Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|October 24, 2002
Charcot-Marie-Tooth disease neurofilament mutations disrupt neurofilament assembly and axonal transportJanet Brownlees, Steven Ackerley, Andrew J Grierson, et al.
Acta Neuropathologica Communications|May 10, 2019
LMTK2 binds to kinesin light chains to mediate anterograde axonal transport of cdk5/p35 and LMTK2 levels are reduced in Alzheimer's disease brainsGábor M Mórotz, Elizabeth B Glennon, Patricia Gomez-Suaga, et al.
The Journal of Biological Chemistry|October 17, 2008
Dexras1 interacts with FE65 to regulate FE65-amyloid precursor protein-dependent transcriptionKwok-Fai Lau, Wing-Man Chan, Michael S Perkinton, et al.
Human Molecular Genetics|September 12, 2009
X11beta rescues memory and long-term potentiation deficits in Alzheimer's disease APPswe Tg2576 miceJacqueline C Mitchell, Belall B Ariff, Darran M Yates, et al.
The Journal of Biological Chemistry|September 13, 2003
The neuronal adaptor protein X11alpha reduces Abeta levels in the brains of Alzheimer's APPswe Tg2576 transgenic miceJu-Hyun Lee, Kwok-Fai Lau, Michael S Perkinton, et al.
Frontiers in Cell and Developmental Biology|September 19, 2022
The PTPIP51 coiled-coil domain is important in VAPB binding, formation of ER-mitochondria contacts and IP3 receptor delivery of Ca<sup>2+</sup> to mitochondriaGábor M Mórotz, Sandra M Martín-Guerrero, Andrea Markovinovic, et al.
The Journal of Biological Chemistry|February 22, 2005
BACE1 cytoplasmic domain interacts with the copper chaperone for superoxide dismutase-1 and binds copperBarbara Angeletti, Kevin J Waldron, Katie B Freeman, et al.
Acta Neuropathologica Communications|March 8, 2019
The VAPB-PTPIP51 endoplasmic reticulum-mitochondria tethering proteins are present in neuronal synapses and regulate synaptic activityPatricia Gómez-Suaga, Beatriz G Pérez-Nievas, Elizabeth B Glennon, et al.
Acta Neuropathologica Communications|February 23, 2024
Stimulating VAPB-PTPIP51 ER-mitochondria tethering corrects FTD/ALS mutant TDP43 linked Ca<sup>2+</sup> and synaptic defectsAndrea Markovinovic, Sandra M Martín-Guerrero, Gábor M Mórotz, et al.
Pageof 7