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Science (New York, N.Y.)|November 6, 2025
The need for a global effort to attend to human neural organoid and assembloid researchSergiu P Pașca, Paola Arlotta, Philip Campbell, et al.
Molecular Psychiatry|February 22, 2025
YY1 mutations disrupt corticogenesis through a cell type specific rewiring of cell-autonomous and non-cell-autonomous transcriptional programsMarlene F Pereira, Veronica Finazzi, Ludovico Rizzuti, et al.
Nature Methods|December 9, 2024
Multiplexing cortical brain organoids for the longitudinal dissection of developmental traits at single-cell resolutionNicolò Caporale, Davide Castaldi, Marco Tullio Rigoli, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
YY1 mutations disrupt corticogenesis through a cell-type specific rewiring of cell-autonomous and non-cell-autonomous transcriptional programsMarlene F Pereira, Veronica Finazzi, Ludovico Rizzuti, et al.
Autophagy|July 21, 2021
Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disordersKatrin Linda, Elly I Lewerissa, Anouk H A Verboven, et al.
Nature Genetics|December 16, 2014
7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineagesAntonio Adamo, Sina Atashpaz, Pierre-Luc Germain, et al.
Stem Cell Reports|October 15, 2019
Human Cortical Organoids Expose a Differential Function of GSK3 on Cortical NeurogenesisAlejandro López-Tobón, Carlo Emanuele Villa, Cristina Cheroni, et al.
Scientific Reports|June 26, 2024
Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patientsClaudio Peter D'Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
Genome Medicine|October 30, 2020
A cell-of-origin epigenetic tracer reveals clinically distinct subtypes of high-grade serous ovarian cancerPietro Lo Riso, Carlo Emanuele Villa, Gilles Gasparoni, et al.
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