Identification and functional analysis of a novel TRPC6 mutation associated with late onset familial focal segmental glomerulosclerosis in Chinese patients
- 12 May 2009
- journal article
- research article
- Published by Elsevier BV in Mutation Research - Reviews in Mutation Research
- Vol. 664 (1-2), 84-90
- https://doi.org/10.1016/j.mrfmmm.2008.11.021
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Isoform-specific Inhibition of TRPC4 Channel by Phosphatidylinositol 4,5-BisphosphatePublished by Elsevier BV ,2008
- hTRPC1‐associated α‐actinin, and not hTRPC1 itself, is tyrosine phosphorylated during human platelet activationJournal of Thrombosis and Haemostasis, 2007
- Direct binding of α‐actinin enhances TRPP3 channel activityJournal of Neurochemistry, 2007
- BMP gradients steer nerve growth cones by a balancing act of LIM kinase and Slingshot phosphatase on ADF/cofilinThe Journal of cell biology, 2007
- Gαq-TRPC6-mediated Ca2+ Entry Induces RhoA Activation and Resultant Endothelial Cell Shape Change in Response to ThrombinPublished by Elsevier BV ,2007
- Proteomic analysis of TRPC5- and TRPC6-binding partners reveals interaction with the plasmalemmal Na+/K+-ATPasePflügers Archiv - European Journal of Physiology, 2005
- TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal functionNature Genetics, 2005
- The Canonical Transient Receptor Potential 6 Channel as a Putative Phosphatidylinositol 3,4,5-Trisphosphate-Sensitive Calcium Entry SystemBiochemistry, 2004
- α-Actinin-4-Mediated FSGS: An Inherited Kidney Disease Caused by an Aggregated and Rapidly Degraded Cytoskeletal ProteinPLoS Biology, 2004
- Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic SyndromeMolecular Cell, 1998