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Murat Gunel

Showing results (31-40 of 118) with videos related to

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Neurosurgery|October 22, 2005
Hypertension, age, and location predict rupture of small intracranial aneurysmsBrian V Nahed, Michael L DiLuna, Thomas Morgan, et al.
Journal of Neurosurgery|August 4, 2004
Krev1 interaction trapped-1/cerebral cavernous malformation-1 protein expression during early angiogenesisOzlem Guzeloglu-Kayisli, Umit A Kayisli, Nduka M Amankulor, et al.
Journal of Human Genetics|August 9, 2020
METAP1 mutation is a novel candidate for autosomal recessive intellectual disabilityAhmet Okay Caglayan, Fesih Aktar, Kaya Bilguvar, et al.
Stroke|February 25, 2006
Molecular genetic analysis of two large kindreds with intracranial aneurysms demonstrates linkage to 11q24-25 and 14q23-31Ali K Ozturk, Brian V Nahed, Mohamad Bydon, et al.
Science Signaling|January 22, 2015
Heparin is an activating ligand of the orphan receptor tyrosine kinase ALKPhillip B Murray, Irit Lax, Andrey Reshetnyak, et al.
Plos One|September 8, 2017
Functional differences between PD-1+ and PD-1- CD4+ effector T cells in healthy donors and patients with glioblastoma multiformeBrittany A Goods, Amanda L Hernandez, Daniel E Lowther, et al.
Frontiers in Oncology|December 11, 2025
Case Report: Genomic characterization of a rare skull-base plasmacytomaHasan Alanya, Sreekar Kasturi, Kanat Yalcin, et al.
Human Mutation|August 7, 2007
Rapid identification of disease-causing mutations using copy number analysis within linkage intervalsFatih Bayrakli, Kaya Bilguvar, Christopher E Mason, et al.
Stroke|January 14, 2021
Genetically Determined Smoking Behavior and Risk of Nontraumatic Subarachnoid HemorrhageJulián N Acosta, Natalia Szejko, Cameron P Both, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 2, 2009
A novel heterozygous deletion within the 3' region of the PAX6 gene causing isolated aniridia in a large family groupFatih Bayrakli, Ilter Guney, Yasar Bayri, et al.
Pageof 12

Showing results (31-40 of 118) with videos related to

Sort By:
Pageof 12
Neurosurgery|October 22, 2005
Hypertension, age, and location predict rupture of small intracranial aneurysmsBrian V Nahed, Michael L DiLuna, Thomas Morgan, et al.
Journal of Neurosurgery|August 4, 2004
Krev1 interaction trapped-1/cerebral cavernous malformation-1 protein expression during early angiogenesisOzlem Guzeloglu-Kayisli, Umit A Kayisli, Nduka M Amankulor, et al.
Journal of Human Genetics|August 9, 2020
METAP1 mutation is a novel candidate for autosomal recessive intellectual disabilityAhmet Okay Caglayan, Fesih Aktar, Kaya Bilguvar, et al.
Stroke|February 25, 2006
Molecular genetic analysis of two large kindreds with intracranial aneurysms demonstrates linkage to 11q24-25 and 14q23-31Ali K Ozturk, Brian V Nahed, Mohamad Bydon, et al.
Science Signaling|January 22, 2015
Heparin is an activating ligand of the orphan receptor tyrosine kinase ALKPhillip B Murray, Irit Lax, Andrey Reshetnyak, et al.
Plos One|September 8, 2017
Functional differences between PD-1+ and PD-1- CD4+ effector T cells in healthy donors and patients with glioblastoma multiformeBrittany A Goods, Amanda L Hernandez, Daniel E Lowther, et al.
Frontiers in Oncology|December 11, 2025
Case Report: Genomic characterization of a rare skull-base plasmacytomaHasan Alanya, Sreekar Kasturi, Kanat Yalcin, et al.
Human Mutation|August 7, 2007
Rapid identification of disease-causing mutations using copy number analysis within linkage intervalsFatih Bayrakli, Kaya Bilguvar, Christopher E Mason, et al.
Stroke|January 14, 2021
Genetically Determined Smoking Behavior and Risk of Nontraumatic Subarachnoid HemorrhageJulián N Acosta, Natalia Szejko, Cameron P Both, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 2, 2009
A novel heterozygous deletion within the 3' region of the PAX6 gene causing isolated aniridia in a large family groupFatih Bayrakli, Ilter Guney, Yasar Bayri, et al.
Pageof 12