Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafness

Proceedings of the National Academy of Sciences of the United States of America

Volumn 103, Issue 13, 2006, Pages 5213-5218

  Abrams, Charles K ^a   Freidin, Mona M ^a   Verselis, Vytas K ^a   Bargiello, Thaddeus A ^a   Kelsell, David P ^b   Richard, Gabriele ^c   Bennett, Michael V L ^a   Bukauskas, Feliksas F ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^c GENEDX   (United States)

Author keywords

Electrical coupling; Erythrokeratodermia variabilis; Gap junction; Intercellular communication

Indexed keywords

4',6 DIAMIDINO 2 PHENYLINDOLE; ALEXA FLUOR 350; ALKANOL; CONNEXIN 31; DYE; ETHIDIUM BROMIDE; LUCIFER YELLOW; UNCLASSIFIED DRUG;

ARTICLE; CELL COMMUNICATION; CHANNEL GATING; CONDUCTANCE; CONTROLLED STUDY; GAP JUNCTION; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN FAMILY; SKIN DISEASE;

ANIMALS; CELL LINE, TUMOR; CELL MEMBRANE PERMEABILITY; CONNEXINS; DEAFNESS; ELECTROPHYSIOLOGY; GAP JUNCTIONS; GENE EXPRESSION REGULATION; GENETIC PREDISPOSITION TO DISEASE; HUMANS; ION CHANNEL GATING; MICE; PATCH-CLAMP TECHNIQUES; SKIN DISEASES;

ALEXA;

EID: 33645509670     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0511091103     Document Type: Article

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