serine has been researched along with Asymmetric Septal Hypertrophy, Familial in 4 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "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 | 4 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| 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 |
| Burkart, EM | 1 |
| Arteaga, GM | 1 |
| Sumandea, MP | 1 |
| Prabhakar, R | 1 |
| Wieczorek, DF | 1 |
| Solaro, RJ | 1 |
| Deng, Y | 1 |
| Schmidtmann, A | 1 |
| Kruse, S | 1 |
| Filatov, V | 1 |
| Heilmeyer, LM | 1 |
| Jaquet, K | 1 |
| Thieleczek, R | 1 |
| Li, MX | 1 |
| Wang, X | 1 |
| Lindhout, DA | 1 |
| Buscemi, N | 1 |
| Van Eyk, JE | 1 |
| Sykes, BD | 1 |
4 other studies available for serine 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, | 2003 |
Altered signaling surrounding the C-lobe of cardiac troponin C in myofilaments containing an alpha-tropomyosin mutation linked to familial hypertrophic cardiomyopathy.
Topics: Animals; Blotting, Western; Calcium; Cardiomyopathy, Hypertrophic, Familial; Dose-Response Relations | 2003 |
Phosphorylation of human cardiac troponin I G203S and K206Q linked to familial hypertrophic cardiomyopathy affects actomyosin interaction in different ways.
Topics: Actin Cytoskeleton; Actomyosin; Adenosine Triphosphatases; Animals; Antibodies, Monoclonal; Calcium; | 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 |