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Dirk Troost

Showing results (61-70 of 65) with videos related to

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EMBO Reports|March 19, 2021
Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signalingLaura Mediani, Francesco Antoniani, Veronica Galli, et al.
Acta Neuropathologica|April 3, 2019
FUS pathology in ALS is linked to alterations in multiple ALS-associated proteins and rescued by drugs stimulating autophagyLara Marrone, Hannes C A Drexler, Jie Wang, et al.
The American Journal of Pathology|June 27, 2007
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusionsNigel J Cairns, Manuela Neumann, Eileen H Bigio, et al.
Nature Communications|January 25, 2018
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formationMarcel Naumann, Arun Pal, Anand Goswami, et al.
Orphanet Journal of Rare Diseases|February 15, 2014
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlationsVeerle Rc Eggens, Peter G Barth, Jikke-Mien F Niermeijer, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
EMBO Reports|March 19, 2021
Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signalingLaura Mediani, Francesco Antoniani, Veronica Galli, et al.
Acta Neuropathologica|April 3, 2019
FUS pathology in ALS is linked to alterations in multiple ALS-associated proteins and rescued by drugs stimulating autophagyLara Marrone, Hannes C A Drexler, Jie Wang, et al.
The American Journal of Pathology|June 27, 2007
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusionsNigel J Cairns, Manuela Neumann, Eileen H Bigio, et al.
Nature Communications|January 25, 2018
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formationMarcel Naumann, Arun Pal, Anand Goswami, et al.
Orphanet Journal of Rare Diseases|February 15, 2014
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlationsVeerle Rc Eggens, Peter G Barth, Jikke-Mien F Niermeijer, et al.
Pageof 7