157 related articles for article (PubMed ID: 12691705)
1. Relationship between complement components C4A and C4B diversities and two TNFA promoter polymorphisms in two healthy Caucasian populations.
Vatay A; Yang Y; Chung EK; Zhou Bi; Blanchong CA; Kovács M; Karádi I; Füst G; Romics L L; Varga L; Yu CY; Szalai C
Hum Immunol; 2003 May; 64(5):543-52. PubMed ID: 12691705
[TBL] [Abstract][Full Text] [Related]
2. Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease.
Blanchong CA; Zhou B; Rupert KL; Chung EK; Jones KN; Sotos JF; Zipf WB; Rennebohm RM; Yung Yu C
J Exp Med; 2000 Jun; 191(12):2183-96. PubMed ID: 10859342
[TBL] [Abstract][Full Text] [Related]
3. Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4.
Blanchong CA; Chung EK; Rupert KL; Yang Y; Yang Z; Zhou B; Moulds JM; Yu CY
Int Immunopharmacol; 2001 Mar; 1(3):365-92. PubMed ID: 11367523
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. An unequal crossover between the RCCX modules of the human MHC leading to the presence of a CYP21B gene and a tenascin TNXB/TNXA-RP2 recombinant between C4A and C4B genes in a patient with juvenile rheumatoid arthritis.
Rupert KL; Rennebohm RM; Yu CY
Exp Clin Immunogenet; 1999; 16(2):81-97. PubMed ID: 10343159
[TBL] [Abstract][Full Text] [Related]
6. Sensitive and specific real-time polymerase chain reaction assays to accurately determine copy number variations (CNVs) of human complement C4A, C4B, C4-long, C4-short, and RCCX modules: elucidation of C4 CNVs in 50 consanguineous subjects with defined HLA genotypes.
Wu YL; Savelli SL; Yang Y; Zhou B; Rovin BH; Birmingham DJ; Nagaraja HN; Hebert LA; Yu CY
J Immunol; 2007 Sep; 179(5):3012-25. PubMed ID: 17709516
[TBL] [Abstract][Full Text] [Related]
7. Determining the one, two, three, or four long and short loci of human complement C4 in a major histocompatibility complex haplotype encoding C4A or C4B proteins.
Chung EK; Yang Y; Rupert KL; Jones KN; Rennebohm RM; Blanchong CA; Yu CY
Am J Hum Genet; 2002 Oct; 71(4):810-22. PubMed ID: 12224044
[TBL] [Abstract][Full Text] [Related]
8. Fine-tuned characterization of RCCX copy number variants and their relationship with extended MHC haplotypes.
Bánlaki Z; Doleschall M; Rajczy K; Fust G; Szilágyi A
Genes Immun; 2012 Oct; 13(7):530-5. PubMed ID: 22785613
[TBL] [Abstract][Full Text] [Related]
9. Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations.
Saxena K; Kitzmiller KJ; Wu YL; Zhou B; Esack N; Hiremath L; Chung EK; Yang Y; Yu CY
Mol Immunol; 2009 Apr; 46(7):1289-303. PubMed ID: 19135723
[TBL] [Abstract][Full Text] [Related]
10. Genetic basis of tobacco smoking: strong association of a specific major histocompatibility complex haplotype on chromosome 6 with smoking behavior.
Füst G; Arason GJ; Kramer J; Szalai C; Duba J; Yang Y; Chung EK; Zhou B; Blanchong CA; Lokki ML; Bödvarsson S; Prohászka Z; Karádi I; Vatay A; Kovács M; Romics L; Thorgeirsson G; Yu CY
Int Immunol; 2004 Oct; 16(10):1507-14. PubMed ID: 15339882
[TBL] [Abstract][Full Text] [Related]
11. Complete complement components C4A and C4B deficiencies in human kidney diseases and systemic lupus erythematosus.
Yang Y; Lhotta K; Chung EK; Eder P; Neumair F; Yu CY
J Immunol; 2004 Aug; 173(4):2803-14. PubMed ID: 15294999
[TBL] [Abstract][Full Text] [Related]
12. Linkage analysis of the C4A/C4B copy number variation and polymorphisms of the adjacent steroid 21-hydroxylase gene in a healthy population.
Blaskó B; Bánlaki Z; Gyapay G; Pozsonyi E; Sasvári-Székely M; Rajczy K; Füst G; Szilágyi A
Mol Immunol; 2009 Aug; 46(13):2623-9. PubMed ID: 19505723
[TBL] [Abstract][Full Text] [Related]
13. Structure and genetics of the partially duplicated gene RP located immediately upstream of the complement C4A and the C4B genes in the HLA class III region. Molecular cloning, exon-intron structure, composite retroposon, and breakpoint of gene duplication.
Shen L; Wu LC; Sanlioglu S; Chen R; Mendoza AR; Dangel AW; Carroll MC; Zipf WB; Yu CY
J Biol Chem; 1994 Mar; 269(11):8466-76. PubMed ID: 8132574
[TBL] [Abstract][Full Text] [Related]
14. The intricate role of complement component C4 in human systemic lupus erythematosus.
Yang Y; Chung EK; Zhou B; Lhotta K; Hebert LA; Birmingham DJ; Rovin BH; Yu CY
Curr Dir Autoimmun; 2004; 7():98-132. PubMed ID: 14719377
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations.
Chen JY; Wu YL; Mok MY; Wu YJ; Lintner KE; Wang CM; Chung EK; Yang Y; Zhou B; Wang H; Yu D; Alhomosh A; Jones K; Spencer CH; Nagaraja HN; Lau YL; Lau CS; Yu CY
Arthritis Rheumatol; 2016 Jun; 68(6):1442-1453. PubMed ID: 26814708
[TBL] [Abstract][Full Text] [Related]
17. Dancing with complement C4 and the RP-C4-CYP21-TNX (RCCX) modules of the major histocompatibility complex.
Yu CY; Chung EK; Yang Y; Blanchong CA; Jacobsen N; Saxena K; Yang Z; Miller W; Varga L; Fust G
Prog Nucleic Acid Res Mol Biol; 2003; 75():217-92. PubMed ID: 14604014
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Human MHC class III genes, BF and C4. Polymorphism, complotypes and HLA class I and II associations in the Lombardy population (Italy).
De Paoli F; Cuccia Belvedere M; Martinetti M; Abbal M
Gene Geogr; 1987 Aug; 1(2):121-9. PubMed ID: 3155297
[TBL] [Abstract][Full Text] [Related]
20. Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease associations.
Yang Z; Mendoza AR; Welch TR; Zipf WB; Yu CY
J Biol Chem; 1999 Apr; 274(17):12147-56. PubMed ID: 10207042
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]