isoleucine has been researched along with Deafness in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (75.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cranston, T; Gaynor, KU; Gomes, T; Gortner, L; Grigorieva, IV; Nesbit, MA; Thakker, RV | 1 |
Belintani Piatto, V; LĂșcia Sartorato, E; Maria Goloni Bertollo, E; Victor Maniglia, J | 1 |
Blanton, SH; Brown, SD; Liang, CY; Liu, XZ; Nance, WE; Pandya, A; Steel, KP; Xia, XJ; Xu, LR | 1 |
Albert, J; Collombel, C; David, M; Guerrier, G; Guibaud, P; Jeune, M; Michel, M | 1 |
4 other study(ies) available for isoleucine and Deafness
Article | Year |
---|---|
A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome.
Topics: Amino Acid Sequence; Blotting, Western; Deafness; DNA Mutational Analysis; Electrophoretic Mobility Shift Assay; Fluorescent Antibody Technique; GATA3 Transcription Factor; Humans; Hypoparathyroidism; Immunohistochemistry; Infant; Isoleucine; Kidney; Kidney Diseases; Male; Molecular Sequence Data; Mutation, Missense; Syndrome; Threonine | 2009 |
Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness.
Topics: Brazil; Connexin 26; Connexins; Deafness; Female; Gene Deletion; Gene Frequency; Guanine; Hearing Loss, Sensorineural; Heterozygote; Humans; Isoleucine; Male; Minisatellite Repeats; Mutation; Valine | 2004 |
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss.
Topics: Adult; Amino Acid Motifs; Child; China; Connexin 26; Connexins; Deafness; Female; Genes, Dominant; Genes, Recessive; Heterozygote; Humans; Isoleucine; Male; Mutation; Pedigree; Polymorphism, Single-Stranded Conformational; Sequence Analysis, DNA | 2000 |
[Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy].
Topics: Amino Acid Metabolism, Inborn Errors; Auditory Cortex; Child, Preschool; Deafness; Electroencephalography; Evoked Potentials; Female; Humans; Infant; Isoleucine; Leucine; Leukocytes; Male; Proline; Retinal Degeneration; Transaminases | 1970 |