- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2045-2322
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Quantitative immuno-mass spectrometry imaging of skeletal muscle dystrophin ; volume:11 ; number:1 ; day:13 ; month:1 ; year:2021 ; pages:1-11 ; date:12.2021
Scientific reports ; 11, Heft 1 (13.1.2021), 1-11, 12.2021
- Creator
-
Bishop, David P.
Westerhausen, Mika T.
Barthelemy, Florian
Lockwood, Thomas
Cole, Nerida
Gibbs, Elizabeth M.
Crosbie, Rachelle H.
Nelson, Stanley F.
Miceli, M. Carrie
Doble, Philip A.
Wanagat, Jonathan
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41598-020-80495-8
- URN
-
urn:nbn:de:101:1-2021020723482409306053
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:30 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Bishop, David P.
- Westerhausen, Mika T.
- Barthelemy, Florian
- Lockwood, Thomas
- Cole, Nerida
- Gibbs, Elizabeth M.
- Crosbie, Rachelle H.
- Nelson, Stanley F.
- Miceli, M. Carrie
- Doble, Philip A.
- Wanagat, Jonathan
- SpringerLink (Online service)
Other Objects (12)
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Pluripotent stem cell-induced skeletal muscle progenitor cells with givinostat promote myoangiogenesis and restore dystrophin in injured Duchenne dystrophic muscle
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Skeletal muscle
GRAF1 deficiency blunts sarcolemmal injury repair and exacerbates cardiac and skeletal muscle pathology in dystrophin-deficient mice
Development and Validation of a Western Blot Method to Quantify Mini-Dystrophin in Human Skeletal Muscle Biopsies
Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice
DRP-1-mediated apoptosis induces muscle degeneration in dystrophin mutants
mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies
Transcriptomic analysis of dystrophin RNAi knockdown reveals a central role for dystrophin in muscle differentiation and contractile apparatus organization
Dystrophin and mini-dystrophin quantification by mass spectrometry in skeletal muscle for gene therapy development in Duchenne muscular dystrophy
Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice
Rapid restitution of contractile dysfunction by synthetic copolymers in dystrophin-deficient single live skeletal muscle fibers
Pluripotent stem cell-induced skeletal muscle progenitor cells with givinostat promote myoangiogenesis and restore dystrophin in injured Duchenne dystrophic muscle
Skeletal muscle
Skeletal muscle
GRAF1 deficiency blunts sarcolemmal injury repair and exacerbates cardiac and skeletal muscle pathology in dystrophin-deficient mice
Development and Validation of a Western Blot Method to Quantify Mini-Dystrophin in Human Skeletal Muscle Biopsies
Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice
DRP-1-mediated apoptosis induces muscle degeneration in dystrophin mutants
mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies
Transcriptomic analysis of dystrophin RNAi knockdown reveals a central role for dystrophin in muscle differentiation and contractile apparatus organization
Dystrophin and mini-dystrophin quantification by mass spectrometry in skeletal muscle for gene therapy development in Duchenne muscular dystrophy
Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice
Rapid restitution of contractile dysfunction by synthetic copolymers in dystrophin-deficient single live skeletal muscle fibers
Pluripotent stem cell-induced skeletal muscle progenitor cells with givinostat promote myoangiogenesis and restore dystrophin in injured Duchenne dystrophic muscle
Skeletal muscle
Skeletal muscle
GRAF1 deficiency blunts sarcolemmal injury repair and exacerbates cardiac and skeletal muscle pathology in dystrophin-deficient mice
Development and Validation of a Western Blot Method to Quantify Mini-Dystrophin in Human Skeletal Muscle Biopsies
Nanopolymers improve delivery of exon skipping oligonucleotides and concomitant dystrophin expression in skeletal muscle of mdx mice
DRP-1-mediated apoptosis induces muscle degeneration in dystrophin mutants
mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies