- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2044-5040
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
miR-146a deficiency does not aggravate muscular dystrophy in mdx mice ; volume:9 ; number:1 ; day:14 ; month:8 ; year:2019 ; pages:1-17 ; date:12.2019
Skeletal muscle ; 9, Heft 1 (14.8.2019), 1-17, 12.2019
- Creator
-
Bronisz-Budzyńska, Iwona
Chwalenia, Katarzyna
Mucha, Olga
Podkalicka, Paulina
Karolina-Bukowska-Strakova
Józkowicz, Alicja
Łoboda, Agnieszka
Kozakowska, Magdalena
Dulak, Józef
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13395-019-0207-0
- URN
-
urn:nbn:de:101:1-2019123119390025321884
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:53 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
- Bronisz-Budzyńska, Iwona
- Chwalenia, Katarzyna
- Mucha, Olga
- Podkalicka, Paulina
- Karolina-Bukowska-Strakova
- Józkowicz, Alicja
- Łoboda, Agnieszka
- Kozakowska, Magdalena
- Dulak, Józef
- SpringerLink (Online service)
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Inactivation of Sirt6 ameliorates muscular dystrophy in mdx mice by releasing suppression of utrophin expression
Biomarkers for Duchenne muscular dystrophy progression: impact of age in the mdx tongue spared muscle
Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice
Increased plasma lipid levels exacerbate muscle pathology in the mdx mouse model of Duchenne muscular dystrophy
Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophy
Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia
Differential effects of PDE5 inhibitors on cardiac dysfunction in the MDX ouse model of Duchenne muscular dystrophy
Altered social behavior and ultrasonic communication in the dystrophin-deficient mdx mouse model of Duchenne muscular dystrophy
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Supplementation with a selective amino acid formula ameliorates muscular dystrophy in mdx mice
Moderate exercise improves function and increases adiponectin in the mdx mouse model of muscular dystrophy
Proteomic profiling of liver tissue from the mdx-4cv mouse model of Duchenne muscular dystrophy
Inactivation of Sirt6 ameliorates muscular dystrophy in mdx mice by releasing suppression of utrophin expression
Biomarkers for Duchenne muscular dystrophy progression: impact of age in the mdx tongue spared muscle
Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice
Increased plasma lipid levels exacerbate muscle pathology in the mdx mouse model of Duchenne muscular dystrophy
Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophy
Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia
Differential effects of PDE5 inhibitors on cardiac dysfunction in the MDX ouse model of Duchenne muscular dystrophy
Altered social behavior and ultrasonic communication in the dystrophin-deficient mdx mouse model of Duchenne muscular dystrophy