leucine and Muscular Atrophy, Spinal

leucine has been researched along with Muscular Atrophy, Spinal in 2 studies

Research

Studies (2)

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

Authors	Studies
Li, XJ; Ma, L; Mou, Y; Tian, Y; Trinh, J; Wang, Y; Xu, C; Zhang, B; Zhang, X; Zhou, S	1
Bird, LE; Cader, MZ; James, PA; Ren, J; Stammers, DK; Talbot, K	1

Other Studies

2 other study(ies) available for leucine and Muscular Atrophy, Spinal

Article	Year
Drug screening with human SMN2 reporter identifies SMN protein stabilizers to correct SMA pathology. Life science alliance, 2019, Volume: 2, Issue:2 Topics: Animals; Blood-Brain Barrier; Cysteine Proteinase Inhibitors; Dipeptides; Disease Models, Animal; Drug Evaluation, Preclinical; Genes, Reporter; HEK293 Cells; Humans; Ketones; Leucine; Mice; Mitochondria; Motor Neurons; Muscular Atrophy, Spinal; Protective Agents; Protein Stability; Proteolysis; Signal Transduction; Survival of Motor Neuron 2 Protein; Transfection; Treatment Outcome	2019
Crystal structure of human wildtype and S581L-mutant glycyl-tRNA synthetase, an enzyme underlying distal spinal muscular atrophy. FEBS letters, 2007, Jun-26, Volume: 581, Issue:16 Topics: Amino Acid Substitution; Binding Sites; Crystallography, X-Ray; Dimerization; Distal Myopathies; Glycine-tRNA Ligase; Humans; Leucine; Models, Molecular; Muscular Atrophy, Spinal; Mutant Proteins; Mutation, Missense; RNA-Binding Proteins; Serine; Transfer RNA Aminoacylation	2007

Article

Year

Drug screening with human SMN2 reporter identifies SMN protein stabilizers to correct SMA pathology.

Life science alliance, 2019, Volume: 2, Issue:2

Topics: Animals; Blood-Brain Barrier; Cysteine Proteinase Inhibitors; Dipeptides; Disease Models, Animal; Drug Evaluation, Preclinical; Genes, Reporter; HEK293 Cells; Humans; Ketones; Leucine; Mice; Mitochondria; Motor Neurons; Muscular Atrophy, Spinal; Protective Agents; Protein Stability; Proteolysis; Signal Transduction; Survival of Motor Neuron 2 Protein; Transfection; Treatment Outcome

2019

Crystal structure of human wildtype and S581L-mutant glycyl-tRNA synthetase, an enzyme underlying distal spinal muscular atrophy.

FEBS letters, 2007, Jun-26, Volume: 581, Issue:16

Topics: Amino Acid Substitution; Binding Sites; Crystallography, X-Ray; Dimerization; Distal Myopathies; Glycine-tRNA Ligase; Humans; Leucine; Models, Molecular; Muscular Atrophy, Spinal; Mutant Proteins; Mutation, Missense; RNA-Binding Proteins; Serine; Transfer RNA Aminoacylation

2007