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R A Mackenzie

Showing results (101-110 of 155) with videos related to

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Muscle & Nerve|June 15, 2010
Fus gene mutations in familial and sporadic amyotrophic lateral sclerosisRosa Rademakers, Heather Stewart, Mariely Dejesus-Hernandez, et al.
Epilepsia|September 1, 1993
Corpus callosotomy for intractable epilepsy: seizure outcome and prognostic factorsD C Reutens, A M Bye, I J Hopkins, et al.
Acta Neuropathologica|May 24, 2011
Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutationIan R A Mackenzie, Olaf Ansorge, Michael Strong, et al.
Brain : a Journal of Neurology|April 26, 2023
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypesCristina T Vicente, Jolien Perneel, Sarah Wynants, et al.
The EMBO Journal|September 13, 2012
Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUSDorothee Dormann, Tobias Madl, Chiara F Valori, et al.
Acta Neuropathologica|October 6, 2006
Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotypeIan R A Mackenzie, Atik Baborie, Stuart Pickering-Brown, et al.
Nature Neuroscience|September 17, 2013
Interaction of FUS and HDAC1 regulates DNA damage response and repair in neuronsWen-Yuan Wang, Ling Pan, Susan C Su, et al.
Acta Neuropathologica|May 12, 2023
Limbic-predominant age-related TDP-43 proteinopathy (LATE-NC) is associated with abundant TMEM106B pathologyManuela Neumann, Jolien Perneel, Simon Cheung, et al.
Acta Neuropathologica|January 6, 2023
Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and agingJolien Perneel, Manuela Neumann, Bavo Heeman, et al.
The Journal of Comparative Neurology|August 26, 2010
Progranulin expression in the developing and adult murine brainTerri L Petkau, S J Neal, P C Orban, et al.
Pageof 16

Showing results (101-110 of 155) with videos related to

Sort By:
Pageof 16
Muscle & Nerve|June 15, 2010
Fus gene mutations in familial and sporadic amyotrophic lateral sclerosisRosa Rademakers, Heather Stewart, Mariely Dejesus-Hernandez, et al.
Epilepsia|September 1, 1993
Corpus callosotomy for intractable epilepsy: seizure outcome and prognostic factorsD C Reutens, A M Bye, I J Hopkins, et al.
Acta Neuropathologica|May 24, 2011
Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutationIan R A Mackenzie, Olaf Ansorge, Michael Strong, et al.
Brain : a Journal of Neurology|April 26, 2023
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypesCristina T Vicente, Jolien Perneel, Sarah Wynants, et al.
The EMBO Journal|September 13, 2012
Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUSDorothee Dormann, Tobias Madl, Chiara F Valori, et al.
Acta Neuropathologica|October 6, 2006
Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotypeIan R A Mackenzie, Atik Baborie, Stuart Pickering-Brown, et al.
Nature Neuroscience|September 17, 2013
Interaction of FUS and HDAC1 regulates DNA damage response and repair in neuronsWen-Yuan Wang, Ling Pan, Susan C Su, et al.
Acta Neuropathologica|May 12, 2023
Limbic-predominant age-related TDP-43 proteinopathy (LATE-NC) is associated with abundant TMEM106B pathologyManuela Neumann, Jolien Perneel, Simon Cheung, et al.
Acta Neuropathologica|January 6, 2023
Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and agingJolien Perneel, Manuela Neumann, Bavo Heeman, et al.
The Journal of Comparative Neurology|August 26, 2010
Progranulin expression in the developing and adult murine brainTerri L Petkau, S J Neal, P C Orban, et al.
Pageof 16