Compounds > tyrosine

tyrosine and Cochlear Hearing Loss

tyrosine 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's1 (20.00)29.6817
2010's4 (80.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Arberas, C; Armando, R; Ballerini, MG; Barros, ÁC; Bergadá, I; Braslavsky, D; Casali, B; Cassinelli, H; Castro, JF; Del Rey, G; Domené, H; Domené, S; Gutiérrez, M; Jasper, H; Keselman, AC; Landi, E; Lapunzina-Badía, P; Martin, A; Nevado Blanco, J; Pennisi, PA; Ramirez, L; Rey, RA; Ropelato, MG; Sanguineti, NM; Scaglia, PA1
Walenkamp, MJE; Wit, JM1
He, Q; Jia, Z; Li, F; Shan, C1
Ando, F; Hibi, T; Kato, K; Nakashima, T; Nishio, N; Otake, H; Shimokata, H; Sone, M; Sugiura, S; Tagaya, M; Teranishi, M; Uchida, Y; Yoshida, T1
Abbate, R; Bruschettini, A; Cecchi, E; Fatini, C; Gensini, GF; Leprini, E; Mannini, L; Pagnini, P; Prisco, D; Sticchi, E1

Other Studies

5 other study(ies) available for tyrosine and Cochlear Hearing Loss

ArticleYear
A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.
    European journal of endocrinology, 2019, Volume: 181, Issue:5

    Topics: Abnormalities, Multiple; Cell Proliferation; Computational Biology; Computer Simulation; Fetal Growth Retardation; Growth Disorders; Hearing Loss, Sensorineural; HEK293 Cells; Homozygote; Humans; Infant; Insulin-Like Growth Factor I; Male; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Receptor, IGF Type 1; Receptors, Somatomedin; Tyrosine

2019
A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.
    European journal of endocrinology, 2019, Volume: 181, Issue:6

    Topics: Growth Disorders; Hearing Loss, Sensorineural; Humans; Insulin-Like Growth Factor I; Mutation; Tyrosine

2019
Tauroursodeoxycholic acid attenuates gentamicin-induced cochlear hair cell death in vitro.
    Toxicology letters, 2018, Sep-15, Volume: 294

    Topics: Animals; Anti-Bacterial Agents; Apoptosis; Biomarkers; Cell Line; Cell Survival; Cochlea; Endoplasmic Reticulum Stress; Gene Expression Regulation; Gentamicins; Hair Cells, Auditory; Hearing Loss, Sensorineural; Humans; Mice, Inbred BALB C; Microscopy, Electron, Scanning; Nitric Oxide Synthase Type II; Protective Agents; Protein Processing, Post-Translational; Protein Synthesis Inhibitors; Taurochenodeoxycholic Acid; Tissue Culture Techniques; Tyrosine

2018
Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes.
    Gene, 2012, May-10, Volume: 499, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Case-Control Studies; Complement Factor H; Diabetes Complications; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Hearing Loss, Sudden; Histidine; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Tyrosine; Young Adult

2012
eNOS gene affects red cell deformability: role of T-786C, G894T, and 4a/4b polymorphisms.
    Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis, 2005, Volume: 11, Issue:4

    Topics: Adult; Aged; Aged, 80 and over; Alleles; Erythrocyte Deformability; Erythrocytes; Female; Genotype; Glycine; Hearing Loss, Sensorineural; Hemorheology; Humans; Male; Middle Aged; Nitric Oxide Synthase Type III; Polymorphism, Genetic; Tyrosine

2005