Functional Domain Mapping and Selective Trans-dominant Effects Exhibited by Cx26 Disease-causing Mutations

Journal of Biological Chemistry

Volumn 279, Issue 18, 2004, Pages 19157-19168

  Thomas, Tamsin ^a   Telford, Debra ^a   Laird, Dale W ^a,b  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

^b Dental Science Building ^*  (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CELLS; DISEASES; FLUORESCENCE; PROTEINS;

GREEN FLUORESCENT PROTEINS (GFP); SKIN DISEASES;

BIOCHEMISTRY;

ALANINE; ASPARTIC ACID; BREFELDIN A; CONNEXIN 26; CONNEXIN 32; CONNEXIN 43; FLUORESCENT DYE; GLYCINE; GREEN FLUORESCENT PROTEIN; HISTIDINE;

ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CELL SURFACE; CONTROLLED STUDY; DISEASE SEVERITY; GAP JUNCTION; GENE EXPRESSION; GENE FUNCTION; GENE MAPPING; GENE MUTATION; HUMAN; HUMAN CELL; NONHUMAN; PERCEPTION DEAFNESS; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN LOCALIZATION; PROTEIN TRANSPORT; RAT; SKIN DISEASE; TRANS GOLGI NETWORK;

AMINO ACID SUBSTITUTION; ANIMALS; CELL LINE; CELL MEMBRANE; CELL MEMBRANE PERMEABILITY; CONNEXINS; GENES, DOMINANT; GENETIC PREDISPOSITION TO DISEASE; HEARING LOSS, SENSORINEURAL; HELA CELLS; HUMANS; MUTATION; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; RATS; SKIN DISEASES; TRANS-GOLGI NETWORK; TRANSFECTION;

ANIMALIA;

EID: 2442502595     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M314117200     Document Type: Article

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