[HTML][HTML] Genetic predictors of human chronic pain conditions

K Zorina-Lichtenwalter, CB Meloto, S Khoury… - Neuroscience, 2016 - Elsevier
Chronic pain conditions are multifactorial disorders with a high frequency in the population.
Their pathophysiology is often unclear, and treatment is inefficient. During the last 20 years …

Dopamine and migraine: biology and clinical implications

S Akerman, PJ Goadsby - Cephalalgia, 2007 - journals.sagepub.com
In the last 30 years dopamine has been considered as playing a role in the pathogenesis of
migraine. The literature indicates that migraineurs are hypersensitive to dopamine agonists …

Locked nucleic acid (LNA) single nucleotide polymorphism (SNP) genotype analysis and validation using real‐time PCR

MP Johnson, LM Haupt, LR Griffiths - Nucleic acids research, 2004 - academic.oup.com
With an increased emphasis on genotyping of single nucleotide polymorphisms (SNPs) in
disease association studies, the genotyping platform of choice is constantly evolving. In …

[PDF][PDF] A susceptibility locus for migraine with aura, on chromosome 4q24

M Wessman, M Kallela, MA Kaunisto, P Marttila… - The American Journal of …, 2002 - cell.com
Migraine is a complex neurovascular disorder with substantial evidence supporting a
genetic contribution. Prior attempts to localize susceptibility loci for common forms of …

Pathophysiological basis of migraine prophylaxis

F Galletti, LM Cupini, I Corbelli, P Calabresi… - Progress in …, 2009 - Elsevier
Several cellular and molecular mechanisms have been implicated in migraine
pathophysiology including abnormal neuronal excitability and vascular events. Drugs from …

The polymorphism A118G of the human mu-opioid receptor gene decreases the pupil constrictory effect of morphine-6-glucuronide but not that of morphine

J Lötsch, C Skarke, S Grösch, J Darimont… - Pharmacogenetics …, 2002 - journals.lww.com
Large individual differences in the clinical response to morphine therapy have been known
for a long time by clinicians. The recent advances in genomic research encourage the …

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura

RA Lea, M Ovcaric, J Sundholm, J MacMillan… - BMC medicine, 2004 - Springer
Abstract Background The C677T variant in the methylenetetrahydrofolate reductase
(MTHFR) gene is associated with increased levels of circulating homocysteine and is a mild …

Dopamine beta-hydroxylase deficiency. A genetic disorder of cardiovascular regulation.

D Robertson, V Haile, SE Perry, RM Robertson… - …, 1991 - Am Heart Assoc
Dopamine beta-hydroxylase (DBH) deficiency is a genetic disorder in which affected
patients cannot synthesize norepinephrine, epinephrine, and octopamine in either the …

Pathophysiology of migraine

FM Cutrer - Seminars in neurology, 2010 - thieme-connect.com
Our understanding of migraine pathophysiology is a work in progress. As more is learned
about migraine, it seems that the probability of identifying a single unifying explanation for …

Meta-analysis of genome-wide association for migraine in six population-based European cohorts

L Ligthart, B De Vries, AV Smith, MA Ikram… - European Journal of …, 2011 - nature.com
Migraine is a common neurological disorder with a genetically complex background. This
paper describes a meta-analysis of genome-wide association (GWA) studies on migraine …