Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome

Biochimica et Biophysica Acta - Biomembranes

Volumn 1818, Issue 8, 2012, Pages 2014-2019

  Levit, Noah A ^a,b   Mese, Gulistan ^a,d   Basaly, Mena George R ^c   White, Thomas W ^a  

^a STONY BROOK UNIVERSITY   (United States)

^b STONY BROOK UNIVERSITY   (United States)

^c Ward Melville High School   (United States)

^d IZMIR INSTITUTE OF TECHNOLOGY   (Turkey)

Author keywords

Channel; Connexin; Epidermis; Genetic disease; Mutation

Indexed keywords

2 AMINOETHOXYDIPHENYLBORANE; 5 NITRO 2 (3 PHENYLPROPYLAMINO) BENZOATE; BENZOIC ACID DERIVATIVE; CONNEXIN 26; FLUFENAMIC ACID; MUTANT PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; BIOPHYSICS; CELL COMMUNICATION; CELL COMPONENT; CELL DIFFERENTIATION; CELL MEMBRANE CONDUCTANCE; CELL MEMBRANE TRANSPORT; CELL PROLIFERATION; CONNEXIN HEMICHANNEL; DISEASE ASSOCIATION; EPIDERMIS; GAP JUNCTION; GENETIC DISORDER; HEARING IMPAIRMENT; HUMAN; KERATINOCYTE; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN MODIFICATION; REVIEW; SKIN DISEASE; SYNDROME KID;

ANIMALS; BIOPHYSICS; CONNEXINS; CYTOPLASM; DEAFNESS; GAP JUNCTIONS; HUMANS; ICHTHYOSIS; KERATITIS; MODELS, BIOLOGICAL; MODELS, CHEMICAL; MODELS, MOLECULAR; MOLECULAR CONFORMATION; MUTATION; XENOPUS;

RUMEX;

EID: 84055168825     PISSN: 00052736     EISSN: 18792642     Source Type: Journal    
DOI: 10.1016/j.bbamem.2011.09.003     Document Type: Review

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