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David R Borchelt

Showing results (51-60 of 159) with videos related to

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Acta Neuropathologica|December 10, 2015
Prion-like propagation of mutant SOD1 misfolding and motor neuron disease spread along neuroanatomical pathwaysJacob I Ayers, Susan E Fromholt, Veronica M O'Neal, et al.
Acta Neuropathologica Communications|February 27, 2026
Rigorous evaluation of pathological α-synucleinopathy transmissibility between animals in an experimental modelAmanda N Sacino, Todd E Golde, David R Borchelt, et al.
Plos One|September 9, 2008
Receptor-associated protein (RAP) plays a central role in modulating Abeta deposition in APP/PS1 transgenic miceGuilian Xu, Celeste Karch, Ning Li, et al.
Neuroscience Letters|December 21, 2020
Novel SOD1 monoclonal antibodies against the electrostatic loop preferentially detect misfolded SOD1 aggregatesYuxing Xia, Zhijuan Chen, Guilian Xu, et al.
Acta Neuropathologica Communications|October 27, 2023
Human tauopathy strains defined by phosphorylation in R1-R2 repeat domains of tauEthan D Smith, Quan Vo, Benoit I Giasson, et al.
Neurobiology of Disease|May 14, 2003
Normal cognitive behavior in two distinct congenic lines of transgenic mice hyperexpressing mutant APP SWEAlena V Savonenko, Guilian M Xu, Donald L Price, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 15, 2009
Immature copper-zinc superoxide dismutase and familial amyotrophic lateral sclerosisSai V Seetharaman, Mercedes Prudencio, Celeste Karch, et al.
Journal of Neurochemistry|February 16, 2012
A novel variant of human superoxide dismutase 1 harboring amyotrophic lateral sclerosis-associated and experimental mutations in metal-binding residues and free cysteines lacks toxicity in vivoMercedes Prudencio, Herman Lelie, Hilda H Brown, et al.
Scientific Reports|December 1, 2020
IL-10 based immunomodulation initiated at birth extends lifespan in a familial mouse model of amyotrophic lateral sclerosisMichael R Strickland, Kristen R Ibanez, Mariya Yaroshenko, et al.
Glia|February 26, 2021
Reactive astrocytes as treatment targets in Alzheimer's disease-Systematic review of studies using the APPswePS1dE9 mouse modelTamar Smit, Natasja A C Deshayes, David R Borchelt, et al.
Pageof 16

Showing results (51-60 of 159) with videos related to

Sort By:
Pageof 16
Acta Neuropathologica|December 10, 2015
Prion-like propagation of mutant SOD1 misfolding and motor neuron disease spread along neuroanatomical pathwaysJacob I Ayers, Susan E Fromholt, Veronica M O'Neal, et al.
Acta Neuropathologica Communications|February 27, 2026
Rigorous evaluation of pathological α-synucleinopathy transmissibility between animals in an experimental modelAmanda N Sacino, Todd E Golde, David R Borchelt, et al.
Plos One|September 9, 2008
Receptor-associated protein (RAP) plays a central role in modulating Abeta deposition in APP/PS1 transgenic miceGuilian Xu, Celeste Karch, Ning Li, et al.
Neuroscience Letters|December 21, 2020
Novel SOD1 monoclonal antibodies against the electrostatic loop preferentially detect misfolded SOD1 aggregatesYuxing Xia, Zhijuan Chen, Guilian Xu, et al.
Acta Neuropathologica Communications|October 27, 2023
Human tauopathy strains defined by phosphorylation in R1-R2 repeat domains of tauEthan D Smith, Quan Vo, Benoit I Giasson, et al.
Neurobiology of Disease|May 14, 2003
Normal cognitive behavior in two distinct congenic lines of transgenic mice hyperexpressing mutant APP SWEAlena V Savonenko, Guilian M Xu, Donald L Price, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 15, 2009
Immature copper-zinc superoxide dismutase and familial amyotrophic lateral sclerosisSai V Seetharaman, Mercedes Prudencio, Celeste Karch, et al.
Journal of Neurochemistry|February 16, 2012
A novel variant of human superoxide dismutase 1 harboring amyotrophic lateral sclerosis-associated and experimental mutations in metal-binding residues and free cysteines lacks toxicity in vivoMercedes Prudencio, Herman Lelie, Hilda H Brown, et al.
Scientific Reports|December 1, 2020
IL-10 based immunomodulation initiated at birth extends lifespan in a familial mouse model of amyotrophic lateral sclerosisMichael R Strickland, Kristen R Ibanez, Mariya Yaroshenko, et al.
Glia|February 26, 2021
Reactive astrocytes as treatment targets in Alzheimer's disease-Systematic review of studies using the APPswePS1dE9 mouse modelTamar Smit, Natasja A C Deshayes, David R Borchelt, et al.
Pageof 16