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Ronald Wetzel

Showing results (71-80 of 83) with videos related to

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Journal of Molecular Biology|January 29, 2013
β-hairpin-mediated nucleation of polyglutamine amyloid formationKarunakar Kar, Cody L Hoop, Kenneth W Drombosky, et al.
Nature Communications|May 25, 2017
Fibril polymorphism affects immobilized non-amyloid flanking domains of huntingtin exon1 rather than its polyglutamine coreHsiang-Kai Lin, Jennifer C Boatz, Inge E Krabbendam, et al.
Journal of Molecular Biology|December 18, 2016
Backbone Engineering within a Latent β-Hairpin Structure to Design Inhibitors of Polyglutamine Amyloid FormationKarunakar Kar, Matthew A Baker, George A Lengyel, et al.
Acta Neuropathologica Communications|April 15, 2021
Correlative light and electron microscopy suggests that mutant huntingtin dysregulates the endolysosomal pathway in presymptomatic Huntington's diseaseYa Zhou, Thomas R Peskett, Christian Landles, et al.
The Journal of Biological Chemistry|December 9, 2017
RAD52 is required for RNA-templated recombination repair in post-mitotic neuronsStarr Welty, Yaqun Teng, Zhuobin Liang, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2016
Huntingtin exon 1 fibrils feature an interdigitated β-hairpin-based polyglutamine coreCody L Hoop, Hsiang-Kai Lin, Karunakar Kar, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2005
Absence of behavioral abnormalities and neurodegeneration in vivo despite widespread neuronal huntingtin inclusionsElizabeth J Slow, Rona K Graham, Alexander P Osmand, et al.
Biochimica Et Biophysica Acta|December 3, 2014
Triosephosphate isomerase I170V alters catalytic site, enhances stability and induces pathology in a Drosophila model of TPI deficiencyBartholomew P Roland, Christopher G Amrich, Charles J Kammerer, et al.
Nature Structural & Molecular Biology|March 10, 2009
Polyglutamine disruption of the huntingtin exon 1 N terminus triggers a complex aggregation mechanismAshwani K Thakur, Murali Jayaraman, Rakesh Mishra, et al.
Nature Reviews. Disease Primers|May 19, 2016
Huntington diseaseGillian P Bates, Ray Dorsey, James F Gusella, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Journal of Molecular Biology|January 29, 2013
β-hairpin-mediated nucleation of polyglutamine amyloid formationKarunakar Kar, Cody L Hoop, Kenneth W Drombosky, et al.
Nature Communications|May 25, 2017
Fibril polymorphism affects immobilized non-amyloid flanking domains of huntingtin exon1 rather than its polyglutamine coreHsiang-Kai Lin, Jennifer C Boatz, Inge E Krabbendam, et al.
Journal of Molecular Biology|December 18, 2016
Backbone Engineering within a Latent β-Hairpin Structure to Design Inhibitors of Polyglutamine Amyloid FormationKarunakar Kar, Matthew A Baker, George A Lengyel, et al.
Acta Neuropathologica Communications|April 15, 2021
Correlative light and electron microscopy suggests that mutant huntingtin dysregulates the endolysosomal pathway in presymptomatic Huntington's diseaseYa Zhou, Thomas R Peskett, Christian Landles, et al.
The Journal of Biological Chemistry|December 9, 2017
RAD52 is required for RNA-templated recombination repair in post-mitotic neuronsStarr Welty, Yaqun Teng, Zhuobin Liang, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2016
Huntingtin exon 1 fibrils feature an interdigitated β-hairpin-based polyglutamine coreCody L Hoop, Hsiang-Kai Lin, Karunakar Kar, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2005
Absence of behavioral abnormalities and neurodegeneration in vivo despite widespread neuronal huntingtin inclusionsElizabeth J Slow, Rona K Graham, Alexander P Osmand, et al.
Biochimica Et Biophysica Acta|December 3, 2014
Triosephosphate isomerase I170V alters catalytic site, enhances stability and induces pathology in a Drosophila model of TPI deficiencyBartholomew P Roland, Christopher G Amrich, Charles J Kammerer, et al.
Nature Structural & Molecular Biology|March 10, 2009
Polyglutamine disruption of the huntingtin exon 1 N terminus triggers a complex aggregation mechanismAshwani K Thakur, Murali Jayaraman, Rakesh Mishra, et al.
Nature Reviews. Disease Primers|May 19, 2016
Huntington diseaseGillian P Bates, Ray Dorsey, James F Gusella, et al.
Pageof 9