Pages that link to "Q33908230"

The following pages link to Analysis of Transcriptional Regulatory Pathways of Photoreceptor Genes by Expression Profiling of the Otx2-Deficient Retina (Q33908230):

Displaying 35 items.

• The role of homeobox genes in retinal development and disease (Q27021998) (← links)
• Regulation of a novel isoform of Receptor Expression Enhancing Protein REEP6 in rod photoreceptors by bZIP transcription factor NRL (Q28589672) (← links)
• Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development (Q31126223) (← links)
• Sterile alpha motif containing 7 (samd7) is a novel crx-regulated transcriptional repressor in the retina (Q33289398) (← links)
• Genome-wide analysis of Müller glial differentiation reveals a requirement for Notch signaling in postmitotic cells to maintain the glial fate (Q33988540) (← links)
• Derivation of human differential photoreceptor cells from adult human dermal fibroblasts by defined combinations of CRX, RAX, OTX2 and NEUROD. (Q34542838) (← links)
• Tropisms of AAV for subretinal delivery to the neonatal mouse retina and its application for in vivo rescue of developmental photoreceptor disorders (Q34555831) (← links)
• Emergence of differentially regulated pathways associated with the development of regional specificity in chicken skin (Q35078793) (← links)
• Mechanistically distinct mouse models for CRX-associated retinopathy (Q35091262) (← links)
• Differentiation of retinal ganglion cells and photoreceptor precursors from mouse induced pluripotent stem cells carrying an Atoh7/Math5 lineage reporter (Q35424411) (← links)
• Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease (Q35470460) (← links)
• Dnmt1-dependent DNA methylation is essential for photoreceptor terminal differentiation and retinal neuron survival (Q36525127) (← links)
• ASCL1 reprograms mouse Muller glia into neurogenic retinal progenitors (Q36883237) (← links)
• Integrative subcellular proteomic analysis allows accurate prediction of human disease-causing genes (Q36893782) (← links)
• Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa (Q37335630) (← links)
• OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness (Q37524324) (← links)
• Gene expression changes during retinal development and rod specification (Q38301080) (← links)
• RB1 gene inactivation by chromothripsis in human retinoblastoma (Q38457744) (← links)
• A modulatory role of the Rax homeobox gene in mature pineal gland function: Investigating the photoneuroendocrine circadian system of a Rax conditional knockout mouse. (Q38694551) (← links)
• Mechanisms of Photoreceptor Patterning in Vertebrates and Invertebrates (Q38951133) (← links)
• OTX2 and CRX rescue overlapping and photoreceptor-specific functions in the Drosophila eye (Q42325776) (← links)
• Navigating the Functional Landscape of Transcription Factors via Non-Negative Tensor Factorization Analysis of MEDLINE Abstracts (Q47141181) (← links)
• Samd7 is a cell type-specific PRC1 component essential for establishing retinal rod photoreceptor identity (Q47814577) (← links)
• Prdm13 regulates subtype specification of retinal amacrine interneurons and modulates visual sensitivity. (Q48184612) (← links)
• Stage-specific reference genes significant for quantitative PCR during mouse retinal development (Q50583104) (← links)
• Mef2d is essential for the maturation and integrity of retinal photoreceptor and bipolar cells. (Q50596815) (← links)
• Developmental origin of the posterior pigmented epithelium of iris (Q50626899) (← links)
• G9a histone methyltransferase activity in retinal progenitors is essential for proper differentiation and survival of mouse retinal cells. (Q50771427) (← links)
• Casz1 controls higher-order nuclear organization in rod photoreceptors (Q58802918) (← links)
• Ultraviolet B-induced Otx2 expression in lens epithelial cells promotes epithelial-mesenchymal transition (Q64235991) (← links)
• -regulatory basis of sister cell type divergence in the vertebrate retina (Q83227762) (← links)
• Foxn4 is a temporal identity factor conferring mid/late-early retinal competence and involved in retinal synaptogenesis (Q89766638) (← links)
• Otx2 enhances transdifferentiation of Müller cells-derived retinal stem cells into photoreceptor-like cells (Q93206743) (← links)
• OTX2 represses sister cell fate choices in the developing retina to promote photoreceptor specification (Q94456293) (← links)
• Developmental changes in the accessible chromatin, transcriptome and Ascl1-binding correlate with the loss in Müller Glial regenerative potential (Q98394771) (← links)