The role of an inwardly rectifying K+ channel (Kir4.1) in the inner ear and hearing loss

Neuroscience

Volumn 265, Issue , 2014, Pages 137-146

  Chen, J ^a,b   Zhao, H B ^b  

^a CHINA THREE GORGES UNIVERSITY   (China)

^b UNIVERSITY OF KENTUCKY MEDICAL CENTER   (United States)

Author keywords

Deafness; EAST; Endocochlear potential; KCNJ10; SeSAME; Spiral ganglion

Indexed keywords

INWARDLY RECTIFYING POTASSIUM CHANNEL; INWARDLY RECTIFYING POTASSIUM CHANNEL KIR4.1; INWARDLY RECTIFYING POTASSIUM CHANNEL KIR5.1; UNCLASSIFIED DRUG; KCNJ10 (CHANNEL);

APICAL MEMBRANE; COCHLEA POTENTIAL; ENDOLYMPH; GENE MUTATION; GLIA CELL; HEARING IMPAIRMENT; HUMAN; INNER EAR; KCNJ10 GENE; MUTATOR GENE; NERVE EXCITABILITY; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PENDRED SYNDROME; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN TARGETING; REVIEW; SATELLITE CELL; STRIA VASCULARIS; STRUCTURE ACTIVITY RELATION; VESTIBULE AQUEDUCT; ANIMAL; COCHLEA; DEFICIENCY; GENETICS; METABOLISM; PHYSIOLOGY;

ANIMALS; COCHLEA; EAR, INNER; HEARING LOSS; HUMANS; POTASSIUM CHANNELS, INWARDLY RECTIFYING;

EID: 84896712860     PISSN: 03064522     EISSN: 18737544     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2014.01.036     Document Type: Review

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