Isolating and characterizing three alternatively spliced mu opioid receptor variants: mMOR-1A, mMOR-1O, and mMOR-1P
Author:
Affiliation:
1. Molecular Pharmacology and Chemistry Program; Memorial Sloan-Kettering Cancer Center; New York New York 10065
2. Department of Neurology; Memorial Sloan-Kettering Cancer Center; New York New York 10065
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience
Reference56 articles.
1. Immunohistochemical localization of the carboxy terminus of the novel mu opioid receptor splice variant MOR-1C within the human spinal cord;Abbadie;Neuroreport,2000a
2. Comparative immunohistochemical distributions of carboxy terminus epitopes from the mu-opioid receptor splice variants MOR-1D, MOR-1 and MOR-1C in the mouse and rat CNS;Abbadie;Neuroscience,2000b
3. Differential distribution in rat brain of mu opioid receptor carboxy terminal splice variants MOR-1C-like and MOR-1-like immunoreactivity: Evidence for region-specific processing;Abbadie;J Comp Neurol,2000c
4. Comparative immunhistochemical distributions of carboxy terminus epitopes from the mu opioid receptor splice variants MOR-1D, MOR-1 and MOR-1C in the mouse and rat central nervous systems;Abbadie;Neuroscience,2000d
5. Differential distribution in rat brain of mu opioid receptor carboxy terminal splice variants MOR-1C and MOR-1-like immunoreactivity: Evidence for region-specific processing;Abbadie;J Comp Neurol,2000e
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