Published in Mol Vis on February 28, 2007
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Identification of candidate genes for human retinal degeneration loci using differentially expressed genes from mouse photoreceptor dystrophy models. Mol Vis (2008) 0.87
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Complex phenotype of mice homozygous for a null mutation in the Sp4 transcription factor gene. Genes Cells (2001) 1.08
Sp4 is expressed in retinal neurons, activates transcription of photoreceptor-specific genes, and synergizes with Crx. J Biol Chem (2005) 1.06
The novel transcription factor gene Sp5 exhibits a dynamic and highly restricted expression pattern during mouse embryogenesis. Mech Dev (2001) 1.00
The rod cGMP-phosphodiesterase beta-subunit promoter is a specific target for Sp4 and is not activated by other Sp proteins or CRX. J Biol Chem (2002) 0.96
A substitution of G to C in the cone cGMP-phosphodiesterase gamma subunit gene found in a distinctive form of cone dystrophy. Ophthalmology (2005) 0.96
Disruption of the gene encoding the beta1-subunit of transducin in the Rd4/+ mouse. Invest Ophthalmol Vis Sci (2006) 0.93
Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa. Hum Mutat (2001) 0.92
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Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerations. Invest Ophthalmol Vis Sci (1999) 0.80
Transfer of microRNAs by embryonic stem cell microvesicles. PLoS One (2009) 2.64
Identification and subcellular localization of the RP1 protein in human and mouse photoreceptors. Invest Ophthalmol Vis Sci (2002) 1.58
Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene. Proc Natl Acad Sci U S A (2002) 1.51
GAP-independent termination of photoreceptor light response by excess gamma subunit of the cGMP-phosphodiesterase. J Neurosci (2006) 1.30
Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20. Genet Med (2007) 1.22
Evidence for retinal remodelling in retinitis pigmentosa caused by PDE6B mutation. Br J Ophthalmol (2007) 1.20
Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice. Am J Hum Genet (2009) 1.16
Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness. Hum Mutat (2007) 1.15
Retinoschisin, a photoreceptor-secreted protein, and its interaction with bipolar and muller cells. J Neurosci (2003) 1.14
Electroretinographic evidence for altered phototransduction gain and slowed recovery from photobleaches in albino mice with a MET450 variant in RPE65. Exp Eye Res (2003) 1.11
Sp4 is expressed in retinal neurons, activates transcription of photoreceptor-specific genes, and synergizes with Crx. J Biol Chem (2005) 1.06
Evaluation of techniques using amplified nucleic acid probes for gene expression profiling. Biomol Eng (2003) 1.01
Involvement of OA1, an intracellular GPCR, and G alpha i3, its binding protein, in melanosomal biogenesis and optic pathway formation. Invest Ophthalmol Vis Sci (2008) 1.00
The rod cGMP-phosphodiesterase beta-subunit promoter is a specific target for Sp4 and is not activated by other Sp proteins or CRX. J Biol Chem (2002) 0.96
A substitution of G to C in the cone cGMP-phosphodiesterase gamma subunit gene found in a distinctive form of cone dystrophy. Ophthalmology (2005) 0.96
A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration. Mol Vis (2008) 0.95
Disruption of the gene encoding the beta1-subunit of transducin in the Rd4/+ mouse. Invest Ophthalmol Vis Sci (2006) 0.93
Morphological characterization of the retinal degeneration in three strains of mice carrying the rd-3 mutation. Vis Neurosci (2006) 0.93
The positive role of the carboxyl terminus of the gamma subunit of retinal cGMP-phosphodiesterase in maintaining phosphodiesterase activity in vivo. Vision Res (2002) 0.91
Early markers of retinal degeneration in rd/rd mice. Mol Vis (2005) 0.90
Embryonic stem cell-derived microvesicles induce gene expression changes in Müller cells of the retina. PLoS One (2012) 0.90
A novel RDS/peripherin gene mutation associated with diverse macular phenotypes. Ophthalmic Genet (2004) 0.85
Glial transcytosis of a photoreceptor-secreted signaling protein, retinoschisin. Glia (2005) 0.85
ZBED4, a BED-type zinc-finger protein in the cones of the human retina. Invest Ophthalmol Vis Sci (2009) 0.84
Specific interaction of Gαi3 with the Oa1 G-protein coupled receptor controls the size and density of melanosomes in retinal pigment epithelium. PLoS One (2011) 0.83
Molecular analysis of the ABCA4 gene in Turkish patients with Stargardt disease and retinitis pigmentosa. Hum Mutat (2004) 0.83
Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog. Mol Vis (2002) 0.82
ZBED4, a cone and Müller cell protein in human retina, has a different cellular expression in mouse. Mol Vis (2011) 0.81
Non-invasive gene transfer by iontophoresis for therapy of an inherited retinal degeneration. Exp Eye Res (2008) 0.81
Expression of cone photoreceptor cGMP-phosphodiesterase alpha' subunit in Chinese hamster ovary, 293 human embryonic kidney, and Y79 retinoblastoma cells. Mol Vis (2003) 0.80
Two forms of the large tumor suppressor gene (Lats1) protein expressed in the vertebrate retina. Biochim Biophys Acta (2005) 0.80
Sequence-specific binding of recombinant Zbed4 to DNA: insights into Zbed4 participation in gene transcription and its association with other proteins. PLoS One (2012) 0.80
Differential expression of rod photoreceptor cGMP-phosphodiesterase alpha and beta subunits: mRNA and protein levels. J Biol Chem (2003) 0.79
Translational regulation of the rod photoreceptor cGMP-phosphodiesterase: the role of the 5'- and 3'-untranslated regions. Exp Eye Res (2006) 0.79
Dynamics of the rhomboid-like protein RHBDD2 expression in mouse retina and involvement of its human ortholog in retinitis pigmentosa. J Biol Chem (2013) 0.79
Regulation of retinoschisin secretion in Weri-Rb1 cells by the F-actin and microtubule cytoskeleton. PLoS One (2011) 0.78
Influence of a quantitative trait locus on mouse chromosome 19 to the light-adapted electroretinogram. Invest Ophthalmol Vis Sci (2008) 0.77
A constitutively active Gαi3 protein corrects the abnormal retinal pigment epithelium phenotype of Oa1-/- mice. PLoS One (2013) 0.77
Identification and characterization of genes expressed in cone photoreceptors. Adv Exp Med Biol (2008) 0.76
Transcriptional and post-transcriptional regulation of the rod cGMP-phosphodiesterase beta-subunit gene. Recent advances and current concepts. Adv Exp Med Biol (2006) 0.76
Regulatory sequences in the 3' untranslated region of the human cGMP-phosphodiesterase beta-subunit gene. Invest Ophthalmol Vis Sci (2009) 0.75
Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice. Mol Vis (2010) 0.75