serine has been researched along with Muscular Dystrophy in 8 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "A defect of the gene for p94 (calpain 3), a skeletal muscle-specific calpain, is responsible for limb girdle muscular dystrophy type 2A (LGMD2A), or 'calpainopathy', which is an autosomal recessive and progressive neuromuscular disorder." | 7.70 | Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A. ( Arahata, K; Fukuda, R; Hata, S; Hayashi, Y; Ishiura, S; Karasuyama, H; Katsui, Y; Nakagawa, M; Nonaka, I; Ono, Y; Seyama, Y; Sorimachi, H; Suzuki, K; Tagawa, K; Taya, C; Toyama-Sorimachi, N; Yonekawa, H, 2000) |
| "A defect of the gene for p94 (calpain 3), a skeletal muscle-specific calpain, is responsible for limb girdle muscular dystrophy type 2A (LGMD2A), or 'calpainopathy', which is an autosomal recessive and progressive neuromuscular disorder." | 3.70 | Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A. ( Arahata, K; Fukuda, R; Hata, S; Hayashi, Y; Ishiura, S; Karasuyama, H; Katsui, Y; Nakagawa, M; Nonaka, I; Ono, Y; Seyama, Y; Sorimachi, H; Suzuki, K; Tagawa, K; Taya, C; Toyama-Sorimachi, N; Yonekawa, H, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (62.50) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Oliveira-Santos, A | 1 |
| Dagda, M | 1 |
| Wittmann, J | 1 |
| Smalley, R | 1 |
| Burkin, DJ | 1 |
| Melis, MA | 1 |
| Muntoni, F | 1 |
| Cau, M | 1 |
| Loi, D | 1 |
| Puddu, A | 1 |
| Boccone, L | 1 |
| Mateddu, A | 1 |
| Cianchetti, C | 1 |
| Cao, A | 1 |
| Tagawa, K | 1 |
| Taya, C | 1 |
| Hayashi, Y | 1 |
| Nakagawa, M | 1 |
| Ono, Y | 1 |
| Fukuda, R | 1 |
| Karasuyama, H | 1 |
| Toyama-Sorimachi, N | 1 |
| Katsui, Y | 1 |
| Hata, S | 1 |
| Ishiura, S | 1 |
| Nonaka, I | 1 |
| Seyama, Y | 1 |
| Arahata, K | 1 |
| Yonekawa, H | 1 |
| Sorimachi, H | 1 |
| Suzuki, K | 1 |
| Katsunuma, N | 1 |
| Sanada, Y | 2 |
| Katunuma, N | 1 |
| Yasogawa, N | 1 |
| Kito, K | 1 |
| Kawai, H | 1 |
| Miyoshi, K | 1 |
| Gusev, EI | 1 |
| Desai, ID | 1 |
| Maskaleris, ML | 1 |
| Gross, S | 1 |
| Milhorat, AT | 1 |
8 other studies available for serine and Muscular Dystrophy
| Article | Year |
|---|---|
Vemurafenib improves muscle histopathology in a mouse model of LAMA2-related congenital muscular dystrophy.
Topics: Animals; Fibrosis; Laminin; Mice; Muscle, Skeletal; Muscular Dystrophies; Protein Serine-Threonine K | 2023 |
Novel nonsense mutation (C-->A nt 10512) in exon 72 of dystrophin gene leading to exon skipping in a patient with a mild dystrophinopathy.
Topics: Child, Preschool; Codon, Terminator; DNA Mutational Analysis; DNA, Complementary; Dystrophin; Exons; | 1998 |
Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A.
Topics: Animals; Binding Sites; Body Weight; Calpain; Connectin; Cysteine; Female; Immunohistochemistry; Mic | 2000 |
[Muscular dystrophy and serine protease].
Topics: Adult; Aged; Animals; Binding Sites; Child; Child, Preschool; Endopeptidases; Humans; Mice; Middle A | 1977 |
Abnormal expression of a serine protease in human dystrophic muscle.
Topics: Adult; Aged; Amyotrophic Lateral Sclerosis; Child; Child, Preschool; Endopeptidases; Humans; L-Lacta | 1978 |
[Hyperaminoaciduria in children suffering from progressive muscular dystrophy].
Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Child; Child, Pr | 1967 |
Beneficial and ineffective levels of selenium for growth and muscular dystrophy.
Topics: Animals; Animals, Newborn; Chickens; Cystine; Growth; Male; Muscular Dystrophies; Selenium; Serine; | 1968 |
Urinary amino acid and peptide excretion patterns in patients with muscular dystrophy (Duchenne). A preliminary study with the autoanalyzer.
Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Autoanalysis; Child; Child | 1969 |