Gene defect in ectodermal dysplasia implicates a death domain adapter in development

Nature

Volumn 414, Issue 6866, 2001, Pages 913-916

  Headon, Denis J ^a   Emmal, Stephanie A ^b   Ferguson, Betsy M ^b   Tucker, Abigail S ^c   Justice, Monica J ^a   Sharpe, Paul T ^c   Zonana, Jonathan ^b   Overbeek, Paul A ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c GUY S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MUTAGENESIS; PROTEINS; TUMORS;

ECTODERMAL DERIVATIVES;

GENES;

LIGAND; TUMOR NECROSIS FACTOR RECEPTOR;

DISEASE;

APOPTOSIS; ARTICLE; CONTROLLED STUDY; DEVELOPMENT; GENE MUTATION; HYPOHIDROTIC ECTODERMAL DYSPLASIA; MISSENSE MUTATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; SCANTY HAIR; SWEAT GLAND; TOOTH MALFORMATION;

AMINO ACID SEQUENCE; ANIMALS; CELL LINE; ECTODERMAL DYSPLASIA; EDAR RECEPTOR; GENE EXPRESSION; HUMANS; MEMBRANE PROTEINS; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; MOLECULAR SEQUENCE DATA; MUTATION; NF-KAPPA B; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; RECEPTORS, ECTODYSPLASIN; RECEPTORS, TUMOR NECROSIS FACTOR; SEQUENCE HOMOLOGY, AMINO ACID; SIGNAL TRANSDUCTION;

MAMMALIA;

EID: 0035924366     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/414913a     Document Type: Article

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