• 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

相似文献

1
Characterization of 108 Genomic DNA Reference Materials for 11 Human Leukocyte Antigen Loci: A GeT-RM Collaborative Project.11 个人白细胞抗原基因座 108 个基因组 DNA 参考物质的特征分析:一个 GeT-RM 合作项目。
J Mol Diagn. 2018 Sep;20(5):703-715. doi: 10.1016/j.jmoldx.2018.05.009. Epub 2018 Jun 26.
2
New Resources to Identify Characterized DNA Reference Materials for Pharmacogenetic (PGx) and Human Leukocyte Antigen (HLA) Testing: The Genetic Testing Reference Material (GeT-RM) Program PGx Search Tool and GeT-RM Consolidated PGx and HLA Table.用于识别药物遗传学(PGx)和人类白细胞抗原(HLA)检测的特征性DNA参考物质的新资源:基因检测参考物质(GeT-RM)计划PGx搜索工具和GeT-RM综合PGx与HLA表格。
J Mol Diagn. 2025 Jun;27(6):457-464. doi: 10.1016/j.jmoldx.2025.02.008. Epub 2025 Mar 21.
3
Allele and haplotype frequencies of human leukocyte antigen-A, -B, -C, -DRB1, -DRB3/4/5, -DQA1, -DQB1, -DPA1, and -DPB1 by next generation sequencing-based typing in Koreans in South Korea.韩国人群中基于下一代测序的 HLA-A、-B、-C、-DRB1、-DRB3/4/5、-DQA1、-DQB1、-DPA1 和 -DPB1 等位基因和单体型频率。
PLoS One. 2021 Jun 21;16(6):e0253619. doi: 10.1371/journal.pone.0253619. eCollection 2021.
4
HLA-DRB1, -DRB3, -DRB4 and -DRB5 genotyping at a super-high resolution level by long range PCR and high-throughput sequencing.通过长距离PCR和高通量测序对HLA-DRB1、-DRB3、-DRB4和-DRB5进行超高分辨率基因分型。
Tissue Antigens. 2014 Jan;83(1):10-6. doi: 10.1111/tan.12258. Epub 2013 Nov 30.
5
HLA high-resolution typing by next-generation sequencing in Pandemrix-induced narcolepsy.应用新一代测序技术对 Pandemrix 诱发的发作性睡病进行 HLA 高分辨率分型。
PLoS One. 2019 Oct 2;14(10):e0222882. doi: 10.1371/journal.pone.0222882. eCollection 2019.
6
Characterization of 107 genomic DNA reference materials for CYP2D6, CYP2C19, CYP2C9, VKORC1, and UGT1A1: a GeT-RM and Association for Molecular Pathology collaborative project.107 份 CYP2D6、CYP2C19、CYP2C9、VKORC1 和 UGT1A1 基因组 DNA 参考品的特征分析:GeT-RM 和分子病理学协会合作项目。
J Mol Diagn. 2010 Nov;12(6):835-46. doi: 10.2353/jmoldx.2010.100090. Epub 2010 Oct 1.
7
Development of genomic reference materials for cystic fibrosis genetic testing.用于囊性纤维化基因检测的基因组参考物质的开发。
J Mol Diagn. 2009 May;11(3):186-93. doi: 10.2353/jmoldx.2009.080149. Epub 2009 Apr 9.
8
[The Polymorphism Analysis of HLA Class II Alleles Based on Next-Generation Sequencing and Prevention Strategy for Allele Dropout].基于下一代测序技术的HLA II类等位基因多态性分析及等位基因丢失预防策略
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Apr;32(2):603-609. doi: 10.19746/j.cnki.issn.1009-2137.2024.02.042.
9
Next-generation sequencing reveals new information about HLA allele and haplotype diversity in a large European American population.下一代测序揭示了大型欧洲裔人群中 HLA 等位基因和单倍型多样性的新信息。
Hum Immunol. 2019 Oct;80(10):807-822. doi: 10.1016/j.humimm.2019.07.275. Epub 2019 Jul 22.
10
Next-generation HLA typing of 382 International Histocompatibility Working Group reference B-lymphoblastoid cell lines: Report from the 17th International HLA and Immunogenetics Workshop.382 个国际组织相容性工作组参考 B 淋巴细胞系的下一代 HLA 分型:第 17 届国际 HLA 和免疫遗传学研讨会报告。
Hum Immunol. 2019 Jul;80(7):449-460. doi: 10.1016/j.humimm.2019.03.001. Epub 2019 Mar 4.

