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在费尔蒂综合征中发现的C4无效等位基因的分子特征分析。

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

作者信息

Hillarby M C, Strachan T, Grennan D M

机构信息

Rheumatic Diseases Centre, Hope Hospital, Salford.

出版信息

Ann Rheum Dis. 1990 Oct;49(10):763-7. doi: 10.1136/ard.49.10.763.

Abstract

A higher prevalence of C4B null alleles is found in Felty's syndrome. The molecular basis of C4 null alleles was investigated by studying restriction fragment length polymorphisms (RFLPs) obtained with C4 and 21-hydroxylase (21-OH) DNA probes and by pulsed field gel electrophoresis in 30 subjects with Felty's syndrome. C4A null alleles were found in 10 subjects, and in five of these were associated with a deletion that included C4A and adjacent 21-OHA gene sequences. A 6.4 kilobase C4B-5'-specific Taq I fragment usually provided a reliable guide to the presence of a C4A deletion but unusually in one instance this fragment was found to be a marker of a functioning C4A gene. A C4B null allele was found in 17 subjects and was associated with a deletion involving C4B and 21-OHA gene sequences on only two occasions. There were no instances in which deletion of the 21-OHB gene occurred.

摘要

在费尔蒂综合征中发现C4B无效等位基因的患病率更高。通过研究用C4和21-羟化酶(21-OH)DNA探针获得的限制性片段长度多态性(RFLP)以及对30例费尔蒂综合征患者进行脉冲场凝胶电泳,研究了C4无效等位基因的分子基础。在10名患者中发现了C4A无效等位基因,其中5名与包括C4A和相邻的21-OHA基因序列的缺失有关。一个6.4千碱基的C4B-5'-特异性Taq I片段通常能可靠地指示C4A缺失的存在,但在一个不寻常的例子中,发现该片段是一个功能正常的C4A基因的标记。在17名患者中发现了C4B无效等位基因,只有两次与涉及C4B和21-OHA基因序列的缺失有关。没有出现21-OHB基因缺失的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f08/1004227/5e19c3fa814f/annrheumd00444-0027-a.jpg

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