Nerve growth factor (NGF) induces neurite outgrowth and promotes survival of embryonic sensory and sympathetic neurons. TRKA, a receptor tyrosine kinase cloned from a human colon cancer was later found to be expressed in the nervous system and phosphorylated in response to NGF. Somatic rearrangement(s) of the TRKA gene (also designated NTRK1) are responsible for formation of some oncogenes. Genetic defects in TRKA are responsible for a human disorder, congenital insensitivity to pain with anhidrosis (CIPA). We report here isolation and characterization of the TRKA gene which spans at least 23 kb and is split into 17 exons. Exon sizes range from 18 to 394 bp and intron sizes range from 170 bp to at least 3.3 kb. Sizes and boundaries of the e...
The Trk family is composed of three principal members (A, B and C), also termed neurotrophin tyrosin...
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder chara...
Congenital insensitivity to pain with anhidrosis is an autosomal recessive hereditary disorder chara...
Nerve growth factor (NGF) induces neurite outgrowth and promotes survival of embryonic sensory and s...
Congenital insensitivity to pain with anhidrosis (CIPA) is characterized by recurrent episodes of un...
SummaryCongenital insensitivity to pain with anhidrosis (CIPA) is characterized by recurrent episode...
Human TRKA (NTRK1) encodes the receptor tyrosine kinases (RTKs) for nerve growth factor (NGF) and is...
The human TRKA gene encodes a high-affinity tyrosine kinase receptor for nerve growth factor. Congen...
Congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropat...
Congenital insensitivity to pain with anhidrosis (CIPA; MIM 256800) is an autosomal-recessive disord...
Publisher Copyright: © 2015 Luberg et al.Background: Tropomyosin-related kinase A (TRKA) is a nerve ...
A nerve growth factor receptor encoded by the TRKA gene plays an important part in the formation of ...
Congenital insensitivity to pain with anhidrosis (CIPA), also referred to as hereditary sensory and ...
Novel transcripts reveal a complex structure of the human TRKA gene and imply the presence of multip...
Congenital insensitivity to pain with anhidrosis is an autosomal recessive hereditary disorder chara...
The Trk family is composed of three principal members (A, B and C), also termed neurotrophin tyrosin...
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder chara...
Congenital insensitivity to pain with anhidrosis is an autosomal recessive hereditary disorder chara...
Nerve growth factor (NGF) induces neurite outgrowth and promotes survival of embryonic sensory and s...
Congenital insensitivity to pain with anhidrosis (CIPA) is characterized by recurrent episodes of un...
SummaryCongenital insensitivity to pain with anhidrosis (CIPA) is characterized by recurrent episode...
Human TRKA (NTRK1) encodes the receptor tyrosine kinases (RTKs) for nerve growth factor (NGF) and is...
The human TRKA gene encodes a high-affinity tyrosine kinase receptor for nerve growth factor. Congen...
Congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropat...
Congenital insensitivity to pain with anhidrosis (CIPA; MIM 256800) is an autosomal-recessive disord...
Publisher Copyright: © 2015 Luberg et al.Background: Tropomyosin-related kinase A (TRKA) is a nerve ...
A nerve growth factor receptor encoded by the TRKA gene plays an important part in the formation of ...
Congenital insensitivity to pain with anhidrosis (CIPA), also referred to as hereditary sensory and ...
Novel transcripts reveal a complex structure of the human TRKA gene and imply the presence of multip...
Congenital insensitivity to pain with anhidrosis is an autosomal recessive hereditary disorder chara...
The Trk family is composed of three principal members (A, B and C), also termed neurotrophin tyrosin...
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder chara...
Congenital insensitivity to pain with anhidrosis is an autosomal recessive hereditary disorder chara...