Absence epilepsy in tottering mutant mice is associated with calcium channel defects
about
Cloning, characterization, and chromosomal location of a novel human K+-Cl- cotransporterSpinocerebellar ataxia type 6 mutation alters P-type calcium channel functionMolecular characterization of a neuronal low-voltage-activated T-type calcium channelStructural elements in domain IV that influence biophysical and pharmacological properties of human alpha1A-containing high-voltage-activated calcium channels.Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden micePhysio-pathological roles of transglutaminase-catalyzed reactionsSynaptic targeting of N-type calcium channels in hippocampal neuronsLinkage and association analysis of CACNG3 in childhood absence epilepsyThe basal ganglia and cerebellum interact in the expression of dystonic movementThe ducky(2J) mutation in Cacna2d2 results in reduced spontaneous Purkinje cell activity and altered gene expressionProgressive ataxia due to a missense mutation in a calcium-channel geneFamilial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16'Medusa head ataxia': the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 2: Anti-PKC-gamma, anti-GluR-delta2, anti-Ca/ARHGAP26 and anti-VGCCPurkinje cell stripes and long-term depression at the parallel fiber-Purkinje cell synapseDisruption of learned timing in P/Q calcium channel mutantsModal gating of human CaV2.1 (P/Q-type) calcium channels: I. The slow and the fast gating modes and their modulation by beta subunitsThree new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kineticsAssociation of neuronal calcium channels with modular adaptor proteinsDelayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraineSpecific 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 traumaAutosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?Protein mutated in paroxysmal dyskinesia interacts with the active zone protein RIM and suppresses synaptic vesicle exocytosisProtein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiPMutations in EFHC1 cause juvenile myoclonic epilepsySuppression of inflammatory and neuropathic pain symptoms in mice lacking the N-type Ca2+ channel.Characterization of acute somatosensory pain transmission in P/Q-type Ca(2+) channel mutant mice, leanerSingle tottering mutations responsible for the neuropathic phenotype of the P-type calcium channelIncreased serotonergic innervation of lumbosacral motoneurons of rolling mouse Nagoya in correlation with abnormal hindlimb extensionAltered calcium homeostasis in cerebellar Purkinje cells of leaner mutant micedsu functions in a MYO5A-independent pathway to suppress the coat color of dilute miceFGF14 regulates presynaptic Ca2+ channels and synaptic transmissionClass A calcium channel variants in pancreatic islets and their role in insulin secretionNovel Cav2.1 splice variants isolated from Purkinje cells do not generate P-type Ca2+ currentAltered expression and assembly of N-type calcium channel alpha1B and beta subunits in epileptic lethargic (lh/lh) mouseExcitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalamiAblation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunitA perforated patch-clamp study of calcium currents and exocytosis in chromaffin cells of wild-type and alpha(1A) knockout miceA mutation in Rab27a causes the vesicle transport defects observed in ashen miceThe ß subunit of voltage-gated Ca2+ channelsRole of voltage-gated calcium channels in epilepsy.
P2860
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P2860
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
description
1996 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1996
@ast
im November 1996 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1996/11/15)
@sk
vědecký článek publikovaný v roce 1996
@cs
wetenschappelijk artikel (gepubliceerd op 1996/11/15)
@nl
наукова стаття, опублікована в листопаді 1996
@uk
مقالة علمية (نشرت في 15-11-1996)
@ar
name
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@ast
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@en
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@nl
type
label
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@ast
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@en
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@nl
prefLabel
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@ast
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@en
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@nl
P2093
P3181
P1433
P1476
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
@en
P2093
C. F. Fletcher
C. M. Lutz
J. D. Shaughnessy
N. A. Jenkins
N. G. Copeland
T. N. O'Sullivan
W. N. Frankel
P304
P3181
P356
10.1016/S0092-8674(00)81381-1
P407
P577
1996-11-15T00:00:00Z