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Search results 1 to 100 out of 382 for Cacna1a

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Type Details Score
Publication
17146767 | J:117062
First Author: Todorov B
Year: 2006
Journal: Genesis
Title: Conditional inactivation of the Cacna1a gene in transgenic mice.
Volume: 44
Issue: 12
Pages: 589-94
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Publication
22952933 | J:191648
First Author: Li W
Year: 2012
Journal: PLoS One
Title: New ataxic tottering-6j mouse allele containing a Cacna1a gene mutation.
Volume: 7
Issue: 8
Pages: e44230
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Publication
15003170 | J:88693
First Author: van den Maagdenberg AM
Year: 2004
Journal: Neuron
Title: A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Volume: 41
Issue: 5
Pages: 701-10
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Publication
23827678 | J:199996
First Author: Du X
Year: 2013
Journal: Cell
Title: Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6.
Volume: 154
Issue: 1
Pages: 118-33
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Publication
30649209 | J:294560
First Author: Loonen ICM
Year: 2019
Journal: Brain
Title: Brainstem spreading depolarization and cortical dynamics during fatal seizures in Cacna1a S218L mice.
Volume: 142
Issue: 2
Pages: 412-425
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Publication
21411672 | J:170451
First Author: Mark MD
Year: 2011
Journal: J Neurosci
Title: Delayed postnatal loss of P/Q-type calcium channels recapitulates the absence epilepsy, dyskinesia, and ataxia phenotypes of genomic Cacna1a mutations.
Volume: 31
Issue: 11
Pages: 4311-26
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Publication
24583041 | J:210330
 
First Author: Hullugundi SK
Year: 2014
Journal: Neuroscience
Title: A hyperexcitability phenotype in mouse trigeminal sensory neurons expressing the R192Q Cacna1a missense mutation of familial hemiplegic migraine type-1.
Volume: 266
Pages: 244-54
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Publication
11344116 | J:76459
First Author: Fletcher CF
Year: 2001
Journal: FASEB J
Title: Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.
Volume: 15
Issue: 7
Pages: 1288-90
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Publication
19854154 | J:155607
First Author: Saito H
Year: 2009
Journal: Biochem Biophys Res Commun
Title: Knockdown of Cav2.1 calcium channels is sufficient to induce neurological disorders observed in natural occurring Cacna1a mutants in mice.
Volume: 390
Issue: 3
Pages: 1029-33
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Publication
31800012 | J:293639
First Author: Miao QL
Year: 2020
Journal: Brain
Title: Adult loss of Cacna1a in mice recapitulates childhood absence epilepsy by distinct thalamic bursting mechanisms.
Volume: 143
Issue: 1
Pages: 161-174
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Publication
22005682 | J:191542
First Author: Fioretti B
Year: 2011
Journal: J Physiol
Title: Trigeminal ganglion neuron subtype-specific alterations of Ca(V)2.1 calcium current and excitability in a Cacna1a mouse model of migraine.
Volume: 589
Issue: Pt 23
Pages: 5879-95
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Publication
14657414 | -
First Author: Catterall WA
Year: 2003
Journal: Pharmacol Rev
Title: International Union of Pharmacology. XL. Compendium of voltage-gated ion channels: calcium channels.
Volume: 55
Issue: 4
Pages: 579-81
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Publication
11031246 | -
 
First Author: Catterall WA
Year: 2000
Journal: Annu Rev Cell Dev Biol
Title: Structure and regulation of voltage-gated Ca2+ channels.
Volume: 16
Pages: 521-55
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Publication
10774722 | J:61466
First Author: Ertel EA
Year: 2000
Journal: Neuron
Title: Nomenclature of voltage-gated calcium channels.
Volume: 25
Issue: 3
Pages: 533-5
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Publication
8825650 | -
First Author: Diriong S
Year: 1995
Journal: Genomics
Title: Chromosomal localization of the human genes for alpha 1A, alpha 1B, and alpha 1E voltage-dependent Ca2+ channel subunits.
Volume: 30
Issue: 3
Pages: 605-9
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Publication
16111830 | J:104354
First Author: Kaja S
Year: 2005
Journal: Neuroscience
Title: Gene dosage-dependent transmitter release changes at neuromuscular synapses of CACNA1A R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness.
Volume: 135
Issue: 1
Pages: 81-95
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Publication
23516282 | J:196594
First Author: Maejima T
Year: 2013
Journal: J Neurosci
Title: Postnatal loss of P/Q-type channels confined to rhombic-lip-derived neurons alters synaptic transmission at the parallel fiber to purkinje cell synapse and replicates genomic Cacna1a mutation phenotype of ataxia and seizures in mice.
Volume: 33
Issue: 12
Pages: 5162-74
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Publication
31628185 | J:282371
First Author: Jansen NA
Year: 2019
Journal: J Neurosci
Title: Apnea Associated with Brainstem Seizures in Cacna1a S218L Mice Is Caused by Medullary Spreading Depolarization.
Volume: 39
Issue: 48
Pages: 9633-9644
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Publication
- | J:198844
     
