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Goal was to assess protein linkers between microtubules and dystrophin (specifically dystrophin regions R4-15 and R20-23). Two paired 10-plex TMT experiments were used to compare sixteen unique Dystrophin Glycoprotein Complex (or microtubule) enrichments (four genotypes, each with n=4) plus four poo...
ORGANISM(S): Mus musculus (Mouse) 
2020-09-21 | PXD021088 | Pride
Dysfunction of the dystrophin-glycoprotein complex (DGC) is a frequent cause of hereditary forms of muscular dystrophy. Although DGC function in maintaining skeletal muscle integrity has been well characterized, little is known about how the DGC complex is coordinately regulated at the transcription...
ORGANISM(S): Mus musculus 
Signaling through the insulin receptor governs central physiological functions related to cell growth and metabolism. Here we show by tandem native protein complex purification approach and super-resolution STED microscopy that insulin receptor activity requires association with the fundamental stru...
ORGANISM(S): Mus musculus (Mouse) 
2020-03-19 | PXD016989 | Pride
Dysfunction of the dystrophin-glycoprotein complex (DGC) is a frequent cause of hereditary forms of muscular dystrophy. Although DGC function in maintaining skeletal muscle integrity has been well characterized, little is known about how the DGC complex is coordinately regulated at the transcription...
ORGANISM(S): Mus musculus 
2008-03-25 | GSE10678 | GEO
Signaling through the dystrophin glycoprotein complex affects the stress-dependent transcriptome in Drosophila
Histone deacetylase 4 represses dystrophin-glycoprotein (DGC) complex expression
Deficiencies in the human dystrophin glycoprotein complex (DGC), which links the extracellular matrix with the intracellular cytoskeleton, cause muscular dystrophies, a group of incurable disorders associated with heterogeneous muscle, brain and eye abnormalities. Stresses such as nutrient deprivati...
ORGANISM(S): Drosophila melanogaster 
2023-01-31 | GSE223505 | GEO
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