Nephrocystin Specifically Localizes to the Transition Zone of Renal and Respiratory Cilia and Photoreceptor Connecting Cilia-Reference-Cited by-同舟云学术

Nephrocystin Specifically Localizes to the Transition Zone of Renal and Respiratory Cilia and Photoreceptor Connecting Cilia

Published:2006-08-02 Issue:9 Volume:17 Page:2424-2433
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Fliegauf Manfred,Horvath Judit,von Schnakenburg Christian,Olbrich Heike,Müller Dominik,Thumfart Julia,Schermer Bernhard,Pazour Gregory J.,Neumann Hartmut P.H.,Zentgraf Hanswalter,Benzing Thomas,Omran Heymut

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference45 articles.

1. New insights: nephronophthisis-medullary cystic kidney disease

2. Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

3. A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

4. A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisis

5. A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution

Cited by 127 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. Immunofluorescence analyses of respiratory epithelial cells aid the diagnosis of nephronophthisis;Pediatric Nephrology;2024-08-05

2. A case report of intrahepatic bile duct dilatation caused by WDR19 gene mutation and presented as Caroli syndrome;Translational Pediatrics;2024-04

3. Transport and barrier mechanisms that regulate ciliary compartmentalization and ciliopathies;Nature Reviews Nephrology;2023-10-23

4. Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4;American Journal of Ophthalmology;2023-08

5. A genotype-to-phenotype approach suggests under-reporting of single nucleotide variants in nephrocystin-1 (NPHP1) related disease (UK 100,000 Genomes Project);Scientific Reports;2023-06-09