Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice. - Wikidata - awgldk - TriplyDB

Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.

Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.

http://www.wikidata.org/entity/Q30502426

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Pharmacological targeting of spreading depression in migraine ASICs as therapeutic targets for migraine Familial hemiplegic migraine and spreading depression Glial Hsp70 protects K+ homeostasis in the Drosophila brain during repetitive anoxic depolarization Spreading Depression, Spreading Depolarizations, and the Cerebral Vasculature Cortical spreading depression impairs oxygen delivery and metabolism in mice Leaky RyR2 channels unleash a brainstem spreading depolarization mechanism of sudden cardiac death.Calcium channels and synaptic transmission in familial hemiplegic migraine type 1 animal models.Migraine strikes as neuronal excitability reaches a tipping point Spreading depression transiently disrupts myelin via interferon-gamma signaling.Migraine mutations impair hippocampal learning despite enhanced long-term potentiation Large-scale mass spectrometry imaging investigation of consequences of cortical spreading depression in a transgenic mouse model of migraine.Critical role of calcitonin gene-related peptide receptors in cortical spreading depression.Triptans disrupt brain networks and promote stress-induced CSD-like responses in cortical and subcortical areas.Susceptibility of Primary Sensory Cortex to Spreading Depolarizations.Genes and primary headaches: discovering new potential therapeutic targets.Vagus nerve stimulation inhibits cortical spreading depression In vivo imaging reveals that pregabalin inhibits cortical spreading depression and propagation to subcortical brain structures.Ophthalmoplegia starting with a headache circumscribed in a line-shaped area: a subtype of ophthalmoplegic migraine?Pearls and pitfalls in experimental models of spreading depression.Temporal fate specification and neural progenitor competence during development.Stress, glucocorticoid receptors, and adult neurogenesis: a balance between excitation and inhibition?Spreading depolarization may link migraine and stroke.Migraine and stroke: in search of shared mechanisms.Initiation of spreading depression by synaptic and network hyperactivity: Insights into trigger mechanisms of migraine aura.Animal models of monogenic migraine.Spreading Depolarizations: A Therapeutic Target Against Delayed Cerebral Ischemia After Subarachnoid Hemorrhage.Migraine genetics: current findings and future lines of research.Synaptic gain-of-function effects of mutant Cav2.1 channels in a mouse model of familial hemiplegic migraine are due to increased basal [Ca2+]i Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation.Abnormal cortical synaptic transmission in CaV2.1 knockin mice with the S218L missense mutation which causes a severe familial hemiplegic migraine syndrome in humans.Effect of cortical spreading depression on basal and evoked traffic in the trigeminovascular sensory system.Enhanced susceptibility to cortical spreading depression in two types of Na+,K+-ATPase α2 subunit-deficient mice as a model of familial hemiplegic migraine 2.Activation of pial and dural macrophages and dendritic cells by CSD (67 chrs).Structural abnormalities in the thalamus of migraineurs with aura: a multiparametric study at 3 T.A critical evaluation of validity and utility of translational imaging in pain and analgesia: Utilizing functional imaging to enhance the process.Biphasic neurovascular changes in prolonged migraine aura in familial hemiplegic migraine type 2.Propagation of cortical spreading depression into the hippocampus: The role of the entorhinal cortex.Involvement of AMPA receptors in CSD-induced impairment of LTP in the hippocampus.Possible Involvement of the CACNA1E Gene in Migraine: A Search for Single Nucleotide Polymorphism in Different Clinical Phenotypes.

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P2860

Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.

http://www.wikidata.org/entity/Q30502426

description

2011 nî lūn-bûn

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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2011 թվականի ապրիլին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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Enhanced subcortical spreading ...... c migraine type 1 mutant mice.

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Enhanced subcortical spreading ...... c migraine type 1 mutant mice.

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Enhanced subcortical spreading ...... c migraine type 1 mutant mice.

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Enhanced subcortical spreading ...... c migraine type 1 mutant mice.

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Enhanced subcortical spreading ...... c migraine type 1 mutant mice.

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Enhanced subcortical spreading ...... c migraine type 1 mutant mice.

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JNEUROSCI.5346-10.2011

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Enhanced subcortical spreading ...... c migraine type 1 mutant mice.

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Ergin Dilekoz

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Izumi Yuzawa

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Katharina Eikermann-Haerter

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Kwangyeol Baek

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Michael A Moskowitz

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Tao Qin

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Ulrike Hoffmann

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Young Ro Kim

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Yumei Wang

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P2860

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

Effects of Ca2+ channel blockers on cortical hypoperfusion and expression of c-Fos-like immunoreactivity after cortical spreading depression in rats

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

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10.1523/JNEUROSCI.5346-10.2011

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Michel D. Ferrari

Arn van den Maagdenberg

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Christian Waeber

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migraine disorder

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3135337

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