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Times Cited: 582
Times Cited: 582
Times Cited
Times Co-cited
Similarity
Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit.
K Jun, E S Piedras-Rentería, S M Smith, D B Wheeler, S B Lee, T G Lee, H Chin, M E Adams, R H Scheller, R W Tsien,[...]. Proc Natl Acad Sci U S A 1999
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Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering.
J L Noebels, R L Sidman. Science 1979
J L Noebels, R L Sidman. Science 1979
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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
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22
Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel.
M Wakamori, K Yamazaki, H Matsunodaira, T Teramoto, I Tanaka, T Niidome, K Sawada, Y Nishizawa, N Sekiguchi, E Mori,[...]. J Biol Chem 1998
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Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
A Jouvenceau, L H Eunson, A Spauschus, V Ramesh, S M Zuberi, D M Kullmann, M G Hanna. Lancet 2001
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18
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
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Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.
D L Burgess, J M Jones, M H Meisler, J L Noebels. Cell 1997
D L Burgess, J M Jones, M H Meisler, J L Noebels. Cell 1997
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Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol)).
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Role of the alpha1G T-type calcium channel in spontaneous absence seizures in mutant mice.
Inseon Song, Daesoo Kim, Soonwook Choi, Minjeong Sun, Yeongin Kim, Hee-Sup Shin. J Neurosci 2004
Inseon Song, Daesoo Kim, Soonwook Choi, Minjeong Sun, Yeongin Kim, Hee-Sup Shin. J Neurosci 2004
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Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a.
T A Zwingman, P E Neumann, J L Noebels, K Herrup. J Neurosci 2001
T A Zwingman, P E Neumann, J L Noebels, K Herrup. J Neurosci 2001
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Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia.
Joy T Walter, Karina Alviña, Mary D Womack, Carolyn Chevez, Kamran Khodakhah. Nat Neurosci 2006
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Presynaptic Ca(2+) influx at a mouse central synapse with Ca(2+) channel subunit mutations.
J Qian, J L Noebels. J Neurosci 2000
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Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
Paola Imbrici, Stephen L Jaffe, Louise H Eunson, Nicholas P Davies, Colin Herd, Robert Robertson, Dimitri M Kullmann, Michael G Hanna. Brain 2004
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Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy.
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13
Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.
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Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalami.
S J Caddick, C Wang, C F Fletcher, N A Jenkins, N G Copeland, D A Hosford. J Neurophysiol 1999
S J Caddick, C Wang, C F Fletcher, N A Jenkins, N G Copeland, D A Hosford. J Neurophysiol 1999
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Mutations in high-voltage-activated calcium channel genes stimulate low-voltage-activated currents in mouse thalamic relay neurons.
Yi Zhang, Mayra Mori, Daniel L Burgess, Jeffrey L Noebels. J Neurosci 2002
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Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.
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Cortical focus drives widespread corticothalamic networks during spontaneous absence seizures in rats.
Hanneke K M Meeren, Jan Pieter M Pijn, Egidius L J M Van Luijtelaar, Anton M L Coenen, Fernando H Lopes da Silva. J Neurosci 2002
Hanneke K M Meeren, Jan Pieter M Pijn, Egidius L J M Van Luijtelaar, Anton M L Coenen, Fernando H Lopes da Silva. J Neurosci 2002
12
Delayed postnatal loss of P/Q-type calcium channels recapitulates the absence epilepsy, dyskinesia, and ataxia phenotypes of genomic Cacna1a mutations.
Melanie D Mark, Takashi Maejima, Denise Kuckelsberg, Jong W Yoo, Robert A Hyde, Viral Shah, Davina Gutierrez, Rosa L Moreno, Wolfgang Kruse, Jeffrey L Noebels,[...]. J Neurosci 2011
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20
Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells.
J Barclay, N Balaguero, M Mione, S L Ackerman, V A Letts, J Brodbeck, C Canti, A Meir, K M Page, K Kusumi,[...]. J Neurosci 2001
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Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner.
