Gene defect in ectodermal dysplasia implicates a death domain adapter in development-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Gene defect in ectodermal dysplasia implicates a death domain adapter in development

Published:2001-12 Issue:6866 Volume:414 Page:913-916
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Headon Denis J.,Emmal Stephanie A.,Ferguson Betsy M.,Tucker Abigail S.,Justice Monica J.,Sharpe Paul T.,Zonana Jonathan,Overbeek Paul A.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/414913a.pdf

Reference28 articles.

1. Ashkenazi, A. & Dixit, V. M. Death receptors: signaling and modulation. Science 281, 1305–1308 (1998).

2. Locksley, R. M., Killeen, N. & Lenardo, M. J. The TNF and TNF receptor superfamilies: Integrating mammalian biology. Cell 104, 487–501 (2001).

3. Headon, D. J. & Overbeek, P. A. Involvement of a novel Tnf receptor homologue in hair follicle induction. Nature Genet. 22, 370–374 (1999).

4. Monreal, A. W. et al. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nature Genet. 22, 366–369 (1999).

5. Kere, J. et al. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nature Genet. 13, 409–416 (1996).

Cited by 330 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. Identification of costimulatory molecule signatures for evaluating prognostic risk in non-small cell lung cancer;Heliyon;2024-09

2. Three-dimensional genome architecture persists in a 52,000-year-old woolly mammoth skin sample;Cell;2024-07

3. EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia;Genes;2024-06-28

4. Novel homozygous frameshift insertion variant in the last exon of the EDARADD causing hypohidrotic ectodermal dysplasia in two siblings: case report and review of the literature;Italian Journal of Pediatrics;2024-06-05

5. A Novel Ectodysplasin a Gene mutation of X-Linked Hypohidrotic Ectodermal Dysplasia;Clinical, Cosmetic and Investigational Dermatology;2024-06

同舟云学术

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