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Annals of Clinical and Translational Neurology|January 7, 2016
Young-onset frontotemporal dementia in a homozygous tau R406W mutation carrierAdeline S L Ng, Ana C Sias, Peter S Pressman, et al.Frontiers in Cellular Neuroscience|August 22, 2012
Lipocalin 2 is present in the EAE brain and is modulated by natalizumabFernanda Marques, Sandro D Mesquita, João C Sousa, et al.NPJ Genomic Medicine|December 18, 2024
Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathologySimone Montalbano, Morten Dybdahl Krebs, Anders Rosengren, et al.Focus (American Psychiatric Publishing)|February 5, 2020
Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic OverlapMichael J Gandal, Jillian R Haney, Neelroop N Parikshak, et al.Cell Reports|November 18, 2020
Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and ImmunosuppressionJessica E Rexach, Damon Polioudakis, Anna Yin, et al.Neuron|July 31, 2012
Subcellular knockout of importin β1 perturbs axonal retrograde signalingRotem Ben-Tov Perry, Ella Doron-Mandel, Elena Iavnilovitch, et al.American Journal of Human Genetics|June 26, 2012
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disordersRui Luo, Stephan J Sanders, Yuan Tian, et al.Autism : the International Journal of Research and Practice|September 5, 2022
Maternal obesity, diabetes, preeclampsia, and asthma during pregnancy and likelihood of autism spectrum disorder with gastrointestinal disturbances in offspringSarah A Carter, Jane C Lin, Ting Chow, et al.Archives of Neurology|May 21, 2003
Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementiaMaria-Jesús Sobrido, Bruce L Miller, Necat Havlioglu, et al.Nature Medicine|November 29, 2011
Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndromeSergiu P Paşca, Thomas Portmann, Irina Voineagu, et al.Pageof 65