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Iscience|October 21, 2020
Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal NeuralgiaWeilai Dong, Sheng Chih Jin, August Allocco, et al.Neuron|December 23, 2018
Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen MalformationDaniel Duran, Xue Zeng, Sheng Chih Jin, et al.Neuron|July 10, 2018
De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital HydrocephalusCharuta Gavankar Furey, Jungmin Choi, Sheng Chih Jin, et al.JAMA Neurology|June 14, 2021
DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya DiseaseAdam J Kundishora, Samuel T Peters, Amélie Pinard, et al.Biorxiv : the Preprint Server for Biology|July 29, 2026
A cargo receptor entrapment complex is a therapeutic node for genetically and clinically distinct proteinopathiesMagdalena Riedl Khursigara, Alissa C Goss, Maria Kost-Alimova, et al.Nature Neuroscience|February 24, 2025
PTEN mutations impair CSF dynamics and cortical networks by dysregulating periventricular neural progenitorsTyrone DeSpenza, Emre Kiziltug, Garrett Allington, et al.Journal of the American Society of Nephrology : JASN|October 17, 2020
AKI Treated with Renal Replacement Therapy in Critically Ill Patients with COVID-19Shruti Gupta, Steven G Coca, Lili Chan, et al.Nature Medicine|October 20, 2020
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalusSheng Chih Jin, Weilai Dong, Adam J Kundishora, et al.Biorxiv : the Preprint Server for Biology|March 30, 2023
Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformationsShujuan Zhao, Kedous Y Mekbib, Martijn A van der Ent, et al.Nature Communications|November 17, 2023
Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformationsShujuan Zhao, Kedous Y Mekbib, Martijn A van der Ent, et al.Pageof 27