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Schizophrenia Research|September 23, 2008
Sequence analysis of P21-activated kinase 3 (PAK3) in chronic schizophrenia with cognitive impairmentEric M Morrow, Anna Kane, Donald C Goff, et al.
Nature Neuroscience|April 21, 2026
Genomic approaches for understanding the evolution of the human brainJanet H T Song, Michael E Greenberg, David Reich, et al.
Epilepsia|November 20, 2008
Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutationsElena Parrini, Anna Rita Ferrari, Thomas Dorn, et al.
Journal of Visualized Experiments : Jove|March 26, 2013
Isolation of cerebrospinal fluid from rodent embryos for use with dissected cerebral cortical explantsMauro W Zappaterra, Anthony S LaMantia, Christopher A Walsh, et al.
The Journal of Cell Biology|June 15, 2019
SFI1 promotes centriole duplication by recruiting USP9X to stabilize the microcephaly protein STILAndrew Kodani, Tyler Moyer, Allen Chen, et al.
American Journal of Medical Genetics. Part A|November 3, 2007
A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasiaAnna Rajab, M Chiara Manzini, Ganeshwaran H Mochida, et al.
American Journal of Medical Genetics. Part A|January 16, 2018
Thoracic aortic aneurysm in patients with loss of function Filamin A mutations: Clinical characterization, genetics, and recommendationsMing Hui Chen, Sangita Choudhury, Mami Hirata, et al.
Nature Genetics|February 6, 2004
The hyh mutation uncovers roles for alpha Snap in apical protein localization and control of neural cell fateTeresa H Chae, Seonhee Kim, Karla E Marz, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 9, 2005
Cytoplasmic LEK1 is a regulator of microtubule function through its interaction with the LIS1 pathwayVictor Soukoulis, Samyukta Reddy, Ryan D Pooley, et al.
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