uridine triphosphate has been researched along with Glomerulosclerosis, Focal Segmental in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Burchette, JL; Conlon, PJ; Creazzo, T; Daskalakis, N; Ebersviller, S; Farrington, MK; Hawkins, AF; Howell, DN; Kwan, SY; Lynn, KL; Pericak-Vance, MA; Rosenberg, PB; Vance, JM; Winn, MP | 1 |
1 other study(ies) available for uridine triphosphate and Glomerulosclerosis, Focal Segmental
| Article | Year |
|---|---|
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis.
Topics: Amino Acid Substitution; Angiotensin II; Calcium; Calcium Channels; Calcium Signaling; Carbachol; Cell Line; Cell Membrane; Chromosomes, Human, Pair 11; Exons; Female; Glomerulosclerosis, Focal Segmental; GTP-Binding Protein alpha Subunits, Gq-G11; Haplotypes; Humans; Kidney; Kidney Glomerulus; Kidney Tubules; Male; Mutation, Missense; Patch-Clamp Techniques; Pedigree; Receptor, Angiotensin, Type 1; Sequence Analysis, DNA; Sodium; Transfection; TRPC Cation Channels; TRPC6 Cation Channel; Uridine Triphosphate | 2005 |