arginine has been researched along with Long QT Syndrome in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (22.22) | 18.2507 |
| 2000's | 2 (22.22) | 29.6817 |
| 2010's | 5 (55.56) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bartos, DC; Burgess, DE; Delisle, BP; Elayi, CS; McBride, CM; Powell, J; Reloj, AR; Smith, AM; Smith, JL; Velasco, EJ | 1 |
| Alonso-Orgaz, S; Cinza, R; García-Torrent, MJ; López-Farré, AJ; Macaya, C; Moreno, J; Pérez-Castellano, N; Pérez-Villacastín, J; Zamorano-León, JJ | 1 |
| Morris, CR | 1 |
| Cui, J; Delaloye, K; Nekouzadeh, A; Rudy, Y; Wu, D; Zaydman, MA | 1 |
| Aidery, P; Baldea, I; Becker, R; Gaspar, H; Katus, HA; Kisselbach, J; Schweizer, PA; Thomas, D | 1 |
| Alvarez-Granada, RR; Calatrava-Ledrado, L; Jaime, G; López-Farré, AJ; Macaya, C; Mateos-Cáceres, PJ; Rodriguez-Sierra, P; Yañez, R; Zamorano-León, JJ | 1 |
| Chong, B; Fawkner, M; Hegde, M; Skinner, JR; Webster, DR | 1 |
| Kitabatake, A; Makita, N; Matsuoka, R; Nagashima, M; Shirai, N; Tohse, N; Yamada, Y | 1 |
| Furutani, M; Furutani, Y; Hino, Y; Imamura, S; Kamisago, M; Kimura, M; Kojima, Y; Matsuoka, R; Momma, K; Morikawa, Y; Takao, A; Yamagishi, H | 1 |
1 review(s) available for arginine and Long QT Syndrome
| Article | Year |
|---|---|
Asthma management: reinventing the wheel in sickle cell disease.
Topics: Acute Disease; Adult; Anemia, Sickle Cell; Anti-Asthmatic Agents; Arginase; Arginine; Asthma; Black or African American; Chest Pain; Child; Child, Preschool; Combined Modality Therapy; Comorbidity; Erythrocytes, Abnormal; Genetic Predisposition to Disease; Humans; Hypertension, Pulmonary; Hypoxia; Long QT Syndrome; Nitric Oxide; Oxidative Stress; Oxygen Inhalation Therapy; Prevalence; United States | 2009 |
8 other study(ies) available for arginine and Long QT Syndrome
| Article | Year |
|---|---|
Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that disrupt conserved arginine residues in the voltage sensor.
Topics: Action Potentials; Amino Acid Substitution; Arginine; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Heart Ventricles; HEK293 Cells; Humans; Ion Channel Gating; Long QT Syndrome; Mutation, Missense; Protein Transport | 2013 |
Novel mutation (H402R) in the S1 domain of KCNH2-encoded gene associated with long QT syndrome in a Spanish family.
Topics: Adult; Amino Acid Substitution; Arginine; Arrhythmias, Cardiac; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Female; Genetic Carrier Screening; Histidine; Humans; Long QT Syndrome; Male; Mutation, Missense; Pedigree; Protein Structure, Tertiary; Spain | 2010 |
State-dependent electrostatic interactions of S4 arginines with E1 in S2 during Kv7.1 activation.
Topics: Amino Acid Sequence; Animals; Arginine; Cell Membrane; Cysteine; Ion Channel Gating; KCNQ1 Potassium Channel; Long QT Syndrome; Membrane Potentials; Mesylates; Models, Molecular; Molecular Sequence Data; Mutation; Protein Conformation; Protein Structure, Tertiary; Protein Transport; Sulfhydryl Reagents; Surface Properties; Time Factors; Xenopus | 2010 |
Identification and functional characterization of the novel human ether-a-go-go-related gene (hERG) R744P mutant associated with hereditary long QT syndrome 2.
Topics: Amino Acid Substitution; Animals; Arginine; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Female; Humans; Long QT Syndrome; Mutation, Missense; Patch-Clamp Techniques; Pedigree; Proline; Xenopus laevis | 2012 |
KCNH2 gene mutation: a potential link between epilepsy and long QT-2 syndrome.
Topics: Arginine; DNA Mutational Analysis; Electrocardiography; Electroencephalography; Epilepsy; Family Health; Female; Humans; Long QT Syndrome; Mutation; Small-Conductance Calcium-Activated Potassium Channels; Young Adult | 2012 |
Use of the newborn screening card to define cause of death in a 12-year-old diagnosed with epilepsy.
Topics: Arginine; Autopsy; Child; Cysteine; Death, Sudden, Cardiac; DNA Mutational Analysis; Electrocardiography; Genetic Predisposition to Disease; Humans; Infant, Newborn; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Long QT Syndrome; Male; Molecular Diagnostic Techniques; Mutation, Missense; Neonatal Screening; Pedigree; Potassium Channels, Voltage-Gated | 2004 |
A de novo missense mutation of human cardiac Na+ channel exhibiting novel molecular mechanisms of long QT syndrome.
Topics: Animals; Arginine; Electric Conductivity; Female; Glutamine; Humans; Infant; Long QT Syndrome; Mutagenesis, Site-Directed; Myocardium; NAV1.5 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Sodium; Sodium Channels; Xenopus | 1998 |
A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT sydrome. Mutations in brief no. 140. Online.
Topics: Amino Acid Substitution; Arginine; Female; Glutamine; Humans; Long QT Syndrome; Mutation, Missense; NAV1.5 Voltage-Gated Sodium Channel; Polymorphism, Single-Stranded Conformational; Sequence Deletion; Sodium Channels | 1998 |