N M Lorenzon, C M Lutz, W N Frankel, K G Beam. J Neurosci 1998
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Primary episodic ataxias: diagnosis, pathogenesis and treatment.
J C Jen, T D Graves, E J Hess, M G Hanna, R C Griggs, R W Baloh. Brain 2007
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Childhood absence epilepsy: genes, channels, neurons and networks.
Vincenzo Crunelli, Nathalie Leresche. Nat Rev Neurosci 2002
Vincenzo Crunelli, Nathalie Leresche. Nat Rev Neurosci 2002
10
A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy.
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Molecular physiology of low-voltage-activated t-type calcium channels.
Edward Perez-Reyes. Physiol Rev 2003
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Association between genetic variation of CACNA1H and childhood absence epilepsy.
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Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channels.
R E Westenbroek, T Sakurai, E M Elliott, J W Hell, T V Starr, T P Snutch, W A Catterall. J Neurosci 1995
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10
Deep layer somatosensory cortical neurons initiate spike-and-wave discharges in a genetic model of absence seizures.
Pierre-Olivier Polack, Isabelle Guillemain, Emilie Hu, Colin Deransart, Antoine Depaulis, Stéphane Charpier. J Neurosci 2007
Pierre-Olivier Polack, Isabelle Guillemain, Emilie Hu, Colin Deransart, Antoine Depaulis, Stéphane Charpier. J Neurosci 2007
10
Bidirectional alterations in cerebellar synaptic transmission of tottering and rolling Ca2+ channel mutant mice.
Kaori Matsushita, Minoru Wakamori, Im Joo Rhyu, Tatsuo Arii, Sen-Ichi Oda, Yasuo Mori, Keiji Imoto. J Neurosci 2002
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The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.
V A Letts, R Felix, G H Biddlecome, J Arikkath, C L Mahaffey, A Valenzuela, F S Bartlett, Y Mori, K P Campbell, W N Frankel. Nat Genet 1998
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A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
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The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
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Deletion of the K(V)1.1 potassium channel causes epilepsy in mice.
S L Smart, V Lopantsev, C L Zhang, C A Robbins, H Wang, S Y Chiu, P A Schwartzkroin, A Messing, B L Tempel. Neuron 1998
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Pathophysiological mechanisms of genetic absence epilepsy in the rat.
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Genetic enhancement of thalamocortical network activity by elevating alpha 1g-mediated low-voltage-activated calcium current induces pure absence epilepsy.
Wayne L Ernst, Yi Zhang, Jong W Yoo, Sara J Ernst, Jeffrey L Noebels. J Neurosci 2009
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Selective increase in T-type calcium conductance of reticular thalamic neurons in a rat model of absence epilepsy.
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Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering.
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Increased noise level of purkinje cell activities minimizes impact of their modulation during sensorimotor control.
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Impaired feedforward inhibition of the thalamocortical projection in epileptic Ca2+ channel mutant mice, tottering.
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Absence epilepsy and sinus dysrhythmia in mice lacking the pacemaker channel HCN2.
Andreas Ludwig, Thomas Budde, Juliane Stieber, Sven Moosmang, Christian Wahl, Knut Holthoff, Anke Langebartels, Carsten Wotjak, Thomas Munsch, Xiangang Zong,[...]. EMBO J 2003
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Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures.
R H Wallace, C Marini, S Petrou, L A Harkin, D N Bowser, R G Panchal, D A Williams, G R Sutherland, J C Mulley, I E Scheffer,[...]. Nat Genet 2001
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Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy.
Houman Khosravani, Christophe Altier, Brett Simms, Kevin S Hamming, Terrance P Snutch, Janette Mezeyova, John E McRory, Gerald W Zamponi. J Biol Chem 2004
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8
The neural substrates of rapid-onset Dystonia-Parkinsonism.
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Lack of the burst firing of thalamocortical relay neurons and resistance to absence seizures in mice lacking alpha(1G) T-type Ca(2+) channels.
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8
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.