Ontology highlight
ABSTRACT:
INSTRUMENT(S): Q Exactive
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Whole Body, Mesenchymal Cell
SUBMITTER: Amanda Assoni
LAB HEAD: Mayana Zatz
PROVIDER: PXD003978 | Pride | 2016-12-09
REPOSITORIES: Pride
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Stem cells and development 20161020 3
Duchenne muscular dystrophy (DMD) is a lethal X-linked disorder caused by null mutations in the dystrophin gene. Although the primary defect is the deficiency of muscle dystrophin, secondary events, including chronic inflammation, fibrosis, and muscle regeneration failure are thought to actively contribute to disease progression. Despite several advances, there is still no effective therapy for DMD. Therefore, the potential regenerative capacities, and immune-privileged properties of mesenchymal ...[more]