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Frontiers in Physiology|January 10, 2022
STXBP1 Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEGSimon J Houtman, Hanna C A Lammertse, Annemiek A van Berkel, et al.Genome Medicine|December 22, 2017
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disordersHoang T Nguyen, Julien Bryois, April Kim, et al.The Journal of Cell Biology|January 18, 2018
Quantifying exosome secretion from single cells reveals a modulatory role for GPCR signalingFrederik Johannes Verweij, Maarten P Bebelman, Connie R Jimenez, et al.Brain : a Journal of Neurology|February 22, 2022
Assessing the landscape of STXBP1-related disorders in 534 individualsJulie Xian, Shridhar Parthasarathy, Sarah M Ruggiero, et al.Neuron|February 7, 2020
Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing FactorsLin Luo, Mateusz C Ambrozkiewicz, Fritz Benseler, et al.Neuron|June 8, 2019
SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the SynapseFrank Koopmans, Pim van Nierop, Maria Andres-Alonso, et al.Nature Genetics|August 27, 2013
Genome-wide association analysis identifies 13 new risk loci for schizophreniaStephan Ripke, Colm O'Dushlaine, Kimberly Chambert, et al.Nature|April 9, 2022
Mapping genomic loci implicates genes and synaptic biology in schizophreniaVassily Trubetskoy, Antonio F Pardiñas, Ting Qi, et al.Pageof 18