scholarly article | Q13442814 |
P50 | author | Steven W. Flavell | Q39515961 |
Martin Hemberg | Q88244360 | ||
P2093 | author name string | Michael E Greenberg | |
Elio Raviola | |||
Athar N Malik | |||
Michael A Sandberg | |||
Basil Pawlyk | |||
Milena M Andzelm | |||
David A Harmin | |||
Charlotte Lee | |||
Timothy J Cherry | |||
Annabel C Boeke | |||
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Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo | Q24644531 | ||
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Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation. | Q42834166 | ||
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Myocyte enhancer factor 2 mediates calcium-dependent transcription of the interleukin-2 gene in T lymphocytes: a calcium signaling module that is distinct from but collaborates with the nuclear factor of activated T cells (NFAT) | Q75256528 | ||
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A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1 | Q28118822 | ||
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p300/CBP acts as a coactivator of the cone-rod homeobox transcription factor | Q28138043 | ||
MEF2: a central regulator of diverse developmental programs | Q28254625 | ||
Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes | Q28255968 | ||
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration | Q28258792 | ||
Cooperative activation of muscle gene expression by MEF2 and myogenic bHLH proteins | Q28272422 | ||
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MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function | Q28507026 | ||
Targeted disruption of FSCN2 gene induces retinopathy in mice | Q28512358 | ||
Centronuclear myopathy in mice lacking a novel muscle-specific protein kinase transcriptionally regulated by MEF2 | Q28589432 | ||
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Functional sequestration of transcription factor activity by repetitive DNA | Q30416705 | ||
The cis-regulatory logic of the mammalian photoreceptor transcriptional network | Q33291750 | ||
Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosa | Q34088630 | ||
Transcriptional regulation of rod photoreceptor homeostasis revealed by in vivo NRL targetome analysis | Q34236670 | ||
Mutations in the gene coding for guanylate cyclase-activating protein 2 (GUCA1B gene) in patients with autosomal dominant retinal dystrophies | Q34353825 | ||
Cocaine regulates MEF2 to control synaptic and behavioral plasticity | Q34818266 | ||
Mechanistically distinct mouse models for CRX-associated retinopathy | Q35091262 | ||
The transcription factor neural retina leucine zipper (NRL) controls photoreceptor-specific expression of myocyte enhancer factor Mef2c from an alternative promoter | Q35266364 | ||
Intrinsic circadian clock of the mammalian retina: importance for retinal processing of visual information | Q36088146 | ||
The MEF2D transcription factor mediates stress-dependent cardiac remodeling in mice | Q36249548 | ||
A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia | Q36439306 | ||
Analysis of the myogenin promoter reveals an indirect pathway for positive autoregulation mediated by the muscle-specific enhancer factor MEF-2 | Q36698404 | ||
Tissue-specific splicing of a ubiquitously expressed transcription factor is essential for muscle differentiation | Q36948978 | ||
Genome-wide analysis of MEF2 transcriptional program reveals synaptic target genes and neuronal activity-dependent polyadenylation site selection | Q37070840 | ||
Usher protein functions in hair cells and photoreceptors | Q37677127 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | photoreceptor protein | Q7187894 |
P304 | page(s) | 247-263 | |
P577 | publication date | 2015-03-19 | |
P1433 | published in | Neuron | Q3338676 |
P1476 | title | MEF2D drives photoreceptor development through a genome-wide competition for tissue-specific enhancers | |
P478 | volume | 86 |
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