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Nature Structural & Molecular Biology|December 9, 2022
A critical period of translational control during brain development at codon resolutionDermot Harnett, Mateusz C Ambrozkiewicz, Ulrike Zinnall, et al.Cell Stem Cell|January 31, 2017
Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA DisordersCarmen Lorenz, Pierre Lesimple, Raul Bukowiecki, et al.American Journal of Human Genetics|November 4, 2017
De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial DysfunctionNadja Ehmke, Luitgard Graul-Neumann, Lukasz Smorag, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 7, 2022
Alternative splicing of BUD13 determines the severity of a developmental disorder with lipodystrophy and progeroid featuresUwe Kornak, Namrata Saha, Boris Keren, et al.Pageof 3