Page last updated: 2024-11-08

alanine and Hearing Loss, Sensorineural

alanine has been researched along with Hearing Loss, Sensorineural in 3 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Hearing Loss, Sensorineural: Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Parrock, S1
Hussain, S1
Issler, N1
Differ, AM1
Lench, N1
Guarino, S1
Oosterveld, MJ1
Keijzer-Veen, M1
Brilstra, E1
van Wieringen, H1
Konijnenberg, AY1
Amin-Rasip, S1
Dumitriu, S1
Klootwijk, E1
Knoers, N1
Bockenhauer, D1
Kleta, R1
Zdebik, AA1
Noguchi, Y1
Yashima, T1
Hatanaka, A1
Uzawa, M1
Yasunami, M1
Kimura, A1
Kitamura, K1
Kupka, S1
Tóth, T1
Wróbel, M1
Zeissler, U1
Szyfter, W1
Szyfter, K1
Niedzielska, G1
Bal, J1
Zenner, HP1
Sziklai, I1
Blin, N1
Pfister, M1

Other Studies

3 other studies available for alanine and Hearing Loss, Sensorineural

ArticleYear
KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16.
    Nephron. Physiology, 2013, Volume: 123, Issue:3-4

    Topics: Alanine; Animals; Female; Genotype; Hearing Loss, Sensorineural; Humans; Intellectual Disability; Oo

2013
A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.
    Acta oto-laryngologica, 2005, Volume: 125, Issue:11

    Topics: Adolescent; Adult; Alanine; Amino Acid Substitution; Auditory Threshold; Child; Codon; Deafness; DNA

2005
Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
    Human mutation, 2002, Volume: 19, Issue:3

    Topics: Adult; Aged; Alanine; Amino Acid Substitution; Child; Child, Preschool; Female; Genetic Predispositi

2002