glycine has been researched along with Asymmetric Septal Hypertrophy, Familial in 5 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "An Australian cohort of 252 unrelated familial hypertrophic cardiomyopathy patients were screened for mutations in the Ca(2+) regulatory genes, sorcin (SRI), calstabin (FKBP1B), calsequestrin (CASQ2), phospholamban (PLN), sarcolipin (SLN), calreticulin (CALR3) and calmodulin (CALM)." | 1.34 | Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy. ( Arthur, JW; Chiu, C; Ingles, J; Lind, JM; Semsarian, C; Tebo, M; Yeates, L, 2007) |
| "A major cause of familial hypertrophic cardiomyopathy (FHC) is dominant mutations in cardiac sarcomeric genes." | 1.32 | Familial hypertrophic cardiomyopathy mutations in troponin I (K183D, G203S, K206Q) enhance filament sliding. ( Brenner, B; Chase, PB; Chen, Y; Gordon, AM; Köhler, J; Kraft, T; Martyn, DA; Regnier, M; Rivera, AJ; Wang, CK, 2003) |
| 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 |
|---|---|
| Wang, H | 1 |
| Zou, YB | 1 |
| Song, L | 1 |
| Wang, JZ | 1 |
| Sun, K | 1 |
| Song, XD | 1 |
| Gao, S | 1 |
| Zhang, CN | 1 |
| Hui, RT | 1 |
| Köhler, J | 1 |
| Chen, Y | 1 |
| Brenner, B | 1 |
| Gordon, AM | 1 |
| Kraft, T | 1 |
| Martyn, DA | 1 |
| Regnier, M | 1 |
| Rivera, AJ | 1 |
| Wang, CK | 1 |
| Chase, PB | 1 |
| Li, MX | 1 |
| Wang, X | 1 |
| Lindhout, DA | 1 |
| Buscemi, N | 1 |
| Van Eyk, JE | 1 |
| Sykes, BD | 1 |
| Wernicke, D | 1 |
| Thiel, C | 1 |
| Duja-Isac, CM | 1 |
| Essin, KV | 1 |
| Spindler, M | 1 |
| Nunez, DJ | 1 |
| Plehm, R | 1 |
| Wessel, N | 1 |
| Hammes, A | 1 |
| Edwards, RJ | 1 |
| Lippoldt, A | 1 |
| Zacharias, U | 1 |
| Strömer, H | 1 |
| Neubauer, S | 1 |
| Davies, MJ | 1 |
| Morano, I | 1 |
| Thierfelder, L | 1 |
| Chiu, C | 1 |
| Tebo, M | 1 |
| Ingles, J | 1 |
| Yeates, L | 1 |
| Arthur, JW | 1 |
| Lind, JM | 1 |
| Semsarian, C | 1 |
5 other studies available for glycine 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, Famili | 2009 |
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, | 2003 |
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; Mol | 2003 |
alpha-Tropomyosin mutations Asp(175)Asn and Glu(180)Gly affect cardiac function in transgenic rats in different ways.
Topics: Animals; Animals, Genetically Modified; Asparagine; Aspartic Acid; Biomarkers; Calcium; Cardiomyopat | 2004 |
Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy.
Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; Australia; Calcium; Calcium-Binding Proteins | 2007 |