Compounds > cysteine

cysteine and Deafness

cysteine has been researched along with Deafness in 12 studies

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19901 (8.33)18.7374
1990's4 (33.33)18.2507
2000's5 (41.67)29.6817
2010's2 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Iwers, L; Majdani, O; Maser, F1
Mese, G; Sánchez, HA; Srinivas, M; Verselis, VK; White, TW1
Capone, A; Dailey, W; Drenser, K; Trese, M; Wu, WC1
Bruzzone, R; Chaïb, H; Denoyelle, F; Lévi-Acobas, F; Lina-Granade, G; Petit, C; Plauchu, H; Weil, D1
Ayuso, C; Beneyto, M; Cuevas, JM; Espinós, C; García-Sandoval, B; Millán, JM; Nájera, C; Sánchez, F; Trujillo, MJ1
De Bellis, C; Lago, G; Mut, F; Pedemonte, M; Silveira, A; Suárez, H; Svirsky, M; Velluti, R1
Cucci, RA; Green, GE; Prasad, S; Smith, RJ1
Barberá, R; del Castillo, I; Hernández-Calvín, FJ; Herraiz, C; Moreno, F; Moreno-Pelayo, MA; Navas, C; Romero, L; Villamar, M1
Calais, C; Chaventre, A; Gayet, M; Le Caignec, C; Lefevre, M; Moisan, JP; Schott, JJ1
Goto, Yi; Nishino, I; Nonaka, I; Oka, Y; Tsukuda, K; Yamasoba, T1
Achatz, H; Berger, W; Cremers, F; Dörner, C; Gal, A; Haasemann, M; Hellebrand, H; Meindl, A; Meitinger, T; van de Pol, D1
Giul'khasian, AA1

Other Studies

12 other study(ies) available for cysteine and Deafness

ArticleYear
[The LEOPARD-syndrome].
    Laryngo- rhino- otologie, 2010, Volume: 89, Issue:10

    Topics: Adolescent; Amino Acid Substitution; Chromosomes, Human, Pair 12; Cochlear Implantation; Cysteine; Deafness; Diagnosis, Differential; DNA Mutational Analysis; Exons; Female; Humans; LEOPARD Syndrome; Point Mutation; Protein Tyrosine Phosphatase, Non-Receptor Type 12; Tyrosine

2010
Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome.
    The Journal of general physiology, 2010, Volume: 136, Issue:1

    Topics: Amino Acid Substitution; Animals; Barium; Calcium; Cell Line, Tumor; Chelating Agents; Chloride Channels; Connexin 26; Connexins; Cysteine; Deafness; Electrophysiological Phenomena; Ethylenediamines; Gap Junctions; Humans; Ion Channel Gating; Keratitis; Membrane Potentials; Mesylates; Mice; Mutation, Missense; Oocytes; Permeability; RNA, Messenger; Streptomyces; Sulfhydryl Reagents; Syndrome; Transfection; Xenopus laevis

2010
Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene.
    Archives of ophthalmology (Chicago, Ill. : 1960), 2007, Volume: 125, Issue:2

    Topics: Amino Acid Sequence; Blindness; Child, Preschool; Cysteine; Deafness; DNA Mutational Analysis; Eye Diseases, Hereditary; Eye Proteins; Female; Genotype; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Molecular Sequence Data; Mutation; Nerve Tissue Proteins; Phenotype; Polymerase Chain Reaction; Retina; Vitreoretinopathy, Proliferative

2007
Connexin 26 gene linked to a dominant deafness.
    Nature, 1998, May-28, Volume: 393, Issue:6683

    Topics: Chromosomes, Human, Pair 13; Connexin 26; Connexins; Cysteine; Deafness; DNA Mutational Analysis; Genes, Dominant; Humans; Mutation; Polymorphism, Genetic

1998
Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type Ib.
    Molecular and cellular probes, 1998, Volume: 12, Issue:6

    Topics: Codon, Terminator; Cysteine; Deafness; DNA; DNA Mutational Analysis; Dyneins; Exons; Female; Genes, Recessive; Humans; Male; Middle Aged; Mutation; Myosin VIIa; Myosins; Pedigree; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Retinitis Pigmentosa; Syndrome

1998
Changes in the cerebral blood flow in postlingual cochlear implant users.
    Acta oto-laryngologica, 1999, Volume: 119, Issue:2

    Topics: Adult; Brain; Cerebrovascular Circulation; Cochlear Implants; Cysteine; Deafness; Female; Humans; Male; Middle Aged; Organotechnetium Compounds; Radiopharmaceuticals; Speech Perception; Tomography, Emission-Computed, Single-Photon

1999
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
A cysteine substitution in the zona pellucida domain of alpha-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family.
    Journal of medical genetics, 2001, Volume: 38, Issue:5

    Topics: Adolescent; Adult; Amino Acid Sequence; Base Sequence; Child; Cysteine; Deafness; Extracellular Matrix Proteins; Female; Gene Frequency; Genes, Dominant; GPI-Linked Proteins; Haplotypes; Humans; Lod Score; Male; Membrane Glycoproteins; Microsatellite Repeats; Molecular Sequence Data; Mutation, Missense; Pedigree; Phenotype; Spain; Zona Pellucida

2001
Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.
    American journal of human genetics, 2002, Volume: 71, Issue:1

    Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Animals; Arcus Senilis; Base Sequence; Calcium-Binding Proteins; Cysteine; Deafness; DNA; Female; Genes, Dominant; Heart Defects, Congenital; Humans; Intercellular Signaling Peptides and Proteins; Jagged-1 Protein; Male; Membrane Proteins; Molecular Sequence Data; Mutation; Pedigree; Protein Structure, Tertiary; Proteins; Sequence Homology, Amino Acid; Serrate-Jagged Proteins

2002
Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene.
    Neuromuscular disorders : NMD, 2002, Volume: 12, Issue:5

    Topics: Adult; Alanine; Anti-Bacterial Agents; Audiology; Cysteine; Cytochrome b Group; Deafness; DNA, Mitochondrial; Female; Glycine; Hearing; Humans; Male; Middle Aged; Muscle, Skeletal; Mutation; Pedigree; Point Mutation; RNA; RNA, Mitochondrial; RNA, Ribosomal; Streptomycin; Threonine

2002
Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins.
    Nature genetics, 1992, Volume: 2, Issue:2

    Topics: Adult; Amino Acid Sequence; Base Sequence; Blindness; Child; Child, Preschool; Chromosome Mapping; Cysteine; Deafness; DNA; DNA Mutational Analysis; Exons; Genetic Linkage; Humans; Infant; Intellectual Disability; Introns; Male; Molecular Sequence Data; Mucins; Point Mutation; Sequence Homology, Amino Acid; X Chromosome

1992
[Effects of some drugs used for reduction of the ototoxic action of some antibiotics and saluzide in experimental conditions].
    Zhurnal eksperimental'noi i klinicheskoi meditsiny, 1971, Volume: 11, Issue:1

    Topics: Adenosine Triphosphate; Animals; Antitubercular Agents; Cysteine; Deafness; Guinea Pigs; Hearing Disorders; Heparin; Neomycin; Neuritis; Nicotinic Acids; Streptomycin; Vestibulocochlear Nerve

1971