alanine has been researched along with Atrophy, Muscular, Peroneal in 5 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Grosse, GM | 1 |
| Bauer, C | 1 |
| Kopp, B | 1 |
| Schrader, C | 1 |
| Osmanovic, A | 1 |
| Nadol, JB | 1 |
| Hedley-Whyte, ET | 1 |
| Amr, SS | 1 |
| O Apos Malley, JT | 1 |
| Kamakura, T | 1 |
| Baker, SK | 1 |
| Reith, CC | 1 |
| Ainsworth, PJ | 1 |
| Luigetti, M | 1 |
| Fabrizi, GM | 1 |
| Taioli, F | 1 |
| Conte, A | 1 |
| Del Grande, A | 1 |
| Sabatelli, M | 1 |
| Kochanski, A | 1 |
| Drac, H | 1 |
| Kabzińska, D | 1 |
| Hausmanowa-Petrusewicz, I | 1 |
5 other studies available for alanine and Atrophy, Muscular, Peroneal
| Article | Year |
|---|---|
Identification of a rare SEPT9 variant in a family with autosomal dominant Charcot-Marie-Tooth disease.
Topics: Adult; Alanine; Amino Acid Substitution; Charcot-Marie-Tooth Disease; Family; Female; Gene Frequency | 2020 |
Histopathology of the Inner Ear in Charcot-Marie-Tooth Syndrome Caused by a Missense Variant (p.Thr65Ala) in the MPZ Gene.
Topics: Aged; Alanine; Charcot-Marie-Tooth Disease; Chromosome Aberrations; Cochlear Nerve; Ear, Inner; Exom | 2018 |
Novel 95G>A (R32K) somatic mosaic connexin 32 mutation.
Topics: Adult; Alanine; Arginine; Charcot-Marie-Tooth Disease; Connexins; DNA Mutational Analysis; Gap Junct | 2008 |
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation.
Topics: Adult; Alanine; Charcot-Marie-Tooth Disease; Electrodiagnosis; Female; GTP Phosphohydrolases; Humans | 2011 |
A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin.
Topics: Adult; Alanine; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; Female; Hand Deformities; Huma | 2004 |