A citation-based method for searching scientific literature

Kimberley M Dorval, Brian P Bobechko, K Farid Ahmad, Rod Bremner. J Biol Chem 2005
Times Cited: 44







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



Times Cited
  Times     Co-cited
Similarity


Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation.
M Burmeister, J Novak, M Y Liang, S Basu, L Ploder, N L Hawes, D Vidgen, F Hoover, D Goldman, V I Kalnins,[...]. Nat Genet 1996
417
56

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
E Ferda Percin, L A Ploder, J J Yu, K Arici, D J Horsford, A Rutherford, B Bapat, D W Cox, A M Duncan, V I Kalnins,[...]. Nat Genet 2000
209
34


Chx10 is required to block photoreceptor differentiation but is dispensable for progenitor proliferation in the postnatal retina.
Izzy Livne-Bar, Marek Pacal, Melissa C Cheung, Mark Hankin, Judy Trogadis, Danian Chen, Kimberley M Dorval, Rod Bremner. Proc Natl Acad Sci U S A 2006
72
34

Negative regulation of Vsx1 by its paralog Chx10/Vsx2 is conserved in the vertebrate retina.
Anna M Clark, Sanghee Yun, Eric S Veien, Yuan Y Wu, Robert L Chow, Richard I Dorsky, Edward M Levine. Brain Res 2008
48
34

CHX10 targets a subset of photoreceptor genes.
Kimberley M Dorval, Brian P Bobechko, Hiroki Fujieda, Shiming Chen, Don J Zack, Rod Bremner. J Biol Chem 2006
45
31


Chx10 repression of Mitf is required for the maintenance of mammalian neuroretinal identity.
D Jonathan Horsford, Minh-Thanh T Nguyen, Grant C Sellar, Rashmi Kothary, Heinz Arnheiter, Roderick R McInnes. Development 2005
144
27

Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cells.
R L Chow, B Snow, J Novak, J Looser, C Freund, D Vidgen, L Ploder, R R McInnes. Mech Dev 2001
78
27

Regulation of retinal cone bipolar cell differentiation and photopic vision by the CVC homeobox gene Vsx1.
Akihira Ohtoshi, Steven W Wang, Hidetaka Maeda, Shannon M Saszik, Laura J Frishman, William H Klein, Richard R Behringer. Curr Biol 2004
77
27

Control of late off-center cone bipolar cell differentiation and visual signaling by the homeobox gene Vsx1.
Robert L Chow, Bela Volgyi, Rachel K Szilard, David Ng, Colin McKerlie, Stewart A Bloomfield, David G Birch, Roderick R McInnes. Proc Natl Acad Sci U S A 2004
116
27

Transdifferentiation of the retina into pigmented cells in ocular retardation mice defines a new function of the homeodomain gene Chx10.
Sheldon Rowan, C-M Amy Chen, Tracy L Young, David E Fisher, Constance L Cepko. Development 2004
120
25

VSX1: a gene for posterior polymorphous dystrophy and keratoconus.
Elise Héon, Alex Greenberg, Kelly K Kopp, David Rootman, Andrea L Vincent, Gail Billingsley, Megan Priston, Kimberley M Dorval, Robert L Chow, Roderick R McInnes,[...]. Hum Mol Genet 2002
207
25


Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development.
Akihiro Nishida, Akiko Furukawa, Chieko Koike, Yasuo Tano, Shinichi Aizawa, Isao Matsuo, Takahisa Furukawa. Nat Neurosci 2003
412
22



VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells.
Helen A Mintz-Hittner, Elena V Semina, Laura J Frishman, Thomas C Prager, Jeffrey C Murray. Ophthalmology 2004
38
23

Vsx-1 and Vsx-2: differential expression of two paired-like homeobox genes during zebrafish and goldfish retinogenesis.
M A Passini, E M Levine, A K Canger, P A Raymond, N Schechter. J Comp Neurol 1997
77
20



Pax6 is required for the multipotent state of retinal progenitor cells.
T Marquardt, R Ashery-Padan, N Andrejewski, R Scardigli, F Guillemot, P Gruss. Cell 2001
679
18

Partial rescue of the ocular retardation phenotype by genetic modifiers.
C Bone-Larson, S Basu, J D Radel, M Liang, T Perozek, N Kapousta-Bruneau, D G Green, M Burmeister, M H Hankin. J Neurobiol 2000
32
21


VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation.
Luigi Bisceglia, Marilena Ciaschetti, Patrizia De Bonis, Pablo Alberto Perafan Campo, Costantina Pizzicoli, Costanza Scala, Michele Grifa, Pio Ciavarella, Nicola Delle Noci, Filippo Vaira,[...]. Invest Ophthalmol Vis Sci 2005
94
15


H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family.
Sophie Valleix, Brigitte Nedelec, Florence Rigaudiere, Paul Dighiero, Yves Pouliquen, Gilles Renard, Jean-François Le Gargasson, Marc Delpech. Invest Ophthalmol Vis Sci 2006
30
23


Roles of homeobox and bHLH genes in specification of a retinal cell type.
J Hatakeyama, K Tomita, T Inoue, R Kageyama. Development 2001
187
13

Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes.
S Chen, Q L Wang, Z Nie, H Sun, G Lennon, N G Copeland, D J Gilbert, N A Jenkins, D J Zack. Neuron 1997
549
13




The subcellular localization of Otx2 is cell-type specific and developmentally regulated in the mouse retina.
D Baas, K M Bumsted, J A Martinez, F M Vaccarino, K C Wikler, C J Barnstable. Brain Res Mol Brain Res 2000
86
13



No VSX1 gene mutations associated with keratoconus.
Anthony J Aldave, Vivek S Yellore, Andrew K Salem, Gina L Yoo, Sylvia A Rayner, Huiying Yang, George Y Tang, Yoana Piconell, Yaron S Rabinowitz. Invest Ophthalmol Vis Sci 2006
77
13

Functional roles of Otx2 transcription factor in postnatal mouse retinal development.
Chieko Koike, Akihiro Nishida, Shinji Ueno, Hiromitsu Saito, Rikako Sanuki, Shigeru Sato, Akiko Furukawa, Shinichi Aizawa, Isao Matsuo, Noboru Suzuki,[...]. Mol Cell Biol 2007
133
13

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.
T Furukawa, E M Morrow, T Li, F C Davis, C L Cepko. Nat Genet 1999
414
13

Vertebrate neural cell-fate determination: lessons from the retina.
F J Livesey, C L Cepko. Nat Rev Neurosci 2001
702
13

Alternative promoter use in eye development: the complex role and regulation of the transcription factor MITF.
Kapil Bharti, Wenfang Liu, Tamas Csermely, Stefano Bertuzzi, Heinz Arnheiter. Development 2008
98
13


Cooperative dimerization of paired class homeo domains on DNA.
D Wilson, G Sheng, T Lecuit, N Dostatni, C Desplan. Genes Dev 1993
342
11

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.
C L Freund, C Y Gregory-Evans, T Furukawa, M Papaioannou, J Looser, L Ploder, J Bellingham, D Ng, J A Herbrick, A Duncan,[...]. Cell 1997
438
11

Vsx-1 and Vsx-2: two Chx10-like homeobox genes expressed in overlapping domains in the adult goldfish retina.
E M Levine, M Passini, P F Hitchcock, E Glasgow, N Schechter. J Comp Neurol 1997
45
11

Cloning of zebrafish vsx1: expression of a paired-like homeobox gene during CNS development.
M A Passini, A L Kurtzman, A K Canger, W S Asch, G A Wray, P A Raymond, N Schechter. Dev Genet 1998
41
12

Cell fate determination in the vertebrate retina.
C L Cepko, C P Austin, X Yang, M Alexiades, D Ezzeddine. Proc Natl Acad Sci U S A 1996
767
11

Delayed expression of the Crx gene and photoreceptor development in the Chx10-deficient retina.
Adam D Rutherford, Nathalie Dhomen, Hazel K Smith, Jane C Sowden. Invest Ophthalmol Vis Sci 2004
21
23

Nrl is required for rod photoreceptor development.
A J Mears, M Kondo, P K Swain, Y Takada, R A Bush, T L Saunders, P A Sieving, A Swaroop. Nat Genet 2001
671
11

Retinal cell fate determination and bHLH factors.
Jun Hatakeyama, Ryoichiro Kageyama. Semin Cell Dev Biol 2004
193
11


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.