Compounds > isoleucine

isoleucine and Cochlear Hearing Loss

isoleucine has been researched along with Cochlear Hearing Loss in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Cang, X; Fu, Y; Guan, MX; Lin, J; Lin, T; Mao, X; Meng, F; Wang, M; Xiao, Y; Ye, Z; Zheng, J; Zhou, M1
Dockter, G; Gomes, TS; Gortner, L; Leitner, D; Rohrer, T; Thakker, RV1
Belintani Piatto, V; Lúcia Sartorato, E; Maria Goloni Bertollo, E; Victor Maniglia, J1
Charoenpipop, D; Duggal, P; Jariengprasert, C; Limwongse, C; Pho-iam, T; Thawil, C; Thongnoppakhun, W; Thongpradit, S; Tocharoenthanaphol, C; Wattanasirichaigoon, D; Yenchitsomanus, PT1

Other Studies

4 other study(ies) available for isoleucine and Cochlear Hearing Loss

ArticleYear
A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation.
    Nucleic acids research, 2021, 01-25, Volume: 49, Issue:2

    Topics: Adenosine Triphosphate; Adult; Archaeal Proteins; Autophagy; Base Sequence; Cell Line; DNA, Mitochondrial; Ethnicity; Female; Genetic Pleiotropy; Hearing Loss, Sensorineural; Humans; Isoleucine; Male; Maternal Inheritance; Membrane Potential, Mitochondrial; Methanocaldococcus; Methylation; Middle Aged; Mitochondria; Molecular Dynamics Simulation; Nucleic Acid Conformation; Oxidative Phosphorylation; Pedigree; Point Mutation; Protein Biosynthesis; Recombinant Proteins; RNA Processing, Post-Transcriptional; RNA, Transfer, Ile; Transfer RNA Aminoacylation; tRNA Methyltransferases; Young Adult

2021
HDR syndrome: a follow-up genotype-phenotype analysis of a de novo missense Thr272Ile mutation in exon 4 of GATA3.
    Klinische Padiatrie, 2012, Volume: 224, Issue:7

    Topics: Child; Child, Preschool; Combined Modality Therapy; Developmental Disabilities; DNA Mutational Analysis; Exons; Follow-Up Studies; GATA3 Transcription Factor; Genetic Carrier Screening; Genotype; Hearing Loss, Sensorineural; Humans; Hypoparathyroidism; Infant; Isoleucine; Male; Mutation, Missense; Nephrosis; Phenotype; Threonine

2012
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
High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals.
    Clinical genetics, 2004, Volume: 66, Issue:5

    Topics: Adolescent; Amino Acid Substitution; Asian People; Child; Child, Preschool; Connexin 26; Connexins; Female; Hearing Loss, Sensorineural; Humans; Infant; Isoleucine; Male; Mutation, Missense; Prevalence; Thailand; Valine

2004