4.8 Article

Reduction of toxic RNAs in myotonic dystrophies type 1 and type 2 by the RNA helicase p68/DDX5

Related references

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

Molecular mechanisms of muscle atrophy in myotonic dystrophies

Lubov Timchenko

INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2013)

Article Medicine, Research & Experimental

GSK3β mediates muscle pathology in myotonic dystrophy

Karlie Jones et al.

JOURNAL OF CLINICAL INVESTIGATION (2012)

Article Biochemistry & Molecular Biology

New function for the RNA helicase p68/DDX5 as a modifier of MBNL1 activity on expanded CUG repeats

Francois-Xavier Laurent et al.

NUCLEIC ACIDS RESEARCH (2012)

Article Biochemistry & Molecular Biology

Expanded CUG Repeats Dysregulate RNA Splicing by Altering the Stoichiometry of the Muscleblind 1 Complex

Sharan Paul et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2011)

Review Biochemistry & Molecular Biology

RNA-dominant diseases

Robert J. Osborne et al.

HUMAN MOLECULAR GENETICS (2006)

Article Multidisciplinary Sciences

The structural basis of myotonic dystrophy from the crystal structure of CUG repeats

BHM Mooers et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)

Article Biochemistry & Molecular Biology

The ATPase, RNA unwinding, and RNA binding activities of recombinant p68 RNA helicase

YL Huang et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2002)

Article Multidisciplinary Sciences

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

CL Liquori et al.

SCIENCE (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)