4.8 Article

Dantrolene Enhances Antisense-Mediated Exon Skipping in Human and Mouse Models of Duchenne Muscular Dystrophy

Related references

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

Exon-skipping drug pulls ahead in muscular dystrophy field

Alisa Opar

NATURE MEDICINE (2012)

Article Biochemistry & Molecular Biology

Diaphragm rescue alone prevents heart dysfunction in dystrophic mice

Alastair Crisp et al.

HUMAN MOLECULAR GENETICS (2011)

Article Medicine, General & Internal

Systemic Administration of PRO051 in Duchenne's Muscular Dystrophy

Nathalie M. Goemans et al.

NEW ENGLAND JOURNAL OF MEDICINE (2011)

Review Genetics & Heredity

Genetic therapies for RNA mis-splicing diseases

Suzan M. Hammond et al.

TRENDS IN GENETICS (2011)

Article Multidisciplinary Sciences

Chemical treatment enhances skipping of a mutated exon in the dystrophin gene

Atsushi Nishida et al.

NATURE COMMUNICATIONS (2011)

Article Biotechnology & Applied Microbiology

Guanine Analogues Enhance Antisense Oligonucleotide-induced Exon Skipping in Dystrophin Gene In Vitro and In Vivo

Yihong Hu et al.

MOLECULAR THERAPY (2010)

Article Clinical Neurology

Efficacy of Systemic Morpholino Exon-Skipping in Duchenne Dystrophy Dogs

Toshifumi Yokota et al.

ANNALS OF NEUROLOGY (2009)

Article Biochemistry & Molecular Biology

The influence of calcium signaling on the regulation of alternative splicing

Joachim Krebs

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2009)

Article Biotechnology & Applied Microbiology

Dosing Regimen Has a Significant Impact on the Efficiency of Morpholino Oligomer-Induced Exon Skipping in mdx Mice

Alberto Malerba et al.

HUMAN GENE THERAPY (2009)

Article Biochemistry & Molecular Biology

Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle

Andrew M. Bellinger et al.

NATURE MEDICINE (2009)

Article Biochemistry & Molecular Biology

Reference genes for normalization of gene expression studies in human osteoarthritic articular cartilage

Manuel Pombo-Suarez et al.

BMC MOLECULAR BIOLOGY (2008)

Article Clinical Neurology

Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene

Akinorl Nakamura et al.

JOURNAL OF CLINICAL NEUROSCIENCE (2008)

Article Multidisciplinary Sciences

Generation of human induced pluripotent stem cells from dermal fibroblasts

W. E. Lowry et al.

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

Article Medicine, General & Internal

Local dystrophin restoration with antisense oligonucleotide PRO051

Judith C. van Deutekom et al.

NEW ENGLAND JOURNAL OF MEDICINE (2007)

Article Clinical Neurology

Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human

Marcella Neri et al.

NEUROMUSCULAR DISORDERS (2007)

Review Clinical Neurology

Pharmacotherapy of spasticity in children with cerebral palsy

A Verrotti et al.

PEDIATRIC NEUROLOGY (2006)

Article Biochemistry & Molecular Biology

Dantrolene stabilizes domain interactions within the ryanodine receptor

S Kobayashi et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2005)

Article Medicine, Research & Experimental

Therapeutic potential of antisense oligonucleotides as modulators of alternative splicing

P Sazani et al.

JOURNAL OF CLINICAL INVESTIGATION (2003)

Article Biochemistry & Molecular Biology

Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse

QL Lu et al.

NATURE MEDICINE (2003)

Review Physiology

Ryanodine receptor calcium release channels

M Fill et al.

PHYSIOLOGICAL REVIEWS (2002)

Article Clinical Neurology

Recombinant micro-genes and dystrophin viral vectors

G Dickson et al.

NEUROMUSCULAR DISORDERS (2002)

Review Medicine, General & Internal

The muscular dystrophies

AEH Emery

LANCET (2002)

Article Biochemistry & Molecular Biology

Dantrolene inhibition of ryanodine receptor Ca2+ release channels -: Molecular mechanism and isoform selectivity

FY Zhao et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2001)