glycine has been researched along with Adult Spinal Muscular Atrophy in 7 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "The SMN protein, which is linked to spinal muscular atrophy (SMA), plays an important role in the assembly of the spliceosomal small nuclear ribonucleoprotein complexes." | 1.32 | High-resolution X-ray and NMR structures of the SMN Tudor domain: conformational variation in the binding site for symmetrically dimethylated arginine residues. ( Groves, MR; Sattler, M; Sinning, I; Sprangers, R, 2003) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Son, YS | 1 |
| Choi, K | 1 |
| Lee, H | 1 |
| Kwon, O | 1 |
| Jung, KB | 1 |
| Cho, S | 2 |
| Baek, J | 1 |
| Son, B | 1 |
| Kang, SM | 1 |
| Kang, M | 1 |
| Yoon, J | 1 |
| Shen, H | 1 |
| Lee, S | 1 |
| Oh, JH | 1 |
| Lee, HA | 1 |
| Lee, MO | 1 |
| Cho, HS | 1 |
| Jung, CR | 1 |
| Kim, J | 1 |
| Son, MY | 1 |
| Marcuzzo, S | 1 |
| Zucca, I | 1 |
| Mastropietro, A | 1 |
| de Rosbo, NK | 1 |
| Cavalcante, P | 1 |
| Tartari, S | 1 |
| Bonanno, S | 1 |
| Preite, L | 1 |
| Mantegazza, R | 1 |
| Bernasconi, P | 1 |
| Sprangers, R | 1 |
| Groves, MR | 1 |
| Sinning, I | 1 |
| Sattler, M | 1 |
| Mancuso, M | 1 |
| Filosto, M | 1 |
| Hirano, M | 1 |
| DiMauro, S | 1 |
| Côté, J | 1 |
| Richard, S | 1 |
| Talbot, K | 1 |
| Ponting, CP | 1 |
| Theodosiou, AM | 1 |
| Rodrigues, NR | 1 |
| Surtees, R | 1 |
| Mountford, R | 1 |
| Davies, KE | 1 |
| Friesen, WJ | 1 |
| Dreyfuss, G | 1 |
7 other studies available for glycine and Adult Spinal Muscular Atrophy
| Article | Year |
|---|---|
A SMN2 Splicing Modifier Rescues the Disease Phenotypes in an In Vitro Human Spinal Muscular Atrophy Model.
Topics: Alternative Splicing; Animals; Cell Line; Glycine; Humans; Mice; Mice, Transgenic; Models, Neurologi | 2019 |
Hind limb muscle atrophy precedes cerebral neuronal degeneration in G93A-SOD1 mouse model of amyotrophic lateral sclerosis: a longitudinal MRI study.
Topics: Alanine; Amyotrophic Lateral Sclerosis; Animals; Brain; Disease Models, Animal; Glycine; Hindlimb; H | 2011 |
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; Glycin | 2003 |
Spinal muscular atrophy and mitochondrial DNA depletion. Response to Berber et al. (2003) Acta Neuropathol 105:245-251.
Topics: beta-Galactosidase; Child; Creatine Kinase; Cysteine; Diagnosis, Differential; DNA, Mitochondrial; E | 2003 |
Tudor domains bind symmetrical dimethylated arginines.
Topics: Amino Acid Sequence; Arginine; Binding Sites; Genetic Vectors; Glycine; Humans; Methionine; Molecula | 2005 |
Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism?
Topics: Amino Acid Sequence; Animals; Caenorhabditis elegans; Cloning, Molecular; Conserved Sequence; Cyclic | 1997 |
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; H | 2000 |