A citation-based method for searching scientific literature

Daniela Pietrobon. Mol Neurobiol 2002
Times Cited: 140







List of co-cited articles
1457 articles co-cited >1



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  Times     Co-cited
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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
31

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
28

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
585
26

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
354
24

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

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
450
19

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
333
18

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
467
18

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
173
17

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
129
14

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
264
14


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
136
13

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
805
12


The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
371
12

Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia.
Edwin Wappl, Alexandra Koschak, Michael Poteser, Martina J Sinnegger, Doris Walter, Andreas Eberhart, Klaus Groschner, Hartmut Glossmann, Richard L Kraus, Manfred Grabner,[...]. J Biol Chem 2002
77
15

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
151
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
83
13

P-type calcium channels in rat central and peripheral neurons.
I M Mintz, M E Adams, B P Bean. Neuron 1992
721
11



International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels.
William A Catterall, Edward Perez-Reyes, Terrance P Snutch, Joerg Striessnig. Pharmacol Rev 2005
853
11

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine.
M Hans, S Luvisetto, M E Williams, M Spagnolo, A Urrutia, A Tottene, P F Brust, E C Johnson, M M Harpold, K A Stauderman,[...]. J Neurosci 1999
190
11


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
285
11

Systematic identification of splice variants in human P/Q-type channel alpha1(2.1) subunits: implications for current density and Ca2+-dependent inactivation.
Tuck Wah Soong, Carla D DeMaria, Rebecca S Alvania, Larry S Zweifel, Mui Cheng Liang, Scott Mittman, William S Agnew, David T Yue. J Neurosci 2002
108
10

Nomenclature of voltage-gated calcium channels.
E A Ertel, K P Campbell, M M Harpold, F Hofmann, Y Mori, E Perez-Reyes, A Schwartz, T P Snutch, T Tanabe, L Birnbaumer,[...]. Neuron 2000
686
10

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
96
10


C-termini of P/Q-type Ca2+ channel alpha1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity.
Holly B Kordasiewicz, Randall M Thompson, H Brent Clark, Christopher M Gomez. Hum Mol Genet 2006
97
10

Neurobiology of migraine.
Daniela Pietrobon, Jörg Striessnig. Nat Rev Neurosci 2003
387
10


Developmental activation of calmodulin-dependent facilitation of cerebellar P-type Ca2+ current.
Dipayan Chaudhuri, Badr A Alseikhan, Siao Yun Chang, Tuck Wah Soong, David T Yue. J Neurosci 2005
52
17

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
764
9

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
72
12

Auxiliary subunits: essential components of the voltage-gated calcium channel complex.
Jyothi Arikkath, Kevin P Campbell. Curr Opin Neurobiol 2003
370
9


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
206
9

Ca2+/calmodulin binds to and modulates P/Q-type calcium channels.
A Lee, S T Wong, D Gallagher, B Li, D R Storm, T Scheuer, W A Catterall. Nature 1999
396
9

Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels.
J Platzer, J Engel, A Schrott-Fischer, K Stephan, S Bova, H Chen, H Zheng, J Striessnig. Cell 2000
623
9

Calcium control of transmitter release at a cerebellar synapse.
I M Mintz, B L Sabatini, W G Regehr. Neuron 1995
429
9

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.
Angelita Tottene, Tommaso Fellin, Stefano Pagnutti, Siro Luvisetto, Joerg Striessnig, Colin Fletcher, Daniela Pietrobon. Proc Natl Acad Sci U S A 2002
183
9

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
109
9

Altered properties of quantal neurotransmitter release at endplates of mice lacking P/Q-type Ca2+ channels.
Francisco J Urbano, Erika S Piedras-Rentería, Kisun Jun, Hee-Sup Shin, Osvaldo D Uchitel, Richard W Tsien. Proc Natl Acad Sci U S A 2003
103
9

The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution.
John E McRory, Jawed Hamid, Clinton J Doering, Esperanza Garcia, Robin Parker, Kevin Hamming, Lina Chen, Michael Hildebrand, Aaron M Beedle, Laura Feldcamp,[...]. J Neurosci 2004
146
8

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
A Ducros, C Denier, A Joutel, K Vahedi, A Michel, F Darcel, M Madigand, D Guerouaou, F Tison, J Julien,[...]. Am J Hum Genet 1999
118
8



Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
E E Kors, G M Terwindt, F L Vermeulen, R B Fitzsimons, P E Jardine, P Heywood, S Love, A M van den Maagdenberg, J Haan, R R Frants,[...]. Ann Neurol 2001
236
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.