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Ian R Mackenzie

Showing results (71-80 of 134) with videos related to

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Human Molecular Genetics|October 29, 2013
Targeted manipulation of the sortilin-progranulin axis rescues progranulin haploinsufficiencyWing C Lee, Sandra Almeida, Mercedes Prudencio, et al.
Molecular Neurodegeneration|March 18, 2020
Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiencyJonathan Frew, Alireza Baradaran-Heravi, Aruna D Balgi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 2014
Intercellular propagated misfolding of wild-type Cu/Zn superoxide dismutase occurs via exosome-dependent and -independent mechanismsLeslie I Grad, Justin J Yerbury, Bradley J Turner, et al.
Journal of Neurochemistry|June 8, 2013
TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementiaAlexandra M Nicholson, Nicole A Finch, Aleksandra Wojtas, et al.
Journal of Neuroinflammation|April 24, 2025
A 3D human iPSC-derived multi-cell type neurosphere system to model cellular responses to chronic amyloidosisStefan Wendt, Ada J Lin, Sarah N Ebert, et al.
Science (New York, N.Y.)|October 7, 2006
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosisManuela Neumann, Deepak M Sampathu, Linda K Kwong, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS familyAdam L Boxer, Ian R Mackenzie, Bradley F Boeve, et al.
American Journal of Human Genetics|November 20, 2010
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasmaMinerva M Carrasquillo, Alexandra M Nicholson, NiCole Finch, et al.
American Journal of Human Genetics|May 26, 2015
Jump from pre-mutation to pathologic expansion in C9orf72Zhengrui Xi, Marka van Blitterswijk, Ming Zhang, et al.
Nature|July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.
Pageof 14

Showing results (71-80 of 134) with videos related to

Sort By:
Pageof 14
Human Molecular Genetics|October 29, 2013
Targeted manipulation of the sortilin-progranulin axis rescues progranulin haploinsufficiencyWing C Lee, Sandra Almeida, Mercedes Prudencio, et al.
Molecular Neurodegeneration|March 18, 2020
Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiencyJonathan Frew, Alireza Baradaran-Heravi, Aruna D Balgi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 2014
Intercellular propagated misfolding of wild-type Cu/Zn superoxide dismutase occurs via exosome-dependent and -independent mechanismsLeslie I Grad, Justin J Yerbury, Bradley J Turner, et al.
Journal of Neurochemistry|June 8, 2013
TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementiaAlexandra M Nicholson, Nicole A Finch, Aleksandra Wojtas, et al.
Journal of Neuroinflammation|April 24, 2025
A 3D human iPSC-derived multi-cell type neurosphere system to model cellular responses to chronic amyloidosisStefan Wendt, Ada J Lin, Sarah N Ebert, et al.
Science (New York, N.Y.)|October 7, 2006
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosisManuela Neumann, Deepak M Sampathu, Linda K Kwong, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS familyAdam L Boxer, Ian R Mackenzie, Bradley F Boeve, et al.
American Journal of Human Genetics|November 20, 2010
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasmaMinerva M Carrasquillo, Alexandra M Nicholson, NiCole Finch, et al.
American Journal of Human Genetics|May 26, 2015
Jump from pre-mutation to pathologic expansion in C9orf72Zhengrui Xi, Marka van Blitterswijk, Ming Zhang, et al.
Nature|July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.
Pageof 14