glutamic acid has been researched along with Electrocardiogram QT Prolonged 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 | 2 (40.00) | 29.6817 |
2010's | 3 (60.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Andersen, J; Bernstein, JA; Birey, F; Fan, HC; Hallmayer, J; Huber, N; Huguenard, JR; Islam, S; Makinson, CD; Metzler, KRC; O'Rourke, NA; Panagiotakos, G; Paşca, SP; Steinmetz, LM; Thom, N; Wei, W | 1 |
Ba, Y; Huang, X; Karush, JM; Lian, J; Liu, N; Lu, X; Mao, H; Wang, Y; Yang, X; Zhou, J | 1 |
Alvarez, M; Amorós, I; Barana, A; Caballero, R; de la Fuente, MG; Delpón, E; Dolz-Gaitón, P; Gómez, R; Jiménez-Jáimez, J; Lorente, JA; Martínez-Espín, E; Melgares, R; Tamargo, J; Tercedor, L | 1 |
Carmeliet, E; Carmeliet, P; Collen, D; Devriendt, K; Gewillig, M; Heidbüchel, H; Jongbloed, RJ; Mubagwa, K; Rossenbacker, T; Vereecke, J | 1 |
Art, JJ; Bajic, S; Chen, L; Itoh, H; Kawano, T; Kaziro, Y; Nakajima, S; Nakajima, Y | 1 |
5 other study(ies) available for glutamic acid and Electrocardiogram QT Prolonged
Article | Year |
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Assembly of functionally integrated human forebrain spheroids.
Topics: Autistic Disorder; Cell Line; Cell Movement; Cells, Cultured; Female; GABAergic Neurons; Glutamic Acid; Humans; Interneurons; Long QT Syndrome; Male; Models, Biological; Neurogenesis; Neurons; Pluripotent Stem Cells; Prosencephalon; Spheroids, Cellular; Synapses; Syndactyly | 2017 |
Pharmacologic Approach to Defective Protein Trafficking in the E637K-hERG Mutant with PD-118057 and Thapsigargin.
Topics: Amino Acid Substitution; Chlorobenzenes; Endoplasmic Reticulum Stress; ERG1 Potassium Channel; Glutamic Acid; HEK293 Cells; Humans; Long QT Syndrome; Lysine; Mutant Proteins; Mutation, Missense; ortho-Aminobenzoates; Patch-Clamp Techniques; Protein Transport; Thapsigargin; Unfolded Protein Response | 2013 |
Functional effects of a missense mutation in HERG associated with type 2 long QT syndrome.
Topics: Animals; Cricetinae; Cricetulus; Delayed Rectifier Potassium Channels; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Glutamic Acid; Humans; Long QT Syndrome; Mutation, Missense; Patch-Clamp Techniques; Potassium Channels, Voltage-Gated; Protein Transport | 2011 |
Novel mutation in the Per-Arnt-Sim domain of KCNH2 causes a malignant form of long-QT syndrome.
Topics: Adult; Blotting, Western; Cell Line; Death, Sudden, Cardiac; Electrophysiology; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Female; Glutamic Acid; Humans; Kidney; Long QT Syndrome; Lysine; Male; Microscopy, Confocal; Middle Aged; Mutation, Missense; Patch-Clamp Techniques; Pedigree; Peptides; Phenotype; Piperidines; Potassium Channels, Voltage-Gated; Protein Structure, Tertiary; Proteins; Pyridines | 2005 |
A glutamate residue at the C terminus regulates activity of inward rectifier K+ channels: implication for Andersen's syndrome.
Topics: Amino Acid Sequence; Amino Acid Substitution; Cell Line; G Protein-Coupled Inwardly-Rectifying Potassium Channels; Glutamic Acid; Humans; Ion Channel Gating; Long QT Syndrome; Molecular Sequence Data; Mutagenesis, Site-Directed; Paralyses, Familial Periodic; Potassium Channels; Potassium Channels, Inwardly Rectifying; Recombinant Proteins; Transfection | 2002 |