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In vivo E-box-lacZ reporter assay in larval wing discs and activation... | Download Scientific Diagram
Novel Drosophila-based disease model to study | EurekAlert!
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Novel Drosophila-based disease model to study human intellectual disability syndrome
Daughterless, the Drosophila orthologue of TCF4, is required for associative learning and maintenance of synaptic proteome | bioRxiv
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The Fuchs corneal dystrophy-associated CTG repeat expansion in the TCF4 gene affects transcription from its alternative promoters | Scientific Reports
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Nervous system defects in da11B3* homozygous embryos. (a] Wild-type... | Download Scientific Diagram
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Novel Drosophila-based disease model to study human intellectual disability syndrome
Novel Drosophila-based disease model to study human intellectual disability syndrome
Mari PALGI | Postdoctoral Researcher | Ph D | Tallinn University of Technology, Tallinn | TTU | Department of Gene Technology
Daughterless, the Drosophila orthologue of TCF4, is required for associative learning and maintenance of synaptic proteome | bioRxiv
Isoform-Specific Reduction of the Basic Helix-Loop-Helix Transcription Factor TCF4 Levels in Huntington's Disease | eNeuro
The Intellectual Disability and Schizophrenia Associated Transcription Factor TCF4 Is Regulated by Neuronal Activity and Protein Kinase A | Journal of Neuroscience
Common Pathophysiology in Multiple Mouse Models of Pitt–Hopkins Syndrome | Journal of Neuroscience
Novel Drosophila-based disease model to study human intellectual disability syndrome
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