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Murat Gunel

Showing results (41-50 of 118) with videos related to

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Journal of Neurosurgery|December 25, 2007
A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigationKaya Bilguvar, Mohamad Bydon, Fatih Bayrakli, et al.
Scientific Reports|March 9, 2017
Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephalyParaskevi Sgourdou, Ketu Mishra-Gorur, Ichiko Saotome, et al.
American Journal of Medical Genetics. Part A|May 26, 2012
The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditionsMichael J Bamshad, Jay A Shendure, David Valle, et al.
Stroke|November 12, 2025
SLAMF1 as a Risk Biomarker for Nontraumatic SAH: Evidence From a Multiomics StudyDaniela Renedo, Andrew Koo, Nanthiya Sujijantarat, et al.
Annals of Neurology|October 28, 2021
Genetically Determined Low-Density Lipoprotein Cholesterol and Risk of Subarachnoid HemorrhageJulián N Acosta, Cameron P Both, Natalia Szejko, et al.
Cold Spring Harbor Molecular Case Studies|June 21, 2017
<i>ALPK3</i> gene mutation in a patient with congenital cardiomyopathy and dysmorphic featuresAhmet Okay Çağlayan, Rabia Gonul Sezer, Hande Kaymakçalan, et al.
Cold Spring Harbor Molecular Case Studies|June 16, 2018
De novo <i>MYH9</i> mutation in congenital scalp hemangiomaElena I Fomchenko, Daniel Duran, Sheng Chih Jin, et al.
Molecular Genetics & Genomic Medicine|April 28, 2022
Mutation spectrum of congenital heart disease in a consanguineous Turkish populationWeilai Dong, Hande Kaymakcalan, Sheng Chih Jin, et al.
Journal of Child Neurology|January 30, 2010
Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI)Zulfikar Arlier, Yasar Bayri, Luis E Kolb, et al.
Neurology|September 25, 2025
Immune Characterization of Intracranial Aneurysms Using Noninvasive Endoluminal Biopsy With High-Dimensional Single-Cell PhenotypingJoseph Antonios, Batur Gultekin, Brianna Theriault, et al.
Pageof 12

Showing results (41-50 of 118) with videos related to

Sort By:
Pageof 12
Journal of Neurosurgery|December 25, 2007
A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigationKaya Bilguvar, Mohamad Bydon, Fatih Bayrakli, et al.
Scientific Reports|March 9, 2017
Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephalyParaskevi Sgourdou, Ketu Mishra-Gorur, Ichiko Saotome, et al.
American Journal of Medical Genetics. Part A|May 26, 2012
The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditionsMichael J Bamshad, Jay A Shendure, David Valle, et al.
Stroke|November 12, 2025
SLAMF1 as a Risk Biomarker for Nontraumatic SAH: Evidence From a Multiomics StudyDaniela Renedo, Andrew Koo, Nanthiya Sujijantarat, et al.
Annals of Neurology|October 28, 2021
Genetically Determined Low-Density Lipoprotein Cholesterol and Risk of Subarachnoid HemorrhageJulián N Acosta, Cameron P Both, Natalia Szejko, et al.
Cold Spring Harbor Molecular Case Studies|June 21, 2017
<i>ALPK3</i> gene mutation in a patient with congenital cardiomyopathy and dysmorphic featuresAhmet Okay Çağlayan, Rabia Gonul Sezer, Hande Kaymakçalan, et al.
Cold Spring Harbor Molecular Case Studies|June 16, 2018
De novo <i>MYH9</i> mutation in congenital scalp hemangiomaElena I Fomchenko, Daniel Duran, Sheng Chih Jin, et al.
Molecular Genetics & Genomic Medicine|April 28, 2022
Mutation spectrum of congenital heart disease in a consanguineous Turkish populationWeilai Dong, Hande Kaymakcalan, Sheng Chih Jin, et al.
Journal of Child Neurology|January 30, 2010
Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI)Zulfikar Arlier, Yasar Bayri, Luis E Kolb, et al.
Neurology|September 25, 2025
Immune Characterization of Intracranial Aneurysms Using Noninvasive Endoluminal Biopsy With High-Dimensional Single-Cell PhenotypingJoseph Antonios, Batur Gultekin, Brianna Theriault, et al.
Pageof 12