Extracellular polysaccharides purified (Polycan) from Aureobasidium pullulans SM‑2001 improves pathophysiology of dystrophin-deficient mdx mice
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2092-8467
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Extracellular polysaccharides purified (Polycan) from Aureobasidium pullulans SM‑2001 improves pathophysiology of dystrophin-deficient mdx mice ; volume:18 ; number:3 ; day:17 ; month:5 ; year:2022 ; pages:285-297 ; date:7.2022
Molecular & cellular toxicology ; 18, Heft 3 (17.5.2022), 285-297, 7.2022
- Creator
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Kim, Young-Suk
Lim, Jong-Min
Shin, Jae Suk
Kim, Hyun Jun
Park, Kwang-Il
Oh, Tae Woo
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s13273-022-00245-x
- URN
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urn:nbn:de:101:1-2022080821350004268098
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:28 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kim, Young-Suk
- Lim, Jong-Min
- Shin, Jae Suk
- Kim, Hyun Jun
- Park, Kwang-Il
- Oh, Tae Woo
- SpringerLink (Online service)
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Early manifestation of alteration in cardiac function in dystrophin deficient mdx mouse using 3D CMR tagging
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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
Metabolic remodeling agents show beneficial effects in the dystrophin- deficient mdx mouse model
iNOS is not responsible for RyR1 S-nitrosylation in mdx mice with truncated dystrophin
Early manifestation of alteration in cardiac function in dystrophin deficient mdx mouse using 3D CMR tagging
Microbiota dysbiosis influences immune system and muscle pathophysiology of dystrophin‐deficient mice
Altered social behavior and ultrasonic communication in the dystrophin-deficient mdx mouse model of Duchenne muscular dystrophy
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