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Neuron
|
July 19, 2025
Accelerating biomedical discoveries in brain health through transformative neuropathology of aging and neurodegeneration
Melissa E Murray, Colin Smith, Vilas Menon, et al.
Acta Neuropathologica
|
August 10, 2025
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-U
Sara Alidadiani, Júlia Faura, Sarah Wynants, et al.
Acta Neuropathologica
|
May 22, 2010
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
Hazel Urwin, Keith A Josephs, Jonathan D Rohrer, et al.
The Lancet. Neurology
|
April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study
Rebecca R Valentino, William J Scotton, Shanu F Roemer, 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 Palsy
Hui 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 study
Stephanie A Chu, Taru M Flagan, Adam M Staffaroni, et al.
Molecular Neurodegeneration
|
August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Hui 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-haplotypes
Hui 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 Cells
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Nature Aging
|
May 16, 2025
Large-scale network analysis of the cerebrospinal fluid proteome identifies molecular signatures of frontotemporal lobar degeneration
Rowan Saloner, Adam M Staffaroni, Eric B Dammer, et al.
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Search research articles
Search
Showing results (421-430 of 448) with videos related to
Sort By:
Page
of 45
Neuron
|
July 19, 2025
Accelerating biomedical discoveries in brain health through transformative neuropathology of aging and neurodegeneration
Melissa E Murray, Colin Smith, Vilas Menon, et al.
Acta Neuropathologica
|
August 10, 2025
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-U
Sara Alidadiani, Júlia Faura, Sarah Wynants, et al.
Acta Neuropathologica
|
May 22, 2010
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
Hazel Urwin, Keith A Josephs, Jonathan D Rohrer, et al.
The Lancet. Neurology
|
April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study
Rebecca R Valentino, William J Scotton, Shanu F Roemer, 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 Palsy
Hui 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 study
Stephanie A Chu, Taru M Flagan, Adam M Staffaroni, et al.
Molecular Neurodegeneration
|
August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Hui 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-haplotypes
Hui 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 Cells
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Nature Aging
|
May 16, 2025
Large-scale network analysis of the cerebrospinal fluid proteome identifies molecular signatures of frontotemporal lobar degeneration
Rowan Saloner, Adam M Staffaroni, Eric B Dammer, et al.
Page
of 45