FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans
Author:
Funder
National Institute of Allergy and Infectious Diseases
Jeffrey Modell Foundation
UT Southwestern Medical Center
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://www.jci.org/articles/view/127565/files/pdf
Reference57 articles.
1. FOXN1 in thymus organogenesis and development
2. Foxn1 regulates key target genes essential for T cell development in postnatal thymic epithelial cells
3. Mechanisms of thymus organogenesis and morphogenesis
4. Thymic epithelial cells: working class heroes for T cell development and repertoire selection
5. TREC Based Newborn Screening for Severe Combined Immunodeficiency Disease: A Systematic Review
Cited by 34 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Monitoring mouse papillomavirus-associated cancer development using longitudinal Pap smear screening;mBio;2024-08-14
2. Utilization of next-generation sequencing to define the role of heterozygous FOXN1 variants in immunodeficiency;Journal of Allergy and Clinical Immunology: Global;2024-08
3. Peripheral T Cell Development and Immunophenotyping of Twins with Heterozygous FOXN1 Mutations;ImmunoHorizons;2024-07-01
4. Parental Engagement in Identifying Information Needs After Newborn Screening for Families of Infants with Suspected Athymia;Journal of Clinical Immunology;2024-03-08
5. Primary and secondary defects of the thymus;Immunological Reviews;2024-01-16
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3