TALPID3 in Joubert syndrome and related ciliopathy disorders
Author:
Funder
BBSRC
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics
Reference40 articles.
1. Developmental abnormalities in the head region of the talpid3 mutant of the fowl;Ede;J Embryol Exp Morphol,1964
2. Studies on the effects of some genetic lethal factors on the embryonic development of Drosophila melanogaster;Ede;Wilhelm Roux Arch Entwickl Mech Org,1956
3. Utilizing the chicken as an animal model for human craniofacial ciliopathies;Schock;Dev Biol,2016
4. The chick limb: embryology, genetics and teratology;Davey;Int J Dev Biol,2018
5. The talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formation;Yin;Development,2009
Cited by 14 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. Expanding the Phenotypic Spectrum of Pathogenic KIAA0586 Variants: From Joubert Syndrome to Hydrolethalus Syndrome;International Journal of Molecular Sciences;2024-07-19
2. Ccdc66 regulates primary cilium stability, disassembly and signaling important for epithelial organization;2024-06-17
3. Absence of the primary cilia formation gene Talpid3 impairs muscle stem cell function;Communications Biology;2023-11-04
4. Muscle stem cell function is impaired in absence of Talpid3 - a gene required for primary cilia formation;2022-10-14
5. Genotype–phenotype correlates in Joubert syndrome: A review;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2022-03
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