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Alexandra M Nicholson

Showing results (21-30 of 28) with videos related to

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Acta Neuropathologica|May 7, 2015
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron diseaseCyril Pottier, Kevin F Bieniek, NiCole Finch, et al.
Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Neuron|September 28, 2011
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSMariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, et al.
Neurology. Genetics|June 30, 2017
Abnormal expression of homeobox genes and transthyretin in <i>C9ORF72</i> expansion carriersNiCole A Finch, Xue Wang, Matthew C Baker, et al.
Nature Communications|July 1, 2016
Prosaposin is a regulator of progranulin levels and oligomerizationAlexandra M Nicholson, NiCole A Finch, Marcio Almeida, et al.
Nature Genetics|December 27, 2011
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroidsRosa Rademakers, Matt Baker, Alexandra M Nicholson, et al.
Acta Neuropathologica|January 4, 2014
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementiaMarka van Blitterswijk, Bianca Mullen, Alexandra M Nicholson, et al.
Neuron|August 18, 2017
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule DynamicsIan R Mackenzie, Alexandra M Nicholson, Mohona Sarkar, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Acta Neuropathologica|May 7, 2015
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron diseaseCyril Pottier, Kevin F Bieniek, NiCole Finch, et al.
Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Neuron|September 28, 2011
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSMariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, et al.
Neurology. Genetics|June 30, 2017
Abnormal expression of homeobox genes and transthyretin in <i>C9ORF72</i> expansion carriersNiCole A Finch, Xue Wang, Matthew C Baker, et al.
Nature Communications|July 1, 2016
Prosaposin is a regulator of progranulin levels and oligomerizationAlexandra M Nicholson, NiCole A Finch, Marcio Almeida, et al.
Nature Genetics|December 27, 2011
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroidsRosa Rademakers, Matt Baker, Alexandra M Nicholson, et al.
Acta Neuropathologica|January 4, 2014
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementiaMarka van Blitterswijk, Bianca Mullen, Alexandra M Nicholson, et al.
Neuron|August 18, 2017
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule DynamicsIan R Mackenzie, Alexandra M Nicholson, Mohona Sarkar, et al.
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