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Murat Gunel

Showing results (101-110 of 118) with videos related to

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The Journal of Experimental Medicine|January 12, 2021
Neuroinvasion of SARS-CoV-2 in human and mouse brainEric Song, Ce Zhang, Benjamin Israelow, et al.
Annals of Neurology|April 12, 2020
Genetically Elevated LDL Associates with Lower Risk of Intracerebral HemorrhageGuido J Falcone, Elayna Kirsch, Julian N Acosta, et al.
JAMA Neurology|May 1, 2023
Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe EpilepsySattar Khoshkhoo, Yilan Wang, Yasmine Chahine, et al.
Cell|February 21, 2023
The choroid plexus links innate immunity to CSF dysregulation in hydrocephalusStephanie M Robert, Benjamin C Reeves, Emre Kiziltug, et al.
Nature Genetics|March 15, 2011
Genome-wide association study identifies susceptibility loci for IgA nephropathyAli G Gharavi, Krzysztof Kiryluk, Murim Choi, et al.
American Journal of Human Genetics|July 14, 2015
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and OpportunitiesJessica X Chong, Kati J Buckingham, Shalini N Jhangiani, et al.
Nature Genetics|July 18, 2018
Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migrationAshleigh E Schaffer, Martin W Breuss, Ahmet Okay Caglayan, et al.
Nature Genetics|April 8, 2015
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunctionNaiara Akizu, Vincent Cantagrel, Maha S Zaki, 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.
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.
Pageof 12

Showing results (101-110 of 118) with videos related to

Sort By:
Pageof 12
The Journal of Experimental Medicine|January 12, 2021
Neuroinvasion of SARS-CoV-2 in human and mouse brainEric Song, Ce Zhang, Benjamin Israelow, et al.
Annals of Neurology|April 12, 2020
Genetically Elevated LDL Associates with Lower Risk of Intracerebral HemorrhageGuido J Falcone, Elayna Kirsch, Julian N Acosta, et al.
JAMA Neurology|May 1, 2023
Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe EpilepsySattar Khoshkhoo, Yilan Wang, Yasmine Chahine, et al.
Cell|February 21, 2023
The choroid plexus links innate immunity to CSF dysregulation in hydrocephalusStephanie M Robert, Benjamin C Reeves, Emre Kiziltug, et al.
Nature Genetics|March 15, 2011
Genome-wide association study identifies susceptibility loci for IgA nephropathyAli G Gharavi, Krzysztof Kiryluk, Murim Choi, et al.
American Journal of Human Genetics|July 14, 2015
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and OpportunitiesJessica X Chong, Kati J Buckingham, Shalini N Jhangiani, et al.
Nature Genetics|July 18, 2018
Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migrationAshleigh E Schaffer, Martin W Breuss, Ahmet Okay Caglayan, et al.
Nature Genetics|April 8, 2015
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunctionNaiara Akizu, Vincent Cantagrel, Maha S Zaki, 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.
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.
Pageof 12