phenylalanine has been researched along with Muscular Dystrophies, Limb-Girdle in 3 studies
| 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 |
|---|---|
| Defour, A; Diaz Manera, J; Gallardo, E; Hogarth, MW; Jaiswal, JK; Lazarski, C; Nagaraju, K; Partridge, TA | 1 |
| Jagannadham, MV; Nagaraj, R; Sowmya, BL | 1 |
| Berciano, J; Combarros, O; Domínguez-Perles, R; Gallardo, E; García, A; García-Barredo, R; Illa, I; Infante, J | 1 |
3 other study(ies) available for phenylalanine and Muscular Dystrophies, Limb-Girdle
| Article | Year |
|---|---|
Fibroadipogenic progenitors are responsible for muscle loss in limb girdle muscular dystrophy 2B.
Topics: Adipocytes; Adipogenesis; Adipose Tissue; Adolescent; Age of Onset; Animals; Annexin A2; Case-Control Studies; Dysferlin; Elapid Venoms; Female; Fibrosis; Humans; In Vitro Techniques; Male; Mice; Muscle Fibers, Skeletal; Muscle, Skeletal; Muscular Dystrophies, Limb-Girdle; Phenylalanine; Protease Inhibitors; Severity of Illness Index; Stem Cells; Thiophenes; Young Adult | 2019 |
Interaction of synthetic peptides corresponding to the scaffolding domain of Caveolin-3 with model membranes.
Topics: Amino Acid Sequence; Caveolin 3; Humans; Membrane Lipids; Membranes; Molecular Sequence Data; Muscular Dystrophies, Limb-Girdle; Peptides; Phenylalanine; Protein Structure, Tertiary; Tryptophan | 2006 |
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; Connectin; Creatine Kinase; Cytoskeletal Proteins; DNA Mutational Analysis; Electromyography; Exons; Female; Genes, Dominant; Genetic Carrier Screening; Humans; Leg; Magnetic Resonance Imaging; Male; Microfilament Proteins; Middle Aged; Muscle Proteins; Muscle Weakness; Muscle, Skeletal; Muscular Atrophy; Muscular Diseases; Muscular Dystrophies, Limb-Girdle; Mutation, Missense; Neurologic Examination; Pedigree; Phenotype; Phenylalanine; Serine | 2008 |