galactose has been researched along with Deafness in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (25.00) | 18.7374 |
| 1990's | 3 (37.50) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 2 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hanaoka, K; Kato, J; Kawamura, T; Miyazaki, Y; Morimoto, K; Nakashima, A; Sugai, K; Takahashi, D; Takahashi, H; Tanaka, M; Ueda, H; Yamaguchi, Y; Yokoo, T | 1 |
| Chen, B; Gao, J; Guan, M; He, Z; Huang, S; Nan, B; Xiang, H; Yu, X; Zheng, B; Zheng, J | 1 |
| Fischel-Ghodsian, N; Friedman, RA; Guan, MX; Li, X; Schwartz, F; Yan, Q | 1 |
| Attardi, G; Fischel-Ghodsian, N; Guan, MX | 1 |
| Holt, IJ; Jacobs, HT; Reid, FM; Rovio, A | 1 |
| Attardi, G; Enriquez, JA; Fischel-Ghodsian, N; Guan, MX; Lin, CP; Maw, MA; Puranam, RS | 1 |
| Amir, J; de Vries, A; Mintz, U; Pinkhas, J | 1 |
| HEXTER, M | 1 |
8 other study(ies) available for galactose and Deafness
| Article | Year |
|---|---|
Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report.
Topics: Adult; Deafness; Diabetes Mellitus, Type 2; Female; Galactose; Humans; Immunoglobulin A; Mesangial Cells; Mitochondrial Diseases; Pedigree | 2018 |
[Function study of non-syndromic deafness associated mitochondrial 12S rRNA A839G mutation].
Topics: Aminoglycosides; Cell Line; Deafness; DNA, Mitochondrial; Galactose; Hearing Tests; Mitochondria; Mutation; Pedigree; Phylogeny; RNA, Ribosomal | 2014 |
Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness.
Topics: Africa; Base Sequence; Cell Division; Cell Line; Cell Respiration; Deafness; DNA, Mitochondrial; Galactose; Glucose; Hearing Loss, Sensorineural; Humans; Mitochondrial Proteins; Molecular Sequence Data; NADH Dehydrogenase; Pedigree; Point Mutation; RNA, Messenger; RNA, Transfer, Ala; RNA, Transfer, Leu; RNA, Transfer, Ser | 2004 |
Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation.
Topics: Adult; Aged; Aminoglycosides; Anti-Bacterial Agents; Cell Division; Cell Line; Cell Nucleus; Cell Respiration; Deafness; DNA, Mitochondrial; DNA, Ribosomal; Female; Galactose; Humans; Lymphocytes; Male; Middle Aged; Mitochondria; Oxidoreductases; Oxygen Consumption; Pedigree; Point Mutation; Protein Biosynthesis; RNA; RNA, Mitochondrial; RNA, Ribosomal | 1996 |
Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutation.
Topics: Blotting, Northern; Cell Line, Transformed; Cell Respiration; Culture Media; Deafness; Deoxyribonucleases, Type II Site-Specific; DNA, Mitochondrial; Electron Transport Complex IV; Galactose; Genotype; Humans; Mitochondria; Mutation; Polymerase Chain Reaction; Protein Biosynthesis; Protein Synthesis Inhibitors; RNA Precursors; RNA, Transfer, Ser | 1997 |
The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.
Topics: Base Sequence; Binding Sites; Cell Division; Cell Respiration; Culture Media; Deafness; DNA, Mitochondrial; Galactose; Gene Expression Regulation, Enzymologic; Glucose; Humans; Molecular Sequence Data; Mutation; NADH Dehydrogenase; New Zealand; Nucleic Acid Conformation; Pedigree; Protein Biosynthesis; RNA Precursors; RNA Processing, Post-Transcriptional; RNA, Messenger; RNA, Transfer, Ser; Tumor Cells, Cultured | 1998 |
Transient perceptive deafness due to erythromycin lactobionate.
Topics: Aged; Deafness; Endocarditis, Subacute Bacterial; Erythromycin; Female; Galactose; Gluconates; Humans; Injections, Intravenous | 1973 |
The care of deaf-mutes in Israel.
Topics: Deafness; Hexoses; Humans; Israel | 1951 |