Lymphedema-distichiasis syndrome and FOXC2 gene mutation
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference23 articles.
1. Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema;Karkkainen;Nat Genet,2000
2. Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase;Irrthum;Am J Hum Genet,2000
3. Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q;Bull;Am J Hum Genet,2000
4. A gene for lymphedema-distichiasis maps to 16q24.3;Mangion;Am J Hum Genet,1999
5. Mutations in FOXC2(MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome;Fang;Am J Hum Genet,2000
Cited by 39 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. The molecular genetics of anterior segment dysgenesis;Experimental Eye Research;2023-09
2. Differential roles of FOXC2 in the trabecular meshwork and Schlemm’s canal in glaucomatous pathology;Life Science Alliance;2023-07-06
3. Mechanical forces in lymphatic vessel development: Focus on transcriptional regulation;Frontiers in Physiology;2022-11-10
4. Differential roles of neural crest- and endothelial-derived FOXC2 in trabecular meshwork and Schlemm’s Canal in glaucomatous pathology;2022-02-20
5. Shear stimulation of FOXC1 and FOXC2 differentially regulates cytoskeletal activity during lymphatic valve maturation;eLife;2020-06-08
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