cycloheximide has been researched along with Muscular Atrophy, Spinal in 3 studies
| 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 (33.33) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Lan, F; Lin, Y; Zeng, J; Zhang, M; Zhang, X | 1 |
| Edula, MR; Matera, AG; Paris-Davila, T; Raimer, AC; Singh, SS; Spring, AM; Vandadi, V | 1 |
| Ar Rochmah, M; Awano, H; Harahap, NIF; Iijima, K; Lai, PS; Matsuo, M; Morioka, I; Niba, ETE; Nishio, H; Saito, K; Saito, T; Shinohara, M; Wijaya, YOS | 1 |
3 other study(ies) available for cycloheximide and Muscular Atrophy, Spinal
| Article | Year |
|---|---|
Premature termination codons in SMN1 leading to spinal muscular atrophy trigger nonsense-mediated mRNA decay.
Topics: Codon, Nonsense; Cycloheximide; Humans; Muscular Atrophy, Spinal; Nonsense Mediated mRNA Decay; RNA Helicases; RNA, Messenger; Survival of Motor Neuron 1 Protein; Trans-Activators | 2022 |
Temperature-sensitive spinal muscular atrophy-causing point mutations lead to SMN instability, locomotor defects and premature lethality in
Topics: Animals; Cycloheximide; Drosophila melanogaster; Drosophila Proteins; Larva; Longevity; Motor Activity; Muscular Atrophy, Spinal; Mutation, Missense; Phenotype; Point Mutation; Protein Domains; Protein Stability; Pupa; RNA-Binding Proteins; Temperature | 2020 |
Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2.
Topics: Blotting, Western; Cell Nucleus; Cycloheximide; HEK293 Cells; HeLa Cells; Hep G2 Cells; Humans; Introns; Muscular Atrophy, Spinal; Nonsense Mediated mRNA Decay; Protein Synthesis Inhibitors; Reverse Transcriptase Polymerase Chain Reaction; Survival of Motor Neuron 1 Protein; Survival of Motor Neuron 2 Protein | 2018 |