aspartic acid has been researched along with Deafness, Transitory in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (33.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (50.00) | 24.3611 |
2020's | 1 (16.67) | 2.80 |
Authors | Studies |
---|---|
Baker, RE; Basrai, MA; Corbett, AH; Enyenihi, L; Farchi, D; Fasken, MB; Hess, L; Kremsky, I; Lee, RS; Leung, SW; Sterrett, MC; Strassler, SE; van Hoof, A; Withers, ES | 1 |
Barta, H; Jermendy, A; Kolossvary, M; Kozak, LR; Lakatos, A; Meder, U; Rudas, G; Szabo, M | 1 |
Bau, AE; de Zwart-Storm, EA; Foelster-Holst, R; Frank, J; Graziadio, C; Kamps, MA; Martin, PE; Paskulin, GA; Rosa, RF; van Geel, M; van Steensel, MA; Zen, PR | 1 |
Dingerdissen, H; Karagiannis, K; Mazumder, R; Motwani, M; Simonyan, V | 1 |
NAKAHARA, K | 1 |
IGARASHI, Y; SAKABE, N; YOSHIE, N | 1 |
6 other study(ies) available for aspartic acid and Deafness, Transitory
Article | Year |
---|---|
A budding yeast model for human disease mutations in the
Topics: Amino Acid Sequence; Amino Acid Substitution; Aspartic Acid; Dwarfism; Exoribonucleases; Exosome Multienzyme Ribonuclease Complex; Facies; Gene Expression; Glycine; Hearing Loss; Humans; Models, Biological; Models, Molecular; Mutation, Missense; Protein Conformation; Retinitis Pigmentosa; RNA-Binding Proteins; RNA, Fungal; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Homology, Amino Acid; Syndrome | 2021 |
Prognostic value of early, conventional proton magnetic resonance spectroscopy in cooled asphyxiated infants.
Topics: Aspartic Acid; Brain; Creatine; Epilepsy; Female; Hearing Loss; Hospital Mortality; Humans; Hypothermia, Induced; Hypoxia-Ischemia, Brain; Infant, Newborn; Inositol; Male; Neurodevelopmental Disorders; Prognosis; Proton Magnetic Resonance Spectroscopy; Retrospective Studies; Time Factors | 2018 |
Molecular analysis of connexin26 asparagine14 mutations associated with syndromic skin phenotypes.
Topics: Adult; Asparagine; Aspartic Acid; Cell Membrane; Child; Connexin 26; Connexins; Cytoplasm; Endoplasmic Reticulum; Female; Fluoresceins; Gap Junctions; Hearing Loss; HeLa Cells; Humans; Hypertrichosis; Keratoderma, Palmoplantar; Keratosis; Lysine; Male; Mutation, Missense; Nails, Malformed; Protein Transport; Skin; Skin Diseases; Syndrome; Transfection; Tyrosine | 2011 |
Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.
Topics: Abnormalities, Multiple; Amino Acid Substitution; Arginine; Aspartic Acid; Carbohydrate Metabolism; Catalytic Domain; Cluster Analysis; Enzyme Activation; Genetic Variation; Genome, Human; Glycogen Storage Disease; Hearing Loss; Histidine; Humans; Lacrimal Apparatus Diseases; Metabolomics; Molecular Sequence Annotation; Phenylalanine; Polymorphism, Single Nucleotide; Proteome; Proteomics; Structure-Activity Relationship; Syndactyly; Tooth Abnormalities; Tyrosine | 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 |