glutamine has been researched along with Asymmetric Septal Hypertrophy, Familial in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Brenner, B; Chase, PB; Chen, Y; Gordon, AM; Köhler, J; Kraft, T; Martyn, DA; Regnier, M; Rivera, AJ; Wang, CK | 1 |
| Chung, F; Davis, JP; Gillis, TE; Liang, B; Pavlov, D; Qu, Y; Tibbits, GF; Tikunova, SB | 1 |
2 other study(ies) available for glutamine and Asymmetric Septal Hypertrophy, Familial
| Article | Year |
|---|---|
Familial hypertrophic cardiomyopathy mutations in troponin I (K183D, G203S, K206Q) enhance filament sliding.
Topics: Actin Cytoskeleton; Amino Acid Sequence; Amino Acid Substitution; Animals; Calcium; Cardiomyopathy, Hypertrophic, Familial; Cattle; Glutamine; Glycine; Lysine; Male; Myocardium; Point Mutation; Rabbits; Rats; Rats, Sprague-Dawley; Recombinant Proteins; Sarcomeres; Sequence Deletion; Serine; Signal Transduction; Troponin I | 2003 |
Familial hypertrophic cardiomyopathy-related cardiac troponin C mutation L29Q affects Ca2+ binding and myofilament contractility.
Topics: Actin Cytoskeleton; Animals; Biomechanical Phenomena; Calcium; Cardiomyopathy, Hypertrophic, Familial; Cattle; Female; Glutamine; Kinetics; Leucine; Mice; Mice, Inbred C57BL; Mutant Proteins; Mutation; Myocardial Contraction; Sarcomeres; Troponin C | 2008 |