A citation-based method for searching scientific literature

M Wakamori, K Yamazaki, H Matsunodaira, T Teramoto, I Tanaka, T Niidome, K Sawada, Y Nishizawa, N Sekiguchi, E Mori, Y Mori, K Imoto. J. Biol. Chem. 1998
Times Cited: 150







List of co-cited articles
956 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Absence epilepsy in tottering mutant mice is associated with calcium channel defects.
C F Fletcher, C M Lutz, T N O'Sullivan, J D Shaughnessy, R Hawkes, W N Frankel, N G Copeland, N A Jenkins. Cell 1996
492
60

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
42

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
308
37

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
924
36


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
107
33

Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol)).
Y Mori, M Wakamori, S Oda, C F Fletcher, N Sekiguchi, E Mori, N G Copeland, N A Jenkins, K Matsushita, Z Matsuyama,[...]. J. Neurosci. 2000
116
28

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.
C F Fletcher, A Tottene, V A Lennon, S M Wilson, S J Dubel, R Paylor, D A Hosford, L Tessarollo, M W McEnery, D Pietrobon,[...]. FASEB J. 2001
119
25

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
67
35

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
384
24

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
93
25

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
201
24


Structure and regulation of voltage-gated Ca2+ channels.
W A Catterall. Annu. Rev. Cell Dev. Biol. 2000
20


Primary structure and functional expression from complementary DNA of a brain calcium channel.
Y Mori, T Friedrich, M S Kim, A Mikami, J Nakai, P Ruth, E Bosse, F Hofmann, V Flockerzi, T Furuichi. Nature 1991
584
18



Cerebellar cell degeneration in the leaner mutant mouse.
K Herrup, S L Wilczynski. Neuroscience 1982
131
17

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
395
17


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
247
17


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
116
16

Increased noise level of purkinje cell activities minimizes impact of their modulation during sensorimotor control.
F E Hoebeek, J S Stahl, A M van Alphen, M Schonewille, C Luo, M Rutteman, A M J M van den Maagdenberg, P C Molenaar, H H L M Goossens, M A Frens,[...]. Neuron 2005
100
16

Splicing of alpha 1A subunit gene generates phenotypic variants of P- and Q-type calcium channels.
E Bourinet, T W Soong, K Sutton, S Slaymaker, E Mathews, A Monteil, G W Zamponi, J Nargeot, T P Snutch. Nat. Neurosci. 1999
284
15

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
76
18




Calcium control of transmitter release at a cerebellar synapse.
I M Mintz, B L Sabatini, W G Regehr. Neuron 1995
392
13





Localization and functional properties of a rat brain alpha 1A calcium channel reflect similarities to neuronal Q- and P-type channels.
A Stea, W J Tomlinson, T W Soong, E Bourinet, S J Dubel, S R Vincent, T P Snutch. Proc. Natl. Acad. Sci. U.S.A. 1994
254
12

P-type calcium channels blocked by the spider toxin omega-Aga-IVA.
I M Mintz, V J Venema, K M Swiderek, T D Lee, B P Bean, M E Adams. Nature 1992
629
12

Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering.
Brandy E Fureman, H A Jinnah, Ellen J Hess. Pharmacol. Biochem. Behav. 2002
39
30


Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2.
S Guida, F Trettel, S Pagnutti, E Mantuano, A Tottene, L Veneziano, T Fellin, M Spadaro, K Stauderman, M Williams,[...]. Am. J. Hum. Genet. 2001
90
12

P/Q-type calcium channels mediate the activity-dependent feedback of syntaxin-1A.
K G Sutton, J E McRory, H Guthrie, T H Murphy, T P Snutch. Nature 1999
104
11

P-type calcium channels in rat central and peripheral neurons.
I M Mintz, M E Adams, B P Bean. Neuron 1992
578
11

Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha(1A) Ca(2+) channel mutation.
J J Plomp, M N Vergouwe, A M Van den Maagdenberg, M D Ferrari, R R Frants, P C Molenaar. Brain 2000
58
18



Neurotransmitter release from tottering mice nerve terminals with reduced expression of mutated P- and Q-type Ca2+-channels.
A G Miriam Leenders, Arn M J M van den Maagdenberg, Fernando H Lopes da Silva, Zu-Hang Sheng, Peter C Molenaar, Wim E J M Ghijsen. Eur. J. Neurosci. 2002
23
43


Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
J Jen, J Wan, M Graves, H Yu, A F Mock, C J Coulin, G Kim, Q Yue, D M Papazian, R W Baloh. Neurology 2001
78
12


Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function.
S Toru, T Murakoshi, K Ishikawa, H Saegusa, H Fujigasaki, T Uchihara, S Nagayama, M Osanai, H Mizusawa, T Tanabe. J. Biol. Chem. 2000
63
15


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.