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Alexandra M Nicholson

Showing results (11-20 of 28) with videos related to

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Brain Communications|January 25, 2023
The role of neurofilament light in genetic frontotemporal lobar degenerationHenrik Zetterberg, Charlotte Teunissen, John van Swieten, et al.
Neurology|April 29, 2014
Progranulin protein levels are differently regulated in plasma and CSFAlexandra M Nicholson, NiCole A Finch, Colleen S Thomas, et al.
Neurology|February 15, 2013
CSF1R mutations link POLD and HDLS as a single disease entityAlexandra M Nicholson, Matt C Baker, Nicole A Finch, 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.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, 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.
Brain : a Journal of Neurology|June 7, 2020
Loss of TMEM106B leads to myelination deficits: implications for frontotemporal dementia treatment strategiesXiaolai Zhou, Alexandra M Nicholson, Yingxue Ren, et al.
Acta Neuropathologica Communications|June 2, 2018
Loss of Tmem106b is unable to ameliorate frontotemporal dementia-like phenotypes in an AAV mouse model of C9ORF72-repeat induced toxicityAlexandra M Nicholson, Xiaolai Zhou, Ralph B Perkerson, et al.
Brain Pathology (Zurich, Switzerland)|March 12, 2021
Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficitsRosa Rademakers, Alexandra M Nicholson, Yingxue Ren, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Brain Communications|January 25, 2023
The role of neurofilament light in genetic frontotemporal lobar degenerationHenrik Zetterberg, Charlotte Teunissen, John van Swieten, et al.
Neurology|April 29, 2014
Progranulin protein levels are differently regulated in plasma and CSFAlexandra M Nicholson, NiCole A Finch, Colleen S Thomas, et al.
Neurology|February 15, 2013
CSF1R mutations link POLD and HDLS as a single disease entityAlexandra M Nicholson, Matt C Baker, Nicole A Finch, 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.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, 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.
Brain : a Journal of Neurology|June 7, 2020
Loss of TMEM106B leads to myelination deficits: implications for frontotemporal dementia treatment strategiesXiaolai Zhou, Alexandra M Nicholson, Yingxue Ren, et al.
Acta Neuropathologica Communications|June 2, 2018
Loss of Tmem106b is unable to ameliorate frontotemporal dementia-like phenotypes in an AAV mouse model of C9ORF72-repeat induced toxicityAlexandra M Nicholson, Xiaolai Zhou, Ralph B Perkerson, et al.
Brain Pathology (Zurich, Switzerland)|March 12, 2021
Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficitsRosa Rademakers, Alexandra M Nicholson, Yingxue Ren, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
Pageof 3