First Author: Harris BS
Year: 2013
Journal: MGI Direct Data Submission
Title: Small roller: A new recessive neurological mutation that maps to Chromosome 8
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Publication
- | J:267668
     
First Author: Keef J
Year: 2018
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for totter.
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Publication
19484318 | J:164112
First Author: Plomp JJ
Year: 2009
Journal: Cerebellum
Title: The ataxic Cacna1a-mutant mouse rolling nagoya: an overview of neuromorphological and electrophysiological findings.
Volume: 8
Issue: 3
Pages: 222-30
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Publication
18687887 | J:139488
First Author: Watase K
Year: 2008
Journal: Proc Natl Acad Sci U S A
Title: Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.
Volume: 105
Issue: 33
Pages: 11987-92
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Publication
16242631 | J:102801
First Author: Fureman BE
Year: 2005
Journal: Neurobiol Dis
Title: Noradrenergic blockade prevents attacks in a model of episodic dysfunction caused by a channelopathy.
Volume: 20
Issue: 2
Pages: 227-32
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30922876 | J:276254
First Author: Du X
Year: 2019
Journal: Neuron
Title: α1ACT Is Essential for Survival and Early Cerebellar Programming in a Critical Neonatal Window.
Volume: 102
Issue: 4
Pages: 770-785.e7
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Publication
24768804 | J:214010
 
First Author: Salvi J
Year: 2014
Journal: Neurobiol Dis
Title: RNAi silencing of P/Q-type calcium channels in Purkinje neurons of adult mouse leads to episodic ataxia type 2.
Volume: 68
Pages: 47-56
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Publication
34077522 | J:322324
First Author: Bohne P
Year: 2021
Journal: Hum Mol Genet
Title: Cognitive deficits in episodic ataxia type 2 mouse models.
Volume: 30
Issue: 19
Pages: 1811-1832
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Publication
11160387 | J:71860
First Author: Zwingman TA
Year: 2001
Journal: J Neurosci
Title: Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a.
Volume: 21
Issue: 4
Pages: 1169-78
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Publication
14724264 | J:194956
First Author: Stahl JS
Year: 2004
Journal: J Neurophysiol
Title: Eye movements of the murine P/Q calcium channel mutant rocker, and the impact of aging.
Volume: 91
Issue: 5
Pages: 2066-78
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31337678 | J:277450
First Author: Miyoshi C
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Methodology and theoretical basis of forward genetic screening for sleep/wakefulness in mice.
Volume: 116
Issue: 32
Pages: 16062-16067
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Publication
25109669 | J:217557
 
First Author: Rose SJ
Year: 2014
Journal: Exp Neurol
Title: The first knockin mouse model of episodic ataxia type 2.
Volume: 261
Pages: 553-62
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Publication
21870131 | J:234599
First Author: Todorov B
Year: 2012
Journal: Cerebellum
Title: Purkinje cell-specific ablation of Cav2.1 channels is sufficient to cause cerebellar ataxia in mice.
Volume: 11
Issue: 1
Pages: 246-58
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Publication
26887908 | J:278031
First Author: Kim TY
Year: 2016
Journal: Exp Anim
Title: Protein expression pattern in cerebellum of Cav2.1 mutant, tottering-6j mice.
Volume: 65
Issue: 3
Pages: 207-14
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20186955 | J:211767
First Author: van den Maagdenberg AM
Year: 2010
Journal: Ann Neurol
Title: High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.
Volume: 67
Issue: 1
Pages: 85-98
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Publication
19104150 | J:144701
First Author: Eikermann-Haerter K
Year: 2009
Journal: J Clin Invest
Title: Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1.
Volume: 119
Issue: 1
Pages: 99-109
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Publication
22956801 | J:333615
First Author: Inchauspe CG
Year: 2012
Journal: J Neurophysiol
Title: Presynaptic CaV2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held.
Volume: 108
Issue: 11
Pages: 2967-76
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Publication
35238776 | J:321889
   
