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Boris Rogelj

Showing results (71-80 of 82) with videos related to

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Cell Reports|December 3, 2013
Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxicYoun-Bok Lee, Han-Jou Chen, João N Peres, et al.
Brain, Behavior, and Immunity|July 13, 2024
Transcriptomic and proteomic profiling of bi-partite and tri-partite murine iPSC-derived neurospheroids under steady-state and inflammatory conditionJulia Di Stefano, Laura Garcia-Pupo, Federica Di Marco, et al.
Brain : a Journal of Neurology|September 22, 2018
A feedback loop between dipeptide-repeat protein, TDP-43 and karyopherin-α mediates C9orf72-related neurodegenerationDaniel A Solomon, Alan Stepto, Wing Hei Au, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6Caroline Vance, Boris Rogelj, Tibor Hortobágyi, et al.
Frontiers in Immunology|October 1, 2024
Varicella-zoster virus recapitulates its immune evasive behaviour in matured hiPSC-derived neurospheroidsJonas Govaerts, Elise Van Breedam, Sarah De Beuckeleer, et al.
European Journal of Human Genetics : EJHG|June 14, 2012
The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founderBradley N Smith, Stephen Newhouse, Aleksey Shatunov, et al.
Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.
Neurology|September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
Cell Reports|December 3, 2013
Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxicYoun-Bok Lee, Han-Jou Chen, João N Peres, et al.
Brain, Behavior, and Immunity|July 13, 2024
Transcriptomic and proteomic profiling of bi-partite and tri-partite murine iPSC-derived neurospheroids under steady-state and inflammatory conditionJulia Di Stefano, Laura Garcia-Pupo, Federica Di Marco, et al.
Brain : a Journal of Neurology|September 22, 2018
A feedback loop between dipeptide-repeat protein, TDP-43 and karyopherin-α mediates C9orf72-related neurodegenerationDaniel A Solomon, Alan Stepto, Wing Hei Au, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6Caroline Vance, Boris Rogelj, Tibor Hortobágyi, et al.
Frontiers in Immunology|October 1, 2024
Varicella-zoster virus recapitulates its immune evasive behaviour in matured hiPSC-derived neurospheroidsJonas Govaerts, Elise Van Breedam, Sarah De Beuckeleer, et al.
European Journal of Human Genetics : EJHG|June 14, 2012
The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founderBradley N Smith, Stephen Newhouse, Aleksey Shatunov, et al.
Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.
Neurology|September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.
Pageof 9