Progressive development of polycystic kidney disease in the mouse model expressing Pkd1 extracellular domain
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/22/12/2361/14138977/ddt081.pdf
Reference62 articles.
1. Identification and characterization of the tuberous sclerosis gene on chromosome 16;European Chromosome 16 Tuberous Sclerosis Consortium;Cell,1993
2. The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16;The European Polycystic Kidney Disease Consortium;Cell,1994
3. Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat;Burn;Hum. Mol. Genet.,1995
4. Polycystic kidney disease: the complete structure of the PKD1 gene and its protein;The International Polycystic Kidney Disease Consortium;Cell,1995
5. Cleavage of polycystin-1 requires the receptor for egg jelly domain and is disrupted by human autosomal-dominant polycystic kidney disease 1-associated mutations;Qian;Proc. Natl Acad. Sci. USA,2002
Cited by 16 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. Differential regulation of MYC expression by PKHD1/Pkhd1 in human and mouse kidneys: phenotypic implications for recessive polycystic kidney disease;Frontiers in Cell and Developmental Biology;2023-11-17
2. Modeling Pkd1 gene-targeted strategies for correction of polycystic kidney disease;Molecular Therapy - Methods & Clinical Development;2023-06
3. Spheroids, organoids and kidneys-on-chips: how complex human cellular models have assisted in the study of kidney disease and renal ciliopathies;Microfluidics and Nanofluidics;2023-02-17
4. Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression;Scientific Reports;2021-09-14
5. The master regulators Myc and p53 cellular signaling and functions in polycystic kidney disease;Cellular Signalling;2020-07
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