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Ian R Mackenzie

Showing results (81-90 of 134) with videos related to

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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.
Science Translational Medicine|April 14, 2017
Individuals with progranulin haploinsufficiency exhibit features of neuronal ceroid lipofuscinosisMichael E Ward, Robert Chen, Hsin-Yi Huang, 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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 10, 2012
Frontotemporal degeneration, the next therapeutic frontier: molecules and animal models for frontotemporal degeneration drug developmentAdam L Boxer, Michael Gold, Edward Huey, et al.
Cell|April 27, 2016
Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement ActivationHansen Lui, Jiasheng Zhang, Stefanie R Makinson, et al.
JAMA Network Open|October 28, 2020
Rates of Brain Atrophy Across Disease Stages in Familial Frontotemporal Dementia Associated With MAPT, GRN, and C9orf72 Pathogenic VariantsAdam M Staffaroni, Sheng-Yang M Goh, Yann Cobigo, et al.
Acta Neuropathologica|March 18, 2015
PART, a distinct tauopathy, different from classical sporadic Alzheimer diseaseKurt A Jellinger, Irina Alafuzoff, Johannes Attems, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 2, 2021
The contribution of behavioral features to caregiver burden in FTLD spectrum disordersHannah E Silverman, Jeannie M Ake, Masood Manoochehri, 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.
Neurobiology of Aging|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.
Pageof 14

Showing results (81-90 of 134) with videos related to

Sort By:
Pageof 14
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.
Science Translational Medicine|April 14, 2017
Individuals with progranulin haploinsufficiency exhibit features of neuronal ceroid lipofuscinosisMichael E Ward, Robert Chen, Hsin-Yi Huang, 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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 10, 2012
Frontotemporal degeneration, the next therapeutic frontier: molecules and animal models for frontotemporal degeneration drug developmentAdam L Boxer, Michael Gold, Edward Huey, et al.
Cell|April 27, 2016
Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement ActivationHansen Lui, Jiasheng Zhang, Stefanie R Makinson, et al.
JAMA Network Open|October 28, 2020
Rates of Brain Atrophy Across Disease Stages in Familial Frontotemporal Dementia Associated With MAPT, GRN, and C9orf72 Pathogenic VariantsAdam M Staffaroni, Sheng-Yang M Goh, Yann Cobigo, et al.
Acta Neuropathologica|March 18, 2015
PART, a distinct tauopathy, different from classical sporadic Alzheimer diseaseKurt A Jellinger, Irina Alafuzoff, Johannes Attems, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 2, 2021
The contribution of behavioral features to caregiver burden in FTLD spectrum disordersHannah E Silverman, Jeannie M Ake, Masood Manoochehri, 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.
Neurobiology of Aging|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.
Pageof 14