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Human Molecular Genetics|March 24, 2017
Proteomics insights into infantile neuronal ceroid lipofuscinosis (CLN1) point to the involvement of cilia pathology in the diseaseMichal Segal-Salto, Karin Hansson, Tamar Sapir, et al.Nature Communications|July 21, 2022
Heterogeneous nuclear ribonucleoprotein U (HNRNPU) safeguards the developing mouse cortexTamar Sapir, Aditya Kshirsagar, Anna Gorelik, et al.BMC Genomics|July 28, 2006
The evolving doublecortin (DCX) superfamilyOrly Reiner, Frédéric M Coquelle, Bastian Peter, et al.Scientifica|November 27, 2013
LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to MicrotubulesOrly ReinerIscience|January 3, 2023
Evidence of shared transcriptomic dysregulation of HNRNPU-related disorder between human organoids and embryonic miceAndrew K Ressler, Gabriela L A Sampaio, Sarah A Dugger, et al.The EMBO Journal|November 21, 2009
Ndel1 palmitoylation: a new mean to regulate cytoplasmic dynein activityAnat Shmueli, Michal Segal, Tamar Sapir, et al.Neuron|January 3, 2006
Doublecortin-like kinase controls neurogenesis by regulating mitotic spindles and M phase progressionTianzhi Shu, Huang-Chun Tseng, Tamar Sapir, et al.Biorxiv : the Preprint Server for Biology|August 20, 2025
Neural Progenitors as a Novel Pathogenic Mechanism in MicrocephalyRami Yair Tshuva, Jeyoon Bok, Mio Nonaka, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 23, 2015
The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanismHadar Vinograd-Byk, Tamar Sapir, Lara Cantarero, et al.Professional Case Management|November 28, 2023
Growth of Remote Therapeutic Monitoring Lands New Opportunities for Case ManagementKathleen Moreo, Tamar SapirPageof 12