Compounds > isoleucine

isoleucine and Deafness

isoleucine has been researched along with Deafness in 4 studies

Research

Studies (4)

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

Authors	Studies
Cranston, T; Gaynor, KU; Gomes, T; Gortner, L; Grigorieva, IV; Nesbit, MA; Thakker, RV	1
Belintani Piatto, V; Lúcia 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

Other Studies

4 other study(ies) available for isoleucine and Deafness

Article	Year
A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome. The Journal of clinical endocrinology and metabolism, 2009, Volume: 94, Issue:10 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. Hearing research, 2004, Volume: 196, Issue:1-2 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. Human molecular genetics, 2000, Jan-01, Volume: 9, Issue:1 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]. Annales de pediatrie, 1970, Feb-02, Volume: 17, Issue:2 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