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Proceedings of the National Academy of Sciences of the United States of America|October 3, 2008
The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic miceElizabeth A Thomas, Giovanni Coppola, Paula A Desplats, et al.Current Oncology (Toronto, Ont.)|April 6, 2013
Impact of a single-day multidisciplinary clinic on the management of patients with liver tumoursJ Zhang, M N Mavros, D Cosgrove, et al.Neuron|September 11, 2012
Autism-associated promoter variant in MET impacts functional and structural brain networksJeffrey D Rudie, Leanna M Hernandez, Jesse A Brown, et al.Science (New York, N.Y.)|February 27, 2025
4D marmoset brain map reveals MRI and molecular signatures for onset of multiple sclerosis-like lesionsJing-Ping Lin, Alexis Brake, Maxime Donadieu, et al.Experimental Neurology|April 1, 2023
Nav1.7 gain-of-function mutation I228M triggers age-dependent nociceptive insensitivity and C-LTMR dysregulationNivanthika K Wimalasena, Daniel G Taub, Jaehoon Shim, et al.Medrxiv : the Preprint Server for Health Sciences|July 9, 2020
Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health SystemTimothy S Chang, Yi Ding, Malika K Freund, et al.Cerebral Cortex (New York, N.Y. : 1991)|September 13, 2022
A neural stem cell paradigm of pediatric hydrocephalusPhan Q Duy, Pasko Rakic, Seth L Alper, et al.Cancer Research Communications|October 10, 2022
Pathway-based approach reveals differential sensitivity to E2F1 inhibition in glioblastomaAlvaro G Alvarado, Kaleab Tessema, Sree Deepthi Muthukrishnan, et al.American Journal of Human Genetics|August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex FamiliesVirpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.Nature Communications|June 26, 2021
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disordersBenxia Hu, Hyejung Won, Won Mah, et al.Pageof 86