serine has been researched along with Muscular Dystrophies, Limb-Girdle 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.
Muscular Dystrophies, Limb-Girdle: A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ojima, K | 1 |
| Ono, Y | 1 |
| Hata, S | 1 |
| Noguchi, S | 2 |
| Nishino, I | 2 |
| Sorimachi, H | 1 |
| Shalaby, S | 1 |
| Mitsuhashi, H | 1 |
| Matsuda, C | 1 |
| Minami, N | 1 |
| Nonaka, I | 1 |
| Hayashi, YK | 1 |
| Berciano, J | 1 |
| Gallardo, E | 2 |
| Domínguez-Perles, R | 1 |
| García, A | 1 |
| García-Barredo, R | 1 |
| Combarros, O | 1 |
| Infante, J | 1 |
| Illa, I | 1 |
3 other studies available for serine and Muscular Dystrophies, Limb-Girdle
| Article | Year |
|---|---|
Muscle-specific calpain-3 is phosphorylated in its unique insertion region for enrichment in a myofibril fraction.
Topics: Adolescent; Animals; Calpain; Chlorocebus aethiops; COS Cells; Female; Humans; Male; Middle Aged; Mu | 2014 |
Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patient.
Topics: Actinin; Animals; Arginine; Chlorocebus aethiops; Connectin; COS Cells; Cytoskeletal Proteins; DNA M | 2009 |
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype.
Topics: Adipose Tissue; Adult; Aged; Amino Acid Substitution; Atrophy; Biopsy; Chromosome Aberrations; Codon | 2008 |