aspartic acid has been researched along with Deaf Mutism in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (33.33) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fukuda, M; Nagao, Y | 1 |
| Garringer, HJ; Ghetti, B; Gnezda, A; Murrell, J; Sammeta, N; Vidal, R | 1 |
| NAKAHARA, K | 1 |
| IGARASHI, Y; SAKABE, N; YOSHIE, N | 1 |
| Ananthanarayanan, SK; Brosey, CA; Mao, S; Tyska, MJ; Yengo, CM | 1 |
| Bowen, J; Maravilla, K; Richards, T | 1 |
6 other study(ies) available for aspartic acid and Deaf Mutism
| Article | Year |
|---|---|
Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report.
Topics: Arginine; Aspartic Acid; Biomarkers; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Growth Differentiation Factor 15; Humans; Male; MELAS Syndrome; Middle Aged; Mitochondrial Diseases; Mutation | 2019 |
Increased tau phosphorylation and tau truncation, and decreased synaptophysin levels in mutant BRI2/tau transgenic mice.
Topics: Adaptor Proteins, Signal Transducing; Animals; Aspartic Acid; Cataract; Cerebellar Ataxia; Deafness; Dementia; Female; Gene Expression; Hippocampus; Humans; Immunohistochemistry; Male; Membrane Glycoproteins; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Transgenic; Motor Activity; Mutation; Neocortex; Phosphorylation; Reverse Transcriptase Polymerase Chain Reaction; Synaptophysin; tau Proteins | 2013 |
[2 CASES OF SLIGHT PERCEPTIVE DEAFNESS CURED BY ASPARA TABLETS].
Topics: Aspartic Acid; Chondroitin; Deafness; Hearing Loss; Hearing Loss, Sensorineural; Humans; Tablets; Thiamine | 1963 |
[EXPERIENCES WITH THE USE OF ASPARTIC ACID IN THE TREATMENT OF NERVE DEAFNESS AND TINNITUS AURIUM].
Topics: Aspartic Acid; Biomedical Research; Child; Deafness; Drug Therapy; Geriatrics; Hearing Loss; Humans; Retrocochlear Diseases; Tinnitus | 1964 |
Human deafness mutation E385D disrupts the mechanochemical coupling and subcellular targeting of myosin-1a.
Topics: Actin Cytoskeleton; Actins; Animals; Aspartic Acid; Deafness; Dictyostelium; Glutamic Acid; Green Fluorescent Proteins; Humans; Mechanotransduction, Cellular; Mutation; Myosin Heavy Chains; Myosin Type I; Myosin Type II; Protein Transport; Recombinant Fusion Proteins; Subcellular Fractions | 2008 |
MR imaging and proton MR spectroscopy in A-to-G substitution at nucleotide position 3243 of leucine transfer RNA.
Topics: Adult; Amino Acid Substitution; Aspartic Acid; Basal Ganglia; Base Sequence; Brain; Cerebral Cortex; Choline; Creatine; Deafness; Diabetes Mellitus, Type 1; DNA Mutational Analysis; DNA, Mitochondrial; Female; Follow-Up Studies; Genotype; Humans; Lactic Acid; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Middle Aged; Mitochondrial Encephalomyopathies; RNA, Transfer, Leu | 1998 |