First Author: Terpollili NA
Year: 2022
Journal: Elife
Title: CaV2.1 channel mutations causing familial hemiplegic migraine type 1 increase the susceptibility for cortical spreading depolarizations and seizures and worsen outcome after experimental traumatic brain injury.
Volume: 11
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26208839 | J:226272
 
First Author: Kaja S
Year: 2015
Journal: Neuroscience
Title: Differential cerebellar GABAA receptor expression in mice with mutations in CaV2.1 (P/Q-type) calcium channels.
Volume: 304
Pages: 198-208
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25716839 | J:219849
First Author: Dilekoz E
Year: 2015
Journal: J Neurosci
Title: Migraine mutations impair hippocampal learning despite enhanced long-term potentiation.
Volume: 35
Issue: 8
Pages: 3397-402
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21490217 | J:170969
First Author: Eikermann-Haerter K
Year: 2011
Journal: J Neurosci
Title: Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.
Volume: 31
Issue: 15
Pages: 5755-63
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25855180 | J:221681
First Author: Cramer SW
Year: 2015
Journal: J Neurosci
Title: Abnormal excitability and episodic low-frequency oscillations in the cerebral cortex of the tottering mouse.
Volume: 35
Issue: 14
Pages: 5664-79
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24849341 | J:211350
First Author: Di Guilmi MN
Year: 2014
Journal: J Neurosci
Title: 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.
Volume: 34
Issue: 21
Pages: 7047-58
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23115190 | J:192290
First Author: Gao Z
Year: 2012
Journal: J Neurosci
Title: Cerebellar ataxia by enhanced Ca(V)2.1 currents is alleviated by Ca2+-dependent K+-channel activators in Cacna1a(S218L) mutant mice.
Volume: 32
Issue: 44
Pages: 15533-46
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Publication
17513018 | J:140908
First Author: Alonso I
Year: 2008
Journal: Neurobiol Aging
Title: Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant.
Volume: 29
Issue: 11
Pages: 1733-43
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Publication
18093175 | J:132196
First Author: Ovsepian SV
Year: 2008
Journal: Eur J Neurosci
Title: The leaner P/Q-type calcium channel mutation renders cerebellar Purkinje neurons hyper-excitable and eliminates Ca2+-Na+ spike bursts.
Volume: 27
Issue: 1
Pages: 93-103
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Publication
17161543 | J:121290
First Author: Kaja S
Year: 2007
Journal: Neuroscience
Title: Characterization of acetylcholine release and the compensatory contribution of non-Ca(v)2.1 channels at motor nerve terminals of leaner Ca(v)2.1-mutant mice.
Volume: 144
Issue: 4
Pages: 1278-87
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Publication
36078147 | J:329002
 
First Author: Chang HHV
Year: 2022
Journal: Cells
Title: Loss of Flocculus Purkinje Cell Firing Precision Leads to Impaired Gaze Stabilization in a Mouse Model of Spinocerebellar Ataxia Type 6 (SCA6).
Volume: 11
Issue: 17
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Publication
17439489 | J:125038
First Author: Kaja S
Year: 2007
Journal: Eur J Neurosci
Title: Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya.
Volume: 25
Issue: 7
Pages: 2009-20
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Publication
19850086 | J:156904
First Author: Takahashi E
Year: 2010
Journal: Behav Brain Res
Title: Neonatal motor functions in Cacna1a-mutant rolling Nagoya mice.
Volume: 207
Issue: 2
Pages: 273-9
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Publication
17188510 | J:123243
First Author: Saegusa H
Year: 2007
Journal: Mol Cell Neurosci
Title: Properties of human Cav2.1 channel with a spinocerebellar ataxia type 6 mutation expressed in Purkinje cells.
Volume: 34
Issue: 2
Pages: 261-70
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17982453 | J:130784
First Author: Glasscock E
Year: 2007
Journal: Nat Neurosci
Title: Masking epilepsy by combining two epilepsy genes.
Volume: 10
Issue: 12
Pages: 1554-8
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Publication
25481823 | J:237437
 
