A citation-based method for searching scientific literature

Takahiro Seki, Naoko Adachi, Yoshitaka Ono, Hideki Mochizuki, Keiko Hiramoto, Taku Amano, Hiroaki Matsubayashi, Masayasu Matsumoto, Hideshi Kawakami, Naoaki Saito, Norio Sakai. J Biol Chem 2005
Times Cited: 53







List of co-cited articles
311 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
66

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
50


Enzymological analysis of mutant protein kinase Cgamma causing spinocerebellar ataxia type 14 and dysfunction in Ca2+ homeostasis.
Naoko Adachi, Takeshi Kobayashi, Hideyuki Takahashi, Takumi Kawasaki, Yasuhito Shirai, Takehiko Ueyama, Toshio Matsuda, Takahiro Seki, Norio Sakai, Naoaki Saito. J Biol Chem 2008
73
37

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
35

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
52

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
44

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
33

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
33

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
32

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
30

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
40

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
28

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
30

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
73

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
48


A novel H101Q mutation causes PKCgamma loss in spinocerebellar ataxia type 14.
Isabel Alonso, Cristina Costa, André Gomes, Anabela Ferro, Ana I Seixas, Sérgio Silva, Vitor Tedim Cruz, Paula Coutinho, Jorge Sequeiros, Isabel Silveira. J Hum Genet 2005
28
39

Distribution of protein kinase C-like immunoreactive neurons in rat brain.
N Saito, U Kikkawa, Y Nishizuka, C Tanaka. J Neurosci 1988
247
20

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
35

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
18

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
649
16

A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.
Zoran Brkanac, Laura Bylenok, Magali Fernandez, Mark Matsushita, Hillary Lipe, John Wolff, David Nochlin, Wendy H Raskind, Thomas D Bird. Arch Neurol 2002
46
19

Mutation of the highly conserved cysteine residue 131 of the SCA14 associated PRKCG gene in a family with slow progressive cerebellar ataxia.
Andreas Dalski, Beate Mitulla, Katrin Bürk, Christoph Schattenfroh, Eberhard Schwinger, Christine Zühlke. J Neurol 2006
26
34

Protein aggregation and neurodegenerative disease.
Christopher A Ross, Michelle A Poirier. Nat Med 2004
15

Spinocerebellar ataxia 14: novel mutation in exon 2 of PRKCG in a German family.
Dagmar Nolte, Melanie Landendinger, Eberhard Schmitt, Ulrich Müller. Mov Disord 2007
16
50

Another mutation in cysteine 131 in protein kinase C gamma as a cause of spinocerebellar ataxia type 14.
Stephan Klebe, Laurence Faivre, Sylvie Forlani, Christel Dussert, Ayman Tourbah, Alexis Brice, Giovanni Stevanin, Alexandra Durr. Arch Neurol 2007
10
80

Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.
Dineke S Verbeek, Bart P C van de Warrenburg, F A M Hennekam, Dennis Dooijes, P F Ippel, Corien C Verschuuren-Bemelmans, H P H Kremer, Richard J Sinke. Hum Genet 2005
27
29




Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene.
Stefan Wieczorek, Larissa Arning, Elke R Gizewski, Ingrid Alheite, Duymal Timmann. Mov Disord 2007
12
58


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
11


Propagation of gammaPKC translocation along the dendrites of Purkinje cell in gammaPKC-GFP transgenic mice.
Norio Sakai, Hiroshi Tsubokawa, Masanori Matsuzaki, Taketoshi Kajimoto, Eri Takahashi, Yi Ren, Shiho Ohmori, Yasuhito Shirai, Hiroaki Matsubayashi, Jingshan Chen,[...]. Genes Cells 2004
16
37

Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene.
M C Fahey, M A Knight, J H Shaw, R J McK Gardner, D du Sart, P J Lockhart, M B Delatycki, P C Gates, E Storey. J Neurol Neurosurg Psychiatry 2005
18
33

Molecular pathogenesis of spinocerebellar ataxias.
Antoni Matilla Dueñas, Robert Goold, Paola Giunti. Brain 2006
153
11

Protection from ataxia-linked apoptosis by gap junction inhibitors.
Dingbo Lin, Dolores J Takemoto. Biochem Biophys Res Commun 2007
16
37

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
11

Effect of trehalose on the properties of mutant {gamma}PKC, which causes spinocerebellar ataxia type 14, in neuronal cell lines and cultured Purkinje cells.
Takahiro Seki, Nana Abe-Seki, Takahiro Kikawada, Hideyuki Takahashi, Kazuhiro Yamamoto, Naoko Adachi, Shigeru Tanaka, Izumi Hide, Naoaki Saito, Norio Sakai. J Biol Chem 2010
18
33

A candidate gene for human neurodegenerative disorders: a rat PKC gamma mutation causes a Parkinsonian syndrome.
N J Craig, M B Durán Alonso, K L Hawker, P Shiels, T A Glencorse, J M Campbell, N K Bennett, M Canham, D Donald, M Gardiner,[...]. Nat Neurosci 2001
24
20

Protein misfolding in neurodegenerative diseases.
E I Agorogiannis, G I Agorogiannis, A Papadimitriou, G M Hadjigeorgiou. Neuropathol Appl Neurobiol 2004
80
9

Toxic proteins in neurodegenerative disease.
J Paul Taylor, John Hardy, Kenneth H Fischbeck. Science 2002
836
9

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
9

Congo red, an amyloid-inhibiting compound, alleviates various types of cellular dysfunction triggered by mutant protein kinase cγ that causes spinocerebellar ataxia type 14 (SCA14) by inhibiting oligomerization and aggregation.
Takahiro Seki, Hideyuki Takahashi, Kazuhiro Yamamoto, Kota Ogawa, Tomoya Onji, Naoko Adachi, Shigeru Tanaka, Izumi Hide, Naoaki Saito, Norio Sakai. J Pharmacol Sci 2010
9
55

Spinocerebellar ataxia type 14.
Dong-Hui Chen, Wendy H Raskind, Thomas D Bird. Handb Clin Neurol 2012
17
29

Elucidation of the molecular mechanism and exploration of novel therapeutics for spinocerebellar ataxia caused by mutant protein kinase Cγ.
Takahiro Seki, Naoko Adachi, Nana Abe-Seki, Takayuki Shimahara, Hideyuki Takahashi, Kazuhiro Yamamoto, Naoaki Saito, Norio Sakai. J Pharmacol Sci 2011
12
41

Identification and characterization of PKCγ, a kinase associated with SCA14, as an amyloidogenic protein.
Hideyuki Takahashi, Naoko Adachi, Toshihiko Shirafuji, Sally Danno, Takehiko Ueyama, Michele Vendruscolo, Anton N Shuvaev, Takuya Sugimoto, Takahiro Seki, Daizo Hamada,[...]. Hum Mol Genet 2015
11
45



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.