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Nature Neuroscience|December 19, 2018
Widespread RNA editing dysregulation in brains from autistic individualsStephen S Tran, Hyun-Ik Jun, Jae Hoon Bahn, et al.Nature Methods|May 26, 2015
Functional cortical neurons and astrocytes from human pluripotent stem cells in 3D cultureAnca M Paşca, Steven A Sloan, Laura E Clarke, et al.Frontiers in Neuroscience|December 5, 2022
Linear discriminant analysis of phenotypic data for classifying autism spectrum disorder by diagnosis and sexZachary Jacokes, Allison Jack, Catherine A W Sullivan, et al.Plos One|February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genesRavinesh A Kumar, Christian R Marshall, Judith A Badner, et al.Elife|December 14, 2022
The injured sciatic nerve atlas (iSNAT), insights into the cellular and molecular basis of neural tissue degeneration and regenerationXiao-Feng Zhao, Lucas D Huffman, Hannah Hafner, et al.Nature Genetics|June 2, 2022
Genetic correlates of phenotypic heterogeneity in autismVarun Warrier, Xinhe Zhang, Patrick Reed, et al.Nature Genetics|April 11, 2018
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insightsAlexander Gusev, Nicholas Mancuso, Hyejung Won, et al.Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.Nature Communications|June 26, 2021
Conservation and divergence of vulnerability and responses to stressors between human and mouse astrocytesJiwen Li, Lin Pan, William G Pembroke, et al.Human Molecular Genetics|April 25, 2014
Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2Brent L Fogel, Ellen Cho, Amanda Wahnich, et al.Pageof 86