alanine has been researched along with Deaf Mutism 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 | 2 (40.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Noguchi, Y | 1 |
| Yashima, T | 1 |
| Hatanaka, A | 1 |
| Uzawa, M | 1 |
| Yasunami, M | 1 |
| Kimura, A | 1 |
| Kitamura, K | 1 |
| Shimada, T | 1 |
| Sasaki, N | 1 |
| Ohkura, R | 1 |
| Sutoh, K | 1 |
| Yamasoba, T | 1 |
| Goto, Yi | 1 |
| Oka, Y | 1 |
| Nishino, I | 1 |
| Tsukuda, K | 1 |
| Nonaka, I | 1 |
| Dunn, HG | 1 |
| Dolman, CL | 1 |
| Hackett, TN | 1 |
| Bray, PF | 1 |
| Ziter, FA | 1 |
| Nyhan, WL | 1 |
| Creer, KM | 1 |
5 other studies available for alanine and Deaf Mutism
| Article | Year |
|---|---|
A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.
Topics: Adolescent; Adult; Alanine; Amino Acid Substitution; Auditory Threshold; Child; Codon; Deafness; DNA | 2005 |
Alanine scanning mutagenesis of the switch I region in the ATPase site of Dictyostelium discoideum myosin II.
Topics: Adenosine Diphosphate; Adenosine Triphosphatases; Alanine; Animals; Binding Sites; Deafness; Dictyos | 1997 |
Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene.
Topics: Adult; Alanine; Anti-Bacterial Agents; Audiology; Cysteine; Cytochrome b Group; Deafness; DNA, Mitoc | 2002 |
Necrotizing encephalomyelopathy. Report of a case with relapsing polyneuropathy and hyperalaninemia and with manifestations resembling Friedreich's ataxia.
Topics: Alanine; Ataxia; Blindness; Brain; Brain Diseases; Bronchopneumonia; Cerebellar Ataxia; Child; Child | 1969 |
A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness.
Topics: Acidosis; Alanine; Child; Chromatography, Paper; Deafness; Electromyography; Female; Growth Disorder | 1973 |