A citation-based method for searching scientific literature

Naoko Adachi, Takeshi Kobayashi, Hideyuki Takahashi, Takumi Kawasaki, Yasuhito Shirai, Takehiko Ueyama, Toshio Matsuda, Takahiro Seki, Norio Sakai, Naoaki Saito. J Biol Chem 2008
Times Cited: 73







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



Times Cited
  Times     Co-cited
Similarity


Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
Dong-Hui Chen, Zoran Brkanac, Christophe L M J Verlinde, Xiao-Jian Tan, Laura Bylenok, David Nochlin, Mark Matsushita, Hillary Lipe, John Wolff, Magali Fernandez,[...]. Am J Hum Genet 2003
175
43


PKC gamma mutations in spinocerebellar ataxia type 14 affect C1 domain accessibility and kinase activity leading to aberrant MAPK signaling.
Dineke S Verbeek, Joachim Goedhart, Laurie Bruinsma, Richard J Sinke, Eric A Reits. J Cell Sci 2008
50
50

Impaired motor coordination correlates with persistent multiple climbing fiber innervation in PKC gamma mutant mice.
C Chen, M Kano, A Abeliovich, L Chen, S Bao, J J Kim, K Hashimoto, R F Thompson, S Tonegawa. Cell 1995
262
32

TRPC3 channels are required for synaptic transmission and motor coordination.
Jana Hartmann, Elena Dragicevic, Helmuth Adelsberger, Horst A Henning, Martin Sumser, Joel Abramowitz, Robert Blum, Alexander Dietrich, Marc Freichel, Veit Flockerzi,[...]. Neuron 2008
282
31

Impaired synapse elimination during cerebellar development in PKC gamma mutant mice.
M Kano, K Hashimoto, C Chen, A Abeliovich, A Aiba, H Kurihara, M Watanabe, Y Inoue, S Tonegawa. Cell 1995
276
31

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.
Joyce van de Leemput, Jayanth Chandran, Melanie A Knight, Lynne A Holtzclaw, Sonja Scholz, Mark R Cookson, Henry Houlden, Katrina Gwinn-Hardy, Hon-Chung Fung, Xian Lin,[...]. PLoS Genet 2007
192
30

Mutant gammaPKC found in spinocerebellar ataxia type 14 induces aggregate-independent maldevelopment of dendrites in primary cultured Purkinje cells.
Takahiro Seki, Takayuki Shimahara, Kazuhiro Yamamoto, Nana Abe, Taku Amano, Naoko Adachi, Hideyuki Takahashi, Kaori Kashiwagi, Naoaki Saito, Norio Sakai. Neurobiol Dis 2009
43
48

A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice.
Esther B E Becker, Peter L Oliver, Maike D Glitsch, Gareth T Banks, Francesca Achilli, Andrea Hardy, Patrick M Nolan, Elizabeth M C Fisher, Kay E Davies. Proc Natl Acad Sci U S A 2009
136
28

Mutant protein kinase Cgamma found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death.
Takahiro Seki, Naoko Adachi, Yoshitaka Ono, Hideki Mochizuki, Keiko Hiramoto, Taku Amano, Hiroaki Matsubayashi, Masayasu Matsumoto, Hideshi Kawakami, Naoaki Saito,[...]. J Biol Chem 2005
53
37

Aggregate formation of mutant protein kinase C gamma found in spinocerebellar ataxia type 14 impairs ubiquitin-proteasome system and induces endoplasmic reticulum stress.
Takahiro Seki, Hideyuki Takahashi, Naoko Adachi, Nana Abe, Takayuki Shimahara, Naoaki Saito, Norio Sakai. Eur J Neurosci 2007
36
55

Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.
Ichiro Yabe, Hidenao Sasaki, Dong-Hui Chen, Wendy H Raskind, Thomas D Bird, Isao Yamashita, Shoji Tsuji, Seiji Kikuchi, Kunio Tashiro. Arch Neurol 2003
85
26

The clinical and genetic spectrum of spinocerebellar ataxia 14.
D-H Chen, P J Cimino, L P W Ranum, H Y Zoghbi, I Yabe, L Schut, R L Margolis, H P Lipe, A Feleke, M Matsushita,[...]. Neurology 2005
56
33

Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 2.
Jing Liu, Tie-Shan Tang, Huiping Tu, Omar Nelson, Emily Herndon, Duong P Huynh, Stefan M Pulst, Ilya Bezprozvanny. J Neurosci 2009
182
24

Mutant PKCγ in spinocerebellar ataxia type 14 disrupts synapse elimination and long-term depression in Purkinje cells in vivo.
Anton N Shuvaev, Hajime Horiuchi, Takahiro Seki, Hanna Goenawan, Tomohiko Irie, Akira Iizuka, Norio Sakai, Hirokazu Hirai. J Neurosci 2011
58
31

Spectrin mutations cause spinocerebellar ataxia type 5.
Yoshio Ikeda, Katherine A Dick, Marcy R Weatherspoon, Dan Gincel, Karen R Armbrust, Joline C Dalton, Giovanni Stevanin, Alexandra Dürr, Christine Zühlke, Katrin Bürk,[...]. Nat Genet 2006
242
23

