serine has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f 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 | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Marques, W | 2 |
| Neto, JM | 1 |
| Barreira, AA | 1 |
| Thomas, PK | 1 |
| Sweeney, MG | 1 |
| Carr, L | 1 |
| Wood, NW | 1 |
| Ekici, AB | 1 |
| Park, O | 1 |
| Korinthenberg, R | 1 |
| Grehl, H | 1 |
| Rautenstrauss, B | 1 |
3 other studies available for serine and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
| Article | Year |
|---|---|
Dejerine-Sottas' neuropathy caused by the missense mutation PMP22 Ser72Leu.
Topics: Adolescent; Amino Acid Substitution; Axons; DNA Mutational Analysis; Female; Genetic Testing; Heredi | 2004 |
Dejerine-Sottas neuropathy and PMP22 point mutations: a new base pair substitution and a possible "hot spot" on Ser72.
Topics: Adult; Amino Acid Substitution; Child; DNA Mutational Analysis; Exons; Female; Hereditary Sensory an | 1998 |
T>C transition in codon 72 (TCG-->CCG), S72P, a putative hotspot in PMP22.
Topics: Amino Acid Substitution; Codon; Cytosine; Hereditary Sensory and Motor Neuropathy; Humans; Mutation, | 2001 |