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.
91 related articles for article (PubMed ID: 11037899)
1. HLA-B44031;DRB1*1503 and other sub-Saharan African major histocompatibility complex haplotypes in African Americans and Afro-Caribbeans carry C4A gene deletions: implications for ethnicity-specific lupus susceptibility genes. Fraser PA; Lu LY; Ding WZ; Najundaswamy SN; Chen DF; Uko G; Tonks S Arthritis Rheum; 2000 Oct; 43(10):2378-9. PubMed ID: 11037899 [No Abstract] [Full Text] [Related]
2. 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 [TBL] [Abstract][Full Text] [Related]
3. 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 [TBL] [Abstract][Full Text] [Related]
4. Genetically determined partial complement C4 deficiency states are not independent risk factors for SLE in UK and Spanish populations. Boteva L; Morris DL; Cortés-Hernández J; Martin J; Vyse TJ; Fernando MM Am J Hum Genet; 2012 Mar; 90(3):445-56. PubMed ID: 22387014 [TBL] [Abstract][Full Text] [Related]
5. A study of association of the complement C4 mutations with systemic lupus erythematosus in the Malaysian population. Puah SM; Lian LH; Chew CH; Chua KH; Tan SY Lupus; 2007; 16(9):750-4. PubMed ID: 17728371 [TBL] [Abstract][Full Text] [Related]
6. [Influence of alleles and haplotypes of the main histocompatibility complex on the susceptibility to systemic lupus erythematosus in the Mexican population]. Granados J; Zúñiga J; Acuña-Alonzo V; Rosetti F; Vargas-Alarcón G Gac Med Mex; 2006; 142(3):195-9. PubMed ID: 16875346 [TBL] [Abstract][Full Text] [Related]
7. HLA-DRB1 allele frequencies and C4 copy number variation in Finnish sarcoidosis patients and associations with disease prognosis. Wennerström A; Pietinalho A; Vauhkonen H; Lahtela L; Palikhe A; Hedman J; Purokivi M; Varkki E; Seppänen M; Lokki ML; Selroos O; Hum Immunol; 2012 Jan; 73(1):93-100. PubMed ID: 22074998 [TBL] [Abstract][Full Text] [Related]
8. Genetic sophistication of human complement components C4A and C4B and RP-C4-CYP21-TNX (RCCX) modules in the major histocompatibility complex. Chung EK; Yang Y; Rennebohm RM; Lokki ML; Higgins GC; Jones KN; Zhou B; Blanchong CA; Yu CY Am J Hum Genet; 2002 Oct; 71(4):823-37. PubMed ID: 12226794 [TBL] [Abstract][Full Text] [Related]
9. Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genes. Lokki ML; Circolo A; Ahokas P; Rupert KL; Yu CY; Colten HR J Immunol; 1999 Mar; 162(6):3687-93. PubMed ID: 10092831 [TBL] [Abstract][Full Text] [Related]
10. Use of a PCR-based amplification analysis as a substitute for the Southern blot method to determine the C4A and C4B genes. Lee HH; Tseng YT; Lee YJ J Immunol Methods; 2006 Dec; 317(1-2):126-31. PubMed ID: 17095005 [TBL] [Abstract][Full Text] [Related]
11. 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; 69(9):580-7. PubMed ID: 18657583 [TBL] [Abstract][Full Text] [Related]
12. MHC region and risk of systemic lupus erythematosus in African American women. Ruiz-Narvaez EA; Fraser PA; Palmer JR; Cupples LA; Reich D; Wang YA; Rioux JD; Rosenberg L Hum Genet; 2011 Dec; 130(6):807-15. PubMed ID: 21695597 [TBL] [Abstract][Full Text] [Related]
13. Complement C4A gene deletion in patients with systemic lupus erythematosus in France. Cornillet P; Pennaforte JL; Philbert F; Bourgeois P; Kahn MF; Kazatchkine MD; Cohen JH J Rheumatol; 1993 Sep; 20(9):1633-4. PubMed ID: 8164236 [No Abstract] [Full Text] [Related]
14. Real-time PCR quantification of human complement C4A and C4B genes. Szilagyi A; Blasko B; Szilassy D; Fust G; Sasvari-Szekely M; Ronai Z BMC Genet; 2006 Jan; 7():1. PubMed ID: 16403222 [TBL] [Abstract][Full Text] [Related]
15. Complement C4 levels in SLE in relation to null allele status. Wilson WA J Rheumatol; 1994 Mar; 21(3):577-8. PubMed ID: 8043142 [No Abstract] [Full Text] [Related]
16. Unequal expression of complement C4A and C4B genes in rheumatoid synovial cells, human monocytoid and hepatoma-derived cell lines. Falus A; Kramer J; Walcz E; Varga Z; Setalo J; Jobst K; Lakatos T; Merétey K Immunology; 1989 Sep; 68(1):133-6. PubMed ID: 2553583 [TBL] [Abstract][Full Text] [Related]
17. Complement C4 protein and DNA typing methods. Schneider PM; Mauff G Methods Mol Biol; 2003; 210():269-95. PubMed ID: 12412461 [No Abstract] [Full Text] [Related]
19. Relationship between copy number of genes (C4A, C4B) encoding the fourth component of complement and the clinical course of hereditary angioedema (HAE). Blaskó B; Széplaki G; Varga L; Ronai Z; Prohászka Z; Sasvari-Szekely M; Visy B; Farkas H; Füst G Mol Immunol; 2007 Apr; 44(10):2667-74. PubMed ID: 17229465 [TBL] [Abstract][Full Text] [Related]
20. High-throughput analysis of the C4 polymorphism by a combination of MLPA and isotype-specific ELISA's. Wouters D; van Schouwenburg P; van der Horst A; de Boer M; Schooneman D; Kuijpers TW; Aarden LA; Hamann D Mol Immunol; 2009 Feb; 46(4):592-600. PubMed ID: 19062096 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]