serine has been researched along with Electrocardiogram QT Prolonged in 9 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 |
|---|---|---|
| "Congenital long QT syndrome is characterized by a prolongation of ventricular repolarization and recurrent episodes of life-threatening ventricular tachyarrhythmias, often leading to sudden death." | 1.35 | Congenital long QT syndrome caused by the F275S KCNQ1 mutation: mechanism of impaired channel function. ( Chen, XL; Du, R; Guan, SM; Kang, CL; Ke, QM; Li, W; Song, ZF; Tian, L; Wang, B; Wang, QF; Xu, QM; Yang, JG; Zhang, SY, 2009) |
| "Congenital long QT syndrome is a cardiac disorder characterized by prolongation of QT interval on the surface ECG associated with syncopal attacks and a high risk of sudden death." | 1.35 | The G314S KCNQ1 mutation exerts a dominant-negative effect on expression of KCNQ1 channels in oocytes. ( Du, R; Li, W; Song, ZF; Tian, L; Wang, QF; Yang, JG, 2009) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (22.22) | 18.2507 |
| 2000's | 6 (66.67) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yamaguchi, Y | 1 |
| Nishide, K | 1 |
| Kato, M | 1 |
| Hata, Y | 1 |
| Mizumaki, K | 1 |
| Kinoshita, K | 1 |
| Nonobe, Y | 1 |
| Tabata, T | 1 |
| Sakamoto, T | 1 |
| Kataoka, N | 1 |
| Nakatani, Y | 1 |
| Ichida, F | 1 |
| Mori, H | 1 |
| Fukurotani, K | 1 |
| Inoue, H | 1 |
| Nishida, N | 1 |
| Li, W | 2 |
| Wang, QF | 2 |
| Du, R | 2 |
| Xu, QM | 1 |
| Ke, QM | 1 |
| Wang, B | 1 |
| Chen, XL | 1 |
| Tian, L | 2 |
| Zhang, SY | 1 |
| Kang, CL | 1 |
| Guan, SM | 1 |
| Yang, JG | 2 |
| Song, ZF | 2 |
| Huang, H | 1 |
| Millat, G | 1 |
| Rodriguez-Lafrasse, C | 1 |
| Rousson, R | 1 |
| Kugener, B | 1 |
| Chevalier, P | 1 |
| Chahine, M | 1 |
| Delisle, BP | 1 |
| Anderson, CL | 1 |
| Balijepalli, RC | 1 |
| Anson, BD | 1 |
| Kamp, TJ | 1 |
| January, CT | 1 |
| Bian, JS | 1 |
| Cui, J | 1 |
| Melman, Y | 1 |
| McDonald, TV | 1 |
| Tian, XL | 1 |
| Cheng, Y | 1 |
| Zhang, T | 1 |
| Liao, ML | 1 |
| Yong, SL | 1 |
| Wang, QK | 1 |
| Lai, LP | 1 |
| Deng, CL | 1 |
| Moss, AJ | 1 |
| Kass, RS | 1 |
| Liang, CS | 1 |
| Akimoto, K | 1 |
| Furutani, M | 1 |
| Imamura, S | 1 |
| Furutani, Y | 1 |
| Kasanuki, H | 1 |
| Takao, A | 1 |
| Momma, K | 1 |
| Matsuoka, R | 1 |
2 trials available for serine and Electrocardiogram QT Prolonged
| Article | Year |
|---|---|
Glycine/Serine polymorphism at position 38 influences KCNE1 subunit's modulatory actions on rapid and slow delayed rectifier K+ currents.
Topics: Amino Acid Substitution; Female; Glycine; HEK293 Cells; Humans; Ion Transport; Long QT Syndrome; Mal | 2014 |
Polymorphism of the gene encoding a human minimal potassium ion channel (minK).
Topics: Alleles; Animals; Base Sequence; Chromosomes, Human, Pair 11; Codon; DNA Primers; Genetic Carrier Sc | 1994 |
7 other studies available for serine and Electrocardiogram QT Prolonged
| Article | Year |
|---|---|
Congenital long QT syndrome caused by the F275S KCNQ1 mutation: mechanism of impaired channel function.
Topics: Animals; Cell Line; Endoplasmic Reticulum; Humans; KCNQ1 Potassium Channel; Long QT Syndrome; Mutati | 2009 |
Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome.
Topics: Base Sequence; Cell Line; Electrophysiology; Humans; Infant; Ion Channel Gating; Long QT Syndrome; M | 2009 |
The G314S KCNQ1 mutation exerts a dominant-negative effect on expression of KCNQ1 channels in oocytes.
Topics: Action Potentials; Amino Acid Sequence; Animals; Electrophysiological Phenomena; Genes, Dominant; Gl | 2009 |
Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805C.
Topics: Amino Acid Substitution; Asparagine; Aspartic Acid; Cation Transport Proteins; Cell Line; Cell Membr | 2003 |
S641 contributes HERG K+ channel inactivation.
Topics: Amino Acid Sequence; Animals; Biophysics; CHO Cells; Cricetinae; Cricetulus; Electrophysiology; ERG1 | 2004 |
Optical mapping of ventricular arrhythmias in LQTS mice with SCN5A mutation N1325S.
Topics: Animals; Arrhythmias, Cardiac; Asparagine; Cardiac Complexes, Premature; Long QT Syndrome; Mexiletin | 2007 |
Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family.
Topics: Amino Acid Substitution; Cation Transport Proteins; Codon; DNA; DNA Mutational Analysis; DNA-Binding | 1998 |