dapi has been researched along with Bardet-Biedl Syndrome in 1 studies
DAPI: RN given refers to parent cpd.
Bardet-Biedl Syndrome: An autosomal recessive disorder characterized by RETINITIS PIGMENTOSA; POLYDACTYLY; OBESITY; MENTAL RETARDATION; hypogenitalism; renal dysplasia; and short stature. This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME. (From J Med Genet 1997 Feb;34(2):92-8)
| 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 |
|---|---|
| Jacoby, M | 1 |
| Cox, JJ | 1 |
| Gayral, S | 1 |
| Hampshire, DJ | 1 |
| Ayub, M | 1 |
| Blockmans, M | 1 |
| Pernot, E | 1 |
| Kisseleva, MV | 1 |
| Compère, P | 1 |
| Schiffmann, SN | 1 |
| Gergely, F | 1 |
| Riley, JH | 1 |
| Pérez-Morga, D | 1 |
| Woods, CG | 1 |
| Schurmans, S | 1 |
1 other study available for dapi and Bardet-Biedl Syndrome
| Article | Year |
|---|---|
INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse.
Topics: Animals; Bardet-Biedl Syndrome; Cell Line; Cell Nucleus; Cells, Cultured; Chromones; Cilia; Culture | 2009 |