Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1472-6750

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice ; volume:8 ; number:1 ; day:02 ; month:4 ; year:2008 ; pages:1-13 ; date:12.2008
BMC biotechnology ; 8, Heft 1 (02.4.2008), 1-13, 12.2008

Creator: Williams, Jason H.

Contributor: Schray, Rebecca C.
Sirsi, Shashank R.
Lutz, Gordon J.
SpringerLink (Online service)

DOI: 10.1186/1472-6750-8-35

URN: urn:nbn:de:1111-2016072533317

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 11:01 AM CEST

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Williams, Jason H.
Schray, Rebecca C.
Sirsi, Shashank R.
Lutz, Gordon J.
SpringerLink (Online service)

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The Assembly and Evaluation of Antisense Oligonucleotides Applied in Exon Skipping for Titin-based Mutations in Dilated Cardiomyopathy

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Integrative effects of dystrophin loss on metabolic function of the mdx mouse

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

In vivo restoration of dystrophin expression in mdx mice using intra-muscular and intra-arterial injections of hydrogel microsphere carriers of exon skipping antisense oligonucleotides

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy

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Exon skipping for DMD

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An LNA-amide modification that enhances the cell uptake and activity of phosphorothioate exon-skipping oligonucleotides

The Assembly and Evaluation of Antisense Oligonucleotides Applied in Exon Skipping for Titin-based Mutations in Dilated Cardiomyopathy

Electrical impedance myography detects dystrophin-related muscle changes in mdx mice

Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling

Integrative effects of dystrophin loss on metabolic function of the mdx mouse

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

In vivo restoration of dystrophin expression in mdx mice using intra-muscular and intra-arterial injections of hydrogel microsphere carriers of exon skipping antisense oligonucleotides

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy

Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model

Exon skipping for DMD

Hochschulschrift

Kraniofaziale Morphologie bei mdx-Mäusen mit Dystrophin-Mangel

An LNA-amide modification that enhances the cell uptake and activity of phosphorothioate exon-skipping oligonucleotides

The Assembly and Evaluation of Antisense Oligonucleotides Applied in Exon Skipping for Titin-based Mutations in Dilated Cardiomyopathy

Electrical impedance myography detects dystrophin-related muscle changes in mdx mice

Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling

Integrative effects of dystrophin loss on metabolic function of the mdx mouse

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

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Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice

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Other Objects (12)

In vivo restoration of dystrophin expression in mdx mice using intra-muscular and intra-arterial injections of hydrogel microsphere carriers of exon skipping antisense oligonucleotides

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy

Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model

Exon skipping for DMD

Kraniofaziale Morphologie bei mdx-Mäusen mit Dystrophin-Mangel

An LNA-amide modification that enhances the cell uptake and activity of phosphorothioate exon-skipping oligonucleotides

The Assembly and Evaluation of Antisense Oligonucleotides Applied in Exon Skipping for Titin-based Mutations in Dilated Cardiomyopathy

Electrical impedance myography detects dystrophin-related muscle changes in mdx mice

Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling

Integrative effects of dystrophin loss on metabolic function of the mdx mouse

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

In vivo restoration of dystrophin expression in mdx mice using intra-muscular and intra-arterial injections of hydrogel microsphere carriers of exon skipping antisense oligonucleotides

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy

Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model

Exon skipping for DMD

Kraniofaziale Morphologie bei mdx-Mäusen mit Dystrophin-Mangel

An LNA-amide modification that enhances the cell uptake and activity of phosphorothioate exon-skipping oligonucleotides

The Assembly and Evaluation of Antisense Oligonucleotides Applied in Exon Skipping for Titin-based Mutations in Dilated Cardiomyopathy

Electrical impedance myography detects dystrophin-related muscle changes in mdx mice

Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling

Integrative effects of dystrophin loss on metabolic function of the mdx mouse

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

In vivo restoration of dystrophin expression in mdx mice using intra-muscular and intra-arterial injections of hydrogel microsphere carriers of exon skipping antisense oligonucleotides

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy

Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model

Exon skipping for DMD

Kraniofaziale Morphologie bei mdx-Mäusen mit Dystrophin-Mangel

An LNA-amide modification that enhances the cell uptake and activity of phosphorothioate exon-skipping oligonucleotides

The Assembly and Evaluation of Antisense Oligonucleotides Applied in Exon Skipping for Titin-based Mutations in Dilated Cardiomyopathy

Electrical impedance myography detects dystrophin-related muscle changes in mdx mice

Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling

Integrative effects of dystrophin loss on metabolic function of the mdx mouse

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

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