dapi has been researched along with Niemann-Pick Disease, Type A in 1 studies
DAPI: RN given refers to parent cpd.
Niemann-Pick Disease, Type A: The classic infantile form of Niemann-Pick Disease, caused by mutation in SPHINGOMYELIN PHOSPHODIESTERASE. It is characterized by accumulation of SPHINGOMYELINS in the cells of the MONONUCLEAR PHAGOCYTE SYSTEM and other cell throughout the body leading to cell death. Clinical signs include JAUNDICE, hepatosplenomegaly, and severe brain damage.
| 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 |
|---|---|
| Sidman, RL | 1 |
| Li, J | 1 |
| Stewart, GR | 1 |
| Clarke, J | 1 |
| Yang, W | 1 |
| Snyder, EY | 1 |
| Shihabuddin, LS | 1 |
1 other study available for dapi and Niemann-Pick Disease, Type A
| Article | Year |
|---|---|
Injection of mouse and human neural stem cells into neonatal Niemann-Pick A model mice.
Topics: Animals; Animals, Newborn; Cholesterol; Disease Models, Animal; Female; Fetus; Humans; Indoles; Male | 2007 |