Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1755-8794
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy ; volume:4 ; number:1 ; day:20 ; month:4 ; year:2011 ; pages:1-10 ; date:12.2011
BMC medical genomics ; 4, Heft 1 (20.4.2011), 1-10, 12.2011
- Urheber
-
Kemaladewi, Dwi U.
- Beteiligte Personen und Organisationen
-
Hoogaars, Willem MH
van Heiningen, Sandra H.
Terlouw, Samuel
de Gorter, David JJ
den Dunnen, Johan T.
van Ommen, Gert Jan B.
Aartsma-Rus, Annemieke
Dijke, Peter ten
't Hoen, Peter AC
SpringerLink (Online service)
- DOI
-
10.1186/1755-8794-4-36
- URN
-
urn:nbn:de:1111-201607224894
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:59 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Kemaladewi, Dwi U.
- Hoogaars, Willem MH
- van Heiningen, Sandra H.
- Terlouw, Samuel
- de Gorter, David JJ
- den Dunnen, Johan T.
- van Ommen, Gert Jan B.
- Aartsma-Rus, Annemieke
- Dijke, Peter ten
- 't Hoen, Peter AC
- SpringerLink (Online service)
Ähnliche Objekte (12)
Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model
Antisense-induced exon skipping for duplications in Duchenne muscular dystrophy
Applying Lessons Learned from Developing Exon Skipping for Duchenne to Developing Individualized Exon Skipping Therapy for Patients with Neurodegenerative Diseases
Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis
Exon skipping for DMD
Assessment of the feasibility of exon 45–55 multiexon skipping for duchenne muscular dystrophy
Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice
The dilemma of choice for duchenne patients eligible for Exon 51 skipping the European experience
Dystrophin bei Muskeldystrophie vom Typ Duchenne und Becker-Kiener
Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy
Elevated nuclear TDP-43 induces constitutive exon skipping
Exon skipping as a therapeutic strategy in dysferlinopathy
Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model
Antisense-induced exon skipping for duplications in Duchenne muscular dystrophy
Applying Lessons Learned from Developing Exon Skipping for Duchenne to Developing Individualized Exon Skipping Therapy for Patients with Neurodegenerative Diseases
Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis
Exon skipping for DMD
Assessment of the feasibility of exon 45–55 multiexon skipping for duchenne muscular dystrophy
Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice
The dilemma of choice for duchenne patients eligible for Exon 51 skipping the European experience
Dystrophin bei Muskeldystrophie vom Typ Duchenne und Becker-Kiener
Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy
Elevated nuclear TDP-43 induces constitutive exon skipping
Exon skipping as a therapeutic strategy in dysferlinopathy
Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model
Antisense-induced exon skipping for duplications in Duchenne muscular dystrophy
Applying Lessons Learned from Developing Exon Skipping for Duchenne to Developing Individualized Exon Skipping Therapy for Patients with Neurodegenerative Diseases
Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis
Exon skipping for DMD
Assessment of the feasibility of exon 45–55 multiexon skipping for duchenne muscular dystrophy
Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice
The dilemma of choice for duchenne patients eligible for Exon 51 skipping the European experience
Dystrophin bei Muskeldystrophie vom Typ Duchenne und Becker-Kiener
Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy
Elevated nuclear TDP-43 induces constitutive exon skipping