Related references
Note: Only part of the references are listed.Paraspeckles: Where Long Noncoding RNA Meets Phase Separation
Archa H. Fox et al.
TRENDS IN BIOCHEMICAL SCIENCES (2018)
Isogenic FUS-eGFP iPSC Reporter Lines Enable Quantification of FUS Stress Granule Pathology that Is Rescued by Drugs Inducing Autophagy
Lara Marrone et al.
STEM CELL REPORTS (2018)
Biomolecular condensates: organizers of cellular biochemistry
Salman F. Banani et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2017)
Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31
Taro Ishiguro et al.
NEURON (2017)
Intrinsically disordered RGG/RG domains mediate degenerate specificity in RNA binding
Bagdeser A. Ozdilek et al.
NUCLEIC ACIDS RESEARCH (2017)
Liquid phase condensation in cell physiology and disease
Yongdae Shin et al.
SCIENCE (2017)
An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function
Daniel Mateju et al.
EMBO JOURNAL (2017)
Rapid agarose gel electrophoretic mobility shift assay for quantitating protein: RNA interactions
Jennifer A. Ream et al.
ANALYTICAL BIOCHEMISTRY (2016)
Prion-like domains as epigenetic regulators, scaffolds for subcellular organization, and drivers of neurodegenerative disease
Zachary M. March et al.
BRAIN RESEARCH (2016)
Mechanisms of FUS mutations in familial amyotrophic lateral sclerosis
Yulei Shang et al.
BRAIN RESEARCH (2016)
Polar Positioning of Phase-Separated Liquid Compartments in Cells Regulated by an mRNA Competition Mechanism
Shambaditya Saha et al.
CELL (2016)
Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss
Jelena Scekic-Zahirovic et al.
EMBO JOURNAL (2016)
Decoding ALS: from genes to mechanism
J. Paul Taylor et al.
NATURE (2016)
ALS-associated mutant FUS induces selective motor neuron degeneration through toxic gain of function
Aarti Sharma et al.
NATURE COMMUNICATIONS (2016)
CPEB4 is regulated during cell cycle by ERK2/Cdk1-mediated phosphorylation and its assembly into liquid-like droplets
Jordina Guillen-Boixet et al.
ELIFE (2016)
Interaction of RNA with a C-terminal fragment of the amyotrophic lateral sclerosis-associated TDP43 reduces cytotoxicity
Akira Kitamura et al.
SCIENTIFIC REPORTS (2016)
Phase Separation by Low Complexity Domains Promotes Stress Granule Assembly and Drives Pathological Fibrillization
Amandine Molliex et al.
CELL (2015)
A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation
Avinash Patel et al.
CELL (2015)
A Human Interactome in Three Quantitative Dimensions Organized by Stoichiometries and Abundances
Marco Y. Hein et al.
CELL (2015)
RNA Controls PolyQ Protein Phase Transitions
Huaiying Zhang et al.
MOLECULAR CELL (2015)
RNA transcription modulates phase transition-driven nuclear body assembly
Joel Berry et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
The disordered P granule protein LAF-1 drives phase separation into droplets with tunable viscosity and dynamics
Shana Elbaum-Garfinkle et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
The role of FUS gene variants in neurodegenerative diseases
Hao Deng et al.
NATURE REVIEWS NEUROLOGY (2014)
An ALS-associated mutation in the FUS 3′-UTR disrupts a microRNA-FUS regulatory circuitry
Stefano Dini Modigliani et al.
NATURE COMMUNICATIONS (2014)
The RRM domain of human fused in sarcoma protein reveals a non-canonical nucleic acid binding site
Xuehui Liu et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2013)
RNA-binding ability of FUS regulates neurodegeneration, cytoplasmic mislocalization and incorporation into stress granules associated with FUS carrying ALS-linked mutations
J. Gavin Daigle et al.
HUMAN MOLECULAR GENETICS (2013)
Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes
Danielle C. Diaper et al.
HUMAN MOLECULAR GENETICS (2013)
Mutations in the 3′ untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis
Mario Sabatelli et al.
HUMAN MOLECULAR GENETICS (2013)
Inhibition of TDP-43 Aggregation by Nucleic Acid Binding
Yi-Chen Huang et al.
PLOS ONE (2013)
RNA Seeds Higher-Order Assembly of FUS Protein
Jacob C. Schwartz et al.
CELL REPORTS (2013)
Microbial environments confound antibiotic efficacy
Henry H. Lee et al.
NATURE CHEMICAL BIOLOGY (2012)
Characterization of a Family of RanBP2-Type Zinc Fingers that Can Recognize Single-Stranded RNA
Cuong D. Nguyen et al.
JOURNAL OF MOLECULAR BIOLOGY (2011)
RNA targets of wild-type and mutant FET family proteins
Jessica I. Hoell et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2011)
Measuring the complete force field of an optical trap
Marcus Jahnel et al.
OPTICS LETTERS (2011)
Molecular Determinants and Genetic Modifiers of Aggregation and Toxicity for the ALS Disease Protein FUS/TLS
Zhihui Sun et al.
PLOS BIOLOGY (2011)
ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
Dorothee Dormann et al.
EMBO JOURNAL (2010)
Cytoplasmic Mislocalization of TDP-43 Is Toxic to Neurons and Enhanced by a Mutation Associated with Familial Amyotrophic Lateral Sclerosis
Sami J. Barmada et al.
JOURNAL OF NEUROSCIENCE (2010)
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies
Manuela Neumann et al.
ACTA NEUROPATHOLOGICA (2009)
TDP-43 is recruited to stress granules in conditions of oxidative insult
Claudia Colombrita et al.
JOURNAL OF NEUROCHEMISTRY (2009)
An Architectural Role for a Nuclear Noncoding RNA: NEAT1 RNA Is Essential for the Structure of Paraspeckles
Christine M. Clemson et al.
MOLECULAR CELL (2009)
Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
Caroline Vance et al.
SCIENCE (2009)
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
T. J. Kwiatkowski et al.
SCIENCE (2009)
Dynamics of chromatin decondensation reveals the structural integrity of a mechanically prestressed nucleus
Aprotim Mazumder et al.
BIOPHYSICAL JOURNAL (2008)
A quantitative estimation of the global translational activity in logarithmically growing yeast cells
Tobias von der Haar
BMC SYSTEMS BIOLOGY (2008)
Precise measurement of diffusion by multi-color dual-focus fluorescence correlation spectroscopy
C. B. Mueller et al.
EPL (2008)
Structural determinants of the cellular localization and shuttling of TDP-43
Youhna M. Ayala et al.
JOURNAL OF CELL SCIENCE (2008)
BAC TransgeneOmics:: a high-throughput method for exploration of protein function in mammals
Ina Poser et al.
NATURE METHODS (2008)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
RNA-selective, live cell imaging probes for studying nuclear structure and function
Qian Li et al.
CHEMISTRY & BIOLOGY (2006)
Dynamics of the Ras/ERK MAPK cascade as monitored by fluorescent probes
A Fujioka et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Share Paper