First Author: Inchauspe CG
Year: 2015
Journal: Hear Res
Title: Familial hemiplegic migraine type-1 mutated cav2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice.
Volume: 319
Pages: 56-68
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Publication
24355314 | J:211481
 
First Author: Park J
Year: 2014
Journal: Neurobiol Dis
Title: Differential trigeminovascular nociceptive responses in the thalamus in the familial hemiplegic migraine 1 knock-in mouse: a Fos protein study.
Volume: 64
Pages: 1-7
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Publication
23451282 | J:199328
First Author: Stahl JS
Year: 2013
Journal: PLoS One
Title: 4-aminopyridine does not enhance flocculus function in tottering, a mouse model of vestibulocerebellar dysfunction and ataxia.
Volume: 8
Issue: 2
Pages: e57895
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Publication
18597946 | J:137816
First Author: Miki T
Year: 2008
Journal: Neuroscience
Title: Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.
Volume: 155
Issue: 1
Pages: 31-44
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Publication
26758833 | J:228867
First Author: Bomben VC
Year: 2016
Journal: J Neurosci
Title: Isolated P/Q Calcium Channel Deletion in Layer VI Corticothalamic Neurons Generates Absence Epilepsy.
Volume: 36
Issue: 2
Pages: 405-18
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11756409 | J:75166
First Author: Tsunemi T
Year: 2002
Journal: J Biol Chem
Title: Novel Cav2.1 splice variants isolated from Purkinje cells do not generate P-type Ca2+ current.
Volume: 277
Issue: 9
Pages: 7214-21
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17376154 | J:119639
First Author: Xie G
Year: 2007
Journal: Genes Brain Behav
Title: Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A.
Volume: 6
Issue: 8
Pages: 717-27
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24205277 | J:209226
First Author: Mallmann RT
Year: 2013
Journal: PLoS One
Title: Ablation of Ca(V)2.1 voltage-gated Ca²⁺ channels in mouse forebrain generates multiple cognitive impairments.
Volume: 8
Issue: 10
Pages: e78598
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23577145 | J:200145
First Author: Hullugundi SK
Year: 2013
Journal: PLoS One
Title: The mechanism of functional up-regulation of P2X3 receptors of trigeminal sensory neurons in a genetic mouse model of familial hemiplegic migraine type 1 (FHM-1).
Volume: 8
Issue: 4
Pages: e60677
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16381801 | J:135773
First Author: Kaja S
Year: 2006
Journal: J Neurophysiol
Title: Compensatory contribution of Cav2.3 channels to acetylcholine release at the neuromuscular junction of tottering mice.
Volume: 95
Issue: 4
Pages: 2698-704
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23426690 | J:195984
First Author: Koch H
Year: 2013
Journal: J Neurosci
Title: Stable respiratory activity requires both P/Q-type and N-type voltage-gated calcium channels.
Volume: 33
Issue: 8
Pages: 3633-45
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24758835 | J:303241
First Author: Yoshimoto T
Year: 2014
Journal: J Vet Med Sci
Title: Rolling Nagoya mouse strain (PROD-rol/rol) with classic piebald mutation.
Volume: 76
Issue: 8
Pages: 1093-8
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33305180 | J:306911
First Author: Yamashiro K
Year: 2020
Journal: iScience
Title: AUTS2 Governs Cerebellar Development, Purkinje Cell Maturation, Motor Function and Social Communication.
Volume: 23
Issue: 12
Pages: 101820
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Publication
- | J:338850
     
First Author: Meyer KJ
Year: 2023
Journal: MGI Direct Data Submission
Title: Direct Data Submission of Multiple Allele.
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23595603 | J:317577
First Author: Rossignol E
Year: 2013
Journal: Ann Neurol
Title: CaV 2.1 ablation in cortical interneurons selectively impairs fast-spiking basket cells and causes generalized seizures.
Volume: 74
Issue: 2
Pages: 209-22
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10381343 | J:55900
First Author: Takahashi E
Year: 1999
Journal: Biochem Biophys Res Commun
Title: Isolation and functional characterization of the 5'-upstream region of mouse P/Q-type Ca2+ channel alpha1A subunit gene.
Volume: 260
Issue: 1
Pages: 54-9
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35853721 | J:330240
     
First Author: Bohne P
Year: 2022
Journal: J Neurosci
Title: Deletion of the P/Q-type calcium channel from serotonergic neurons drives male aggression in mice.
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28688851 | J:258570
 
