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Deciphering the cis-regulatory architecture of mammalian photoreceptors
PubMed Full text in PMC Similar studies SRA Run Selector
Genome-Wide CRX Binding Sites in adult mouse photoreceptors
PubMed Full text in PMC Similar studies
Otx2 ChIP-seq in the adult mouse Retinal Pigmented Epithelium (RPE) and neural retina
Enhancer transcription identifies cis-regulatory elements for photoreceptor cell types
Transcriptional profiling of the adult mouse retina in wild-type and Nrl deficient mice
Non-coding Transcriptional profiling of the adult mouse retina in wild-type and Nrl deficient mice
Information Content Differentiates Enhancers From Silencers in Mouse Photoreceptors
Transcriptional activity of an MPRA library containing sequences of genomic origin bound by the transcription factor CRX measured in retinas from mice carrying pathogenic CRX variants
Quantification of mouse retinal enhancer activity by massively parallel reporter assay
In vivo function of NR2E3 in establishing photoreceptor identity during mammalian retinal development
PubMed Full text in PMC Similar studies Analyze with GEO2R
Photoreceptor-specific nuclear receptor NR2E3 ectopic expression effect on NRL null retinas
PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet
OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness
Gene expression changes during retinal development and rod specification.
Conditional knockout of p300 and Cbp in mouse rod photoreceptors
Temporal ChIP-on-Chip of RNA-Polymerase-II to detect novel gene activation events during photoreceptor maturation
Transcriptome dynamics of developing photoreceptors in 3-D retina cultures recapitulates temporal sequence of human cone and rod differentiation revealing cell surface markers and gene networks
Graded Expression Changes Determine Phenotype Severity In Mouse Models of CRX-Associated Retinopathy
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms [Spec-seq]
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms [ChIP-seq]
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