A citation-based method for searching scientific literature

Manabu Yoshida, Yuji Harada, Sachiko Kaidzu, Akihiro Ohira, Junichi Masuda, Toru Nabika. Pathol Int 2005
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


Disruption of alpha3 connexin gene leads to proteolysis and cataractogenesis in mice.
X Gong, E Li, G Klier, Q Huang, Y Wu, H Lei, N M Kumar, J Horwitz, N B Gilula. Cell 1997
335
68

A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice.
Bo Chang, Xin Wang, Norman L Hawes, Ryan Ojakian, Muriel T Davisson, Woo-Kuen Lo, Xiaohua Gong. Hum Mol Genet 2002
62
56

Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract.
J Graw, J Löster, D Soewarto, H Fuchs, B Meyer, A Reis, E Wolf, R Balling, M Hrabé de Angelis. Exp Eye Res 2001
43
50

A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract.
E C Steele, M F Lyon, J Favor, P V Guillot, Y Boyd, R L Church. Curr Eye Res 1998
76
43



Connexin46 mutations in autosomal dominant congenital cataract.
D Mackay, A Ionides, Z Kibar, G Rouleau, V Berry, A Moore, A Shiels, S Bhattacharya. Am J Hum Genet 1999
232
43



Knock-in of alpha3 connexin prevents severe cataracts caused by an alpha8 point mutation.
Chun-hong Xia, Debra Cheung, Adam M DeRosa, Bo Chang, Woo-Kuen Lo, Thomas W White, Xiaohua Gong. J Cell Sci 2006
26
43

A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family.
P K F Addison, V Berry, K R Holden, D Espinal, B Rivera, H Su, A K Srivastava, S S Bhattacharya. Mol Vis 2006
33
37

Disruption of Gja8 (alpha8 connexin) in mice leads to microphthalmia associated with retardation of lens growth and lens fiber maturation.
Pei Rong, Xin Wang, Ingrid Niesman, Ying Wu, Lucio E Benedetti, Irene Dunia, Esther Levy, Xiaohua Gong. Development 2002
140
37

The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46.
Lars Hansen, Wenliang Yao, Hans Eiberg, Mikkel Funding, Ruth Riise, Klaus Wilbrandt Kjaer, James Fielding Hejtmancik, Thomas Rosenberg. Mol Vis 2006
35
37

A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract.
Haisong Jiang, Yiping Jin, Lei Bu, Weiying Zhang, Jing Liu, Bin Cui, Xiangyin Kong, Landian Hu. Mol Vis 2003
45
37

Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population.
Ramachandran Ramya Devi, Chandrashekar Reena, Perumalsamy Vijayalakshmi. Mol Vis 2005
42
37


Mapping of A gene responsible for cataract formation and its modifier in the UPL rat.
Satoshi Yamashita, Kayo Furumoto, Asako Nobukiyo, Masashi Kamohara, Toshikazu Ushijima, Toshinori Furukawa. Invest Ophthalmol Vis Sci 2002
11
54

A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.
Kamlesh Guleria, Karl Sperling, Daljit Singh, Raymonda Varon, Jai Rup Singh, Vanita Vanita. Mol Vis 2007
31
37

A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene.
Kamlesh Guleria, Vanita Vanita, Daljit Singh, Jai Rup Singh. Mol Vis 2007
16
31


Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract.
Z W Ma, J Q Zheng, J Li, X R Li, X Tang, X Y Yuan, X M Zhang, H M Sun. Br J Ophthalmol 2005
28
31

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin.
V Berry, D Mackay, S Khaliq, P J Francis, A Hameed, K Anwar, S Q Mehdi, R J Newbold, A Ionides, A Shiels,[...]. Hum Genet 1999
118
31

A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract.
A Arora, P J Minogue, X Liu, M A Reddy, J R Ainsworth, S S Bhattacharya, A R Webster, D M Hunt, L Ebihara, A T Moore,[...]. J Med Genet 2006
67
31

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract.
Surya Prakash G Ponnam, Kekunnaya Ramesha, Sushma Tejwani, Balasubramanya Ramamurthy, Chitra Kannabiran. J Med Genet 2007
57
31

Microphthalmia and cataract in rats with a novel point mutation in connexin 50 - L7Q.
Frantisek Liska, Blanka Chylíková, Jindrich Martínek, Vladimír Kren. Mol Vis 2008
12
41

Genetic factors influence cataract formation in alpha 3 connexin knockout mice.
X Gong, K Agopian, N M Kumar, N B Gilula. Dev Genet 1999
66
31

