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Times Cited: 185
Times Cited: 185
Times Cited
Times Co-cited
Similarity
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
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Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
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ALS Clinical Trials Review: 20 Years of Failure. Are We Any Closer to Registering a New Treatment?
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Molecular Mechanisms of TDP-43 Misfolding and Pathology in Amyotrophic Lateral Sclerosis.
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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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Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice.
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Poly(GR) in C9ORF72-Related ALS/FTD Compromises Mitochondrial Function and Increases Oxidative Stress and DNA Damage in iPSC-Derived Motor Neurons.
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Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial.
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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
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C9orf72-mediated ALS and FTD: multiple pathways to disease.
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Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis.
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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.
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Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
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State of play in amyotrophic lateral sclerosis genetics.
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ALS Genes in the Genomic Era and their Implications for FTD.
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ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43.
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A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group.
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Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation.
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The Overlapping Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia.
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Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons.
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Astrocytes from familial and sporadic ALS patients are toxic to motor neurons.
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Riluzole and edaravone: A tale of two amyotrophic lateral sclerosis drugs.
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Neurotoxic reactive astrocytes are induced by activated microglia.
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The role of mitochondria in amyotrophic lateral sclerosis.
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Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis.
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Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.
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Modeling sporadic ALS in iPSC-derived motor neurons identifies a potential therapeutic agent.
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The changing scene of amyotrophic lateral sclerosis.
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Role of Neuroinflammation in Amyotrophic Lateral Sclerosis: Cellular Mechanisms and Therapeutic Implications.
Jia Liu, Fei Wang. Front Immunol 2017
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ALS/FTD-associated FUS activates GSK-3β to disrupt the VAPB-PTPIP51 interaction and ER-mitochondria associations.
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Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
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Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia.
Axel Freischmidt, Thomas Wieland, Benjamin Richter, Wolfgang Ruf, Veronique Schaeffer, Kathrin Müller, Nicolai Marroquin, Frida Nordin, Annemarie Hübers, Patrick Weydt,[...]. Nat Neurosci 2015
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Gene Therapy for ALS-A Perspective.
Marisa Cappella, Chiara Ciotti, Mathilde Cohen-Tannoudji, Maria Grazia Biferi. Int J Mol Sci 2019
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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
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The inhibition of TDP-43 mitochondrial localization blocks its neuronal toxicity.
Wenzhang Wang, Luwen Wang, Junjie Lu, Sandra L Siedlak, Hisashi Fujioka, Jingjing Liang, Sirui Jiang, Xiaopin Ma, Zhen Jiang, Edroaldo Lummertz da Rocha,[...]. Nat Med 2016
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Genetics of amyotrophic lateral sclerosis: an update.
Sheng Chen, Pavani Sayana, Xiaojie Zhang, Weidong Le. Mol Neurodegener 2013
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Onset and progression in inherited ALS determined by motor neurons and microglia.
Séverine Boillée, Koji Yamanaka, Christian S Lobsiger, Neal G Copeland, Nancy A Jenkins, George Kassiotis, George Kollias, Don W Cleveland. Science 2006
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7
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.