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Transcriptional profiling of mouse cortex tissue comparing control animals with Gtf2i-mutated mouse (Gtf2i+/Δex2 ). Goal was to determine the specific deregulated genes in the cortex of mutated animals. Pools of total RNA derived from five-three mice of each genotype were subjected to microarray an...
ORGANISM(S): Mus musculus 
Copy number variations at 7q11.23 cause neurodevelopmental disorders with shared and opposite manifestations. Deletion leads to Williams-Beuren syndrome (WBS), while duplication causes 7q11.23 microduplication syndrome (7Dup). Converging evidence indicates GTF2I, from the 7q11.23 locus, is a key me...
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD036770 | Pride
Hippocampus RNA-seq in CD x Gtf2i*
The transcriptional regulatory network governing the differentiation and functionality of oligodendrocytes is essential for the formation and maintenance of the myelin sheath, and hence for the proper function of the nervous system. Perturbations in the intricate interplay of transcriptional effecto...
ORGANISM(S): Mus musculus (Mouse) 
2025-07-14 | PXD054341 | Pride
Gtf2i and Gtf2ird1 E13.5 whole brain ChIP-seq and RNA-seq
Mutant GTF2I induces cell transformation and metabolic alterations in thymic epithelial cells
Transcriptional profiling of mouse cortex tissue comparing control animals with Gtf2i-mutated mouse (Gtf2i+/Δex2 ). Goal was to determine the specific deregulated genes in the cortex of mutated animals.
ORGANISM(S): Mus musculus 
2014-10-20 | GSE41251 | GEO
A Knock-in Mouse Model of Thymoma with the GTF2I L424H Mutation
Loss of GTF2I promotes neuronal apoptosis and synaptic reduction in human cellular models of neurodevelopment
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