valdimarsson H, Steinsson K. Arthritis Rheum; 2008 Dec; 58(12):3865-72. PubMed ID: 19035512 [Abstract] [Full Text] [Related]
3. A study of the genetic basis of C4A protein deficiency. Detection of C4A gene deletion by long-range PCR and its associated haplotypes. Kristjánsdóttir H, Steinsson K. Scand J Rheumatol; 2004 Dec; 33(6):417-22. PubMed ID: 15794202 [Abstract] [Full Text] [Related]
4. Complete deficiencies of complement C4A and C4B including 2-bp insertion in codon 1213 are genetic risk factors of systemic lupus erythematosus in Thai populations. Ittiprasert W, Kantachuvesiri S, Pavasuthipaisit K, Verasertniyom O, Chaomthum L, Totemchokchyakarn K, Kitiyanant Y. J Autoimmun; 2005 Aug; 25(1):77-84. PubMed ID: 15998580 [Abstract] [Full Text] [Related]
7. Mannan-binding lectin and complement C4A in Icelandic multicase families with systemic lupus erythematosus. Saevarsdottir S, Kristjansdottir H, Grondal G, Vikingsdottir T, Steinsson K, Valdimarsson H. Ann Rheum Dis; 2006 Nov; 65(11):1462-7. PubMed ID: 16439442 [Abstract] [Full Text] [Related]
8. 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; 44(3):287-92. PubMed ID: 15522921 [Abstract] [Full Text] [Related]
9. Long PCR detection of the C4A null allele in B8-C4AQ0-C4B1-DR3. Grant SF, Kristjánsdóttir H, Steinsson K, Blöndal T, Yuryev A, Stefansson K, Gulcher JR. J Immunol Methods; 2000 Oct 20; 244(1-2):41-7. PubMed ID: 11033017 [Abstract] [Full Text] [Related]
10. Lack of gene deletion for complement C4A deficiency in Japanese patients with systemic lupus erythematosus. Yamada H, Watanabe A, Mimori A, Nakano K, Takeuchi F, Matsuta K, Tanimoto K, Miyamoto T, Yukiyama Y, Tokunaga K. J Rheumatol; 1990 Aug 20; 17(8):1054-7. PubMed ID: 1976809 [Abstract] [Full Text] [Related]
11. C4AQ0 superimposed on a primary defect increases the susceptibility to systemic lupus erythematosus (SLE) in a family with association between C4AQ0 and SLE. Traustadóttir KH, Steinsson K, Erlendsson K. J Rheumatol; 1998 Nov 20; 25(11):2118-25. PubMed ID: 9818652 [Abstract] [Full Text] [Related]
12. Increased number of interleukin-10-producing cells in systemic lupus erythematosus patients and their first-degree relatives and spouses in Icelandic multicase families. Gröndal G, Kristjansdottir H, Gunnlaugsdottir B, Arnason A, Lundberg I, Klareskog L, Steinsson K. Arthritis Rheum; 1999 Aug 20; 42(8):1649-54. PubMed ID: 10446864 [Abstract] [Full Text] [Related]
13. Major histocompatibility complex extended haplotypes in systemic lupus erythematosus. Welch TR, Beischel LS, Balakrishnan K, Quinlan M, West CD. Dis Markers; 1988 Aug 20; 6(4):247-55. PubMed ID: 3266126 [Abstract] [Full Text] [Related]
14. Autoimmune-associated HLA-B8-DR3 haplotypes in Asian Indians are unique in C4 complement gene copy numbers and HSP-2 1267A/G. Kaur G, Kumar N, Szilagyi A, Blasko B, Fust G, Rajczy K, Pozsonyi E, Hosso A, Petranyi G, Tandon N, Mehra N. Hum Immunol; 2008 Sep 20; 69(9):580-7. PubMed ID: 18657583 [Abstract] [Full Text] [Related]
19. A genetic association between systemic lupus erythematosus and tumor necrosis factor alpha. Wilson AG, Gordon C, di Giovine FS, de Vries N, van de Putte LB, Emery P, Duff GW. Eur J Immunol; 1994 Jan 20; 24(1):191-5. PubMed ID: 8020556 [Abstract] [Full Text] [Related]