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Lee-Cyn Ang

Showing results (71-80 of 80) with videos related to

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Acta Neuropathologica|July 31, 2012
Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutationsManuela Neumann, Chiara F Valori, Olaf Ansorge, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|June 22, 2019
Concentration, distribution, and influence of aging on the 18 kDa translocator protein in human brain: Implications for brain imaging studiesJunchao Tong, Belinda Williams, Pablo M Rusjan, et al.
Journal of Neurointerventional Surgery|February 14, 2015
Catheter based selective hypothermia reduces stroke volume during focal cerebral ischemia in swineThomas K Mattingly, Lynn M Denning, Karen L Siroen, et al.
Frontiers in Genetics|January 9, 2019
<i>MECP2</i> Mutation Interrupts Nucleolin-mTOR-P70S6K Signaling in Rett Syndrome PatientsCarl O Olson, Shervin Pejhan, Daniel Kroft, et al.
Brain : a Journal of Neurology|August 23, 2011
FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutationsManuela Neumann, Eva Bentmann, Dorothee Dormann, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
Distinct TAF15 amyloid filament folds define multiple subtypes of FTLD-TAF15Stephan Tetter, Nikhil R Varghese, Alexey G Murzin, et al.
Acta Neuropathologica|August 10, 2025
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-USara Alidadiani, Júlia Faura, Sarah Wynants, et al.
The Lancet. Neurology|April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Nature Genetics|March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusionsWouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences|May 10, 2023
Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's diseaseRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
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Showing results (71-80 of 80) with videos related to

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Pageof 8
You have reached the last page of results.This site can display upto 80 results.
Acta Neuropathologica|July 31, 2012
Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutationsManuela Neumann, Chiara F Valori, Olaf Ansorge, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|June 22, 2019
Concentration, distribution, and influence of aging on the 18 kDa translocator protein in human brain: Implications for brain imaging studiesJunchao Tong, Belinda Williams, Pablo M Rusjan, et al.
Journal of Neurointerventional Surgery|February 14, 2015
Catheter based selective hypothermia reduces stroke volume during focal cerebral ischemia in swineThomas K Mattingly, Lynn M Denning, Karen L Siroen, et al.
Frontiers in Genetics|January 9, 2019
<i>MECP2</i> Mutation Interrupts Nucleolin-mTOR-P70S6K Signaling in Rett Syndrome PatientsCarl O Olson, Shervin Pejhan, Daniel Kroft, et al.
Brain : a Journal of Neurology|August 23, 2011
FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutationsManuela Neumann, Eva Bentmann, Dorothee Dormann, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
Distinct TAF15 amyloid filament folds define multiple subtypes of FTLD-TAF15Stephan Tetter, Nikhil R Varghese, Alexey G Murzin, et al.
Acta Neuropathologica|August 10, 2025
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-USara Alidadiani, Júlia Faura, Sarah Wynants, et al.
The Lancet. Neurology|April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Nature Genetics|March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusionsWouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences|May 10, 2023
Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's diseaseRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
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