From cilia to cyst
- 1 August 2003
- journal article
- editorial
- Published by Springer Nature in Nature Genetics
- Vol. 34 (4), 355-356
- https://doi.org/10.1038/ng0803-355
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationNature Genetics, 2003
- Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosisNature Genetics, 2003
- Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cellsNature Genetics, 2003
- Ciliary signaling goes down the tubesNature Genetics, 2003
- The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystinNature Genetics, 2002
- Nephrocystin-conserved Domains Involved in Targeting to Epithelial Cell-Cell Junctions, Interaction with Filamins, and Establishing Cell PolarityJournal of Biological Chemistry, 2002
- A Proteomic Analysis of Human CiliaMolecular & Cellular Proteomics, 2002
- Nephrocystin interacts with Pyk2, p130 Cas , and tensin and triggers phosphorylation of Pyk2Proceedings of the National Academy of Sciences, 2001
- Cloning of inv, a gene that controls left/right asymmetry and kidney developmentNature, 1998
- A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1Nature Genetics, 1997