173 related articles for article (PubMed ID: 24465950)
1. Investigation of complement component C4 copy number variation in human longevity.
Flachsbart F; Caliebe A; Heinsen FA; Hemming-Karlsen T; Schreiber S; Franke A; Nebel A
PLoS One; 2014; 9(1):e86188. PubMed ID: 24465950
[TBL] [Abstract][Full Text] [Related]
2. Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans.
Yang Y; Chung EK; Wu YL; Savelli SL; Nagaraja HN; Zhou B; Hebert M; Jones KN; Shu Y; Kitzmiller K; Blanchong CA; McBride KL; Higgins GC; Rennebohm RM; Rice RR; Hackshaw KV; Roubey RA; Grossman JM; Tsao BP; Birmingham DJ; Rovin BH; Hebert LA; Yu CY
Am J Hum Genet; 2007 Jun; 80(6):1037-54. PubMed ID: 17503323
[TBL] [Abstract][Full Text] [Related]
3. High-throughput complement component 4 genomic sequence analysis with C4Investigator.
Marin WM; Augusto DG; Wade KJ; Hollenbach JA
HLA; 2024 Jan; 103(1):e15273. PubMed ID: 37899688
[TBL] [Abstract][Full Text] [Related]
4. C4 null alleles and myocardial infarction.
Nityanand S; Hamsten A; Lithell H; Holm G; Lefvert AK
Atherosclerosis; 1999 Apr; 143(2):377-81. PubMed ID: 10217367
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Low C4, C4A and C4B gene copy numbers are stronger risk factors for juvenile-onset than for adult-onset systemic lupus erythematosus.
Pereira KM; Faria AG; Liphaus BL; Jesus AA; Silva CA; Carneiro-Sampaio M; Andrade LE
Rheumatology (Oxford); 2016 May; 55(5):869-73. PubMed ID: 26800705
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Genome-Wide Copy Number Variation Scan Identifies Complement Component C4 as Novel Susceptibility Gene for Crohn's Disease.
Cleynen I; Konings P; Robberecht C; Laukens D; Amininejad L; Théâtre E; Machiels K; Arijs I; Rutgeerts P; Louis E; Franchimont D; De Vos M; Van Steen K; Georges M; Moreau Y; Vermeesch J; Vermeire S
Inflamm Bowel Dis; 2016 Mar; 22(3):505-15. PubMed ID: 26595553
[TBL] [Abstract][Full Text] [Related]
9. Genotypic diversity of complement component C4 does not predict kidney transplant outcome.
Wahrmann M; Döhler B; Ruhenstroth A; Haslacher H; Perkmann T; Exner M; Rees AJ; Böhmig GA
J Am Soc Nephrol; 2011 Feb; 22(2):367-76. PubMed ID: 21164027
[TBL] [Abstract][Full Text] [Related]
10. Molecular heterogeneity of the fourth component of complement (C4) and its genes in vitiligo.
Venneker GT; Westerhof W; de Vries IJ; Drayer NM; Wolthers BG; de Waal LP; Bos JD; Asghar SS
J Invest Dermatol; 1992 Dec; 99(6):853-8. PubMed ID: 1469300
[TBL] [Abstract][Full Text] [Related]
11. Impact of C4, C4A and C4B gene copy number variation in the susceptibility, phenotype and progression of systemic lupus erythematosus.
Pereira KMC; Perazzio S; Faria AGA; Moreira ES; Santos VC; Grecco M; da Silva NP; Andrade LEC
Adv Rheumatol; 2019 Aug; 59(1):36. PubMed ID: 31387635
[TBL] [Abstract][Full Text] [Related]
12. Complement component 4 variations may influence psychopathology risk in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Lao Q; Jardin MD; Jayakrishnan R; Ernst M; Merke DP
Hum Genet; 2018 Dec; 137(11-12):955-960. PubMed ID: 30465166
[TBL] [Abstract][Full Text] [Related]
13. Molecular heterogeneity of second and fourth components of complement and their genes in systemic sclerosis and association of HLA alleles A1, B8 and DR3 with limited and DR5 with diffuse systemic sclerosis.
Venneker GT; van den Hoogen FH; van Meegen M; de Kok-Nazaruk M; Hulsmans RF; Boerbooms AM; de Waal LP; Bos JD; Asghar SS
Exp Clin Immunogenet; 1998; 15(2):90-9. PubMed ID: 9691203
[TBL] [Abstract][Full Text] [Related]
14. Combined heterozygous deficiency of the classical complement pathway proteins C2 and C4.
Hartmann D; Fremeaux-Bacchi V; Weiss L; Meyer A; Blouin J; Hauptmann G; Kazatchkine M; Uring-Lambert B
J Clin Immunol; 1997 Mar; 17(2):176-84. PubMed ID: 9083894
[TBL] [Abstract][Full Text] [Related]
15. Inherited deficiency of the fourth component of human complement.
Hauptmann G; Tappeiner G; Schifferli JA
Immunodefic Rev; 1988; 1(1):3-22. PubMed ID: 3078708
[TBL] [Abstract][Full Text] [Related]
16. Association between copy number variation of complement component C4 and Graves' disease.
Liu YH; Wan L; Chang CT; Liao WL; Chen WC; Tsai Y; Tsai CH; Tsai FJ
J Biomed Sci; 2011 Sep; 18(1):71. PubMed ID: 21943165
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype.
Fasano MB; Winkelstein JA; LaRosa T; Bias WB; McLean RH
J Clin Invest; 1992 Oct; 90(4):1180-4. PubMed ID: 1401055
[TBL] [Abstract][Full Text] [Related]
19. A marked drop in the incidence of the null allele of the B gene of the fourth component of complement (C4B*Q0) in elderly subjects: C4B*Q0 as a probable negative selection factor for survival.
Kramer J; Fülöp T; Rajczy K; Nguyen AT; Füst G
Hum Genet; 1991 Apr; 86(6):595-8. PubMed ID: 2026423
[TBL] [Abstract][Full Text] [Related]
20. Glomerular deposition of the complement C4 isotypes C4A and C4B in glomeruonephritis.
Lhotta K; Schlogl A; Kronenberg F; Joannidis M; Konig P
Nephrol Dial Transplant; 1996 Jun; 11(6):1024-8. PubMed ID: 8671963
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
