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Volumn 277, Issue 8, 2002, Pages 6455-6462

Novel pathogenic mechanisms of congenital insensitivity to pain with anhidrosis genetic disorder unveiled by functional analysis of neurotrophic tyrosine receptor kinase type 1/nerve growth factor receptor mutations

(7) Miranda, Claudia a,b Virgilio, Michela Di a Selleri, Silvia a Zanotti, Giuseppe a Pagliardini, Sonia b Pierotti, Marco A b Greco, Angela a

a NATIONAL CANCER INSTITUTE (Italy)

b UNIVERSITY OF PADOVA (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BIOASSAY; DISEASES; GENES; MUTAGENESIS; NEUROLOGY;

PATHOGENESIS;

ENZYMES;

NERVE GROWTH FACTOR RECEPTOR; NEUROTROPHIC TYROSINE RECEPTOR KINASE 1; PHOSPHOTRANSFERASE; UNCLASSIFIED DRUG;

ANHIDROSIS; ANIMAL CELL; ARTICLE; AUTOPHOSPHORYLATION; CONGENITAL ANALGESIA; FUNCTIONAL ASSESSMENT; GENETIC POLYMORPHISM; HUMAN; HUMAN CELL; MUTATION; NONHUMAN; PATHOGENESIS; POINT MUTATION; PRIORITY JOURNAL; PROTEIN FUNCTION;

AMINO ACID SUBSTITUTION; ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; HUMANS; HYPOHIDROSIS; KINETICS; MUTATION; MUTATION, MISSENSE; NERVE GROWTH FACTOR; PAIN INSENSITIVITY, CONGENITAL; RECEPTOR, NERVE GROWTH FACTOR; RECEPTOR, TRKA; RECOMBINANT PROTEINS; SIGNAL TRANSDUCTION; TRANSFECTION;

ANIMALIA;

EID: 0037155170 PISSN: 00219258 EISSN: None Source Type: Journal
DOI: 10.1074/jbc.M110016200 Document Type: Article

Times cited : (40)

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