Flow cytometry for the analysis of α-dystroglycan glycosylation in fibroblasts from patients with dystroglycanopathies.
α-dystroglycan (α-DG) is a peripheral membrane protein that is an integral component of the dystrophin-glycoprotein complex. In an inherited subset of muscular dystrophies known as dystroglycanopathies, α-DG has reduced glycosylation which results in lower affinity binding to several extracellular m...
Saved in:
| Main Authors: | Elizabeth Stevens, Silvia Torelli, Lucy Feng, Rahul Phadke, Maggie C Walter, Peter Schneiderat, Ayad Eddaoudi, Caroline A Sewry, Francesco Muntoni |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2013-01-01
|
| Series: | PLoS ONE |
| Online Access: | https://doi.org/10.1371/journal.pone.0068958 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Transgenic overexpression of LARGE induces α-dystroglycan hyperglycosylation in skeletal and cardiac muscle.
by: Martin Brockington, et al.
Published: (2010-12-01) -
Neurexin facilitates glycosylation of Dystroglycan to sustain muscle architecture and function in Drosophila
by: Yu Zhao, et al.
Published: (2024-11-01) -
Metabolic Engineering of Glycofusion Bispecific Antibodies for α-Dystroglycanopathies
by: Xiaotian Zhong, et al.
Published: (2024-10-01) -
Muscular Dystrophy-Dystroglycanopathy and Epilepsy
by: J Gordon Millichap
Published: (2013-01-01) -
UDP‐glucose dehydrogenase variants cause dystroglycanopathy
by: Anna M. Reelfs, et al.
Published: (2025-06-01)