Genetic mutations that prevent pain: implications for future pain medication. - Wikidata - awgldk - TriplyDB

Genetic mutations that prevent pain: implications for future pain medication.

Genetic mutations that prevent pain: implications for future pain medication.

http://www.wikidata.org/entity/Q37120834

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Exploring Genetic Susceptibility to Fibromyalgia Neurological diseases and pain Animal models of chronic pain: Advances and challenges for clinical translation.Tolerance and withdrawal from prolonged opioid use in critically ill children.Clinical pharmacology of analgesics assessed with human experimental pain models: bridging basic and clinical research.Low back pain in older adults: risk factors, management options and future directions.Novel diagnostic and prognostic methods for disc degeneration and low back pain In search of analgesia: emerging roles of GPCRs in pain.Pharmacogenetics of new analgesics.Genomics and pain research in sickle cell disease: an explanation of heterogeneity?The delta opioid receptor: an evolving target for the treatment of brain disorders.Polymorphism of the Glutamate Transporter Protein EAAT2 and Migraine Transformation into Chronic Daily Headache.Translating the human genome to manage pediatric postoperative pain.Pain sensitivity and opioid analgesia: a pharmacogenomic twin study Human pain and genetics: some basics Polymorphisms in the GTP cyclohydrolase gene (GCH1) are associated with ratings of capsaicin pain.Current evidence for a modulation of low back pain by human genetic variants.Nerve growth factor, pain, itch and inflammation: lessons from congenital insensitivity to pain with anhidrosis.Genetic variability of pain perception and treatment--clinical pharmacological implications.Screening TRPV1 antagonists for the treatment of pain: lessons learned over a decade.MC1R, the cAMP pathway, and the response to solar UV: extending the horizon beyond pigmentation Genetics of chronic post-surgical pain: a crucial step toward personal pain medicine.Consequences of daily corticosteroid dosing with or without pre-treatment with quinidine on the in vivo cytochrome P450 2D (CYP2D) enzyme in rats: effect on O-demethylation activity of dextromethorphan and expression levels of CYP2D1 mRNA.The A118G single-nucleotide polymorphism of human μ-opioid receptor gene and use of labor analgesia.Genetic susceptibility to postherniotomy pain. The influence of polymorphisms in the Mu opioid receptor, TNF-α, GRIK3, GCH1, BDNF and CACNA2D2 genes.New insights into the genetics of fibromyalgia.

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P2860

Genetic mutations that prevent pain: implications for future pain medication.

http://www.wikidata.org/entity/Q37120834

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on February 2008

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

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name

Genetic mutations that prevent pain: implications for future pain medication.

@en

Genetic mutations that prevent pain: implications for future pain medication.

@nl

type

label

Genetic mutations that prevent pain: implications for future pain medication.

@en

Genetic mutations that prevent pain: implications for future pain medication.

@nl

prefLabel

Genetic mutations that prevent pain: implications for future pain medication.

@en

Genetic mutations that prevent pain: implications for future pain medication.

@nl

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14622416.9.2.179

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Pharmacogenomics

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Genetic mutations that prevent pain: implications for future pain medication.

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Bruno Oertel

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P2860

Initial sequencing and analysis of the human genome

The Sequence of the Human Genome

Single-nucleotide polymorphism in the human mu opioid receptor gene alters beta-endorphin binding and activity: possible implications for opiate addiction

Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates

Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk

Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia

Familial dysautonomia is caused by mutations of the IKAP gene.

Melanocortin-1 receptor gene variants affect pain and mu-opioid analgesia in mice and humans

Increased sensitivity to thermal pain and reduced subcutaneous lidocaine efficacy in redheads

The melanocortin-1 receptor gene mediates female-specific mechanisms of analgesia in mice and humans

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179-194

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scholarly article

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10.2217/14622416.9.2.179

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18370847

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