Related references
Note: Only part of the references are listed.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)
Myofibrillar disruption and RNA-binding protein aggregation in a mouse model of limb-girdle muscular dystrophy 1D
Rocio Bengoechea et al.
HUMAN MOLECULAR GENETICS (2015)
Formation and Maturation of Phase-Separated Liquid Droplets by RNA-Binding Proteins
Yuan Lin et al.
MOLECULAR CELL (2015)
Multisystem proteinopathy Intersecting genetics in muscle, bone, and brain degeneration
J. Paul Taylor
NEUROLOGY (2015)
Pathology of frontotemporal dementia with limb girdle muscular dystrophy caused by a DNAJB6 mutation
Ichiro Yabe et al.
CLINICAL NEUROLOGY AND NEUROSURGERY (2014)
A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G)
Natassia M. Vieira et al.
HUMAN MOLECULAR GENETICS (2014)
Myopathy-causing Mutations in an HSP40 Chaperone Disrupt Processing of Specific Client Conformers
Kevin C. Stein et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy
Julien Couthouis et al.
NEUROMUSCULAR DISORDERS (2014)
ATP-driven molecular chaperone machines
Daniel K. Clare et al.
BIOPOLYMERS (2013)
Eukaryotic Stress Granules Are Cleared by Autophagy and Cdc48/VCP Function
J. Ross Buchan et al.
CELL (2013)
Altered Ribostasis: RNA-Protein Granules in Degenerative Disorders
Mani Ramaswami et al.
CELL (2013)
DNAJ Proteins and Protein Aggregation Diseases
Vaishali Kakkar et al.
CURRENT TOPICS IN MEDICINAL CHEMISTRY (2013)
Stress granules as crucibles of ALS pathogenesis
Yun R. Li et al.
JOURNAL OF CELL BIOLOGY (2013)
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
Hong Joo Kim et al.
NATURE (2013)
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy
Matthew B. Harms et al.
ANNALS OF NEUROLOGY (2012)
The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease
Oliver D. King et al.
BRAIN RESEARCH (2012)
Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis
Julien Couthouis et al.
HUMAN MOLECULAR GENETICS (2012)
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy
Jaakko Sarparanta et al.
NATURE GENETICS (2012)
De novo design of synthetic prion domains
James A. Toombs et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Modulation of Stress Granules and P Bodies during Dicistrovirus Infection
Anthony Khong et al.
JOURNAL OF VIROLOGY (2011)
Heat shock protein 70 kDa chaperone/DnaJ cochaperone complex employs an unusual dynamic interface
Atta Ahmad et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
A yeast functional screen predicts new candidate ALS disease genes
Julien Couthouis et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Search and clustering orders of magnitude faster than BLAST
Robert C. Edgar
BIOINFORMATICS (2010)
Global Analysis of TDP-43 Interacting Proteins Reveals Strong Association with RNA Splicing and Translation Machinery
Brian D. Freibaum et al.
JOURNAL OF PROTEOME RESEARCH (2010)
Tar DNA Binding Protein-43 (TDP-43) Associates with Stress Granules: Analysis of Cultured Cells and Pathological Brain Tissue
Liqun Liu-Yesucevitz et al.
PLOS ONE (2010)
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)
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
Jemeen Sreedharan et al.
SCIENCE (2008)
Inherited myopathies and muscular dystrophies
Michael Cardamone et al.
SEMINARS IN NEUROLOGY (2008)
SQUINT: a multiple alignment program and editor
Matthew G. Goode et al.
BIOINFORMATICS (2007)
The diversity of the DnaJ/Hsp40 family, the crucial partners for Hsp70 chaperones
X-B. Qiu et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2006)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Stress granule assembly is mediated by prion-like aggregation of TIA-1
N Gilks et al.
MOLECULAR BIOLOGY OF THE CELL (2004)
Identification of genes that modify ataxin-1-induced neurodegeneration
P Fernandez-Funez et al.
NATURE (2000)
Share Paper
