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Showing results (301-310 of 328) with videos related to

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Cell|March 15, 2024
Rescue of a lysosomal storage disorder caused by Grn loss of function with a brain penetrant progranulin biologicTodd Logan, Matthew J Simon, Anil Rana, et al.
Neurology|September 25, 2024
Gene-Specific Effects on Brain Volume and Cognition of <i>TMEM106B</i> in Frontotemporal Lobar DegenerationMarijne Vandebergh, Eliana Marisa Ramos, Nick Corriveau-Lecavalier, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 9, 2020
Genetic screening of a large series of North American sporadic and familial frontotemporal dementia casesEliana Marisa Ramos, Deepika Reddy Dokuru, Victoria Van Berlo, et al.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Neurobiology of Aging|October 5, 2019
Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriersQin Chen, Bradley F Boeve, Christopher G Schwarz, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear PalsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Annals of Clinical and Translational Neurology|November 28, 2020
Brain volumetric deficits in MAPT mutation carriers: a multisite studyStephanie A Chu, Taru M Flagan, Adam M Staffaroni, et al.
Molecular Neurodegeneration|October 14, 2024
Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal CellsHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2024
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and <i>MAPT</i> Sub-haplotypesHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Pageof 33

Showing results (301-310 of 328) with videos related to

Sort By:
Pageof 33
Cell|March 15, 2024
Rescue of a lysosomal storage disorder caused by Grn loss of function with a brain penetrant progranulin biologicTodd Logan, Matthew J Simon, Anil Rana, et al.
Neurology|September 25, 2024
Gene-Specific Effects on Brain Volume and Cognition of <i>TMEM106B</i> in Frontotemporal Lobar DegenerationMarijne Vandebergh, Eliana Marisa Ramos, Nick Corriveau-Lecavalier, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 9, 2020
Genetic screening of a large series of North American sporadic and familial frontotemporal dementia casesEliana Marisa Ramos, Deepika Reddy Dokuru, Victoria Van Berlo, et al.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Neurobiology of Aging|October 5, 2019
Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriersQin Chen, Bradley F Boeve, Christopher G Schwarz, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear PalsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Annals of Clinical and Translational Neurology|November 28, 2020
Brain volumetric deficits in MAPT mutation carriers: a multisite studyStephanie A Chu, Taru M Flagan, Adam M Staffaroni, et al.
Molecular Neurodegeneration|October 14, 2024
Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal CellsHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2024
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and <i>MAPT</i> Sub-haplotypesHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Pageof 33