scholarly article | Q13442814 |
P50 | author | Shinya Yamanaka | Q80917 |
Erja Kerkelä | Q39399909 | ||
Jari Hyttinen | Q47236912 | ||
P2093 | author name string | Kimmo Kontula | |
Katriina Aalto-Setälä | |||
Heikki Swan | |||
Olli Silvennoinen | |||
Bruce R Conklin | |||
Anna L Lahti | |||
Ari-Pekka Koivisto | |||
Hugh Chapman | |||
Mari Pekkanen-Mattila | |||
Ville J Kujala | |||
P2860 | cites work | A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome | Q24316980 |
Induced pluripotent stem cell lines derived from human somatic cells | Q27860597 | ||
Induction of pluripotent stem cells from adult human fibroblasts by defined factors | Q27860967 | ||
The genetic basis of long QT and short QT syndromes: a mutation update | Q28262724 | ||
Modelling the long QT syndrome with induced pluripotent stem cells | Q29620092 | ||
Patient-specific induced pluripotent stem-cell models for long-QT syndrome | Q29620353 | ||
Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome | Q30499663 | ||
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. | Q33146000 | ||
Drug-induced prolongation of the QT interval | Q33151147 | ||
Clinical practice. Long-QT syndrome | Q33155879 | ||
High prevalence of four long QT syndrome founder mutations in the Finnish population | Q33401777 | ||
A defined and xeno-free culture method enabling the establishment of clinical-grade human embryonic, induced pluripotent and adipose stem cells | Q33564271 | ||
Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome | Q33910479 | ||
The long QT syndromes: genetic basis and clinical implications | Q33970623 | ||
Drug evaluation in cardiomyocytes derived from human induced pluripotent stem cells carrying a long QT syndrome type 2 mutation | Q34793218 | ||
Relationships between preclinical cardiac electrophysiology, clinical QT interval prolongation and torsade de pointes for a broad range of drugs: evidence for a provisional safety margin in drug development | Q35095735 | ||
Long QT syndrome: reduced repolarization reserve and the genetic link | Q36335258 | ||
Strategies to reduce the risk of drug-induced QT interval prolongation: a pharmaceutical company perspective | Q37171823 | ||
The hERG potassium channel and hERG screening for drug-induced torsades de pointes | Q37212382 | ||
Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases. | Q37793374 | ||
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Generation and characterization of functional cardiomyocytes using induced pluripotent stem cells derived from human fibroblasts | Q39803924 | ||
Baseline values and sotalol-induced changes of ventricular repolarization duration, heterogeneity, and instability in patients with a history of drug-induced torsades de pointes | Q39860280 | ||
Differentiation of human embryonic stem cells to cardiomyocytes: role of coculture with visceral endoderm-like cells | Q40648427 | ||
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Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointes | Q44331873 | ||
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In vitro electrophysiological drug testing using human embryonic stem cell derived cardiomyocytes | Q46569292 | ||
Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland | Q47398470 | ||
Postmortem long QT syndrome genetic testing for sudden unexplained death in the young | Q48480320 | ||
Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation | Q48933322 | ||
Induced pluripotent stem cell technology for the study of human disease. | Q51919490 | ||
Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects. | Q54095734 | ||
Low penetrance in the long-QT syndrome: clinical impact | Q77932863 | ||
Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome | Q79352873 | ||
Isolation and characterization of I(Kr) in cardiac myocytes by Cs+ permeation | Q81356187 | ||
Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients | Q83928276 | ||
The effects of cardioactive drugs on cardiomyocytes derived from human induced pluripotent stem cells | Q84250613 | ||
P4510 | describes a project that uses | UTA.00112.hFF | Q54992201 |
UTA.00514.LQT2 | Q54992206 | ||
UTA.00525.LQT2 | Q54992207 | ||
UTA.01006.WT | Q54992208 | ||
UTA.04602.WT | Q54992209 | ||
P433 | issue | 2 | |
P921 | main subject | long QT syndrome | Q653924 |
cell line | Q21014462 | ||
P304 | page(s) | 220-230 | |
P577 | publication date | 2011-11-03 | |
P1433 | published in | Disease Models & Mechanisms | Q1524006 |
P1476 | title | Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture | |
P478 | volume | 5 |
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