First Author: Dorgans K
Year: 2017
Journal: Neurobiol Dis
Title: Characterization of the dominant inheritance mechanism of Episodic Ataxia type 2.
Volume: 106
Pages: 110-123
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17156361 | J:117068
First Author: Kodama T
Year: 2006
Journal: Eur J Neurosci
Title: A CaV2.1 calcium channel mutation rocker reduces the number of postsynaptic AMPA receptors in parallel fiber-Purkinje cell synapses.
Volume: 24
Issue: 11
Pages: 2993-3007
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28510727 | J:243499
First Author: Aikawa T
Year: 2017
Journal: Hum Mol Genet
Title: Alternative splicing in the C-terminal tail of Cav2.1 is essential for preventing a neurological disease in mice.
Volume: 26
Issue: 16
Pages: 3094-3104
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- | J:275973
     
First Author: Funato H
Year: 2019
Journal: MGI Direct Data Submission
Title: Direct Data Submission for Drowsy
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16890369 | J:113141
First Author: Luvisetto S
Year: 2006
Journal: Neuroscience
Title: Pain sensitivity in mice lacking the Ca(v)2.1alpha1 subunit of P/Q-type Ca2+ channels.
Volume: 142
Issue: 3
Pages: 823-32
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25150573 | J:218311
First Author: Marinelli S
Year: 2015
Journal: Neurobiol Aging
Title: Effects of age-related loss of P/Q-type calcium channels in a mice model of peripheral nerve injury.
Volume: 36
Issue: 1
Pages: 352-64
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Publication
22850483 | J:233263
 
First Author: Raike RS
Year: 2013
Journal: Neurobiol Dis
Title: Limited regional cerebellar dysfunction induces focal dystonia in mice.
Volume: 49
Pages: 200-10
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28786379 | J:258998
   
First Author: Lübbert M
Year: 2017
Journal: Elife
Title: A novel region in the CaV2.1 α1 subunit C-terminus regulates fast synaptic vesicle fusion and vesicle docking at the mammalian presynaptic active zone.
Volume: 6
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33850125 | J:333602
First Author: Tamim I
Year: 2021
Journal: Nat Commun
Title: Spreading depression as an innate antiseizure mechanism.
Volume: 12
Issue: 1
Pages: 2206
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15090043 | J:155724
First Author: Kulik A
Year: 2004
Journal: Eur J Neurosci
Title: Immunocytochemical localization of the alpha 1A subunit of the P/Q-type calcium channel in the rat cerebellum.
Volume: 19
Issue: 8
Pages: 2169-78
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16472880 | J:112757
First Author: Goto J
Year: 2006
Journal: Neurosci Res
Title: Short-term potentiation at the parallel fiber-Purkinje cell synapse.
Volume: 55
Issue: 1
Pages: 28-33
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Publication
26002462 | J:221102
First Author: Kim TY
Year: 2015
Journal: Biochem Biophys Res Commun
Title: Absence-like seizures and their pharmacological profile in tottering-6j mice.
Volume: 463
Issue: 1-2
Pages: 148-53
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Publication
27857685 | J:279634
 
First Author: Jung D
Year: 2016
Journal: Front Behav Neurosci
Title: Conditional Knockout of Cav2.1 Disrupts the Accuracy of Spatial Recognition of CA1 Place Cells and Spatial/Contextual Recognition Behavior.
Volume: 10
Pages: 214
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Publication
22144569 | J:193793
First Author: Eikermann-Haerter K
Year: 2012
Journal: Circulation
Title: Migraine mutations increase stroke vulnerability by facilitating ischemic depolarizations.
Volume: 125
Issue: 2
Pages: 335-45
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Publication
28363781 | J:244073
 
First Author: Eroli F
Year: 2017
Journal: Neuroscience
Title: Hyperpolarization-activated current Ih in mouse trigeminal sensory neurons in a transgenic mouse model of familial hemiplegic migraine type-1.
Volume: 351
Pages: 47-64
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Publication
20937883 | J:165507
First Author: Adams PJ
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: Contribution of calcium-dependent facilitation to synaptic plasticity revealed by migraine mutations in the P/Q-type calcium channel.
Volume: 107
Issue: 43
Pages: 18694-9
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Publication
24907493 | J:214741
 
First Author: Vecchia D
Year: 2014
Journal: Neurobiol Dis
Title: Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2.1 knockin migraine mice.
Volume: 69
Pages: 225-34
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Publication
35863891 | J:330239
     
