Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia. - Wikidata - awgldk - TriplyDB

Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia.

Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia.

http://www.wikidata.org/entity/Q36401909

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Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia Exploring Genetic Susceptibility to Fibromyalgia The comorbidity of insomnia, chronic pain, and depression: dopamine as a putative mechanism Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs.β2- and β3-adrenergic receptors drive COMT-dependent pain by increasing production of nitric oxide and cytokines Effect of catechol-O-methyltransferase polymorphism on response to propranolol therapy in chronic musculoskeletal pain: a randomized, double-blind, placebo-controlled, crossover pilot study.COMT val158met polymorphism and neural pain processing Candidate gene studies of fibromyalgia: a systematic review and meta-analysis.Large candidate gene association study reveals genetic risk factors and therapeutic targets for fibromyalgia.Catechol O-methyltransferase haplotype predicts immediate musculoskeletal neck pain and psychological symptoms after motor vehicle collision.Genetic contributions to clinical pain and analgesia: avoiding pitfalls in genetic research Epistasis between polymorphisms in COMT, ESR1, and GCH1 influences COMT enzyme activity and pain.COMT moderates the relation of daily maladaptive coping and pain in fibromyalgia.Current progress in the pharmacological therapy of fibromyalgia.Meta-analysis reveals a lack of association between a common catechol-O-methyltransferase (COMT) polymorphism val¹⁵⁸met and fibromyalgia The role of the central nervous system in the generation and maintenance of chronic pain in rheumatoid arthritis, osteoarthritis and fibromyalgia Disruptive mRNA folding increases translational efficiency of catechol-O-methyltransferase variant Neuroplasticity underlying the comorbidity of pain and depression Fibromyalgia: When Distress Becomes (Un)sympathetic Pain.Genetic influences on the dynamics of pain and affect in fibromyalgia.Increased Risk of Coronary Heart Disease in Patients with Primary Fibromyalgia and Those with Concomitant Comorbidity-A Taiwanese Population-Based Cohort Study Nocturnal heart rate variability parameters as potential fibromyalgia biomarker: correlation with symptoms severity.The role of benign joint hypermobility in the pain experience in Juvenile Fibromyalgia: an observational study.Comparing Genomic Profiles of Women With and Without Fibromyalgia.Modification of COMT-dependent pain sensitivity by psychological stress and sex.Central pain mechanisms in the rheumatic diseases: future directions.Janus molecule I: dichotomous effects of COMT in neuropathic vs nociceptive pain modalities.Fibromyalgia and sleep-disordered breathing: the missing link Genetic contributions to pain: a review of findings in humans.Programmed symptoms: disparate effects united by purpose.Persistent Catechol-O-methyltransferase-dependent Pain Is Initiated by Peripheral β-Adrenergic Receptors Association between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome.Nature and nurture of human pain.Genetic basis of pain variability: recent advances Genetic variants associated with development of TMD and its intermediate phenotypes: the genetic architecture of TMD in the OPPERA prospective cohort study.Current evidence for a modulation of low back pain by human genetic variants.Variation in the COMT gene: implications for pain perception and pain treatment.Complex multilocus effects of catechol-O-methyltransferase haplotypes predict pain and pain interference 6 weeks after motor vehicle collision.The phenotypic and genetic signatures of common musculoskeletal pain conditions.

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Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia.

http://www.wikidata.org/entity/Q36401909

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A simple salting out procedure for extracting DNA from human nucleated cells

No association between chronic musculoskeletal complaints and Val158Met polymorphism in the Catechol-O-methyltransferase gene. The HUNT study.

Catechol-O-methyltransferase (COMT): biochemistry, molecular biology, pharmacology, and clinical efficacy of the new selective COMT inhibitors.

COMT val158met genotype affects mu-opioid neurotransmitter responses to a pain stressor.

Family study of fibromyalgia.

The fibromyalgia impact questionnaire: development and validation.

Genetic linkage analysis of multicase families with fibromyalgia syndrome.

The burden of musculoskeletal diseases in the general population of Spain: results from a national survey

Fibromyalgia as a sympathetically maintained pain syndrome.

The association between headache and Val158Met polymorphism in the catechol-O-methyltransferase gene: the HUNT Study.

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