methionine has been researched along with Adult Onset Nemaline Myopathy 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 | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abdulrazzak, H; Marston, S; Mirza, M; Sewry, C | 1 |
| Akkari, PA; Cooper, ST; Corbett, MA; Domazetovska, A; Gunning, PW; Hardeman, EC; Laing, NG; North, KN | 1 |
| Corbett, MA; Dunglison, GF; Gunning, PW; Hardeman, EC; Joya, JE; North, KN; Robinson, CS; Schnell, C; Stewart, AW; Yang, N | 1 |
3 other study(ies) available for methionine and Adult Onset Nemaline Myopathy
| Article | Year |
|---|---|
Functional characterisation of a mutant actin (Met132Val) from a patient with nemaline myopathy.
Topics: Actin Cytoskeleton; Actins; Amino Acid Substitution; Base Sequence; Biopsy; DNA Mutational Analysis; Humans; Methionine; Models, Molecular; Muscle Contraction; Muscle, Skeletal; Mutation; Myopathies, Nemaline; Polymers; Protein Structure, Quaternary; RNA, Messenger; Valine | 2004 |
An alphaTropomyosin mutation alters dimer preference in nemaline myopathy.
Topics: Animals; Animals, Newborn; Arginine; Blotting, Northern; Blotting, Western; Dimerization; Disease Models, Animal; DNA Mutational Analysis; Gene Expression Regulation; Humans; Methionine; Mice; Mice, Transgenic; Muscle, Skeletal; Mutation; Myopathies, Nemaline; Promoter Regions, Genetic; Protein Structure, Secondary; Recombinant Proteins; RNA, Messenger; Time Factors; Tropomyosin | 2005 |
A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy.
Topics: Amino Acid Substitution; Animals; Arginine; Disease Models, Animal; Dissection; Female; Glycolysis; Humans; Hypertrophy; Inclusion Bodies; Methionine; Mice; Mice, Inbred Strains; Mice, Transgenic; Microtubules; Muscle Development; Muscle Fibers, Fast-Twitch; Muscle Fibers, Slow-Twitch; Muscle Weakness; Muscle, Skeletal; Myopathies, Nemaline; Oxidation-Reduction; Point Mutation; RNA, Messenger; Sarcoplasmic Reticulum; Strontium; Tropomyosin | 2001 |