21-羟化酶缺乏所致先天性肾上腺皮质增生症中的补体C4同种异型：21-羟化酶基因座存在不同等位基因变异的进一步证据 - Suppr

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超能文献

Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.

作者信息

O'Neill G J, Dupont B, Pollack M S, Levine L S, New M I

出版信息

Clin Immunol Immunopathol. 1982 May;23(2):312-22. doi: 10.1016/0090-1229(82)90117-9.

DOI:10.1016/0090-1229(82)90117-9

PMID:6980755

Abstract

摘要

相似文献

Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.21-羟化酶缺乏所致先天性肾上腺皮质增生症中的补体C4同种异型：21-羟化酶基因座存在不同等位基因变异的进一步证据

Clin Immunol Immunopathol. 1982 May;23(2):312-22. doi: 10.1016/0090-1229(82)90117-9.

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。

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Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.伴有补体C4B蛋白缺失的失盐型先天性肾上腺皮质增生症中的基因转换

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Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia.先天性肾上腺皮质增生症中类固醇21-羟化酶和补体C4基因的缺失

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21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.具有HLA相同的患病和未患病同胞的21-羟化酶缺乏症家族。

J Med Genet. 1989 Jan;26(1):10-7. doi: 10.1136/jmg.26.1.10.

Steroid 21-hydroxylase deficiency and the major histocompatibility complex.类固醇21-羟化酶缺乏症与主要组织相容性复合体

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Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.

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The HLA associations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a Yugoslav population.

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Adrenal 21-hydroxylase cytochrome P-450 genes within the MHC class III region.主要组织相容性复合体III类区域内的肾上腺21-羟化酶细胞色素P-450基因。

Immunol Rev. 1985 Oct;87:123-50. doi: 10.1111/j.1600-065x.1985.tb01148.x.

Frequent deletion and duplication of the steroid 21-hydroxylase genes.类固醇21-羟化酶基因的频繁缺失和重复。

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History of Adrenal Research: From Ancient Anatomy to Contemporary Molecular Biology.肾上腺研究史：从古代解剖学到当代分子生物学。

Endocr Rev. 2023 Jan 12;44(1):70-116. doi: 10.1210/endrev/bnac019.

MHC-linked class III genes. Analysis of C4 gene frequencies, complotypes and associations with distinct HLA haplotypes in German Caucasians.与主要组织相容性复合体（MHC）相关的Ⅲ类基因。德国高加索人群中C4基因频率、补体单倍型及其与不同HLA单倍型的关联分析。

Immunogenetics. 1984;20(1):23-31. doi: 10.1007/BF00373444.

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.与HLA相关的先天性肾上腺皮质增生症是由一个有缺陷的基因引起的，该基因编码一种对类固醇21-羟化作用具有特异性的细胞色素P-450。

Proc Natl Acad Sci U S A. 1984 Dec;81(23):7505-9. doi: 10.1073/pnas.81.23.7505.

Comparison of one-dimensional IEF patterns for serologically detectable HLA-A and B allotypes.血清学可检测的HLA - A和B同种异型的一维等电聚焦图谱比较。

Immunogenetics. 1984;19(3):217-31. doi: 10.1007/BF00364765.

Liver mRNA probes disclose two cytochrome P-450 genes duplicated in tandem with the complement C4 loci of the mouse H-2S region.肝脏mRNA探针揭示了两个与小鼠H-2S区域的补体C4基因座串联重复的细胞色素P-450基因。

Proc Natl Acad Sci U S A. 1985 Jul;82(13):4453-7. doi: 10.1073/pnas.82.13.4453.

C4 uremic variant: an acquired C4 allotype.C4尿毒症变体：一种获得性C4同种异型。

Immunogenetics. 1985;22(6):553-62. doi: 10.1007/BF00430303.

Frequent deletion and duplication of the steroid 21-hydroxylase genes.类固醇21-羟化酶基因的频繁缺失和重复。

Am J Hum Genet. 1986 Oct;39(4):461-9.

Order of class III genes relative to HLA genes determined by the haplotype method.通过单倍型方法确定的Ⅲ类基因相对于HLA基因的顺序。

Immunogenetics. 1986;24(2):79-83. doi: 10.1007/BF00373113.

Comparison of the structure of HLA-Bw47 to HLA-B13 and its relationship to 21-hydroxylase deficiency.

Immunogenetics. 1988;27(4):281-7. doi: 10.1007/BF00376123.

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.编码类固醇21-羟化酶的两个基因位于人类补体第四成分编码基因附近。

Proc Natl Acad Sci U S A. 1985 Feb;82(4):1089-93. doi: 10.1073/pnas.82.4.1089.

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