| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Miguel Estevez | |
| Kathy L. Gardner | |||
| P2860 | cites work | Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2 | Q24293004 |
| Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons | Q24538702 | ||
| Mechanisms of migraine aura revealed by functional MRI in human visual cortex | Q24635174 | ||
| The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells | Q24657270 | ||
| Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions | Q28204791 | ||
| The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel | Q28204946 | ||
| Physical mapping and characterization of the human Na,K-ATPase isoform, ATP1A4 | Q28214737 | ||
| A new locus for hemiplegic migraine maps to chromosome 1q31 | Q28254832 | ||
| A gene for familial hemiplegic migraine maps to chromosome 19 | Q28255425 | ||
| Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity | Q28256929 | ||
| Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics | Q28263620 | ||
| Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome | Q28270270 | ||
| Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 | Q28295213 | ||
| Direct binding of G-protein betagamma complex to voltage-dependent calcium channels | Q28302204 | ||
| Absence epilepsy in tottering mutant mice is associated with calcium channel defects | Q28587452 | ||
| Identification of a specific role for the Na,K-ATPase alpha 2 isoform as a regulator of calcium in the heart | Q28589440 | ||
| The Na,K-ATPase alpha 2 isoform is expressed in neurons, and its absence disrupts neuronal activity in newborn mice | Q28589473 | ||
| Mutant mouse tottering: selective increase of locus ceruleus axons in a defined single-locus mutation | Q28589781 | ||
| Impaired neurotransmitter release and elevated threshold for cortical spreading depression in mice with mutations in the alpha1A subunit of P/Q type calcium channels | Q28594747 | ||
| Abnormal brain processing of cutaneous pain in patients with chronic migraine | Q31123350 | ||
| Neocortical spreading depression provokes the expression of c-fos protein-like immunoreactivity within trigeminal nucleus caudalis via trigeminovascular mechanisms. | Q34662700 | ||
| Genetic heterogeneity of familial hemiplegic migraine | Q35889752 | ||
| A locus for migraine without aura maps on chromosome 14q21.2-q22.3. | Q37205369 | ||
| A susceptibility locus for migraine with aura, on chromosome 4q24. | Q37361279 | ||
| Relations among Na+,K+-ATPase activity, sodium pump activity, transmembrane sodium movement, and cardiac contractility | Q37543825 | ||
| Cell-specific expression of mRNAs encoding Na+,K(+)-ATPase alpha- and beta-subunit isoforms within the rat central nervous system | Q37582993 | ||
| Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine. | Q38294179 | ||
| Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura | Q39416650 | ||
| Comorbidity of migraine and psychiatric disorders | Q40905718 | ||
| Crosstalk between G proteins and protein kinase C mediated by the calcium channel alpha1 subunit. | Q41132629 | ||
| Clinical neurophysiology of headache | Q41371813 | ||
| Dopamine and migraine | Q41598488 | ||
| Familial typical migraine: significant linkage and localization of a gene to Xq24-28. | Q42633527 | ||
| The -141C Ins/Del polymorphism of the dopamine D2 receptor gene is not associated with either migraine or Parkinson's disease | Q43642796 | ||
| Significance of serotonin transporter gene polymorphism in migraine. | Q43645171 | ||
| Differential role of KIR channel and Na(+)/K(+)-pump in the regulation of extracellular K(+) in rat hippocampus | Q43850122 | ||
| Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model | Q43873034 | ||
| Dopamine receptor genes and migraine with and without aura: an association study. | Q44016293 | ||
| A genetic association study of migraine with dopamine receptor 4, dopamine transporter and dopamine-beta-hydroxylase genes | Q44354243 | ||
| Glutathione S-Transferase Polymorphisms: Susceptibility to Migraine without Aura | Q44433696 | ||
| The voltage-gated calcium channel UNC-2 is involved in stress-mediated regulation of tryptophan hydroxylase | Q44693090 | ||
| Evidence for allelic association of the dopamine beta-hydroxylase gene (DBH) with susceptibility to typical migraine | Q44802503 | ||
| Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus | Q46190178 | ||
| Functional MRI-BOLD of visually triggered headache in patients with migraine | Q48210772 | ||
| Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group | Q48480301 | ||
| Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family | Q48553901 | ||
| P/Q-type calcium-channel blockade in the periaqueductal gray facilitates trigeminal nociception: a functional genetic link for migraine? | Q48668592 | ||
| Isoforms of Na,K-ATPase alpha and beta subunits in the rat cerebellum and in granule cell cultures | Q48706993 | ||
| Central serotonergic nerves project to the pial vessels of the brain. | Q48716042 | ||
| Stimulation of the superior sagittal sinus increases metabolic activity and blood flow in certain regions of the brainstem and upper cervical spinal cord of the cat. | Q48744994 | ||
| Migraine association and linkage analyses of the human 5-hydroxytryptamine (5HT2A) receptor gene | Q48875514 | ||
| The occipital cortex is hyperexcitable in migraine: experimental evidence | Q48932532 | ||
| Interictal cortical hyperexcitability in migraine patients demonstrated with transcranial magnetic stimulation | Q48974800 | ||
| An association between migraine and cutaneous allodynia. | Q51402389 | ||
| Expression of c-Fos-like immunoreactivity in the caudal medulla and upper cervical spinal cord following stimulation of the superior sagittal sinus in the cat. | Q51650217 | ||
| Significant linkage to migraine with aura on chromosome 11q24. | Q52010989 | ||
| Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity. | Q53151351 | ||
| Allelic variation in the serotonin 5-HT2C receptor gene and migraine | Q57024868 | ||
| A typical migraine susceptibility region localizes to chromosome 1q31 | Q59590792 | ||
| Familial Migraine: Exclusion of the Susceptibility Gene from the Reported Locus of Familial Hemiplegic Migraine on 19p | Q61819951 | ||
| Investigation of theCACNA1A gene as a candidate for typical migraine susceptibility | Q61982638 | ||
| Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23 | Q63383621 | ||
| Immunofluorescent localization of three Na,K-ATPase isozymes in the rat central nervous system: both neurons and glia can express more than one Na,K-ATPase | Q67912776 | ||
| Serotonin metabolism in migraine | Q69096571 | ||
| Exclusion of 5-HT2A and 5-HT2C receptor genes as candidate genes for migraine | Q71174137 | ||
| Genetic markers: association study in migraine | Q71729576 | ||
| Perfusion weighted imaging during migraine: spontaneous visual aura and headache | Q73202951 | ||
| The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine | Q73307591 | ||
| Absence of linkage between the interleukin-6 gene (-174 G/C) polymorphism and migraine | Q73443706 | ||
| Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles | Q73508519 | ||
| Activity-dependent extracellular K+ accumulation in rat optic nerve: the role of glial and axonal Na+ pumps | Q73540905 | ||
| Cytochrome P450 2D6 and glutathione S-transferase M1 genotypes and migraine | Q73664330 | ||
| Angiotensin-converting enzyme gene deletion polymorphism determines an increase in frequency of migraine attacks in patients suffering from migraine without aura | Q73676409 | ||
| Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura | Q73800890 | ||
| No evidence for involvement of the human inducible nitric oxide synthase (iNOS) gene in susceptibility to typical migraine | Q74094047 | ||
| A polymorphism in the interleukin-1alpha gene influences the clinical features of migraine | Q74236591 | ||
| Tumor necrosis factor gene polymorphism in migraine | Q74236594 | ||
| 5-HT1B receptor polymorphism and clinical response to sumatriptan | Q74574599 | ||
| Association between dopamine receptor genes and migraine without aura in a Sardinian sample | Q77332492 | ||
| Apolipoprotein E gene polymorphisms in patients with migraine | Q77384926 | ||
| Parallel concept of migraine pathogenesis | Q77466605 | ||
| Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13 | Q78347038 | ||
| Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1. | Q78633416 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genetics | Q7162 |
| migraine | Q133823 | ||
| P304 | page(s) | 225-235 | |
| P577 | publication date | 2003-11-18 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Update on the genetics of migraine | |
| P478 | volume | 114 |
| Q46816145 | A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred. |
| Q54560010 | An adenosine A2A receptor gene haplotype is associated with migraine with aura. |
| Q51579082 | Association between a polymorphism in the lymphotoxin-a promoter region and migraine. |
| Q50089675 | Association of MTHFR gene polymorphisms with migraine in North Indian population |
| Q48760342 | Autopsy case of acute encephalopathy linked to familial hemiplegic migraine with cerebellar atrophy and mental retardation |
| Q48465401 | Both insulin and calcium channel signaling are required for developmental regulation of serotonin synthesis in the chemosensory ADF neurons of Caenorhabditis elegans |
| Q46464414 | COMT (Val158Met) polymorphism is not associated to neuropathic pain in a Spanish population |
| Q36697950 | Combined analysis of circulating β-endorphin with gene polymorphisms in OPRM1, CACNAD2 and ABCB1 reveals correlation with pain, opioid sensitivity and opioid-related side effects |
| Q33800231 | Effects of tumor necrosis factor-β (TNF-β) 252A>G polymorphism on the development of migraine: a meta-analysis |
| Q53257053 | Endothelin receptor A -231 G>A polymorphism: no linkage to primary pediatric headache. |
| Q34770974 | Evidence for an association between migraine and the hypocretin receptor 1 gene |
| Q42671135 | Familial risks for migraine and other headaches among siblings based on hospitalizations in Sweden |
| Q57992455 | Family-Based Analysis of Serotonin Transporter Gene Polymorphisms in Migraine With and Without Aura |
| Q45881629 | Genetics and pain |
| Q36574910 | Genetics of migraine: an update |
| Q46011691 | Genomic profiles for human peripheral blood T cells, B cells, natural killer cells, monocytes, and polymorphonuclear cells: comparisons to ischemic stroke, migraine, and Tourette syndrome. |
| Q36574912 | Invertebrate modeling of a migraine channelopathy |
| Q24596291 | Investigating the genetic role of aquaporin4 gene in migraine |
| Q57811769 | Migraine |
| Q33586998 | Migraine headache in affectively ill latino adults of mexican american origin is associated with bipolarity |
| Q36825299 | Migraine: a complex genetic disorder |
| Q57272263 | Migraineurs show a high prevalence of antiphospholipid antibodies |
| Q36995199 | Molecular mechanisms of migraine? |
| Q35601495 | Orofacial pain prospective evaluation and risk assessment study--the OPPERA study. |
| Q28268080 | Rare missense variants in ATP1A2 in families with clustering of common forms of migraine |
| Q30470143 | Targeted mutations in the Na,K-ATPase α 2 isoform confer ouabain resistance and result in abnormal behavior in mice. |
| Q35932365 | The molecular genetics of migraine |
| Q28286980 | The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene |
| Q37171543 | The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations |
| Q41288208 | Tumour necrosis factor gene polymorphisms and migraine in Greek children |
| Q79907235 | [Mechanisms and genetics of migraine] |
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