Page last updated: 2024-11-08

serine and Cochlear Hearing Loss

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

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

Research Excerpts

ExcerptRelevanceReference
"Therefore, we hypothesize that focal palmoplantar keratoderma in gap junction skin disease may be specifically associated with connexin trafficking defects as well as with mutations affecting its extracellular domains, thus broadening the spectrum of GJB2-associated diseases."1.35A novel missense mutation in the second extracellular domain of GJB2, p.Ser183Phe, causes a syndrome of focal palmoplantar keratoderma with deafness. ( de Zwart-Storm, EA; Martin, PE; Steijlen, PM; van Geel, M; van Neer, PA; van Steensel, MA, 2008)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's2 (40.00)29.6817
2010's0 (0.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Fang, H1
Xie, A1
Du, M1
Li, X1
Yang, K1
Fu, Y1
Yuan, X1
Fan, R1
Yu, W1
Zhou, Z1
Sang, T1
Nie, K1
Li, J1
Zhao, Q1
Chen, Z1
Yang, Y1
Hong, C1
Lyu, J1
de Zwart-Storm, EA1
van Geel, M1
van Neer, PA1
Steijlen, PM1
Martin, PE1
van Steensel, MA1
Borck, G1
Roth, C1
Martiné, U1
Wildhardt, G1
Pohlenz, J1
Klein, CJ1
Nakumura, M1
Jacobson, DR1
Lacy, MQ1
Benson, MD1
Petersen, RC1
de Kok, YJ1
Bom, SJ1
Brunt, TM1
Kemperman, MH1
van Beusekom, E1
van der Velde-Visser, SD1
Robertson, NG1
Morton, CC1
Huygen, PL1
Verhagen, WI1
Brunner, HG1
Cremers, CW1
Cremers, FP1

Other Studies

5 other studies available for serine and Cochlear Hearing Loss

ArticleYear
SERAC1 is a component of the mitochondrial serine transporter complex required for the maintenance of mitochondrial DNA.
    Science translational medicine, 2022, 03-02, Volume: 14, Issue:634

    Topics: Animals; Carboxylic Ester Hydrolases; Contracture; DNA, Mitochondrial; Hearing Loss, Sensorineural;

2022
A novel missense mutation in the second extracellular domain of GJB2, p.Ser183Phe, causes a syndrome of focal palmoplantar keratoderma with deafness.
    The American journal of pathology, 2008, Volume: 173, Issue:4

    Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Child, Preschool; Connexin 26; C

2008
Mutations in the PDS gene in German families with Pendred's syndrome: V138F is a founder mutation.
    The Journal of clinical endocrinology and metabolism, 2003, Volume: 88, Issue:6

    Topics: Adolescent; Amino Acid Substitution; Base Sequence; Carrier Proteins; Child; Child, Preschool; Femal

2003
Transthyretin amyloidosis (serine 44) with headache, hearing loss, and peripheral neuropathy.
    Neurology, 1998, Volume: 51, Issue:5

    Topics: Adult; Amino Acid Sequence; Amyloidosis; Base Sequence; Exons; Headache; Hearing Loss, Sensorineural

1998
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 1

1999