Identification of PKDL, a Novel Polycystic Kidney Disease 2-Like Gene Whose Murine Homologue Is Deleted in Mice with Kidney and Retinal Defects-Reference-Cited by-同舟云学术

Identification of PKDL, a Novel Polycystic Kidney Disease 2-Like Gene Whose Murine Homologue Is Deleted in Mice with Kidney and Retinal Defects

Published:1998-10 Issue:40 Volume:273 Page:25967-25973
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Nomura Hideki,Turco Alberto E.,Pei York,Kalaydjieva Luba,Schiavello Tina,Weremowicz Stanislawa,Ji Weizhen,Morton Cynthia C.,Meisler Miriam,Reeders Stephen T.,Zhou Jing

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference39 articles.

1. Autosomal Dominant Polycystic Kidney Disease

2. Evidence for a third genetic locus for autosomal dominant polycystic kidney disease

3. An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene

4. Polycystic kidney disease: The complete structure of the PKD1 gene and its protein

5. The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains

Cited by 147 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. Primary cilia TRP channel regulates hippocampal excitability;Proceedings of the National Academy of Sciences;2023-05-22

2. Energetic landscape of polycystin channel gating;EMBO reports;2023-05-09

3. Inhibition of TRPP3 by calmodulin through Ca2+/calmodulin-dependent protein kinase II;Cell Insight;2023-04

4. Polycystin Channel Complexes;Annual Review of Physiology;2023-02-10

5. Placental ion channels: potential target of chemical exposure;Biology of Reproduction;2022-09-29