• 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

Whole exome sequencing identifies new susceptibility candidates underlying community-acquired pneumonia.

作者信息

Pardo-Seco Jacobo, Viz-Lasheras Sandra, Bello Xabier, Gómez-Carballa Alberto, Camino-Mera Alba, Pischedda Sara, Currás-Tuala María José, Rivero-Calle Irene, Dacosta-Urbieta Ana, Caamaño-Viña Fernando, Rodríguez-Tenreiro Sánchez Carmen, Cifuentes Isabel, Méndez Cristina, Khor Chiea Chuen, Martinón-Torres Federico, Salas Antonio

机构信息

Unidade de Xenética, Instituto de Ciencias Forenses, Facultade de Medicina, Universidade de Santiago de Compostela, and GenPoB Research Group, Instituto de Investigación Sanitaria (IDIS), Hospital Clínico Universitario de Santiago de Compostela (SERGAS), Galicia 15706, Spain.

Genetics, Vaccines and Infections Research Group (GENVIP), Instituto de Investigación Sanitaria de Santiago, Universidade de Santiago de Compostela, Santiago de Compostela, Galicia 15706, Spain.

出版信息

Genes Dis. 2023 Nov 19;11(6):101170. doi: 10.1016/j.gendis.2023.101170. eCollection 2024 Nov.

DOI:10.1016/j.gendis.2023.101170
PMID:39157457
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11327392/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8925/11327392/1870c8d94ccb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8925/11327392/1870c8d94ccb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8925/11327392/1870c8d94ccb/gr1.jpg

相似文献

1
Whole exome sequencing identifies new susceptibility candidates underlying community-acquired pneumonia.全外显子组测序鉴定出社区获得性肺炎潜在的新的易感候选基因。
Genes Dis. 2023 Nov 19;11(6):101170. doi: 10.1016/j.gendis.2023.101170. eCollection 2024 Nov.
2
Whole Exome Sequencing Identifies New Host Genomic Susceptibility Factors in Empyema Caused by Streptococcus pneumoniae in Children: A Pilot Study.全外显子组测序鉴定儿童肺炎链球菌所致脓胸新的宿主基因组易感性因素：一项初步研究
Genes (Basel). 2018 May 3;9(5):240. doi: 10.3390/genes9050240.
3
Whole exome sequencing identifies PLEC, EXO5 and DNAH7 as novel susceptibility genes in testicular cancer.全外显子组测序鉴定出 PLEC、EXO5 和 DNAH7 为睾丸癌的新型易感性基因。
Int J Cancer. 2018 Oct 15;143(8):1954-1962. doi: 10.1002/ijc.31604. Epub 2018 Aug 9.
4
Discovery of Variants Underlying Host Susceptibility to Virus Infection Using Whole-Exome Sequencing.利用全外显子组测序发现宿主对病毒感染易感性的潜在变异体。
Methods Mol Biol. 2017;1656:209-227. doi: 10.1007/978-1-4939-7237-1_14.
5
Whole exome sequencing for familial bicuspid aortic valve identifies putative variants.对家族性二叶式主动脉瓣进行全外显子组测序可识别潜在变异。
Circ Cardiovasc Genet. 2014 Oct;7(5):677-83. doi: 10.1161/CIRCGENETICS.114.000526. Epub 2014 Aug 1.
6
Whole exome sequencing identifies a causal RBM20 mutation in a large pedigree with familial dilated cardiomyopathy.全外显子组测序在一个患有家族性扩张型心肌病的大型家系中鉴定出一个致病的RBM20突变。
Circ Cardiovasc Genet. 2013 Aug;6(4):317-26. doi: 10.1161/CIRCGENETICS.113.000011. Epub 2013 Jul 16.
7
Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene.全外显子组测序确定了嗜铬细胞瘤的突变图谱，并将KMT2D鉴定为一个反复突变的基因。
Genes Chromosomes Cancer. 2015 Sep;54(9):542-54. doi: 10.1002/gcc.22267. Epub 2015 May 29.
8
Novel candidate genes may be possible predisposing factors revealed by whole exome sequencing in familial esophageal squamous cell carcinoma.新型候选基因可能是家族性食管鳞状细胞癌全外显子测序揭示的潜在致病因素。
Tumour Biol. 2017 May;39(5):1010428317699115. doi: 10.1177/1010428317699115.
9
Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinoma.全外显子组测序确定MST1R为鼻咽癌的一个遗传易感基因。
Proc Natl Acad Sci U S A. 2016 Mar 22;113(12):3317-22. doi: 10.1073/pnas.1523436113. Epub 2016 Mar 7.
10
Detecting identity by descent and homozygosity mapping in whole-exome sequencing data.通过全外显子组测序数据中的血缘关系和纯合性映射来检测身份。
PLoS One. 2012;7(10):e47618. doi: 10.1371/journal.pone.0047618. Epub 2012 Oct 11.

本文引用的文献

1
CAPPRIC Study-Characterization of Community-Acquired Pneumonia in Spanish Adults Managed in Primary Care Settings.CAPPRIC研究——西班牙初级保健机构中成年社区获得性肺炎的特征分析
Microorganisms. 2021 Feb 28;9(3):508. doi: 10.3390/microorganisms9030508.
2
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.罕见 CYP39A1 变体与前房眼牵涉的剥脱综合征的关联。
JAMA. 2021 Feb 23;325(8):753-764. doi: 10.1001/jama.2021.0507.
3
Ancestry patterns inferred from massive RNA-seq data.基于大规模 RNA-seq 数据推断的祖源模式。
RNA. 2019 Jul;25(7):857-868. doi: 10.1261/rna.070052.118. Epub 2019 Apr 22.
4
Epidemiology of community-acquired pneumonia in older adults: a population-based study.老年人社区获得性肺炎的流行病学：一项基于人群的研究。
Respir Med. 2009 Feb;103(2):309-16. doi: 10.1016/j.rmed.2008.08.006. Epub 2008 Sep 18.