Cardiac-enriched LIM domain protein fhl2 is required to generate IKs in a heterologous system

Cardiovascular Research

Volumn 56, Issue 1, 2002, Pages 93-103

  Kupershmidt, Sabina ^a   Yang, Iris C H ^b   Sutherland, Margaret ^a   Wells, K Sam ^a   Yang, Tao ^a   Yang, Ping ^a   Balser, Jeffrey R ^a,b   Roden, Dan M ^a,b  

^a VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Arrhythmia (mechanisms); Ion channels; K channel; Long QT syndrome; Ventricular arrhythmias

Indexed keywords

POTASSIUM CHANNEL; PROTEIN; PROTEIN ANTIBODY; PROTEIN FHL2; PROTEIN MINK; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL LINE; CHO CELL; CONTROLLED STUDY; GENETIC TRANSFECTION; HETEROLOGOUS EXPRESSION; HUMAN; HUMAN CELL; IMMUNOCYTOCHEMISTRY; NONHUMAN; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; TWO HYBRID SYSTEM;

ANIMALS; CELL MEMBRANE; CHO CELLS; CRICETINAE; GENETIC ENGINEERING; HOMEODOMAIN PROTEINS; IMMUNOHISTOCHEMISTRY; KCNQ POTASSIUM CHANNELS; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; OLIGONUCLEOTIDES, ANTISENSE; PATCH-CLAMP TECHNIQUES; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; TRANSCRIPTION FACTORS; TRANSFECTION; TWO-HYBRID SYSTEM TECHNIQUES;

EID: 0036775298     PISSN: 00086363     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0008-6363(02)00498-4     Document Type: Article

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