Pages that link to "Q34560191"
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The following pages link to Calcium channels and channelopathies of the central nervous system (Q34560191):
Displaying 50 items.
- Ca2 -dependent modulation of voltage-gated Ca2 channels (Q21564049) (← links)
- C-termini of P/Q-type Ca2 channel alpha1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity (Q24314234) (← links)
- Systematic identification of splice variants in human P/Q-type channel alpha1(2.1) subunits: implications for current density and Ca2 -dependent inactivation (Q24321661) (← links)
- Familial hemiplegic migraine mutations increase Ca(2 ) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons (Q24538702) (← links)
- The cerebellum and migraine (Q24628942) (← links)
- 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) (← links)
- A short history of voltage-gated calcium channels (Q24670360) (← links)
- Genetic neurological channelopathies: molecular genetics and clinical phenotypes (Q26777559) (← links)
- The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential (Q26781422) (← links)
- Cell biology of spinocerebellar ataxia (Q26829511) (← links)
- Modal gating of human CaV2.1 (P/Q-type) calcium channels: I. The slow and the fast gating modes and their modulation by beta subunits (Q27863796) (← links)
- 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 (Q28237739) (← links)
- Gating deficiency in a familial hemiplegic migraine type 1 mutant P/Q-type calcium channel (Q28241997) (← links)
- Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2 channel gating: evidence for beta-subunit isoform-specific effects (Q28284668) (← links)
- The neuronal beta 4 subunit increases the unitary conductance of L-type voltage-gated calcium channels in PC12 cells (Q28572130) (← links)
- Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia (Q28586378) (← links)
- The β Subunit of Voltage-Gated Ca2 Channels (Q30155988) (← links)
- Role of voltage-gated calcium channels in epilepsy. (Q30427731) (← links)
- Ophthalmologic migraine (Q30712143) (← links)
- Neurobiology of migraine. (Q33186891) (← links)
- Migraine: new molecular mechanisms (Q33220839) (← links)
- Familial hemiplegic migraine (Q33280531) (← links)
- Insights into migraine mechanisms and CaV2.1 calcium channel function from mouse models of familial hemiplegic migraine (Q33535616) (← links)
- CaV2.1 channelopathies (Q33537218) (← links)
- Biological science of headache channels (Q33684226) (← links)
- Calcium Channel CaVα₁ Splice Isoforms - Tissue Specificity and Drug Action (Q33719513) (← links)
- Differential regulation of Purkinje cell dendritic spines in rolling mouse Nagoya (tg/tg), P/Q type calcium channel (α1(A)/Ca(v)2.1) mutant (Q33787960) (← links)
- Genetic Analysis of a Synaptic Calcium Channel in Drosophila: Intragenic Modifiers of a Temperature-Sensitive Paralytic Mutant of cacophony (Q34617490) (← links)
- Functional diversity in neuronal voltage-gated calcium channels by alternative splicing of Ca(v)alpha1. (Q34976636) (← links)
- Transcriptomic analysis of the effects of a fish oil enriched diet on murine brains (Q35121792) (← links)
- When calcium goes wrong: genetic alterations of a ubiquitous signaling route (Q35140775) (← links)
- Role of hydrogen sulfide in brain synaptic remodeling (Q35166466) (← links)
- Molecular dynamics and mutational analysis of a channelopathy mutation in the IIS6 helix of Ca V 1.2. (Q35390926) (← links)
- Neurotransmitter modulation of neuronal calcium channels. (Q35682291) (← links)
- In vivo analysis of voltage-dependent calcium channels (Q35682326) (← links)
- Ca2 channels as targets of neurological disease: Lambert-Eaton Syndrome and other Ca2 channelopathies (Q35682330) (← links)
- Future pharmacologic targets for acute and preventive treatments of migraine (Q36106970) (← links)
- Migraine and genetic polymorphisms: an overview (Q36210660) (← links)
- An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation (Q36250792) (← links)
- Altered functional expression of Purkinje cell calcium channels precedes motor dysfunction in tottering mice. (Q36387934) (← links)
- Molecular basis of inherited calcium channelopathies: role of mutations in pore-forming subunits (Q36513343) (← links)
- Voltage-gated calcium channels and idiopathic generalized epilepsies. (Q36525559) (← links)
- The role of botulinum toxin in whiplash injuries (Q36582832) (← links)
- Molecular pathogenesis of spinocerebellar ataxia type 6. (Q36774733) (← links)
- Current trends in migraine prophylaxis (Q36787468) (← links)
- Pathophysiology of HCN channels (Q36840738) (← links)
- The sequence of events that underlie quantal transmission at central glutamatergic synapses (Q36885427) (← links)
- Low-frequency oscillations in the cerebellar cortex of the tottering mouse (Q37086565) (← links)
- Large conductance calcium-activated potassium channels affect both spontaneous firing and intracellular calcium concentration in cerebellar Purkinje neurons (Q37295584) (← links)
- The ataxic Cacna1a-mutant mouse rolling nagoya: an overview of neuromorphological and electrophysiological findings (Q37502776) (← links)