Connexins in lens development and cataractogenesis.
Xiaohua Gong, Catherine Cheng, Chun-hong Xia. J Membr Biol 2007
67
31

Diverse gap junctions modulate distinct mechanisms for fiber cell formation during lens development and cataractogenesis.
Chun-Hong Xia, Haiquan Liu, Debra Cheung, Catherine Cheng, Eddie Wang, Xin Du, Bruce Beutler, Woo-Kuen Lo, Xiaohua Gong. Development 2006
37
31

Congenital cataracts and their molecular genetics.
J Fielding Hejtmancik. Semin Cell Dev Biol 2008
258
31

Connexin46 mutations linked to congenital cataract show loss of gap junction channel function.
J D Pal, X Liu, D Mackay, A Shiels, V M Berthoud, E C Beyer, L Ebihara. Am J Physiol Cell Physiol 2000
72
25

A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts.
A Arora, P J Minogue, X Liu, P K Addison, I Russel-Eggitt, A R Webster, D M Hunt, L Ebihara, E C Beyer, V M Berthoud,[...]. J Med Genet 2008
61
25

Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract.
A V Polyakov, I A Shagina, O V Khlebnikova, O V Evgrafov. Clin Genet 2001
69
25

A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract.
C E Willoughby, Sara Arab, R Gandhi, S Zeinali, Seddigheh Arab, D Luk, G Billingsley, F L Munier, E Héon. J Med Genet 2003
53
25


A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.
K P Burdon, M G Wirth, D A Mackey, I M Russell-Eggitt, J E Craig, J E Elder, J L Dickinson, M M Sale. J Med Genet 2004
50
25

Loss of function and impaired degradation of a cataract-associated mutant connexin50.
Viviana M Berthoud, Peter J Minogue, Jun Guo, Edward K Williamson, Xiaorong Xu, Lisa Ebihara, Eric C Beyer. Eur J Cell Biol 2003
72
25

An aberrant sequence in a connexin46 mutant underlies congenital cataracts.
Peter J Minogue, Xiaoqin Liu, Lisa Ebihara, Eric C Beyer, Viviana M Berthoud. J Biol Chem 2005
50
25


Gap junctional coupling in lenses from alpha(8) connexin knockout mice.
G J Baldo, X Gong, F J Martinez-Wittinghan, N M Kumar, N B Gilula, R T Mathias. J Gen Physiol 2001
75
25

Gap junctional coupling in lenses lacking alpha3 connexin.
X Gong, G J Baldo, N M Kumar, N B Gilula, R T Mathias. Proc Natl Acad Sci U S A 1998
91
25

Genetic background influences cataractogenesis, but not lens growth deficiency, in Cx50-knockout mice.
Dwan A Gerido, Caterina Sellitto, Leping Li, Thomas W White. Invest Ophthalmol Vis Sci 2003
36
25

Absence of alpha3 (Cx46) and alpha8 (Cx50) connexins leads to cataracts by affecting lens inner fiber cells.
Chun-hong Xia, Catherine Cheng, Qingling Huang, Debra Cheung, Lin Li, Irene Dunia, Lucio E Benedetti, Joseph Horwitz, Xiaohua Gong. Exp Eye Res 2006
46
25

A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.
Vanita Vanita, Hans Christian Hennies, Daljit Singh, Peter Nürnberg, Karl Sperling, Jai Rup Singh. Mol Vis 2006
34
18

Transgenic overexpression of connexin50 induces cataracts.
June Chung, Viviana M Berthoud, Layne Novak, Rebecca Zoltoski, Benjamin Heilbrunn, Peter J Minogue, Xiaoqin Liu, Lisa Ebihara, Jer Kuszak, Eric C Beyer. Exp Eye Res 2007
23
18

Molecular solutions to mammalian lens transparency.
P Donaldson, J Kistler, R T Mathias. News Physiol Sci 2001
132
18

The cataract-inducing S50P mutation in Cx50 dominantly alters the channel gating of wild-type lens connexins.
Adam M DeRosa, Chun-Hong Xia, Xiaohua Gong, Thomas W White. J Cell Sci 2007
26
18

Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
Ramachandran Ramya Devi, Perumalsamy Vijayalakshmi. Mol Vis 2006
67
18



Molecular mechanism underlying a Cx50-linked congenital cataract.
J D Pal, V M Berthoud, E C Beyer, D Mackay, A Shiels, L Ebihara. Am J Physiol 1999
62
18


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.