A citation-based method for searching scientific literature

Robert S Raike, Holly B Kordasiewicz, Randall M Thompson, Christopher M Gomez. Mol Cell Neurosci 2007
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity


A destructive interaction mechanism accounts for dominant-negative effects of misfolded mutants of voltage-gated calcium channels.
Alexandre Mezghrani, Arnaud Monteil, Katrin Watschinger, Martina J Sinnegger-Brauns, Christian Barrère, Emmanuel Bourinet, Joël Nargeot, Jörg Striessnig, Philippe Lory. J Neurosci 2008
58
66

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
61

Dominant-negative calcium channel suppression by truncated constructs involves a kinase implicated in the unfolded protein response.
Karen M Page, Fay Heblich, Anthony Davies, Adrian J Butcher, Jerôme Leroy, Federica Bertaso, Wendy S Pratt, Annette C Dolphin. J Neurosci 2004
69
57


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
352
47

Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2.
Chung-Jiuan Jeng, Yu-Ting Chen, Yi-Wen Chen, Chih-Yung Tang. Am J Physiol Cell Physiol 2006
38
47

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
99
42

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
260
42

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
108
42

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134
42

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
177
38

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
75
38

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
38

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
135
33

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
270
33

Dominant-negative synthesis suppression of voltage-gated calcium channel Cav2.2 induced by truncated constructs.
A Raghib, F Bertaso, A Davies, K M Page, A Meir, Y Bogdanov, A C Dolphin. J Neurosci 2001
74
33

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
198
33

Structure and regulation of voltage-gated Ca2+ channels.
W A Catterall. Annu Rev Cell Dev Biol 2000
33

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
33

N terminus is key to the dominant negative suppression of Ca(V)2 calcium channels: implications for episodic ataxia type 2.
Karen M Page, Fay Heblich, Wojciech Margas, Wendy S Pratt, Manuela Nieto-Rostro, Kanchan Chaggar, Kieran Sandhu, Anthony Davies, Annette C Dolphin. J Biol Chem 2010
41
33

CACNA1A mutations causing episodic and progressive ataxia alter channel trafficking and kinetics.
J Wan, R Khanna, M Sandusky, D M Papazian, J C Jen, R W Baloh. Neurology 2005
38
28

Episodic ataxia type 2.
Michael Strupp, Andreas Zwergal, Thomas Brandt. Neurotherapeutics 2007
96
28

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
148
28

Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy.
Yu-Qing Cao, Erika S Piedras-Rentería, Geoffrey B Smith, Gong Chen, Nobutoshi C Harata, Richard W Tsien. Neuron 2004
124
28

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
331
28

Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2.
R A Maselli, J Wan, V Dunne, M Graves, R W Baloh, R L Wollmann, J Jen. Neurology 2003
30
23


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
23

Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.
Kei Watase, Curtis F Barrett, Taisuke Miyazaki, Taro Ishiguro, Kinya Ishikawa, Yuanxin Hu, Toshinori Unno, Yaling Sun, Sayumi Kasai, Masahiko Watanabe,[...]. Proc Natl Acad Sci U S A 2008
104
23

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
92
23

Functional implications of a novel EA2 mutation in the P/Q-type calcium channel.
Sian D Spacey, Michael E Hildebrand, Luke A Materek, Thomas D Bird, Terrance P Snutch. Ann Neurol 2004
54
19

Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic ataxia 2.
E Mantuano, L Veneziano, M Spadaro, P Giunti, S Guida, M G Leggio, L Verriello, N Wood, C Jodice, M Frontali. J Med Genet 2004
33
19


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
583
19

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
19

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.
C Denier, A Ducros, K Vahedi, A Joutel, P Thierry, A Ritz, G Castelnovo, T Deonna, P Gérard, J L Devoize,[...]. Neurology 1999
145
19

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
669
19

Increased expression of alpha 1A Ca2+ channel currents arising from expanded trinucleotide repeats in spinocerebellar ataxia type 6.
E S Piedras-Renteria, K Watase, N Harata, O Zhuchenko, H Y Zoghbi, C C Lee, R W Tsien. J Neurosci 2001
69
19

Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2.
Tracey D Graves, Paola Imbrici, Esther E Kors, Gisela M Terwindt, Louise H Eunson, Rune R Frants, Joost Haan, Michel D Ferrari, Peter J Goadsby, Michael G Hanna,[...]. Neurobiol Dis 2008
19
21

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.
C Jodice, E Mantuano, L Veneziano, F Trettel, G Sabbadini, L Calandriello, A Francia, M Spadaro, F Pierelli, F Salvi,[...]. Hum Mol Genet 1997
212
19

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.
A Escayg, M De Waard, D D Lee, D Bichet, P Wolf, T Mayer, J Johnston, R Baloh, T Sander, M H Meisler. Am J Hum Genet 2000
269
19

Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.
T Miki, T A Zwingman, M Wakamori, C M Lutz, S A Cook, D A Hosford, K Herrup, C F Fletcher, Y Mori, W N Frankel,[...]. Neuroscience 2008
37
19

Knockdown of Cav2.1 calcium channels is sufficient to induce neurological disorders observed in natural occurring Cacna1a mutants in mice.
Hiromitsu Saito, Motohiro Okada, Takafumi Miki, Minoru Wakamori, Akira Futatsugi, Yasuo Mori, Katsuhiko Mikoshiba, Noboru Suzuki. Biochem Biophys Res Commun 2009
15
26


Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
Sanjeev Rajakulendran, Diego Kaski, Michael G Hanna. Nat Rev Neurol 2012
86
19

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
60
19

Calcium control of transmitter release at a cerebellar synapse.
I M Mintz, B L Sabatini, W G Regehr. Neuron 1995
425
14

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
172
14

Motor deficits in homozygous and heterozygous p/q-type calcium channel mutants.
Akira Katoh, Jenelle A Jindal, Jennifer L Raymond. J Neurophysiol 2007
28
14

Alternative splicing as a molecular switch for Ca2+/calmodulin-dependent facilitation of P/Q-type Ca2+ channels.
Dipayan Chaudhuri, Siao-Yun Chang, Carla D DeMaria, Rebecca S Alvania, Tuck Wah Soong, David T Yue. J Neurosci 2004
67
14


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.