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Helen Kim

Showing results (171-180 of 250) with videos related to

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Molecular Genetics & Genomic Medicine|September 7, 2021
Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformationForam Choksi, Shantel Weinsheimer, Jeffrey Nelson, et al.
International Journal of Oncology|July 3, 2010
Raloxifene-stimulated experimental breast cancer with the paradoxical actions of estrogen to promote or prevent tumor growth: a unifying concept in anti-hormone resistanceGregor M Balaburski, Rita C Dardes, Michael Johnson, et al.
Neuroreport|May 31, 2012
Perlecan domain V is upregulated in human brain arteriovenous malformation and could mediate the vascular endothelial growth factor effect in lesional tissueMichael P Kahle, Boyeon Lee, Tony Pourmohamad, et al.
Stroke|February 25, 2012
An admission bioclinical score to predict 1-year outcomes in patients undergoing aneurysm coilingVincent Degos, Christian C Apfel, Paola Sanchez, et al.
Neurology|February 11, 2022
Endoluminal Biopsy for Molecular Profiling of Human Brain Vascular MalformationsEthan Winkler, David Wu, Eugene Gil, et al.
Nature Reviews. Disease Primers|May 19, 2016
Brain arteriovenous malformationsMichael T Lawton, W Caleb Rutledge, Helen Kim, et al.
Cells|January 11, 2024
Increased Collagen I/Collagen III Ratio Is Associated with Hemorrhage in Brain Arteriovenous Malformations in Human and MouseZahra Shabani, Joana Schuerger, Xiaonan Zhu, et al.
Leukemia & Lymphoma|April 23, 2004
Autologous bone marrow transplantation for marginal zone non-Hodgkin's lymphomaJennifer R Brown, Guylaine Gaudet, Jonathan W Friedberg, et al.
World Neurosurgery|September 7, 2018
The Unique Features and Outcomes of Microsurgically Resected Cerebellar Arteriovenous MalformationsPeyton L Nisson, Salman A Fard, Ali Tayebi Meybodi, et al.
American Journal of Human Genetics|March 16, 2025
Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesisEvon DeBose-Scarlett, Andrew K Ressler, Carol J Gallione, et al.
Pageof 25

Showing results (171-180 of 250) with videos related to

Sort By:
Pageof 25
Molecular Genetics & Genomic Medicine|September 7, 2021
Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformationForam Choksi, Shantel Weinsheimer, Jeffrey Nelson, et al.
International Journal of Oncology|July 3, 2010
Raloxifene-stimulated experimental breast cancer with the paradoxical actions of estrogen to promote or prevent tumor growth: a unifying concept in anti-hormone resistanceGregor M Balaburski, Rita C Dardes, Michael Johnson, et al.
Neuroreport|May 31, 2012
Perlecan domain V is upregulated in human brain arteriovenous malformation and could mediate the vascular endothelial growth factor effect in lesional tissueMichael P Kahle, Boyeon Lee, Tony Pourmohamad, et al.
Stroke|February 25, 2012
An admission bioclinical score to predict 1-year outcomes in patients undergoing aneurysm coilingVincent Degos, Christian C Apfel, Paola Sanchez, et al.
Neurology|February 11, 2022
Endoluminal Biopsy for Molecular Profiling of Human Brain Vascular MalformationsEthan Winkler, David Wu, Eugene Gil, et al.
Nature Reviews. Disease Primers|May 19, 2016
Brain arteriovenous malformationsMichael T Lawton, W Caleb Rutledge, Helen Kim, et al.
Cells|January 11, 2024
Increased Collagen I/Collagen III Ratio Is Associated with Hemorrhage in Brain Arteriovenous Malformations in Human and MouseZahra Shabani, Joana Schuerger, Xiaonan Zhu, et al.
Leukemia & Lymphoma|April 23, 2004
Autologous bone marrow transplantation for marginal zone non-Hodgkin's lymphomaJennifer R Brown, Guylaine Gaudet, Jonathan W Friedberg, et al.
World Neurosurgery|September 7, 2018
The Unique Features and Outcomes of Microsurgically Resected Cerebellar Arteriovenous MalformationsPeyton L Nisson, Salman A Fard, Ali Tayebi Meybodi, et al.
American Journal of Human Genetics|March 16, 2025
Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesisEvon DeBose-Scarlett, Andrew K Ressler, Carol J Gallione, et al.
Pageof 25