Compounds > cysteine

cysteine and Cochlear Hearing Loss

cysteine has been researched along with Cochlear Hearing Loss in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (80.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fahlke, C; Fischer, M; Gorinski, N; Guseva, D; Ponimaskin, E; Steinke, KV; Todorov, V; Wojciechowski, D1
Apaydin, F; Aydin, O; Blin, N; Devoto, M; Fransen, E; Kupka, S; Leistenschneider, P; Nürnberg, P; Ozkarakas, H; Pfister, M; Thiele, H; Van Camp, G; Zenner, HP1
Ignatius, J; Kääriäinen, H; Körkkö, J; Löppönen, T; Lundan, T; Seppänen, U1
Aldahmesh, MA; Khan, AO; Meyer, B1
Cucci, RA; Green, GE; Prasad, S; Smith, RJ1

Reviews

1 review(s) available for cysteine and Cochlear Hearing Loss

ArticleYear
Childhood-onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75-Cys mutation in procollagen type II gene (COL2A1).
    Arthritis and rheumatism, 2004, Dec-15, Volume: 51, Issue:6

    Topics: Adult; Arginine; Arthritis, Juvenile; Body Height; Collagen Type II; Cysteine; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Lumbar Vertebrae; Middle Aged; Mutation; Osteoarthritis; Scoliosis; Syndrome

2004

Other Studies

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

ArticleYear
Human CLC-K Channels Require Palmitoylation of Their Accessory Subunit Barttin to Be Functional.
    The Journal of biological chemistry, 2015, Jul-10, Volume: 290, Issue:28

    Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Bartter Syndrome; Chloride Channels; Cysteine; Dogs; Hearing Loss, Sensorineural; HEK293 Cells; Humans; Lipoylation; Madin Darby Canine Kidney Cells; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutant Proteins; Point Mutation; Protein Subunits; Recombinant Proteins; Sequence Homology, Amino Acid

2015
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations.
    Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 2004, Volume: 14, Issue:4-6

    Topics: Age Factors; Amino Acid Sequence; Amino Acid Substitution; Animals; Chromosomes, Human, Pair 11; Cysteine; Exons; Extracellular Matrix Proteins; Female; Genotype; GPI-Linked Proteins; Hearing Loss, Sensorineural; Humans; Male; Membrane Glycoproteins; Microsatellite Repeats; Molecular Sequence Data; Mutation, Missense; Phenotype; Protein Structure, Tertiary; Sex Factors

2004
Correlation of ophthalmic examination with carrier status in females potentially harboring a severe Norrie disease gene mutation.
    Ophthalmology, 2008, Volume: 115, Issue:4

    Topics: Cysteine; Diagnostic Techniques, Ophthalmological; Eye Proteins; Female; Genes, Recessive; Genetic Diseases, X-Linked; Hearing Loss, Sensorineural; Heterozygote; Humans; Intellectual Disability; Male; Molecular Biology; Mutation; Nerve Tissue Proteins; Pedigree; Phenylalanine; Prospective Studies; Retinal Diseases; Severity of Illness Index; Vitreoretinopathy, Proliferative

2008
Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).
    Human mutation, 2000, Volume: 16, Issue:6

    Topics: Alleles; Amino Acid Substitution; Arginine; Connexin 26; Connexins; Cysteine; Deafness; Genetic Testing; Genetic Variation; Hearing Loss, Sensorineural; Humans; Mutation; Sequence Deletion

2000