Page last updated: 2024-08-23

staurosporine and Spastic Paraplegia, Hereditary

staurosporine has been researched along with Spastic Paraplegia, Hereditary in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Arimitsu, N; Baba, T; Enda, Y; Hamamoto, H; Hara-Miyauchi, C; Hasegawa-Ogawa, M; Maemoto, Y; Maruyama, T; Matsumoto, K; Nakanishi, H; Nakao, K; Ohto-Nakanishi, T; Okano, HJ; Sekimizu, K; Tagaya, M; Tani, K; Tokuyama, T; Yanagi, S	1

Other Studies

1 other study(ies) available for staurosporine and Spastic Paraplegia, Hereditary

Article	Year
Loss of DDHD2, whose mutation causes spastic paraplegia, promotes reactive oxygen species generation and apoptosis. Cell death & disease, 2018, 07-23, Volume: 9, Issue:8 Topics: Adenosine Triphosphate; Animals; Apoptosis; Cardiolipins; Cells, Cultured; Disease Models, Animal; Fibroblasts; Humans; Mice; Mice, Knockout; Mitochondria; Motor Neurons; Phospholipases; Phospholipases A1; Reactive Oxygen Species; Spastic Paraplegia, Hereditary; Spinal Cord; Staurosporine	2018

Article

Year

Loss of DDHD2, whose mutation causes spastic paraplegia, promotes reactive oxygen species generation and apoptosis.

Cell death & disease, 2018, 07-23, Volume: 9, Issue:8

Topics: Adenosine Triphosphate; Animals; Apoptosis; Cardiolipins; Cells, Cultured; Disease Models, Animal; Fibroblasts; Humans; Mice; Mice, Knockout; Mitochondria; Motor Neurons; Phospholipases; Phospholipases A1; Reactive Oxygen Species; Spastic Paraplegia, Hereditary; Spinal Cord; Staurosporine

2018