Add to ORKGMost opioid analgesics used clinically, including morphine and fentanyl, as well as the recreational drug heroin, act primarily through the mu opioid receptor, a class A Rhodopsin-like G protein-coupled receptor (GPCR). The single-copy mu opioid receptor gene
Background/Aims: Opiates are potent analgesics but their clinical use is limited by sex-associated s...
Mu-opioid receptor (MOR) belongs to a family of heptahelical G-protein-coupled receptors (GPCRs). St...
The human μ-opioid receptor gene (OPRM1), due to its genetic and structural variation, has been a ta...
Most opioid analgesics used clinically, including morphine and fentanyl, as well as the recreational...
Most opioid analgesics used clinically, including morphine and fentanyl, as well as the recreational...
The µ opioid receptor gene, OPRM1, undergoes extensive alternative pre-mRNA splicing in rodents and ...
The μ-opioid receptor (OPRM1) is the principal receptor target for both endogenous and exogenous opi...
The opioid field and the quest for the ideal analgesics with limited side effects has accumulated de...
A subset of the population receiving opioids for the treatment of acute and chronic clinical pain de...
Abstract: Background: Opioids are the most widely used analgesics for the treatment of clinical pain...
AbstractAlthough MOR-1 encodes a mu opioid receptor, its relationship to the pharmacologically defin...
AbstractThe MOR-1 gene is large, with a recent study reporting nine exons spanning 250 kb which comb...
The 118A>G single nucleotide polymorphism (SNP) in the μ-opioid receptor (OPRM1) gene has been the m...
The human μ-opioid receptor gene (OPRM1), due to its genetic and structural variation, has been a ta...
Relief from pain is a major goal of all branches of medicine, and poorly controlled pain is associat...
Background/Aims: Opiates are potent analgesics but their clinical use is limited by sex-associated s...
Mu-opioid receptor (MOR) belongs to a family of heptahelical G-protein-coupled receptors (GPCRs). St...
The human μ-opioid receptor gene (OPRM1), due to its genetic and structural variation, has been a ta...
Most opioid analgesics used clinically, including morphine and fentanyl, as well as the recreational...
Most opioid analgesics used clinically, including morphine and fentanyl, as well as the recreational...
The µ opioid receptor gene, OPRM1, undergoes extensive alternative pre-mRNA splicing in rodents and ...
The μ-opioid receptor (OPRM1) is the principal receptor target for both endogenous and exogenous opi...
The opioid field and the quest for the ideal analgesics with limited side effects has accumulated de...
A subset of the population receiving opioids for the treatment of acute and chronic clinical pain de...
Abstract: Background: Opioids are the most widely used analgesics for the treatment of clinical pain...
AbstractAlthough MOR-1 encodes a mu opioid receptor, its relationship to the pharmacologically defin...
AbstractThe MOR-1 gene is large, with a recent study reporting nine exons spanning 250 kb which comb...
The 118A>G single nucleotide polymorphism (SNP) in the μ-opioid receptor (OPRM1) gene has been the m...
The human μ-opioid receptor gene (OPRM1), due to its genetic and structural variation, has been a ta...
Relief from pain is a major goal of all branches of medicine, and poorly controlled pain is associat...
Background/Aims: Opiates are potent analgesics but their clinical use is limited by sex-associated s...
Mu-opioid receptor (MOR) belongs to a family of heptahelical G-protein-coupled receptors (GPCRs). St...
The human μ-opioid receptor gene (OPRM1), due to its genetic and structural variation, has been a ta...