First Author: Marchionni I
Year: 2022
Journal: J Neurosci
Title: Enhanced Feedback Inhibition Due to Increased Recruitment of Somatostatin-Expressing Interneurons and Enhanced Cortical Recurrent Excitation in a Genetic Mouse Model of Migraine.
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Publication
15743764 | J:145848
First Author: Tottene A
Year: 2005
Journal: J Biol Chem
Title: 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.
Volume: 280
Issue: 18
Pages: 17678-86
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Publication
25447936 | J:218777
 
First Author: Shyti R
Year: 2015
Journal: Exp Neurol
Title: Stress hormone corticosterone enhances susceptibility to cortical spreading depression in familial hemiplegic migraine type 1 mutant mice.
Volume: 263
Pages: 214-20
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Publication
19285472 | J:157368
First Author: Tottene A
Year: 2009
Journal: Neuron
Title: Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.
Volume: 61
Issue: 5
Pages: 762-73
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Publication
31645463 | J:282327
First Author: Tottene A
Year: 2019
Journal: J Neurosci
Title: Enhanced Thalamocortical Synaptic Transmission and Dysregulation of the Excitatory-Inhibitory Balance at the Thalamocortical Feedforward Inhibitory Microcircuit in a Genetic Mouse Model of Migraine.
Volume: 39
Issue: 49
Pages: 9841-9851
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Publication
- | J:161271
     
First Author: Harris B
Year: 2010
Journal: MGI Direct Data Submission
Title: Cacna1atg-7J; a neurological mutation on Chromosome 8.
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Publication
26755594 | J:229923
First Author: Nanou E
Year: 2016
Journal: Proc Natl Acad Sci U S A
Title: Calcium sensor regulation of the CaV2.1 Ca2+ channel contributes to short-term synaptic plasticity in hippocampal neurons.
Volume: 113
Issue: 4
Pages: 1062-7
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Publication
26755585 | J:229926
First Author: Nanou E
Year: 2016
Journal: Proc Natl Acad Sci U S A
Title: Altered short-term synaptic plasticity and reduced muscle strength in mice with impaired regulation of presynaptic CaV2.1 Ca2+ channels.
Volume: 113
Issue: 4
Pages: 1068-73
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Publication
27799552 | J:279162
First Author: Nanou E
Year: 2016
Journal: Proc Natl Acad Sci U S A
Title: Calcium sensor regulation of the CaV2.1 Ca2+ channel contributes to long-term potentiation and spatial learning.
Volume: 113
Issue: 46
Pages: 13209-13214
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13950100 | J:262
 
First Author: GREEN MC
Year: 1962
Journal: J Hered
Title: Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism.
Volume: 53
Pages: 233-7
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11166370 | J:102977
First Author: Colliver TL
Year: 2001
Journal: J Neurosci Methods
Title: Amperometric analysis of exocytosis at chromaffin cells from genetically distinct mice.
Volume: 105
Issue: 1
Pages: 95-103
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First Author: Sawada K
Year: 2000
Journal: Congenit Anom (Kyoto)
Title: Ataxic mutant mice with defects in Ca2+ channel alpha-1A subunit gene: morphological and functional abnormalities in cerebellar cortical neurons.
Volume: 40
Pages: 99-107
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Publication
16540584 | J:106709
First Author: Sasaki S
Year: 2006
Journal: J Neurosci
Title: Impaired feedforward inhibition of the thalamocortical projection in epileptic Ca2+ channel mutant mice, tottering.
Volume: 26
Issue: 11
Pages: 3056-65
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10686170 | J:102080
 
First Author: Plomp JJ
Year: 2000
Journal: Brain
Title: Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha(1A) Ca(2+) channel mutation.
Volume: 123 Pt 3
Pages: 463-71
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10218773 | J:106598
First Author: Rhyu IJ
Year: 1999
Journal: Neuroscience
Title: An ultrastructural study of granule cell/Purkinje cell synapses in tottering (tg/tg), leaner (tg(la)/tg(la)) and compound heterozygous tottering/leaner (tg/tg(la)) mice.
Volume: 90
Issue: 3
Pages: 717-28
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First Author: Kostopoulos GK
Year: 1992
Journal: J Neural Transm Suppl
Title: Possible mechanisms underlying hyperexcitability in the epileptic mutant mouse tottering.
Volume: 35
Pages: 109-24
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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