4.5 Article

Cellular toxicity of expanded RNA repeats: focus on RNA foci

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

Muscleblind participates in RNA toxicity of expanded CAG and CUG repeats in Caenorhabditis elegans

Li-Chun Wang et al.

CELLULAR AND MOLECULAR LIFE SCIENCES (2011)

Article Cell Biology

Stochastic and reversible aggregation of mRNA with expanded CUG-triplet repeats

Emmanuelle Querido et al.

JOURNAL OF CELL SCIENCE (2011)

Article Biochemistry & Molecular Biology

Selective silencing of mutated mRNAs in DM1 by using modified hU7-snRNAs

Virginie Francois et al.

NATURE STRUCTURAL & MOLECULAR BIOLOGY (2011)

Article Biochemistry & Molecular Biology

Mutant CAG repeats of Huntingtin transcript fold into hairpins, form nuclear foci and are targets for RNA interference

Mateusz de Mezer et al.

NUCLEIC ACIDS RESEARCH (2011)

Article Multidisciplinary Sciences

Long Tract of Untranslated CAG Repeats Is Deleterious in Transgenic Mice

Ren-Jun Hsu et al.

PLOS ONE (2011)

Review Biochemistry & Molecular Biology

CAG repeat RNA as an auxiliary toxic agent in polyglutamine disorders

Marzena Wojciechowska et al.

RNA BIOLOGY (2011)

Article Biochemistry & Molecular Biology

Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients

Chantal Sellier et al.

EMBO JOURNAL (2010)

Review Biochemistry & Molecular Biology

Partners in crime: bidirectional transcription in unstable microsatellite disease

Ranjan Batra et al.

HUMAN MOLECULAR GENETICS (2010)

Article Genetics & Heredity

Spinocerebellar Ataxia Type 31 Is Associated with Inserted Penta-Nucleotide Repeats Containing (TGGAA)n

Nozomu Sato et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2009)

Article Biochemistry & Molecular Biology

Spinocerebellar ataxia type 8 larger triplet expansion alters histone modification and induces RNA foci

I-Cheng Chen et al.

BMC MOLECULAR BIOLOGY (2009)

Review Clinical Neurology

FRAGILE X SYNDROME-FROM GENES TO COGNITION

A. Schneider et al.

DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (2009)

Article Multidisciplinary Sciences

Pentamidine reverses the splicing defects associated with myotonic dystrophy

M. Bryan Warf et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)

Article Multidisciplinary Sciences

Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy

Susan A. M. Mulders et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)

Article Multidisciplinary Sciences

Reversal of RNA Dominance by Displacement of Protein Sequestered on Triplet Repeat RNA

Thurman M. Wheeler et al.

SCIENCE (2009)

Article Genetics & Heredity

RNA Gain-of-Function in Spinocerebellar Ataxia Type 8

Randy S. Daughters et al.

PLOS GENETICS (2009)

Article Multidisciplinary Sciences

RNA toxicity is a component of ataxin-3 degeneration in Drosophila

Ling-Bo Li et al.

NATURE (2008)

Article Multidisciplinary Sciences

Genetic and Chemical Modifiers of a CUG Toxicity Model in Drosophila

Amparo Garcia-Lopez et al.

PLOS ONE (2008)

Article Multidisciplinary Sciences

Cytoplasmic CUG RNA Foci Are Insufficient to Elicit Key DM1 Features

Warunee Dansithong et al.

PLOS ONE (2008)

Article Multidisciplinary Sciences

Expanded CTG repeats within the DMPK 3′ UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy

James P. Orengo et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Article Clinical Neurology

Myotonic dystrophy: RNA-mediated muscle disease

Thurman M. Wheeler et al.

CURRENT OPINION IN NEUROLOGY (2007)

Article Medicine, Research & Experimental

Elevation of RNA-binding protein CUGBP1 is an early event in an inducible heart-specific mouse model of myotonic dystrophy

Guey-Shin Wang et al.

JOURNAL OF CLINICAL INVESTIGATION (2007)

Article Clinical Neurology

Huntington's disease-like 2 is associated with CUG repeat-containing RNA foci

Dobrila D. Rudnicki et al.

ANNALS OF NEUROLOGY (2007)

Review Biochemistry & Molecular Biology

RNA-dominant diseases

Robert J. Osborne et al.

HUMAN MOLECULAR GENETICS (2006)

Article Genetics & Heredity

Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy

Mani S. Mahadevan et al.

NATURE GENETICS (2006)

Article Biochemistry & Molecular Biology

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

Xiaoyan Lin et al.

HUMAN MOLECULAR GENETICS (2006)

Article Biochemistry & Molecular Biology

MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1

Maria de Haro et al.

HUMAN MOLECULAR GENETICS (2006)

Article Cardiac & Cardiovascular Systems

Nuclear RNA foci in the heart in myotonic dystrophy

A Mankodi et al.

CIRCULATION RESEARCH (2005)

Article Biochemistry & Molecular Biology

Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy

TH Ho et al.

HUMAN MOLECULAR GENETICS (2005)

Article Biochemistry & Molecular Biology

Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to Drosophila

JM Houseley et al.

HUMAN MOLECULAR GENETICS (2005)

Article Neurosciences

Recent progress in spinocerebellar ataxia type-10 (SCA10)

X Lin et al.

CEREBELLUM (2005)

Article Biochemistry & Molecular Biology

HnRNP H inhibits nuclear export of mRNA containing expanded CUG repeats and a distal branch point sequence

DH Kim et al.

NUCLEIC ACIDS RESEARCH (2005)

Article Biochemistry & Molecular Biology

Overexpression of CUG triplet repeat-binding protein, CUGBP1, in mice inhibits myogenesis

NA Timchenko et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2004)

Article Clinical Neurology

Sudden cardiac death in myotonic dystrophy type 2

BGH Schoser et al.

NEUROLOGY (2004)

Article Multidisciplinary Sciences

A muscleblind knockout model for myotonic dystrophy

RN Kanadia et al.

SCIENCE (2003)

Article Biotechnology & Applied Microbiology

Hammerhead ribozyme-mediated destruction of nuclear foci in myotonic dystrophy myoblasts

MA Langlois et al.

MOLECULAR THERAPY (2003)

Article Clinical Neurology

Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2

A Mankodi et al.

ANNALS OF NEUROLOGY (2003)

Article Biochemistry & Molecular Biology

Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2

A Mankodi et al.

HUMAN MOLECULAR GENETICS (2001)

Article Biochemistry & Molecular Biology

Defective satellite cells in congenital myotonic dystrophy

D Furling et al.

HUMAN MOLECULAR GENETICS (2001)

Article Multidisciplinary Sciences

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

CL Liquori et al.

SCIENCE (2001)

Article Biochemistry & Molecular Biology

In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts

M Fardaei et al.

NUCLEIC ACIDS RESEARCH (2001)

Article Multidisciplinary Sciences

Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat

A Mankodi et al.

SCIENCE (2000)

Article Biochemistry & Molecular Biology

Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

JW Miller et al.

EMBO JOURNAL (2000)