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pro vyhledávání: '"Caleb J. Hintz"'
Autor:
Corey L Anderson, Catherine E Kuzmicki, Ryan R Childs, Caleb J Hintz, Craig T January, Ravi C Balijepalli
Publikováno v:
Circulation. 132
Introduction: Hundreds of HERG potassium channel mutations are linked to type 2 Long QT Syndrome (LQT2). Most mutations are trafficking defective but correctable by culturing cells at reduced temperature (27 C) or with the pore blocker E4031. For a f
Autor:
Catherine E. Kuzmicki, Craig T. January, Corey L. Anderson, Caleb J. Hintz, Brian P. Delisle, Ryan R. Childs
Publikováno v:
Nature communications
It has been suggested that deficient protein trafficking to the cell membrane is the dominant mechanism associated with type 2 Long QT syndrome (LQT2) caused by Kv11.1 potassium channel missense mutations, and that for many mutations the trafficking