lysine has been researched along with Asymmetric Septal Hypertrophy, Familial in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (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 |
| Bertini, E; Boldrini, R; D'Amico, A; Feng, JJ; Graziano, C; Jacques, A; Laing, N; Limongelli, G; Marston, SB; Nowak, KJ; Pacileo, G; Petrini, S; Porfirio, B; Santorelli, FM; Sewry, CA | 1 |
| Blaudeck, N; Iorga, B; Lopez Davila, AJ; Neulen, A; Pfitzer, G; Solzin, J; Stehle, I; Stehle, R | 1 |
| Bousman, S; Coates, K; Dienel, NH; Hanson, EL; Hershberger, RE; Jakobs, PM; Keegan, H; Litt, M | 1 |
4 other study(ies) available for lysine 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 |
Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation.
Topics: Actinin; Actins; Amino Acid Substitution; Cardiomyopathy, Hypertrophic, Familial; Child, Preschool; DNA Mutational Analysis; Fatal Outcome; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Humans; Lysine; Male; Muscle Contraction; Muscle Fibers, Skeletal; Muscle, Skeletal; Mutation, Missense; Myocardium; Myopathies, Nemaline | 2006 |
Lys184 deletion in troponin I impairs relaxation kinetics and induces hypercontractility in murine cardiac myofibrils.
Topics: Animals; Calcium Signaling; Cardiomyopathy, Hypertrophic, Familial; Diacetyl; Disease Models, Animal; Guinea Pigs; Humans; Kinetics; Lysine; Mice; Mice, Inbred C57BL; Mice, Transgenic; Muscle Contraction; Muscle Strength; Myofibrils; Papillary Muscles; Protein Conformation; Sarcomeres; Sequence Deletion; Troponin I; Ventricular Dysfunction, Left | 2008 |
Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy.
Topics: Cardiomyopathy, Dilated; Cardiomyopathy, Hypertrophic, Familial; Exons; Female; Gene Deletion; Humans; Lysine; Male; Middle Aged; Mutation; Pedigree; Troponin T | 2002 |