nocodazole has been researched along with Niemann-Pick Diseases in 2 studies
Niemann-Pick Diseases: A group of autosomal recessive disorders in which harmful quantities of lipids accumulate in the viscera and the central nervous system. They can be caused by deficiencies of enzyme activities (SPHINGOMYELIN PHOSPHODIESTERASE) or defects in intracellular transport, resulting in the accumulation of SPHINGOMYELINS and CHOLESTEROL. There are various subtypes based on their clinical and genetic differences.
Excerpt | Relevance | Reference |
---|---|---|
"Amiodarone analogues were also studied, including the recently developed derivative dronedarone." | 1.37 | Amiodarone impairs trafficking through late endosomes inducing a Niemann-Pick C-like phenotype. ( Baritussio, A; Bergonzini, V; Bigler, L; Calistri, A; Caretta, CM; Dal Zoppo, D; Del Vecchio, C; Faggin, E; Ha, HR; Nadai, M; Orlando, R; Palù, G; Pettenazzo, A; Piccoli, E; Salata, C, 2011) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Piccoli, E | 1 |
Nadai, M | 1 |
Caretta, CM | 1 |
Bergonzini, V | 1 |
Del Vecchio, C | 1 |
Ha, HR | 1 |
Bigler, L | 1 |
Dal Zoppo, D | 1 |
Faggin, E | 1 |
Pettenazzo, A | 1 |
Orlando, R | 1 |
Salata, C | 1 |
Calistri, A | 1 |
Palù, G | 1 |
Baritussio, A | 1 |
Lange, Y | 1 |
Ye, J | 1 |
Rigney, M | 1 |
Steck, TL | 1 |
2 other studies available for nocodazole and Niemann-Pick Diseases
Article | Year |
---|---|
Amiodarone impairs trafficking through late endosomes inducing a Niemann-Pick C-like phenotype.
Topics: Amiodarone; Androstenes; Animals; Anti-Arrhythmia Agents; Cells, Cultured; Cholesterol; Dose-Respons | 2011 |
Dynamics of lysosomal cholesterol in Niemann-Pick type C and normal human fibroblasts.
Topics: Amphotericin B; Androstenes; Anti-Bacterial Agents; Anticholesteremic Agents; Antineoplastic Agents; | 2002 |