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Bgl II polymorphic site upstream to the human complement component C4A gene.

作者信息

Palsdottir A, Fossdal R, Jensson O, Arnason A

出版信息

Nucleic Acids Res. 1987 Mar 11;15(5):2395. doi: 10.1093/nar/15.5.2395.

DOI:10.1093/nar/15.5.2395
PMID:2882470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC340649/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009e/340649/59dd83ace457/nar00249-0508-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009e/340649/59dd83ace457/nar00249-0508-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009e/340649/59dd83ace457/nar00249-0508-a.jpg

相似文献

1
Bgl II polymorphic site upstream to the human complement component C4A gene.人类补体成分C4A基因上游的Bgl II多态性位点。
Nucleic Acids Res. 1987 Mar 11;15(5):2395. doi: 10.1093/nar/15.5.2395.
2
Bgl II restriction fragment length polymorphism of human complement C4A gene coincides with BF*F allele of factor B.
Immunogenetics. 1988;27(3):225-8. doi: 10.1007/BF00346591.
3
Polymorphism of the human complement component C4.人类补体成分C4的多态性
Exp Clin Immunogenet. 1990;7(1):69-84.
4
Heterogeneity in the structural basis of the human complement C4A null allele (C4A Q0) as revealed by HindIII restriction fragment length polymorphism analysis.通过HindIII限制性片段长度多态性分析揭示的人类补体C4A无效等位基因(C4A Q0)结构基础的异质性。
FEBS Lett. 1987 Jun 8;217(1):65-8. doi: 10.1016/0014-5793(87)81244-9.
5
Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.人类补体C4和类固醇21-羟化酶基因的多态性。揭示结构缺失、同型重复和大小变异的限制性片段长度多态性。
J Clin Invest. 1986 Sep;78(3):650-7. doi: 10.1172/JCI112623.
6
Polymerase chain reaction analysis of the Xba I polymorphism of the human complement C4 genes provides evidence for strong haplotype conservation.对人类补体C4基因Xba I多态性的聚合酶链反应分析为强单倍型保守性提供了证据。
Hum Immunol. 1995 Jul;43(3):165-73. doi: 10.1016/0198-8859(94)00150-o.
7
Correlation between a DNA restriction fragment length polymorphism and C4A6 protein.
Nature. 1983;306(5943):615-6. doi: 10.1038/306615a0.
8
A rare TaqI polymorphism in a human complement C4 gene is caused by an additional restriction site in the first intron.
Immunol Lett. 1992 Oct-Nov;34(2):93-7. doi: 10.1016/0165-2478(92)90233-e.
9
Restriction fragment length polymorphisms of the complement component C4 loci on chromosome 6: studies with emphasis on the determination of gene number.6号染色体上补体成分C4基因座的限制性片段长度多态性:着重于基因数量测定的研究
Ann Hum Genet. 1988 May;52(2):77-84. doi: 10.1111/j.1469-1809.1988.tb01082.x.
10
A rare complement component C4 restriction fragment length polymorphism in two families with systemic lupus erythematosus.两个系统性红斑狼疮家族中罕见的补体成分C4限制性片段长度多态性
J Rheumatol. 1991 Mar;18(3):345-8.

引用本文的文献

1
Bgl II restriction fragment length polymorphism of human complement C4A gene coincides with BF*F allele of factor B.
Immunogenetics. 1988;27(3):225-8. doi: 10.1007/BF00346591.
2
Direct observation of the gene organization of the complement C4 and 21-hydroxylase loci by pulsed field gel electrophoresis.通过脉冲场凝胶电泳直接观察补体C4和21-羟化酶基因座的基因组织。
J Exp Med. 1989 May 1;169(5):1803-18. doi: 10.1084/jem.169.5.1803.

本文引用的文献

1
The structural basis of the multiple forms of human complement component C4.人类补体成分C4多种形式的结构基础。
Cell. 1984 Apr;36(4):907-14. doi: 10.1016/0092-8674(84)90040-0.
2
C2 and factor B: structure and genetics.补体C2和B因子:结构与遗传学
Biochem Soc Symp. 1986;51:7-18.