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Rohan de Silva

Showing results (91-100 of 109) with videos related to

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Annals of Neurology|August 1, 1996
Genetic studies in Alzheimer's disease with an NACP/alpha-synuclein polymorphismY Xia, H A Rohan de Silva, B L Rosi, et al.
Brain : a Journal of Neurology|September 13, 2011
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degenerationJonathan D Rohrer, Tammaryn Lashley, Jonathan M Schott, et al.
Neuron|November 16, 2004
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's diseaseCoro Paisán-Ruíz, Shushant Jain, E Whitney Evans, et al.
Annals of Neurology|August 2, 2018
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotypeEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
Acta Neuropathologica|March 23, 2006
An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodiesRohan de Silva, Tammaryn Lashley, Catherine Strand, 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.
Plos One|August 23, 2013
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locusDaniah Trabzuni, Mina Ryten, Warren Emmett, et al.
Acta Neuropathologica|January 18, 2020
Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregatesHelen Ling, Ellen Gelpi, Karen Davey, et al.
Nature|May 20, 2021
MIR-NATs repress MAPT translation and aid proteostasis in neurodegenerationRoberto Simone, Faiza Javad, Warren Emmett, et al.
Pageof 11

Showing results (91-100 of 109) with videos related to

Sort By:
Pageof 11
Annals of Neurology|August 1, 1996
Genetic studies in Alzheimer's disease with an NACP/alpha-synuclein polymorphismY Xia, H A Rohan de Silva, B L Rosi, et al.
Brain : a Journal of Neurology|September 13, 2011
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degenerationJonathan D Rohrer, Tammaryn Lashley, Jonathan M Schott, et al.
Neuron|November 16, 2004
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's diseaseCoro Paisán-Ruíz, Shushant Jain, E Whitney Evans, et al.
Annals of Neurology|August 2, 2018
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotypeEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
Acta Neuropathologica|March 23, 2006
An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodiesRohan de Silva, Tammaryn Lashley, Catherine Strand, 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.
Plos One|August 23, 2013
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locusDaniah Trabzuni, Mina Ryten, Warren Emmett, et al.
Acta Neuropathologica|January 18, 2020
Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregatesHelen Ling, Ellen Gelpi, Karen Davey, et al.
Nature|May 20, 2021
MIR-NATs repress MAPT translation and aid proteostasis in neurodegenerationRoberto Simone, Faiza Javad, Warren Emmett, et al.
Pageof 11