aspartic acid has been researched along with Electrocardiogram QT Prolonged 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 | 2 (50.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Sesti, F; Swiatkowski, P | 1 |
Fukuda, K; Furukawa, T; Okata, S; Yamane, T; Yuasa, S | 1 |
Cross, JC; Duff, HJ; Lees-Miller, JP; Li, P; London, B; Quinn, FR; Rancourt, DE; Teng, GQ; Zhao, X | 1 |
Anderson, CL; Anson, BD; Balijepalli, RC; Delisle, BP; January, CT; Kamp, TJ | 1 |
4 other study(ies) available for aspartic acid and Electrocardiogram QT Prolonged
Article | Year |
---|---|
Delayed pharyngeal repolarization promotes abnormal calcium buildup in aging muscle.
Topics: Action Potentials; Aging; Animals; Aspartic Acid; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Calcium; Heart Ventricles; Humans; Long QT Syndrome; Models, Biological; Mutation; Myocardium; Pharynx; Potassium Channels; Potassium Channels, Voltage-Gated; Protein Binding; Protein Isoforms; Protein Subunits; Sequence Homology, Amino Acid | 2013 |
The generation of induced pluripotent stem cells from a patient with KCNH2 G603D, without LQT2 disease associated symptom.
Topics: Adenine; Aspartic Acid; Cell Culture Techniques; Child; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Genome, Human; Glycine; Guanine; Homeodomain Proteins; Humans; Long QT Syndrome; Male; Nanog Homeobox Protein; Octamer Transcription Factor-3; Pluripotent Stem Cells; Polymorphism, Single Nucleotide; Sequence Analysis, DNA | 2013 |
Homozygous missense N629D hERG (KCNH2) potassium channel mutation causes developmental defects in the right ventricle and its outflow tract and embryonic lethality.
Topics: Amino Acid Substitution; Animals; Asparagine; Aspartic Acid; Cardiac Output; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Female; Gene Expression Regulation, Developmental; Heart Ventricles; Homozygote; Long QT Syndrome; Mice; Mice, Mutant Strains; Mutation, Missense; Pregnancy; Ventricular Dysfunction, Right | 2008 |
Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805C.
Topics: Amino Acid Substitution; Asparagine; Aspartic Acid; Cation Transport Proteins; Cell Line; Cell Membrane; Cell Nucleus; DNA-Binding Proteins; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Glycine; Humans; Long QT Syndrome; Mutagenesis, Site-Directed; Patch-Clamp Techniques; Potassium Channel Blockers; Potassium Channels; Potassium Channels, Voltage-Gated; Protein Transport; Recombinant Proteins; Serine; Thapsigargin; Trans-Activators; Transcriptional Regulator ERG | 2003 |