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Times Cited: 1769
Times Cited: 1769
Times Cited
Times Co-cited
Similarity
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
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Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.
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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
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TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
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ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import.
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A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation.
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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
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Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.
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Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.
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Decoding ALS: from genes to mechanism.
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State of play in amyotrophic lateral sclerosis genetics.
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Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules.
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14
Mutations of optineurin in amyotrophic lateral sclerosis.
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13
Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons.
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13
The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.
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12
ALS/FTD Mutation-Induced Phase Transition of FUS Liquid Droplets and Reversible Hydrogels into Irreversible Hydrogels Impairs RNP Granule Function.
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12
ALS/FTD-Linked Mutation in FUS Suppresses Intra-axonal Protein Synthesis and Drives Disease Without Nuclear Loss-of-Function of FUS.
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12
Phase Separation of FUS Is Suppressed by Its Nuclear Import Receptor and Arginine Methylation.
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12
A new subtype of frontotemporal lobar degeneration with FUS pathology.
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12
ALS-associated mutant FUS induces selective motor neuron degeneration through toxic gain of function.
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12
Exome sequencing reveals VCP mutations as a cause of familial ALS.
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11
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
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11
Protein aggregation in amyotrophic lateral sclerosis.
Anna M Blokhuis, Ewout J N Groen, Max Koppers, Leonard H van den Berg, R Jeroen Pasterkamp. Acta Neuropathol 2013
Anna M Blokhuis, Ewout J N Groen, Max Koppers, Leonard H van den Berg, R Jeroen Pasterkamp. Acta Neuropathol 2013
11
Phosphorylation of the FUS low-complexity domain disrupts phase separation, aggregation, and toxicity.
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11
Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like Domains.
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11
Amyotrophic lateral sclerosis.
Michael A van Es, Orla Hardiman, Adriano Chio, Ammar Al-Chalabi, R Jeroen Pasterkamp, Jan H Veldink, Leonard H van den Berg. Lancet 2017
Michael A van Es, Orla Hardiman, Adriano Chio, Ammar Al-Chalabi, R Jeroen Pasterkamp, Jan H Veldink, Leonard H van den Berg. Lancet 2017
11
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia.
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10
Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion.
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10
Position-dependent FUS-RNA interactions regulate alternative splicing events and transcriptions.
Shinsuke Ishigaki, Akio Masuda, Yusuke Fujioka, Yohei Iguchi, Masahisa Katsuno, Akihide Shibata, Fumihiko Urano, Gen Sobue, Kinji Ohno. Sci Rep 2012
Shinsuke Ishigaki, Akio Masuda, Yusuke Fujioka, Yohei Iguchi, Masahisa Katsuno, Akihide Shibata, Fumihiko Urano, Gen Sobue, Kinji Ohno. Sci Rep 2012
10
Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations.
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10
ALS Mutations Disrupt Phase Separation Mediated by α-Helical Structure in the TDP-43 Low-Complexity C-Terminal Domain.
Alexander E Conicella, Gül H Zerze, Jeetain Mittal, Nicolas L Fawzi. Structure 2016
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10
Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs.
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Clotilde Lagier-Tourenne, Magdalini Polymenidou, Kasey R Hutt, Anthony Q Vu, Michael Baughn, Stephanie C Huelga, Kevin M Clutario, Shuo-Chien Ling, Tiffany Y Liang, Curt Mazur,[...]. Nat Neurosci 2012
10
Cell-free formation of RNA granules: low complexity sequence domains form dynamic fibers within hydrogels.
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10
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics.
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10
The role of FUS gene variants in neurodegenerative diseases.
Hao Deng, Kai Gao, Joseph Jankovic. Nat Rev Neurol 2014
Hao Deng, Kai Gao, Joseph Jankovic. Nat Rev Neurol 2014
10
Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis.
Giulia E Tyzack, Raphaelle Luisier, Doaa M Taha, Jacob Neeves, Miha Modic, Jamie S Mitchell, Ione Meyer, Linda Greensmith, Jia Newcombe, Jernej Ule,[...]. Brain 2019
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14
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation.
Marcel Naumann, Arun Pal, Anand Goswami, Xenia Lojewski, Julia Japtok, Anne Vehlow, Maximilian Naujock, René Günther, Mengmeng Jin, Nancy Stanslowsky,[...]. Nat Commun 2018
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10
The C9orf72 repeat expansion disrupts nucleocytoplasmic transport.
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9
GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport.
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Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation.
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SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis.
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TDP-43 repression of nonconserved cryptic exons is compromised in ALS-FTD.
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Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9.
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TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity.
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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.
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9
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.