引用本文的文献

1
From Expert Knowledge to Validation Resources: A Case for Using in Silico Approaches to Close the Gap in Available Reference Materials for Common Germline Genetic Tests.从专家知识到验证资源:利用计算机模拟方法填补常见种系基因检测可用参考材料差距的实例
J Mol Diagn. 2025 Aug 20. doi: 10.1016/j.jmoldx.2025.07.006.
2
Clinical impact of pharmacogenomics in pediatric care: insights extracted from clinical exome sequencing.药物基因组学在儿科护理中的临床影响:从临床外显子组测序中提取的见解
Front Genet. 2025 May 29;16:1574325. doi: 10.3389/fgene.2025.1574325. eCollection 2025.
3
New Resources to Identify Characterized DNA Reference Materials for Pharmacogenetic (PGx) and Human Leukocyte Antigen (HLA) Testing: The Genetic Testing Reference Material (GeT-RM) Program PGx Search Tool and GeT-RM Consolidated PGx and HLA Table.用于识别药物遗传学(PGx)和人类白细胞抗原(HLA)检测的特征性DNA参考物质的新资源:基因检测参考物质(GeT-RM)计划PGx搜索工具和GeT-RM综合PGx与HLA表格。
J Mol Diagn. 2025 Jun;27(6):457-464. doi: 10.1016/j.jmoldx.2025.02.008. Epub 2025 Mar 21.
4
Reference Materials for Improving Reliability of Multiomics Profiling.提高多组学分析可靠性的参考材料。
Phenomics. 2024 Mar 6;4(5):487-521. doi: 10.1007/s43657-023-00153-7. eCollection 2024 Oct.
5
Behçet's disease risk-variant HLA-B51/ERAP1-Hap10 alters human CD8 T cell immunity.白塞病风险变体 HLA-B51/ERAP1-Hap10 改变人类 CD8 T 细胞免疫。
Ann Rheum Dis. 2022 Nov;81(11):1603-1611. doi: 10.1136/ard-2022-222277. Epub 2022 Aug 3.
6
Technical Performance of a 430-Gene Preventative Genomics Assay to Identify Multiple Variant Types Associated with Adult-Onset Monogenic Conditions, Susceptibility Loci, and Pharmacogenetic Insights.一种430基因预防基因组检测方法的技术性能,用于识别与成人发病的单基因疾病、易感位点和药物遗传学见解相关的多种变异类型。
J Pers Med. 2022 Apr 21;12(5):667. doi: 10.3390/jpm12050667.

本文引用的文献

1
Missing or altered self: human NK cell receptors that recognize HLA-C.缺失或改变的自身:识别HLA - C的人类自然杀伤细胞受体
Immunogenetics. 2017 Aug;69(8-9):567-579. doi: 10.1007/s00251-017-1001-y. Epub 2017 Jul 10.
2
Introduction: MHC/KIR and governance of specificity.引言:主要组织相容性复合体/杀伤细胞免疫球蛋白样受体与特异性调控
Immunogenetics. 2017 Aug;69(8-9):481-488. doi: 10.1007/s00251-017-0986-6. Epub 2017 Jul 10.
3
Pathogenesis of ankylosing spondylitis - recent advances and future directions.强直性脊柱炎的发病机制——最新进展与未来方向。
Nat Rev Rheumatol. 2017 Jun;13(6):359-367. doi: 10.1038/nrrheum.2017.56. Epub 2017 Apr 27.
4
Applications of Immunogenomics to Cancer.免疫基因组学在癌症中的应用。
Cell. 2017 Feb 9;168(4):600-612. doi: 10.1016/j.cell.2017.01.014.
5
Strategic Use of Epitope Matching to Improve Outcomes.利用表位匹配策略改善结果。
Transplantation. 2016 Oct;100(10):2048-52. doi: 10.1097/TP.0000000000001284.
6
Determining performance characteristics of an NGS-based HLA typing method for clinical applications.确定一种基于二代测序(NGS)的HLA分型方法在临床应用中的性能特征。
HLA. 2016 Mar;87(3):141-52. doi: 10.1111/tan.12736. Epub 2016 Feb 16.
7
Viral infection causes a shift in the self peptide repertoire presented by human MHC class I molecules.病毒感染导致人类 MHC Ⅰ类分子呈递的自身肽库发生改变。
Proteomics Clin Appl. 2015 Dec;9(11-12):1035-52. doi: 10.1002/prca.201500106.
8
Celiac disease: Autoimmunity in response to food antigen.乳糜泻:针对食物抗原的自身免疫反应。
Semin Immunol. 2015 Sep;27(5):343-52. doi: 10.1016/j.smim.2015.11.001. Epub 2015 Nov 18.
9
Allele Frequencies Net Database: Improvements for storage of individual genotypes and analysis of existing data.等位基因频率网络数据库:个体基因型存储及现有数据分析的改进
Hum Immunol. 2016 Mar;77(3):238-248. doi: 10.1016/j.humimm.2015.11.013. Epub 2015 Nov 14.
10
Platelet refractoriness--practical approaches and ongoing dilemmas in patient management.血小板抵抗性——患者管理中的实用方法和持续存在的困境。
Br J Haematol. 2015 Nov;171(3):297-305. doi: 10.1111/bjh.13597. Epub 2015 Jul 20.

