arginine has been researched along with Asymmetric Septal Hypertrophy, Familial in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gao, S; Hui, RT; Song, L; Song, XD; Sun, K; Wang, H; Wang, JZ; Zhang, CN; Zou, YB | 1 |
| Buscemi, N; Li, MX; Lindhout, DA; Sykes, BD; Van Eyk, JE; Wang, X | 1 |
| Gomes, AV; Potter, JD | 1 |
| Arthur, JW; Chiu, C; Ingles, J; Lind, JM; Semsarian, C; Tebo, M; Yeates, L | 1 |
| Gomes, AV; Housmans, PR; Lang, R; Miller, T; Potter, JD; Zhao, J | 1 |
1 review(s) available for arginine and Asymmetric Septal Hypertrophy, Familial
| Article | Year |
|---|---|
Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene.
Topics: Amino Acid Sequence; Animals; Arginine; Base Sequence; Binding Sites; Calcium; Cardiomyopathy, Hypertrophic, Familial; Codon; DNA; Humans; In Vitro Techniques; Mice; Mice, Transgenic; Molecular Sequence Data; Mutation; Mutation, Missense; Myocardial Contraction; Phenotype; Phosphorylation; Sequence Deletion; Sequence Homology, Amino Acid; Troponin I | 2004 |
4 other study(ies) available for arginine and Asymmetric Septal Hypertrophy, Familial
| Article | Year |
|---|---|
[The genotype-phenotype correlation of the MYH7 gene c.1273G > a mutation in familial hypertrophic cardiomyopathy].
Topics: Adult; Amino Acid Sequence; Animals; Arginine; Cardiac Myosins; Cardiomyopathy, Hypertrophic, Familial; Cattle; Dogs; Female; Genetic Predisposition to Disease; Glycine; Humans; Male; Mice; Mutation, Missense; Myosin Heavy Chains; Rats; Sequence Alignment; Swine | 2009 |
Phosphorylation and mutation of human cardiac troponin I deferentially destabilize the interaction of the functional regions of troponin I with troponin C.
Topics: Amino Acid Sequence; Arginine; Calcium; Cardiomyopathy, Hypertrophic, Familial; Glycine; Humans; Molecular Sequence Data; Mutagenesis, Site-Directed; Myocardium; Nuclear Magnetic Resonance, Biomolecular; Peptide Fragments; Phosphorylation; Protein Binding; Protein Structure, Tertiary; Recombinant Proteins; Serine; Threonine; Troponin C; Troponin I; Tryptophan | 2003 |
Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy.
Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; Australia; Calcium; Calcium-Binding Proteins; Calreticulin; Calsequestrin; Cardiomyopathy, Hypertrophic, Familial; Cohort Studies; Consensus Sequence; Conserved Sequence; Female; Genetic Testing; Glutamic Acid; Glutathione; Glycine; Humans; Male; Models, Genetic; Models, Molecular; Molecular Sequence Data; Pedigree; Protein Structure, Tertiary | 2007 |
Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy.
Topics: Adenosine Triphosphatases; Amino Acid Sequence; Animals; Arginine; Binding Sites; Calcium; Cardiomyopathy, Hypertrophic, Familial; Circular Dichroism; Dose-Response Relationship, Drug; Humans; Models, Theoretical; Molecular Sequence Data; Muscle Contraction; Muscle Fibers, Skeletal; Mutation; Mutation, Missense; Myocardium; Myosins; Stress, Mechanical; Swine; Temperature; Time Factors; Troponin; Troponin I | 2002 |