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Matt Baker

Showing results (61-70 of 88) 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.
Human Molecular Genetics|August 30, 2008
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementiaRosa Rademakers, Jason L Eriksen, Matt Baker, 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.
Acta Neuropathologica|July 29, 2003
The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathyMarion Hogg, Zoran M Grujic, Matt Baker, et al.
Neurobiology of Aging|October 24, 2007
Prominent phenotypic variability associated with mutations in ProgranulinBrendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.
Human Molecular Genetics|October 1, 2005
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsyRosa Rademakers, Stacey Melquist, Marc Cruts, et al.
American Journal of Human Genetics|March 16, 2007
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsStacey Melquist, David W Craig, Matthew J Huentelman, et al.
Medicine|June 16, 2023
The SERPINA5 coding variant E228Q does not contribute to clinicopathologic characteristics in Alzheimer's disease: A cross-sectional studyBillie J Matchett, Sarah J Lincoln, Matt Baker, et al.
Neurobiology of Aging|September 24, 2016
TYROBP genetic variants in early-onset Alzheimer's diseaseCyril Pottier, Thomas A Ravenscroft, Patricia H Brown, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
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.
Human Molecular Genetics|August 30, 2008
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementiaRosa Rademakers, Jason L Eriksen, Matt Baker, 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.
Acta Neuropathologica|July 29, 2003
The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathyMarion Hogg, Zoran M Grujic, Matt Baker, et al.
Neurobiology of Aging|October 24, 2007
Prominent phenotypic variability associated with mutations in ProgranulinBrendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.
Human Molecular Genetics|October 1, 2005
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsyRosa Rademakers, Stacey Melquist, Marc Cruts, et al.
American Journal of Human Genetics|March 16, 2007
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsStacey Melquist, David W Craig, Matthew J Huentelman, et al.
Medicine|June 16, 2023
The SERPINA5 coding variant E228Q does not contribute to clinicopathologic characteristics in Alzheimer's disease: A cross-sectional studyBillie J Matchett, Sarah J Lincoln, Matt Baker, et al.
Neurobiology of Aging|September 24, 2016
TYROBP genetic variants in early-onset Alzheimer's diseaseCyril Pottier, Thomas A Ravenscroft, Patricia H Brown, et al.
Pageof 9