11 个人白细胞抗原基因座 108 个基因组 DNA 参考物质的特征分析:一个 GeT-RM 合作项目。

Characterization of 108 Genomic DNA Reference Materials for 11 Human Leukocyte Antigen Loci: A GeT-RM Collaborative Project.

机构信息

Immunogenetics Laboratory, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.

Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

出版信息

J Mol Diagn. 2018 Sep;20(5):703-715. doi: 10.1016/j.jmoldx.2018.05.009. Epub 2018 Jun 26.

DOI:10.1016/j.jmoldx.2018.05.009
PMID:29959025
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6939753/
Abstract

The highly polymorphic human leukocyte antigen (HLA) genes, located in the human major histocompatibility complex, encode the class I and II antigen-presenting molecules, which are centrally involved in the immune response. HLA typing is used for several clinical applications, such as transplantation, pharmacogenetics, and diagnosis of autoimmune disease. HLA typing is highly complex because of the homology of HLA genes and pseudogenes and the extensive polymorphism in the population. The Centers for Disease Control and Prevention established the Genetic Testing Reference Materials Coordination Program (GeT-RM) in partnership with the genetics community to improve the availability of genomic DNA reference materials necessary for quality assurance of genetic laboratory testing. The GeT-RM together with three clinical laboratories and the Coriell Cell Repositories have characterized genomic DNA obtained from a panel of 108 cell lines for all HLA classic polymorphic loci: HLA-A, B, C, DRB1, DRB3, DRB4, DRB5, DQA1, DQB1, DPA1, and DPB1. The goal was to develop a publicly available and renewable source of well-characterized genomic DNA reference materials to support molecular HLA typing assay development, validation, and verification, quality control, and proficiency testing. These genomic DNA samples are publicly available from the National Institutes of General Medical Science Repository at the Coriell Cell Repositories.

摘要

高度多态性的人类白细胞抗原 (HLA) 基因位于人类主要组织相容性复合体中,编码 I 类和 II 类抗原呈递分子,这些分子在免疫反应中起着核心作用。HLA 分型用于多种临床应用,如移植、药物遗传学和自身免疫性疾病的诊断。由于 HLA 基因和假基因的同源性以及人群中广泛的多态性,HLA 分型非常复杂。疾病控制和预防中心与遗传学社区合作建立了遗传测试参考材料协调计划 (GeT-RM),以提高遗传实验室测试质量保证所需的基因组 DNA 参考材料的可用性。GeT-RM 与三个临床实验室和科里尔细胞库一起,对来自 108 个细胞系的基因组 DNA 进行了所有 HLA 经典多态性位点的特征描述:HLA-A、B、C、DRB1、DRB3、DRB4、DRB5、DQA1、DQB1、DPA1 和 DPB1。目标是开发一种可公开获得和可再生的、经过充分表征的基因组 DNA 参考材料来源,以支持分子 HLA 分型测定的开发、验证和验证、质量控制和能力验证。这些基因组 DNA 样本可从科里尔细胞库的国立普通医学科学研究所知识库中公开获得。