• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在英国白种人群中通过光分型法(PCR-SSP)检测到的两个新型HLA-B等位基因的完整编码区:B*5108和B*5002。

Complete coding regions of two novel HLA-B alleles detected by phototyping (PCR-SSP) in the British caucasoid population: B*5108 and B*5002.

作者信息

Vilches C, Bunce M, de Pablo R, Murray A K, McIntyre C A, Kreisler M

机构信息

Servicio de Inmunología, Clínica Puerta de Hierro, Madrid, Spain.

出版信息

Tissue Antigens. 1997 Jul;50(1):38-41. doi: 10.1111/j.1399-0039.1997.tb02831.x.

DOI:10.1111/j.1399-0039.1997.tb02831.x
PMID:9243753
Abstract

Two previously reported PCR-SSP variants of the HLA-B locus, B51GAC and B45v, were investigated by RT-PCR cloning and nucleotide sequence analysis of their complete coding regions. They have been shown to correspond to the new alleles B5108 and B5002, both of which differ from the common B5101 and B5001 subtypes, respectively, by amino acid replacements at their alpha-2 domain alpha-helices. The primary structure of B5002, intermediate between those of B4501 and B5001, raises further concern about the current classification of B45 as a B12 rather than as a B*50 subtype.

摘要

通过对HLA - B位点的两个先前报道的PCR - SSP变体B51GAC和B45v的完整编码区进行逆转录聚合酶链反应(RT - PCR)克隆和核苷酸序列分析,对它们展开了研究。结果表明它们分别对应新等位基因B5108和B5002,这两个新等位基因在其α - 2结构域α - 螺旋处的氨基酸替换,使其分别与常见的B5101和B5001亚型有所不同。B5002的一级结构处于B4501和B5001之间,这进一步引发了对于当前将B45归类为B12而非B*50亚型的质疑。

相似文献

1
Complete coding regions of two novel HLA-B alleles detected by phototyping (PCR-SSP) in the British caucasoid population: B*5108 and B*5002.在英国白种人群中通过光分型法(PCR-SSP)检测到的两个新型HLA-B等位基因的完整编码区:B*5108和B*5002。
Tissue Antigens. 1997 Jul;50(1):38-41. doi: 10.1111/j.1399-0039.1997.tb02831.x.
2
Complementary DNA sequence of the novel HLA-B*3704 allele.
Tissue Antigens. 2002 Feb;59(2):142-4. doi: 10.1034/j.1399-0039.2002.590213.x.
3
Identification of a new HLA-B*15 allele, HLA-B*1569.一种新的HLA - B*15等位基因HLA - B*1569的鉴定。
Tissue Antigens. 2002 Feb;59(2):151-3. doi: 10.1034/j.1399-0039.2002.590216.x.
4
A novel HLA-B*51 allele (B*5116) identified by nucleotide sequencing.通过核苷酸测序鉴定出一种新型HLA - B*51等位基因(B*5116)。
Tissue Antigens. 2000 Feb;55(2):182-4. doi: 10.1034/j.1399-0039.2000.550214.x.
5
A discrepancy between serological and molecular typing results led to identification of a novel HLA-B*57 allele: HLA-B*5728N.血清学和分子分型结果之间的差异导致了一个新的 HLA-B*57 等位基因的鉴定:HLA-B*5728N。
Int J Immunogenet. 2010 Aug;37(4):299-300. doi: 10.1111/j.1744-313X.2010.00922.x. Epub 2010 May 27.
6
A novel HLA-B*420502 allele identified by PCR-SSO/SSP routine typing and confirmed by Sequencing-based typing.通过聚合酶链反应-序列特异性寡核苷酸探针/序列特异性引物常规分型鉴定并经测序分型确认的一种新型HLA-B*420502等位基因。
Tissue Antigens. 2005 Mar;65(3):275-7. doi: 10.1111/j.1399-0039.2005.00376.x.
7
A new HLA-B51 allele, B*5107 in RCE55 detected and characterized by PCR-SSOP, cloning and nucleotide sequence determination.
Tissue Antigens. 1996 Sep;48(3):228-30. doi: 10.1111/j.1399-0039.1996.tb02636.x.
8
Complementary DNA sequence of the HLA-B*3924 allele.HLA - B*3924等位基因的互补DNA序列。
Eur J Immunogenet. 2003 Feb;30(1):11-2. doi: 10.1046/j.1365-2370.2003.00362.x.
9
HLA-B*4413 identified in a UK Caucasoid potential bone marrow donor.在一名英国白种人潜在骨髓供者中鉴定出HLA - B*4413。
Tissue Antigens. 2000 Feb;55(2):185-7. doi: 10.1034/j.1399-0039.2000.550215.x.
10
Complete cDNA sequence of B*4406, an HLA-B allele containing sequences of B*5101 and B*4402.
Tissue Antigens. 1996 May;47(5):431-4. doi: 10.1111/j.1399-0039.1996.tb02581.x.

引用本文的文献

1
How ERAP1 and ERAP2 Shape the Peptidomes of Disease-Associated MHC-I Proteins.内质网氨肽酶 1 和 2 如何塑造与疾病相关的 MHC-I 蛋白的肽组。
Front Immunol. 2018 Oct 30;9:2463. doi: 10.3389/fimmu.2018.02463. eCollection 2018.
2
The Behçet's disease-associated variant of the aminopeptidase ERAP1 shapes a low-affinity HLA-B*51 peptidome by differential subpeptidome processing.与白塞病相关的氨肽酶ERAP1变体通过差异亚肽组加工形成低亲和力的HLA - B*51肽组。
J Biol Chem. 2017 Jun 9;292(23):9680-9689. doi: 10.1074/jbc.M117.789180. Epub 2017 Apr 26.