Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Restoration of Human Dystrophin Following Transplantation of Exon-Skipping-Engineered DMD Patient Stem Cells into Dystrophic Mice

1 Dec 2007

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Muscle Physiology and Disorders
Share to Tissue Engineering and Regenerative Medicine
Share to Virus-based gene therapy research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18371406
DOI: 10.1016/j.stem.2007.09.016

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Restoration of Human Dystrophin Following Transplantation of Exon-Skipping-Engineered DMD Patient Stem Cells into Dystrophic MicePMID 18371406Read ↗

Human ES- and iPS-Derived Myogenic Progenitors Restore DYSTROPHIN and Improve Contractility upon Transplantation in Dystrophic MiceSemantic proximity Read ↗

Restoring Dystrophin Expression in Duchenne Muscular Dystrophy MuscleSemantic proximity Read ↗

Restoration of Dystrophin Protein Expression by Exon Skipping Utilizing CRISPR-Cas9 in Myoblasts Derived from DMD Patient iPS Cells.Semantic proximity Read ↗

Empowering Muscle Stem Cells for the Treatment of Duchenne Muscular DystrophySemantic proximity Read ↗

Exon skipping and gene transfer restore dystrophin expression in human induced pluripotent stem cells-cardiomyocytes harboring DMD mutations.Semantic proximity Read ↗

Four new Duchenne muscular dystrophy mouse models with clinically relevant exon deletions in the human <i>DMD</i> geneSemantic proximity Read ↗

Molecular, cellular, and pharmacological therapies for Duchenne/Becker muscular dystrophies.Semantic proximity Read ↗

Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and miceSemantic proximity Read ↗

Non-uniform dystrophin re-expression after CRISPR-mediated exon excision in the dystrophin/utrophin double-knockout mouse model of DMDSemantic proximity Read ↗

Gene Therapy in Large Animal Models of Muscular DystrophySemantic proximity Read ↗

Targeting muscle stem cell intrinsic defects to treat Duchenne muscular dystrophySemantic proximity Read ↗

Generation of allogeneic and xenogeneic functional muscle stem cells for intramuscular transplantationSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.