A citation-based method for searching scientific literature

Pei Rong, Xin Wang, Ingrid Niesman, Ying Wu, Lucio E Benedetti, Irene Dunia, Esther Levy, Xiaohua Gong. Development 2002
Times Cited: 141







List of co-cited articles
1243 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
337
58


Lens gap junctions in growth, differentiation, and homeostasis.
Richard T Mathias, Thomas W White, Xiaohua Gong. Physiol Rev 2010
159
36



Connexin50 is essential for normal postnatal lens cell proliferation.
Caterina Sellitto, Leping Li, Thomas W White. Invest Ophthalmol Vis Sci 2004
59
45


Physiological properties of the normal lens.
R T Mathias, J L Rae, G J Baldo. Physiol Rev 1997
313
25


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
63
36

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
92
25

The lens circulation.
Richard T Mathias, Joerg Kistler, Paul Donaldson. J Membr Biol 2007
190
22

Optimal lens epithelial cell proliferation is dependent on the connexin isoform providing gap junctional coupling.
Thomas W White, Yang Gao, Leping Li, Caterina Sellitto, Miduturu Srinivas. Invest Ophthalmol Vis Sci 2007
45
48

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
76
27

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
73
26

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
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
51

A mutant connexin50 with enhanced hemichannel function leads to cell death.
Peter J Minogue, Jun-Jie Tong, Anita Arora, Isabelle Russell-Eggitt, David M Hunt, Anthony T Moore, Lisa Ebihara, Eric C Beyer, Viviana M Berthoud. Invest Ophthalmol Vis Sci 2009
67
28

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
18

Heteromeric connexons in lens gap junction channels.
J X Jiang, D A Goodenough. Proc Natl Acad Sci U S A 1996
216
18



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
77
22

Connexins in lens development and cataractogenesis.
Xiaohua Gong, Catherine Cheng, Chun-hong Xia. J Membr Biol 2007
69
24

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
36

Plasma membrane channels formed by connexins: their regulation and functions.
Juan C Saez, Viviana M Berthoud, Maria C Branes, Agustin D Martinez, Eric C Beyer. Physiol Rev 2003
892
16

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
68
23

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
44
36

Connexin mutants and cataracts.
Eric C Beyer, Lisa Ebihara, Viviana M Berthoud. Front Pharmacol 2013
68
23


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
24

Connexin channel permeability to cytoplasmic molecules.
Andrew L Harris. Prog Biophys Mol Biol 2007
334
15

Functional characterization of a naturally occurring Cx50 truncation.
Adam M DeRosa, Rickie Mui, Miduturu Srinivas, Thomas W White. Invest Ophthalmol Vis Sci 2006
41
36

Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
Ramachandran Ramya Devi, Perumalsamy Vijayalakshmi. Mol Vis 2006
67
20

Molecular solutions to mammalian lens transparency.
P Donaldson, J Kistler, R T Mathias. News Physiol Sci 2001
133
14


Connexin disorders of the ear, skin, and lens.
Dwan A Gerido, Thomas W White. Biochim Biophys Acta 2004
124
14

Connections between connexins, calcium, and cataracts in the lens.
Junyuan Gao, Xiurong Sun, Francisco J Martinez-Wittinghan, Xiaohua Gong, Thomas W White, Richard T Mathias. J Gen Physiol 2004
96
14


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
13


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
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
50


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
26

Dominant cataracts result from incongruous mixing of wild-type lens connexins.
Francisco J Martinez-Wittinghan, Caterina Sellitto, Leping Li, Xiaohua Gong, Peter R Brink, Richard T Mathias, Thomas W White. J Cell Biol 2003
48
27

Lens gap junctional coupling is modulated by connexin identity and the locus of gene expression.
Francisco J Martinez-Wittinghan, Caterina Sellitto, Thomas W White, Richard T Mathias, David Paul, Daniel A Goodenough. Invest Ophthalmol Vis Sci 2004
37
35


A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.
Vanita Vanita, Jai Rup Singh, Daljit Singh, Raymonda Varon, Karl Sperling. Mol Vis 2008
36
36


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.