Compounds > proline

proline and Cochlear Hearing Loss

proline 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's1 (25.00)18.2507
2000's3 (75.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Berman, Z; Leshinsky-Silver, E; Lev, D; Vinkler, C; Yannov-Sharav, M1
Abe, S; Asamura, K; Fukuoka, H; Nakamura, Y; Usami, S1
Büsse-Ratzka, M; Collmann, H; Hoppe, F; Krauss, J; Kress, W; Kunz, J; Lieb, G; Pahnke, J; Petersen, B; Reinhart, E; Schäfer, WD; Schropp, C; Sold, J; Sörensen, N; Trusen, A1
Bom, SJ; Brunner, HG; Brunt, TM; Cremers, CW; Cremers, FP; de Kok, YJ; Huygen, PL; Kemperman, MH; Morton, CC; Robertson, NG; van Beusekom, E; van der Velde-Visser, SD; Verhagen, WI1

Other Studies

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

ArticleYear
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness.
    Hearing research, 2005, Volume: 202, Issue:1-2

    Topics: Alleles; Base Sequence; Child; Connexin 26; Connexins; Conserved Sequence; Cytosine; Female; Genes, Recessive; Hearing Loss, Sensorineural; Homozygote; Humans; Leucine; Mutation, Missense; Point Mutation; Polymorphism, Restriction Fragment Length; Proline; Thymine

2005
Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients.
    Auris, nasus, larynx, 2005, Volume: 32, Issue:2

    Topics: Amino Acid Sequence; Aspartic Acid; Base Sequence; Cochlea; Collagen Type IX; DNA Mutational Analysis; Gene Deletion; Glutamic Acid; Glycine; Hearing Loss, Sensorineural; Humans; Molecular Sequence Data; Mutation; Mutation, Missense; Pedigree; Proline

2005
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
    European journal of human genetics : EJHG, 2006, Volume: 14, Issue:1

    Topics: Acrocephalosyndactylia; Adolescent; Amino Acid Substitution; Arginine; Child, Preschool; Ear; Hearing Loss, Sensorineural; Humans; Intellectual Disability; Intracranial Pressure; Mutation; Nuclear Proteins; Pedigree; Proline; Receptor, Fibroblast Growth Factor, Type 3; Repetitive Sequences, Nucleic Acid; Syndrome; Synostosis; Twist-Related Protein 1

2006
A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.
    Human molecular genetics, 1999, Volume: 8, Issue:2

    Topics: Age of Onset; Amino Acid Substitution; Base Sequence; Chromosome Mapping; Chromosomes, Human, Pair 14; Deafness; DNA; DNA Mutational Analysis; Extracellular Matrix Proteins; Female; Genes, Dominant; Genetic Linkage; Hearing Loss, Sensorineural; Humans; Male; Microsatellite Repeats; Pedigree; Point Mutation; Proline; Proteins; Serine; Vestibular Diseases

1999