Utility of hERG Assays as Surrogate Markers of Delayed Cardiac Repolarization and QT Safety [PDF]
Gary A. Gintant +3 more
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Homozygous Missense N629D hERG (KCNH2) Potassium Channel Mutation Causes Developmental Defects in the Right Ventricle and Its Outflow Tract and Embryonic Lethality [PDF]
Guo Qi Teng +8 more
openalex +1 more source
KCNQ1 Expression Modulates Herg Current by Removing Inactivation [PDF]
Carlos G. Vanoye +2 more
openalex +1 more source
Analysis of the human KCNH2(HERG) gene: Identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion Communicated by: Mark H. Paalman Online Citation: Human Mutation, Mutation in Brief #325 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/325.pdf [PDF]
Aimée Paulussen +10 more
openalex +1 more source
Molecular Determinants in K+ Channel hERG Inactivation Gating [PDF]
David A. Köpfer +6 more
openalex +1 more source
Molecular Determinants of Pentamidine-Induced hERG Trafficking Inhibition [PDF]
Adrienne T. Dennis +5 more
openalex +1 more source
Reassessing the Conduct of Patch Clamp Cardiac Ion Channel Assays to Improve Nonclinical Data Translation to Clinical ECG Changes and Proarrythmia Risk. [PDF]
Alvarez Baron C +6 more
europepmc +1 more source
HERG potassium channels are more frequently expressed in human endometrial cancer as compared to non-cancerous endometrium [PDF]
Alessia Cherubini +14 more
openalex +1 more source
KCNH2-L693P Causes Long QT Syndrome Type 2 Through hERG Channel Dysfunction: Functional Validation of a Variant of Uncertain Significance. [PDF]
Zheng XF +4 more
europepmc +1 more source

