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Human Molecular Genetics|March 21, 2013
Cytosolic proteins lose solubility as amyloid deposits in a transgenic mouse model of Alzheimer-type amyloidosisGuilian Xu, Stanley M Stevens, Brenda D Moore, et al.
Zeitschrift Fur Gerontologie Und Geriatrie|June 26, 2002
[Agreement on the Barthel Index. A rapid analysis of other and self-assessment in elderly stroke patients]S Gauggel, G Lämmler, M Borchelt, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 22, 2007
Alzheimer's-type amyloidosis in transgenic mice impairs survival of newborn neurons derived from adult hippocampal neurogenesisLaure Verret, Joanna L Jankowsky, Guilian M Xu, et al.
Journal of Neuropathology and Experimental Neurology|May 8, 2010
Partial depletion of CREB-binding protein reduces life expectancy in a mouse model of Huntington diseaseAlexandra M Klevytska, Andrew T N Tebbenkamp, Alena V Savonenko, et al.
Analytical Chemistry|May 13, 2015
Characterization of Protein Structural Changes in Living Cells Using Time-Lapsed FTIR ImagingPaul Gelfand, Randy J Smith, Eli Stavitski, et al.
Prion|February 17, 2026
Efficient induction of motor neuron disease in transgenic G93A SOD1 mice by prion-like seedingGuilian Xu, Amanda Lopez, Selma Brkic, et al.
Frontiers in Aging Neuroscience|July 2, 2014
Metal-deficient aggregates and diminished copper found in cells expressing SOD1 mutations that cause ALSMegan W Bourassa, Hilda H Brown, David R Borchelt, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 23, 1998
Caspase-1 is activated in neural cells and tissue with amyotrophic lateral sclerosis-associated mutations in copper-zinc superoxide dismutaseP Pasinelli, D R Borchelt, M K Houseweart, et al.
Current Neurology and Neuroscience Reports|August 10, 2002
Transgenic mouse models of neurodegenerative disease: opportunities for therapeutic developmentJoanna L Jankowsky, Alena Savonenko, Gabriele Schilling, et al.
Muscle & Nerve|August 23, 2008
MnSOD deficiency has a differential effect on disease progression in two different ALS mutant mouse modelsFlorian L Muller, Yuhong Liu, Amanda Jernigan, et al.
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