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Biorxiv : the Preprint Server for Biology|June 12, 2026
iAstrocytes model cytokine influences on complement expression and neuronal network synchronizationNader Morshed, Matthew Demers, Ana Gonzalez-Ramos, et al.American Journal of Medical Genetics. Part A|October 30, 2019
Duplication 2p16 is associated with perisylvian polymicrogyriaDina Amrom, Annapurna Poduri, Jennifer S Goldman, et al.The FEBS Journal|October 10, 2013
G-protein coupled receptor 56 promotes myoblast fusion through serum response factor- and nuclear factor of activated T-cell-mediated signalling but is not essential for muscle development in vivoMelissa P Wu, Jamie R Doyle, Brenda Barry, et al.Biorxiv : the Preprint Server for Biology|January 30, 2023
Contrasting patterns of somatic mutations in neurons and glia reveal differential predisposition to disease in the aging human brainJavier Ganz, Lovelace J Luquette, Sara Bizzotto, et al.Neuron|January 6, 2022
Brain ventricles as windows into brain development and diseasePhan Q Duy, Pasko Rakic, Seth L Alper, et al.American Journal of Medical Genetics. Part A|August 5, 2015
A novel 2q37 microdeletion containing human neural progenitors genes including STK25 results in severe developmental delay, epilepsy, and microcephalyJaime Imitola, Divya S Khurana, Nadiya M Teplyuk, et al.Clinical Genetics|April 2, 2023
A recurrent de novo variant in NUSAP1 escapes nonsense-mediated decay and leads to microcephaly, epilepsy, and developmental delayAlisa Mo, Emuna Paz-Ebstein, Shira Yanovsky-Dagan, et al.Biorxiv : the Preprint Server for Biology|October 17, 2024
Perinatal Reduction of Genetically Aberrant Neurons from Human Cerebral CortexDiane D Shao, Yifan Zhao, Urmi Ghosh, et al.Nature Biotechnology|January 8, 2020
Accurate detection of mosaic variants in sequencing data without matched controlsYanmei Dou, Minseok Kwon, Rachel E Rodin, et al.American Journal of Human Genetics|December 17, 2009
A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephalyGaneshwaran H Mochida, Muhammad Mahajnah, Anthony D Hill, et al.Pageof 41