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Results: 1 to 20 of 121

1.
2.

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. Review.

PMID:
11367523
[PubMed - indexed for MEDLINE]
3.
4.
5.

A promoter within intron 35 of the human C4A gene initiates abundant adrenal-specific transcription of a 1 kb RNA: location of a cryptic CYP21 promoter element?

Tee MK, Babalola GO, Aza-Blanc P, Speek M, Gitelman SE, Miller WL.

Hum Mol Genet. 1995 Nov;4(11):2109-16.

PMID:
8589688
[PubMed - indexed for MEDLINE]
6.

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. doi: 10.1016/j.molimm.2009.04.033. Epub 2009 Jun 7.

PMID:
19505723
[PubMed - indexed for MEDLINE]
7.

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 15;173(4):2803-14.

PMID:
15294999
[PubMed - indexed for MEDLINE]
Free Article
8.
9.

Polymerase chain reaction analysis of the Xba I polymorphism of the human complement C4 genes provides evidence for strong haplotype conservation.

Witzel K, Chu X, Rittner C, Schneider PM.

Hum Immunol. 1995 Jul;43(3):165-73.

PMID:
7558933
[PubMed - indexed for MEDLINE]
10.

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 19;191(12):2183-96.

PMID:
10859342
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Characterisation of the novel gene G11 lying adjacent to the complement C4A gene in the human major histocompatibility complex.

Sargent CA, Anderson MJ, Hsieh SL, Kendall E, Gomez-Escobar N, Campbell RD.

Hum Mol Genet. 1994 Mar;3(3):481-8.

PMID:
8012361
[PubMed - indexed for MEDLINE]
13.

Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region.

Carroll MC, Palsdottir A, Belt KT, Porter RR.

EMBO J. 1985 Oct;4(10):2547-52.

PMID:
2996881
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression.

Barba G, Rittner C, Schneider PM.

J Clin Invest. 1993 Apr;91(4):1681-6.

PMID:
8473511
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Polymorphism of the human complement component C4.

Campbell RD, Dunham I, Kendall E, Sargent CA.

Exp Clin Immunogenet. 1990;7(1):69-84. Review.

PMID:
1971760
[PubMed - indexed for MEDLINE]
16.

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.

PMID:
15998580
[PubMed - indexed for MEDLINE]
17.

Null alleles of human complement C4. Evidence for pseudogenes at the C4A locus and for gene conversion at the C4B locus.

Braun L, Schneider PM, Giles CM, Bertrams J, Rittner C.

J Exp Med. 1990 Jan 1;171(1):129-40.

PMID:
2295875
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

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. doi: 10.1016/j.molimm.2008.07.028. Epub 2008 Dec 5.

PMID:
19062096
[PubMed - indexed for MEDLINE]
19.

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 15;162(6):3687-93.

PMID:
10092831
[PubMed - indexed for MEDLINE]
Free Article

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