staurosporine has been researched along with ALS - Amyotrophic Lateral Sclerosis in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 4 (57.14) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Boccanfuso, LM; Dobson-Stone, C; Fitzpatrick, L; Hallupp, M; Kwok, JB; Oyston, LJ; Ubiparipovic, S | 1 |
| Bénardais, K; Claus, P; Dengler, R; Hensel, N; Huang, D; Petri, S; Stangel, M; Stanslowsky, N; Sun, H; Thau-Habermann, N | 1 |
| Lee, K; Matsuoka, M; Suzuki, H | 1 |
| Armstrong, EJ; Brooks, BR; Hemendinger, RA; Radio, N | 1 |
| Bruestle, DA; Chigurupati, S; Greig, NH; Harvey, BK; Holloway, HW; Lahiri, DK; Li, Y; Mattson, MP; Mughal, M; Ray, B; Tweedie, D; Wang, Y | 1 |
| Coffin, R; Collaco Moraes, Y; de Belleroche, J; Latchman, D; Patel, Y | 1 |
| de Belleroche, J; Latchman, DS; Patel, YJ; Payne Smith, MD | 1 |
7 other study(ies) available for staurosporine and ALS - Amyotrophic Lateral Sclerosis
| Article | Year |
|---|---|
Rapid in vitro quantification of TDP-43 and FUS mislocalisation for screening of gene variants implicated in frontotemporal dementia and amyotrophic lateral sclerosis.
Topics: Amyotrophic Lateral Sclerosis; Animals; Cell Line; Cytoplasm; Deubiquitinating Enzyme CYLD; DNA-Binding Proteins; Frontotemporal Dementia; Genetic Testing; Humans; Mutation; Neurons; RNA-Binding Protein FUS; Staurosporine | 2021 |
Therapeutic potential of mesenchymal stromal cells and MSC conditioned medium in Amyotrophic Lateral Sclerosis (ALS)--in vitro evidence from primary motor neuron cultures, NSC-34 cells, astrocytes and microglia.
Topics: Amyotrophic Lateral Sclerosis; Animals; Apoptosis; Astrocytes; Cells, Cultured; Chemokine CX3CL1; Ciliary Neurotrophic Factor; Culture Media, Conditioned; Glial Cell Line-Derived Neurotrophic Factors; Humans; Mesenchymal Stem Cells; Mice; Microglia; Motor Neurons; Staurosporine | 2013 |
TDP-43-induced death is associated with altered regulation of BIM and Bcl-xL and attenuated by caspase-mediated TDP-43 cleavage.
Topics: Amyotrophic Lateral Sclerosis; Animals; Apoptosis Regulatory Proteins; Bcl-2-Like Protein 11; bcl-X Protein; Caspases; Cell Death; Cell Line; DNA-Binding Proteins; Endoplasmic Reticulum; Enzyme Inhibitors; Frontotemporal Lobar Degeneration; Gene Expression Regulation; Humans; Inclusion Bodies; Membrane Proteins; Mice; Mice, Inbred ICR; Neurons; Proto-Oncogene Proteins; Staurosporine; Ubiquitin; Unfolded Protein Response | 2011 |
Neurotoxic injury pathways in differentiated mouse motor neuron-neuroblastoma hybrid (NSC-34D) cells in vitro--limited effect of riluzole on thapsigargin, but not staurosporine, hydrogen peroxide and homocysteine neurotoxicity.
Topics: Amyotrophic Lateral Sclerosis; Animals; Apoptosis; Calcium; Caspase 3; Caspase 7; Cell Line; Dose-Response Relationship, Drug; Endoplasmic Reticulum; Homocysteine; Hybrid Cells; Hydrogen Peroxide; Mice; Motor Neurons; Neuroblastoma; Neuroprotective Agents; Neurotoxins; Riluzole; Staurosporine; Thapsigargin | 2012 |
Exendin-4 ameliorates motor neuron degeneration in cellular and animal models of amyotrophic lateral sclerosis.
Topics: Amyotrophic Lateral Sclerosis; Animals; Apoptosis; Cell Line; Choline O-Acetyltransferase; Disease Models, Animal; Exenatide; Glucagon-Like Peptide 1; Glucose Tolerance Test; Hydrogen Peroxide; Hypoglycemic Agents; Insulin; Male; Mice; Motor Neurons; Oxidative Stress; Peptides; Spinal Cord; Staurosporine; Superoxide Dismutase; Superoxide Dismutase-1; Venoms | 2012 |
Neuroprotective effects of copper/zinc-dependent superoxide dismutase against a wide variety of death-inducing stimuli and proapoptotic effect of familial amyotrophic lateral sclerosis mutations.
Topics: Amyotrophic Lateral Sclerosis; Animals; Apoptosis; Cell Line; Cell Survival; Culture Media, Serum-Free; Enzyme Inhibitors; Genetic Vectors; Humans; In Situ Nick-End Labeling; Interferon-gamma; Mutagenesis, Site-Directed; Neurons; Neuroprotective Agents; Staurosporine; Superoxide Dismutase | 2002 |
Hsp27 and Hsp70 administered in combination have a potent protective effect against FALS-associated SOD1-mutant-induced cell death in mammalian neuronal cells.
Topics: Amino Acid Chloromethyl Ketones; Amyotrophic Lateral Sclerosis; Analysis of Variance; Animals; Animals, Newborn; Blotting, Western; Cell Death; Cells, Cultured; Cricetinae; Culture Media, Serum-Free; Disease Models, Animal; Drug Combinations; Drug Interactions; Enzyme Inhibitors; Ganglia, Spinal; Genetic Vectors; Green Fluorescent Proteins; Heat-Shock Proteins; HIV-1; HSP27 Heat-Shock Proteins; HSP70 Heat-Shock Proteins; In Situ Nick-End Labeling; Mutagenesis; Mutation; Neoplasm Proteins; Neurons; Neuroprotective Agents; Rats; Staurosporine; Superoxide Dismutase; Superoxide Dismutase-1; Time Factors; Transfection | 2005 |