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Bgl II restriction fragment length polymorphism of human complement C4A gene coincides with BF*F allele of factor B.

作者信息

Schneider P M, Rittner C

机构信息

Children's Hospital, Department of Pediatrics, Boston, MA 02115.

出版信息

Immunogenetics. 1988;27(3):225-8. doi: 10.1007/BF00346591.

DOI:10.1007/BF00346591
PMID:2892787
Abstract
摘要

相似文献

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
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.
3
Human MHC class III genes, Bf and C4. Polymorphism, complotypes and association with MHC class I genes in the Finnish population.人类主要组织相容性复合体III类基因、B因子和C4。芬兰人群中的多态性、补体单倍型及与主要组织相容性复合体I类基因的关联
Hum Hered. 1986;36(5):269-75. doi: 10.1159/000153642.
4
DNA polymorphism of the C2 and factor B genes. Detection of a restriction fragment length polymorphism which subdivides haplotypes carrying the C2C and factor B F alleles.C2和B因子基因的DNA多态性。检测一种限制性片段长度多态性，该多态性可细分携带C2C和B因子F等位基因的单倍型。
Immunogenetics. 1985;21(1):39-48. doi: 10.1007/BF00372240.
5
A DNA restriction fragment length polymorphism in the complement region of the human MHC shows an absolute correlation with polymorphism of complement factor B(Bf) defined by isoelectric focusing.人类主要组织相容性复合体（MHC）补体区域的DNA限制性片段长度多态性与通过等电聚焦定义的补体因子B（Bf）多态性呈现出绝对相关性。
J Immunogenet. 1985 Dec;12(6):321-6.
6
A new TaqI polymorphism of the complement factor B gene.补体因子B基因的一种新的TaqI多态性
Nucleic Acids Res. 1988 Dec 23;16(24):11851. doi: 10.1093/nar/16.24.11851.
7
Genetic mapping of C4 and Bf complement genes in the rat major histocompatibility complex.大鼠主要组织相容性复合体中C4和Bf补体基因的遗传图谱
Immunogenetics. 1988;28(1):57-60. doi: 10.1007/BF00372531.
8
Complement polymorphism in Colombia.哥伦比亚的补体多态性。
Ann Hum Biol. 1985 May-Jun;12(3):261-5. doi: 10.1080/03014468500007761.
9
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.
10
Complement C2, C3, C4 and factor B allele distribution in the Gipsy population in Hungary.匈牙利吉卜赛人群中补体C2、C3、C4及B因子的等位基因分布
Immunol Lett. 1990 Mar-Apr;24(1):11-2. doi: 10.1016/0165-2478(90)90029-p.

引用本文的文献

1
Possible association of sudden infant death with partial complement C4 deficiency revealed by post-mortem DNA typing of HLA class II and III genes.通过对HLA II类和III类基因进行尸检DNA分型揭示婴儿猝死与部分补体C4缺乏之间可能存在的关联。
Eur J Pediatr. 1989 Dec;149(3):170-4. doi: 10.1007/BF01958273.
2
Major-histocompatibility-complex gene markers and restriction-fragment analysis of steroid 21-hydroxylase (CYP21) and complement C4 genes in classical congenital adrenal hyperplasia patients in a single population.单一人群中经典型先天性肾上腺皮质增生症患者的主要组织相容性复合体基因标记以及类固醇21-羟化酶（CYP21）和补体C4基因的限制性片段分析
Am J Hum Genet. 1989 May;44(5):660-70.

本文引用的文献

1
Statement on the nomenclature of human C4 allotypes.关于人类C4同种异型命名的声明。
Immunobiology. 1983 Mar;164(2):184-91. doi: 10.1016/s0171-2985(83)80009-6.
2
DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex.C4基因的DNA多态性。一种用于分析主要组织相容性复合体的新标记。
N Engl J Med. 1984 Jan 12;310(2):88-91. doi: 10.1056/NEJM198401123100204.
3
A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B.连接补体基因C4、C2和B因子的人类主要组织相容性复合体III类区域的分子图谱。
Nature. 1984;307(5948):237-41. doi: 10.1038/307237a0.
4
Serum complement 'supergenes' of the major histocompatibility complex in man (complotypes).人类主要组织相容性复合体的血清补体“超级基因”（补体型）
Vox Sang. 1983;45(1):62-7. doi: 10.1111/j.1423-0410.1983.tb04124.x.
5
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.
6
Correlation between a DNA restriction fragment length polymorphism and C4A6 protein.
Nature. 1983;306(5943):615-6. doi: 10.1038/306615a0.
7
Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.人类主要组织相容性复合体HLA中，类固醇21-羟化酶基因与补体成分C4基因的定位。
Proc Natl Acad Sci U S A. 1985 Jan;82(2):521-5. doi: 10.1073/pnas.82.2.521.
8
Complotype genetic loci segregate more frequently with HLA-DR than with HLA-B.补体型遗传位点与HLA - DR的分离比与HLA - B的分离更频繁。
Immunogenetics. 1985;21(1):25-31. doi: 10.1007/BF00372238.
9
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.
10
C4B gene polymorphism detected in a human cosmid clone.
Immunogenetics. 1986;23(4):274-6. doi: 10.1007/BF00373024.