Results 71 to 80 of about 51,631 (223)

ALS mutant FUS disrupts nuclear localization and sequesters wild-type FUS within cytoplasmic stress granules [PDF]

open access: yes, 2013
Mutations in the gene encoding Fused in Sarcoma (FUS) cause amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disorder. FUS is a predominantly nuclear DNA- and RNA-binding protein that is involved in RNA processing.
Miller, CC   +40 more
core   +1 more source

Synaptic accumulation of FUS triggers age-dependent misregulation of inhibitory synapses in ALS-FUS mice [PDF]

open access: yes, 2020
FUS is a primarily nuclear RNA-binding protein with important roles in RNA processing and transport. FUS mutations disrupting its nuclear localization characterize a subset of amyotrophic lateral sclerosis (ALS-FUS) patients, through an unidentified ...
Pérez-Berlanga, Manuela   +10 more
core   +1 more source

FUS transgenic rats develop the phenotypes of amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

open access: yesPLoS Genetics, 2011
Fused in Sarcoma (FUS) proteinopathy is a feature of frontotemporal lobar dementia (FTLD), and mutation of the fus gene segregates with FTLD and amyotrophic lateral sclerosis (ALS).
Cao Huang   +7 more
doaj   +1 more source

The FUS(s) about splicing

open access: yes, 2014
Fused in sarcoma (FUS), also called translocated in liposarcoma (TLS), is a ubiquitously expressed DNA/RNA binding protein belonging to the TET family and predominantly localized in the nucleus.
Ruepp, Marc-David
core  

Transportin 1 co-localisation with FUS inclusions is not characteristic for ALS-FUS confirming disrupted nuclear import of mutant FUS and distinguishing it from FTLD-FUS

open access: yes, 2012
Aims:  Transportin 1 (TNPO 1) is an abundant component of the Fused in Sarcoma (FUS)-immunopositive inclusions seen in a subgroup of frontotemporal lobar degeneration (FTLD-FUS).
Al-Sarraj, Safa   +5 more
core   +1 more source

Nuclear import factor transportin and arginine methyltransferase 1 modify FUS neurotoxicity in Drosophila

open access: yesNeurobiology of Disease, 2015
Inclusions containing Fused in Sarcoma (FUS) are found in familial and sporadic cases of the incurable progressive motor neuron disease amyotrophic lateral sclerosis and in a common form of dementia, frontotemporal dementia.
Sandra Jäckel   +9 more
doaj   +1 more source

Number of differentially expressed genes by mutant FUS, FUS overexpression, and FUS knock-down.

open access: yes, 2013
Number of differentially expressed genes by mutant FUS, FUS overexpression, and FUS knock-down.
John E. Landers (172264)   +9 more
core   +1 more source

HSP60 interacts with FUS, mediating FUS mitochondrial localization.

open access: yes, 2016
(A) FUS-HSP60 interaction was detected by co-immunoprecipitation assay. Western blotting (WB) was performed using corresponding specific antibodies following immunoprecipitation of cell lysates with anti-GFP.(B)FUS-HSP60 interaction was detected by co ...
Marsel Mesulam (2207017)   +14 more
core   +1 more source

FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees

open access: yes, 2021
Mutations in FUS and TBK1 often cause aggressive early-onset amyotrophic lateral sclerosis (ALS) or a late-onset ALS and/or frontotemporal dementia (FTD) phenotype, respectively.
Ludolph, Albert C.,   +21 more
core   +1 more source

The role of FUS in splicing regulation

open access: yes, 2014
Fused in sarcoma (FUS), also called translocated in liposarcoma (TLS), is a ubiquitously expressed DNA/RNA binding protein belonging to the TET family and predominantly localized in the nucleus.
Ruepp, Marc-David
core  

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