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IPSC derived cardiac fibroblasts of DMD patients show compromised actin microfilaments, metabolic sh...

IPSC derived cardiac fibroblasts of DMD patients show compromised actin microfilaments, metabolic sh...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_bf3a762253b14d5b8a3a2000997579d2

IPSC derived cardiac fibroblasts of DMD patients show compromised actin microfilaments, metabolic shift and pro-fibrotic phenotype

About this item

Full title

IPSC derived cardiac fibroblasts of DMD patients show compromised actin microfilaments, metabolic shift and pro-fibrotic phenotype

Publisher

England: BioMed Central Ltd

Journal title

Biology direct, 2023-07, Vol.18 (1), p.41-41, Article 41

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Duchenne muscular dystrophy (DMD) is a severe form of muscular dystrophy caused by mutations in the dystrophin gene. We characterized which isoforms of dystrophin were expressed by human induced pluripotent stem cell (hiPSC)-derived cardiac fibroblasts obtained from control and DMD patients. Distinct dystrophin isoforms were observed; however, high...

Alternative Titles

Full title

IPSC derived cardiac fibroblasts of DMD patients show compromised actin microfilaments, metabolic shift and pro-fibrotic phenotype

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_bf3a762253b14d5b8a3a2000997579d2

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_bf3a762253b14d5b8a3a2000997579d2

Other Identifiers

ISSN

1745-6150

E-ISSN

1745-6150

DOI

10.1186/s13062-023-00398-2

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