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Showing results (621-630 of 632) with videos related to

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American Journal of Human Genetics|September 10, 2019
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital ArthrogryposisPamela Magini, Daphne J Smits, Laura Vandervore, et al.
Frontiers in Neurology|September 27, 2021
Excessive White Matter Hyperintensity Increases Susceptibility to Poor Functional Outcomes After Acute Ischemic StrokeSungmin Hong, Anne-Katrin Giese, Markus D Schirmer, et al.
Cancer Cell|May 30, 2025
The pan-cancer proteome atlas, a mass spectrometry-based landscape for discovering tumor biology, biomarkers, and therapeutic targetsJaco C Knol, Mengge Lyu, Franziska Böttger, et al.
The New England Journal of Medicine|October 23, 2009
Multicenter analysis of glucocerebrosidase mutations in Parkinson's diseaseE Sidransky, M A Nalls, J O Aasly, et al.
Brain Communications|March 14, 2022
Sex-specific lesion pattern of functional outcomes after strokeAnna K Bonkhoff, Martin Bretzner, Sungmin Hong, et al.
Stroke|January 7, 2016
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2Yu-Ching Cheng, Tara M Stanne, Anne-Katrin Giese, et al.
Nature Genetics|November 25, 2014
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissectionStéphanie Debette, Yoichiro Kamatani, Tiina M Metso, et al.
Plos One|November 2, 2018
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic strokeJohn W Cole, Huichun Xu, Kathleen Ryan, et al.
Journal of Medical Genetics|April 6, 2017
<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspectsKonrad Platzer, Hongjie Yuan, Hannah Schütz, et al.
Brain : a Journal of Neurology|August 1, 2024
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease studyAna Westenberger, Volha Skrahina, Tatiana Usnich, et al.
Pageof 64

Showing results (621-630 of 632) with videos related to

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Pageof 64
American Journal of Human Genetics|September 10, 2019
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital ArthrogryposisPamela Magini, Daphne J Smits, Laura Vandervore, et al.
Frontiers in Neurology|September 27, 2021
Excessive White Matter Hyperintensity Increases Susceptibility to Poor Functional Outcomes After Acute Ischemic StrokeSungmin Hong, Anne-Katrin Giese, Markus D Schirmer, et al.
Cancer Cell|May 30, 2025
The pan-cancer proteome atlas, a mass spectrometry-based landscape for discovering tumor biology, biomarkers, and therapeutic targetsJaco C Knol, Mengge Lyu, Franziska Böttger, et al.
The New England Journal of Medicine|October 23, 2009
Multicenter analysis of glucocerebrosidase mutations in Parkinson's diseaseE Sidransky, M A Nalls, J O Aasly, et al.
Brain Communications|March 14, 2022
Sex-specific lesion pattern of functional outcomes after strokeAnna K Bonkhoff, Martin Bretzner, Sungmin Hong, et al.
Stroke|January 7, 2016
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2Yu-Ching Cheng, Tara M Stanne, Anne-Katrin Giese, et al.
Nature Genetics|November 25, 2014
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissectionStéphanie Debette, Yoichiro Kamatani, Tiina M Metso, et al.
Plos One|November 2, 2018
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic strokeJohn W Cole, Huichun Xu, Kathleen Ryan, et al.
Journal of Medical Genetics|April 6, 2017
<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspectsKonrad Platzer, Hongjie Yuan, Hannah Schütz, et al.
Brain : a Journal of Neurology|August 1, 2024
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease studyAna Westenberger, Volha Skrahina, Tatiana Usnich, et al.
Pageof 64