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Items: 1 to 20 of 272

1.

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.

2.
3.

Restriction fragment analysis of duplication of the fourth component of complement (C4A).

McLean RH, Donohoue PA, Jospe N, Bias WB, Van Dop C, Migeon CJ.

Genomics. 1988 Jan;2(1):76-85.

PMID:
2838414
4.

Adrenal 21-hydroxylase cytochrome P-450 genes within the MHC class III region.

White PC, New MI, Dupont B.

Immunol Rev. 1985 Oct;87:123-50. Review.

PMID:
3902620
5.

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.

White PC, Grossberger D, Onufer BJ, Chaplin DD, New MI, Dupont B, Strominger JL.

Proc Natl Acad Sci U S A. 1985 Feb;82(4):1089-93.

6.
7.

Gene organization of haplotypes expressing two different C4A allotypes.

Palsdottir A, Arnason A, Fossdal R, Jensson O.

Hum Genet. 1987 Jul;76(3):220-4.

PMID:
3036685
8.

Molecular heterogeneity of complement component C4-null and 21-hydroxylase genes in systemic lupus erythematosus.

Goldstein R, Arnett FC, McLean RH, Bias WB, Duvic M.

Arthritis Rheum. 1988 Jun;31(6):736-44.

PMID:
3260100
9.

C4B gene polymorphism detected in a human cosmid clone.

Prentice HL, Schneider PM, Strominger JL.

Immunogenetics. 1986;23(4):274-6. No abstract available.

PMID:
3009318
11.

Molecular genetics of the fourth component of human complement.

Carroll MC, Palsdottir A, Belt KT, Yu CY.

Biochem Soc Symp. 1986;51:29-36.

PMID:
3101699
12.
14.

Major histocompatibility complex (MHC) class III genetics in two Amerindian tribes from southern Brazil: the Kaingang and the Guarani.

Weg-Remers S, Brenden M, Schwarz E, Witzel K, Schneider PM, Guerra LK, Rehfeldt IR, Lima MT, Hartmann D, Petzl-Erler ML, de Messias IJ, Mauff G.

Hum Genet. 1997 Oct;100(5-6):548-56.

PMID:
9341869
15.

Complement component C4 deficiencies and gene alterations in patients with systemic lupus erythematosus.

Fan Q, Uring-Lambert B, Weill B, Gautreau C, Menkes CJ, Delpech M.

Eur J Immunogenet. 1993 Feb;20(1):11-21.

PMID:
8095158
16.

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
17.

Molecular characterisation of C4 null alleles found in Felty's syndrome.

Hillarby MC, Strachan T, Grennan DM.

Ann Rheum Dis. 1990 Oct;49(10):763-7.

18.

Steroid 21-hydroxylase deficiency and the major histocompatibility complex.

White PC, Werkmeister J, New MI, Dupont B.

Hum Immunol. 1986 Apr;15(4):404-15.

PMID:
3009365

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