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ProteomicsGeneration of dystrophin short product-specific tag-insertion mouse: distinct Dp71 glycoprotein complexes at inhibitory postsynapse and glia limitans
Duchenne muscular dystrophy (DMD), the most severe form of dystrophinopathies, is a fatal X-linked recessive neuromuscular disorder characterized by progressive muscle degeneration and various extents of intellectual disabilities. Physiological and pathological roles of the responsible gene, dystrop...
ORGANISM(S): Mus Musculus (mouse) 
2026-08-04 | PXD080658 | JPOST Repository
UnknownRescue of Defective Electroretinographic Responses in Dp71-Null Mice With AAV-Mediated Reexpression of Dp71.
Not available
S-EPMC7326481 | biostudies-literature
UnknownDecreased Dp71 expression is associated with gastric adenocarcinoma prognosis.
Not available
S-EPMC5288215 | biostudies-literature
UnknownKnockdown of dystrophin Dp71 impairs PC12 cells cycle: localization in the spindle and cytokinesis structures implies a role for Dp71 in cell division.
Not available
S-EPMC3158767 | biostudies-literature
UnknownEvidence of the involvement of dystrophin Dp71 in corneal angiogenesis.
Not available
S-EPMC6857772 | biostudies-literature
UnknownDP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient.
Not available
S-EPMC6334379 | biostudies-literature
UnknownDystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells.
Not available
S-EPMC8468555 | biostudies-literature
UnknownExpression of Dystrophin Dp71 Splice Variants Is Temporally Regulated During Rodent Brain Development.
Not available
S-EPMC11584426 | biostudies-literature
UnknownDp71, utrophin and beta-dystroglycan expression and distribution in PC12/L6 cell cocultures.
Not available
S-EPMC2580073 | biostudies-literature
UnknownSocial and emotional alterations in mice lacking the short dystrophin-gene product, Dp71.
Not available
S-EPMC11344925 | biostudies-literature
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