New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.
Stephan Klebe, Alexandra Durr, Alexander Rentschler, Valerie Hahn-Barma, Michael Abele, Naima Bouslam, Ludger Schöls, Pierre Jedynak, Sylvie Forlani, Elodie Denis,[...]. Ann Neurol 2005
62
25


Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16.
A Iwaki, Y Kawano, S Miura, H Shibata, D Matsuse, W Li, H Furuya, Y Ohyagi, T Taniwaki, J Kira,[...]. J Med Genet 2008
90
21

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
20

Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice.
Heliane G Serra, Courtney E Byam, Jeffrey D Lande, Susan K Tousey, Huda Y Zoghbi, Harry T Orr. Hum Mol Genet 2004
130
20


Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family.
B P C van de Warrenburg, D S Verbeek, S J Piersma, F A M Hennekam, P L Pearson, N V A M Knoers, H P H Kremer, R J Sinke. Neurology 2003
77
19

Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin.
Hirohide Asai, Makito Hirano, Keiji Shimada, Takao Kiriyama, Yoshiko Furiya, Masanori Ikeda, Takaaki Iwamoto, Toshio Mori, Kazuto Nishinaka, Noboru Konishi,[...]. Hum Mol Genet 2009
28
50


Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
649
17

Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
Giovanni Stevanin, Valérie Hahn, Ebba Lohmann, Naima Bouslam, Michel Gouttard, Caroline Soumphonphakdy, Marie-Laure Welter, Elisabeth Ollagnon-Roman, Arnaud Lemainque, Merle Ruberg,[...]. Arch Neurol 2004
70
18


Distribution of protein kinase C-like immunoreactive neurons in rat brain.
N Saito, U Kikkawa, Y Nishizuka, C Tanaka. J Neurosci 1988
247
16

Molecular pathogenesis of spinocerebellar ataxias.
Antoni Matilla Dueñas, Robert Goold, Paola Giunti. Brain 2006
153
16


Negative regulation of TRPC3 channels by protein kinase C-mediated phosphorylation of serine 712.
Mohamed Trebak, Nadine Hempel, Barbara J Wedel, Jeremy T Smyth, Gary St J Bird, James W Putney. Mol Pharmacol 2005
104
15

RORalpha-mediated Purkinje cell development determines disease severity in adult SCA1 mice.
Heliane G Serra, Lisa Duvick, Tao Zu, Kerri Carlson, Sam Stevens, Nathan Jorgensen, Alana Lysholm, Eric Burright, Huda Y Zoghbi, H Brent Clark,[...]. Cell 2006
149
15

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
15

Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.
K Hara, A Shiga, H Nozaki, J Mitsui, Y Takahashi, H Ishiguro, H Yomono, H Kurisaki, J Goto, T Ikeuchi,[...]. Neurology 2008
91
15

Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 3.
Xi Chen, Tie-Shan Tang, Huiping Tu, Omar Nelson, Mark Pook, Robert Hammer, Nobuyuki Nukina, Ilya Bezprozvanny. J Neurosci 2008
151
15

Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling.
Stephanie Schorge, Joyce van de Leemput, Andrew Singleton, Henry Houlden, John Hardy. Trends Neurosci 2010
61
18

Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagy.
Kazuhiro Yamamoto, Takahiro Seki, Naoko Adachi, Tetsuya Takahashi, Shigeru Tanaka, Izumi Hide, Naoaki Saito, Norio Sakai. Genes Cells 2010
19
57


Increased protein kinase C gamma activity induces Purkinje cell pathology in a mouse model of spinocerebellar ataxia 14.
Jingmin Ji, Melanie L Hassler, Etsuko Shimobayashi, Nagendher Paka, Raphael Streit, Josef P Kapfhammer. Neurobiol Dis 2014
26
42


Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
Keiko Hiramoto, Hideshi Kawakami, Kimiko Inoue, Takahiro Seki, Hirofumi Maruyama, Hiroyuki Morino, Masayasu Matsumoto, Kaoru Kurisu, Norio Sakai. Mov Disord 2006
27
37

Emerging pathogenic pathways in the spinocerebellar ataxias.
Kerri M Carlson, J Michael Andresen, Harry T Orr. Curr Opin Genet Dev 2009
55
18

Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptor.
M Matsumoto, T Nakagawa, T Inoue, E Nagata, K Tanaka, H Takano, O Minowa, J Kuno, S Sakakibara, M Yamada,[...]. Nature 1996
330
13

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
S M Pulst, A Nechiporuk, T Nechiporuk, S Gispert, X N Chen, I Lopes-Cendes, S Pearlman, S Starkman, G Orozco-Diaz, A Lunkes,[...]. Nat Genet 1996
867
13



Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: expanding the phenotype.
Monique H M Vlak, Richard J Sinke, Gwenda M Rabelink, Berry P H Kremer, Bart P C van de Warrenburg. Mov Disord 2006
37
24

A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter.
I Yamashita, H Sasaki, I Yabe, T Fukazawa, S Nogoshi, K Komeichi, A Takada, K Shiraishi, Y Takiyama, M Nishizawa,[...]. Ann Neurol 2000
83
12

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
Henry Houlden, Janel Johnson, Christopher Gardner-Thorpe, Tammaryn Lashley, Dena Hernandez, Paul Worth, Andrew B Singleton, David A Hilton, Janice Holton, Tamas Revesz,[...]. Nat Genet 2007
115
12


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.