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MYT1L is an autism spectrum disorder (ASD)-associated transcription factor that is expressed in virtually all neurons throughout life. How MYT1L mutations cause neurological phenotypes and whether they can be targeted remains enigmatic. Here, we examine the effects of MYT1L deficiency in human neuro...
ORGANISM(S): Mus musculus (Mouse) 
2023-02-20 | PXD037867 | Pride
Bulk transcriptome analysis of Myt1l mutant mouse cortices across development.
Bulk transcriptome analysis of Myt1l mutant mouse neuron primary cultures.
Single-cell transcriptome analysis of Myt1l mutant mouse cortices at birth.
MYT1L deficiency impairs excitatory neuron trajectory during cortical development [P21]
MYT1L deficiency impairs excitatory neuron trajectory during cortical development [P1]
MYT1L deficiency impairs excitatory neuron trajectory during cortical development [E14]
Brain transcriptome analysis of Myt1l heterozygote mutation mice (RNA-Seq I)
Bulk transcriptome analysis of conditional MYT1L-mutant ESC-derived human induced neurons.
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