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Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum.
Smith, Jennifer L; Reloj, Allison R; Nataraj, Parvathi S; Bartos, Daniel C; Schroder, Elizabeth A; Moss, Arthur J; Ohno, Seiko; Horie, Minoru; Anderson, Corey L; January, Craig T; Delisle, Brian P.
Affiliation
  • Smith JL; Center for Muscle Biology, Department of Physiology, University of Kentucky, Lexington, Kentucky;
Am J Physiol Cell Physiol ; 305(9): C919-30, 2013 Nov 01.
Article in En | MEDLINE | ID: mdl-23864605

Full text: 1 Database: MEDLINE Main subject: Long QT Syndrome / Mutation, Missense / Endoplasmic Reticulum / Ether-A-Go-Go Potassium Channels Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Am J Physiol Cell Physiol Journal subject: FISIOLOGIA Year: 2013 Type: Article

Full text: 1 Database: MEDLINE Main subject: Long QT Syndrome / Mutation, Missense / Endoplasmic Reticulum / Ether-A-Go-Go Potassium Channels Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Am J Physiol Cell Physiol Journal subject: FISIOLOGIA Year: 2013 Type: Article