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Showing results (481-490 of 500) with videos related to

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Neurology|October 5, 2012
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathologyDebby Tsuang, James B Leverenz, Oscar L Lopez, et al.
Cell Reports|January 16, 2025
Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathyMari Aikio, Hana M Odeh, Heike J Wobst, et al.
Cell Reports|February 20, 2025
Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathyMari Aikio, Hana M Odeh, Heike J Wobst, et al.
JAMA Neurology|February 15, 2013
APOE ε4 increases risk for dementia in pure synucleinopathiesDebby Tsuang, James B Leverenz, Oscar L Lopez, et al.
Iscience|November 8, 2021
An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients, Jonathan Li, Ryan G Lim, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
A foundational atlas of autism protein interactions reveals molecular convergenceBelinda Wang, Rasika Vartak, Yefim Zaltsman, et al.
Archives of Neurology|April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationAlice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
JAMA Neurology|October 19, 2020
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysisBrian W Kunkle, Michael Schmidt, Hans-Ulrich Klein, et al.
Nature Neuroscience|February 4, 2022
Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell linesEmily G Baxi, Terri Thompson, Jonathan Li, et al.
Nature Genetics|February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Pageof 50

Showing results (481-490 of 500) with videos related to

Sort By:
Pageof 50
Neurology|October 5, 2012
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathologyDebby Tsuang, James B Leverenz, Oscar L Lopez, et al.
Cell Reports|January 16, 2025
Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathyMari Aikio, Hana M Odeh, Heike J Wobst, et al.
Cell Reports|February 20, 2025
Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathyMari Aikio, Hana M Odeh, Heike J Wobst, et al.
JAMA Neurology|February 15, 2013
APOE ε4 increases risk for dementia in pure synucleinopathiesDebby Tsuang, James B Leverenz, Oscar L Lopez, et al.
Iscience|November 8, 2021
An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients, Jonathan Li, Ryan G Lim, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
A foundational atlas of autism protein interactions reveals molecular convergenceBelinda Wang, Rasika Vartak, Yefim Zaltsman, et al.
Archives of Neurology|April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationAlice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
JAMA Neurology|October 19, 2020
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysisBrian W Kunkle, Michael Schmidt, Hans-Ulrich Klein, et al.
Nature Neuroscience|February 4, 2022
Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell linesEmily G Baxi, Terri Thompson, Jonathan Li, et al.
Nature Genetics|February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Pageof 50