Closing the gap on autosomal dominant connexin-26 and connexin-43 mutants linked to human disease

Journal of Biological Chemistry

Volumn 283, Issue 6, 2008, Pages 2997-3001

  Laird, Dale W ^a  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AUDITION; ENCODING (SYMBOLS); GALLIUM ALLOYS; GENE ENCODING; GENES; HISTOLOGY; HUMAN COMPUTER INTERACTION; MOLECULAR BIOLOGY;

AUTOSOMAL DOMINANT MUTATIONS; AUTOSOMAL DOMINANTS; DEVELOPMENTAL DISORDERS; GAP JUNCTION PROTEINS; GAP JUNCTIONS; GENE ABLATIONS; GENES ENCODING; GERM LINE MUTATIONS; HEARING LOSSES; HUMAN BODIES; HUMAN DISEASES; HUMAN TISSUES; MOLECULAR GENETICS; MOUSE MODELS; OCULODENTODIGITAL DYSPLASIAS; ORGAN FUNCTIONS; SENSORINEURAL HEARING LOSSES; SKIN DISEASES;

ANIMAL CELL CULTURE;

CONNEXIN 26; CONNEXIN 43; GAP JUNCTION PROTEIN;

AUTOSOMAL DOMINANT INHERITANCE; CELL PROLIFERATION; GENE DELETION; GENE EXPRESSION; GENE MUTATION; HEARING LOSS; HUMAN; ICHTHYOSIS; IMMUNOPRECIPITATION; KERATINOCYTE; KERATITIS; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SHORT SURVEY; ANIMAL; BIOLOGICAL MODEL; CELL JUNCTION; CELL LINE; DISEASE MODEL; DOMINANT GENE; GENETIC DISORDER; GENETICS; MOUSE; MUTATION; PHYSIOLOGY; REVIEW;

ANIMALS; CELL LINE; CONNEXIN 43; CONNEXINS; DISEASE MODELS, ANIMAL; GAP JUNCTIONS; GENES, DOMINANT; GENETIC DISEASES, INBORN; GERM-LINE MUTATION; HUMANS; MICE; MODELS, BIOLOGICAL; MODELS, GENETIC; MUTATION; PHENOTYPE;

EID: 41249084806     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.R700041200     Document Type: Short Survey

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