Trk A Monoclonal Antibody, 100ul In vitro Transcription Deficiency of this enzyme may

Deficiency of this enzyme may contribute to hepatic dysfunction

NBPF1 is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1

Two transcripts| resulting from the use of alternate polyadenylation signals| have been identified for this gene

DIRAS1 belongs to a distinct branch of the functionally diverse Ras (see HRAS

belongs to the DEAD box helicase family

Trk A Monoclonal Antibody, 100ul In vitro Transcription Deficiency of this enzyme mayThis gene encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family. This kinase is a membrane bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. The presence of this kinase leads to cell differentiation and may play a role in specifying sensory neuron subtypes. Mutations in this gene have been associated with congenital insensitivity to pain, anhidrosis, self mutilating behavior,