Cellular and molecular mechanisms of autosomal dominant form of progressive hearing loss, DFNA2

Journal of Biological Chemistry

Volumn 286, Issue 2, 2011, Pages 1517-1527

  Kim, Hyo Jeong ^a   Lv, Ping ^a   Sihn, Choong Ryoul ^a   Yamoah, Ebenezer N ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANTS; CELL SURFACE EXPRESSION; CELLULAR MECHANISMS; CURRENT MAGNITUDES; DOMINANT-NEGATIVE EFFECTS; ENDOPLASMIC RETICULUM; FUNCTIONAL FEATURES; FUNCTIONAL MECHANISMS; HEARING LOSS; HETEROLOGOUS EXPRESSION; MOLECULAR MECHANISM; NON-FUNCTIONAL; POINT MUTATIONS; PORE REGION; TETRAMERIC CHANNELS; TRANSMEMBRANES; WILD TYPES;

CELL MEMBRANES;

AUDITION;

POTASSIUM CHANNEL KCNQ; TETRAMER;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT PROGRESSIVE HEARING LOSS; CARBOXY TERMINAL SEQUENCE; CELL FUNCTION; CELL SURFACE; ENDOPLASMIC RETICULUM; GENE EXPRESSION; HEARING LOSS; MOLECULAR MECHANICS; NONHUMAN; POINT MUTATION; POTASSIUM CURRENT; PRIORITY JOURNAL; PROTEIN POLYMORPHISM; WILD TYPE;

ANIMALS; CHO CELLS; CRICETINAE; CRICETULUS; DISEASE PROGRESSION; ENDOPLASMIC RETICULUM; GENES, DOMINANT; HEARING LOSS, SENSORINEURAL; HUMANS; KCNQ POTASSIUM CHANNELS; MEMBRANE POTENTIALS; MEMBRANE PROTEINS; POINT MUTATION; PROTEIN STRUCTURE, TERTIARY; TRANSFECTION;

EID: 78651402896     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.179010     Document Type: Article

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