serine has been researched along with Deafness, Transitory in 3 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Xie, WR | 1 |
| Jen, HI | 1 |
| Seymour, ML | 1 |
| Yeh, SY | 1 |
| Pereira, FA | 1 |
| Groves, AK | 1 |
| Klisch, TJ | 1 |
| Zoghbi, HY | 1 |
| Almontashiri, NAM | 1 |
| Rodan, LH | 1 |
| Peake, RWA | 1 |
| Yuan, H | 1 |
| Chen, J | 1 |
| Liu, X | 1 |
| Cheng, J | 1 |
| Wang, X | 1 |
| Yang, L | 1 |
| Yang, S | 1 |
| Cao, J | 1 |
| Kang, D | 1 |
| Dai, P | 1 |
| Zhai, S | 1 |
| Han, D | 1 |
| Young, WY | 1 |
| Guan, MX | 1 |
3 other studies available for serine and Deafness, Transitory
| Article | Year |
|---|---|
An Atoh1-S193A Phospho-Mutant Allele Causes Hearing Deficits and Motor Impairment.
Topics: Aging; Alleles; Animals; Basic Helix-Loop-Helix Transcription Factors; Female; Gene Knock-In Techniq | 2017 |
Serine Deficiency in a Child with Neurological Presentation, Hearing Loss, and Multiple Congenital Anomalies.
Topics: Child, Preschool; Congenital Abnormalities; Hearing Loss; Humans; Male; Serine | 2018 |
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.
Topics: Aminoglycosides; China; Cyclooxygenase 1; DNA, Mitochondrial; Female; Hearing Loss; Humans; Male; Mu | 2007 |