The role of inactivation in open-channel block of the sodium channel: Studies with inactivation-deficient mutant channels

Molecular Pharmacology

Volumn 50, Issue 6, 1996, Pages 1643-1650

  Grant, Augustus O ^a,d   John, J Edward ^b   Nesterenko, Vladislav V ^c   Starmer, C Frank ^a   Moorman, J Randall ^b  

^a DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF VIRGINIA   (United States)

^c MASONIC MEDICAL RESEARCH LABORATORY   (United States)

^d DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DISOPYRAMIDE; GLUTAMINE; LIDOCAINE; LOCAL ANESTHETIC AGENT; MUTANT PROTEIN; PHENYLALANINE; SODIUM CHANNEL; SODIUM CHANNEL BLOCKING AGENT; SODIUM ION;

ANIMAL CELL; ARTICLE; CELL MEMBRANE DEPOLARIZATION; CHANNEL GATING; CONTROLLED STUDY; FROG; LOCAL ANESTHESIA; MOLECULAR CLONING; NONHUMAN; OOCYTE; PRIORITY JOURNAL; PROTEIN DOMAIN; SITE DIRECTED MUTAGENESIS; SODIUM CURRENT;

CLONING, MOLECULAR; DISOPYRAMIDE; GLUTAMINE; ION CHANNEL GATING; KINETICS; MUTAGENESIS, SITE-DIRECTED; PHENYLALANINE; SODIUM CHANNEL BLOCKERS; SODIUM CHANNELS;

EID: 0030473474     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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