arginine has been researched along with Adult Spinal Muscular Atrophy in 11 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 7 (63.64) | 29.6817 |
2010's | 3 (27.27) | 24.3611 |
2020's | 1 (9.09) | 2.80 |
Authors | Studies |
---|---|
Binda, O; Corpet, A; Côté, J; Fradet-Turcotte, A; Galloy, M; Jacquet, K; Kimenyi Ishimwe, AB; Lomonte, P | 1 |
Ciara, E; Dębek, E; Gasperowicz, P; Gos, M; Halat, P; Jędrzejowska, M; Jezela-Stanek, A; Kostera-Pruszczyk, A; Kowalczyk, B; Rydzanicz, M | 1 |
Albertyn, CH; Bryer, A; Corrigall, A; Heckmann, JM; Meissner, P; Sonderup, M | 1 |
Peng, C; Wong, CC | 1 |
Autexier, C; Bachand, F; Boisvert, FM; Boulanger, MC; Cleroux, P; Cote, J; Richard, S | 1 |
Groves, MR; Sattler, M; Sinning, I; Sprangers, R | 1 |
Androphy, EJ; Coon, K; Francis, JW; Lince, D; Lorson, CL; Young, PJ | 1 |
Côté, J; Richard, S | 1 |
Boisvenue, S; Côté, J; Deschênes-Furry, J; Tadesse, H | 1 |
Dreyfuss, G; Friesen, WJ | 1 |
Dreyfuss, G; Friesen, WJ; Massenet, S; Paushkin, S; Wyce, A | 1 |
1 review(s) available for arginine and Adult Spinal Muscular Atrophy
Article | Year |
---|---|
The story of protein arginine methylation: characterization, regulation, and function.
Topics: Arginine; Cardiovascular Diseases; DNA Repair; Humans; Mass Spectrometry; Methylation; Multiple Sclerosis; Muscular Atrophy, Spinal; Neoplasms; Protein Processing, Post-Translational; Protein-Arginine N-Methyltransferases; Proteins; Proteomics; Signal Transduction | 2017 |
10 other study(ies) available for arginine and Adult Spinal Muscular Atrophy
Article | Year |
---|---|
The TUDOR domain of SMN is an H3K79
Topics: Arginine; Histone Code; Humans; Infant; Lysine; Muscular Atrophy, Spinal; RNA Polymerase II; Survival of Motor Neuron 1 Protein; Transcription Factors | 2023 |
The remarkable phenotypic variability of the p.Arg269HiS variant in the TRPV4 gene.
Topics: Adult; Arginine; Child, Preschool; Creatine Kinase; Family Health; Female; Heterozygote; Histidine; Humans; Male; Muscular Atrophy, Spinal; Mutation; Transaminases; TRPV Cation Channels | 2019 |
Acute intermittent porphyria presenting as progressive muscular atrophy in a young black man.
Topics: Arginine; Heme; Humans; Hydroxymethylbilane Synthase; Male; Muscular Atrophy, Spinal; Porphyria, Acute Intermittent; Young Adult | 2014 |
Symmetrical dimethylarginine methylation is required for the localization of SMN in Cajal bodies and pre-mRNA splicing.
Topics: Antibodies; Arginine; Cell Nucleus; Coiled Bodies; DNA; Dose-Response Relationship, Drug; Down-Regulation; Electrophoresis, Polyacrylamide Gel; Enzyme-Linked Immunosorbent Assay; Fibroblasts; Fluorescent Antibody Technique, Indirect; HeLa Cells; Humans; Mass Spectrometry; Methylation; Microscopy, Fluorescence; Muscular Atrophy, Spinal; Precipitin Tests; RNA Splicing; RNA, Messenger; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Transfection | 2002 |
High-resolution X-ray and NMR structures of the SMN Tudor domain: conformational variation in the binding site for symmetrically dimethylated arginine residues.
Topics: Arginine; Binding Sites; Crystallography, X-Ray; Cyclic AMP Response Element-Binding Protein; Glycine; Humans; Methylation; Models, Molecular; Muscular Atrophy, Spinal; Nerve Tissue Proteins; Nuclear Magnetic Resonance, Biomolecular; Protein Binding; Protein Conformation; Protein Folding; Protein Structure, Tertiary; RNA-Binding Proteins; SMN Complex Proteins | 2003 |
The Ewing's sarcoma protein interacts with the Tudor domain of the survival motor neuron protein.
Topics: Animals; Arginine; Binding Sites; Cell Line, Tumor; Cell Nucleus; Cells, Cultured; Cyclic AMP Response Element-Binding Protein; Exons; Humans; Methylation; Muscular Atrophy, Spinal; Nerve Tissue Proteins; Neurons; Peptides; Protein Binding; Protein Structure, Tertiary; Rats; RNA-Binding Protein EWS; RNA-Binding Proteins; RNA, Antisense; SMN Complex Proteins; Survival of Motor Neuron 1 Protein | 2003 |
Tudor domains bind symmetrical dimethylated arginines.
Topics: Amino Acid Sequence; Arginine; Binding Sites; Genetic Vectors; Glycine; Humans; Methionine; Molecular Sequence Data; Muscular Atrophy, Spinal; Polymerase Chain Reaction; Recombinant Fusion Proteins; RNA-Binding Proteins; Sequence Alignment; Sequence Homology, Amino Acid | 2005 |
KH-type splicing regulatory protein interacts with survival motor neuron protein and is misregulated in spinal muscular atrophy.
Topics: Amino Acid Sequence; Animals; Arginine; Base Sequence; Binding Sites; Cell Line; Cyclic AMP Response Element-Binding Protein; DNA Primers; Gene Expression Regulation; Humans; Methylation; Mice; Mice, Knockout; Mice, Mutant Strains; Molecular Chaperones; Molecular Sequence Data; Motor Neurons; Muscular Atrophy, Spinal; Mutation; Nerve Tissue Proteins; Protein Structure, Tertiary; Protein-Arginine N-Methyltransferases; RNA Stability; RNA-Binding Proteins; RNA, Messenger; Sequence Homology, Amino Acid; SMN Complex Proteins; Survival of Motor Neuron 1 Protein; Trans-Activators | 2008 |
Specific sequences of the Sm and Sm-like (Lsm) proteins mediate their interaction with the spinal muscular atrophy disease gene product (SMN).
Topics: Amino Acid Sequence; Arginine; Autoantigens; Cyclic AMP Response Element-Binding Protein; Glycine; Humans; Molecular Sequence Data; Muscular Atrophy, Spinal; Nerve Tissue Proteins; Protein Binding; Ribonucleoproteins, Small Nuclear; RNA-Binding Proteins; SMN Complex Proteins; snRNP Core Proteins; Structure-Activity Relationship | 2000 |
SMN, the product of the spinal muscular atrophy gene, binds preferentially to dimethylarginine-containing protein targets.
Topics: Amino Acid Sequence; Arginine; Autoantigens; Cyclic AMP Response Element-Binding Protein; Enzyme Inhibitors; HeLa Cells; Humans; Methylation; Molecular Sequence Data; Muscular Atrophy, Spinal; Nerve Tissue Proteins; Protein Binding; Recombinant Fusion Proteins; Ribonucleoproteins, Small Nuclear; RNA-Binding Proteins; SMN Complex Proteins; snRNP Core Proteins; Substrate Specificity | 2001 |