[HTML][HTML] The roles of the dystrophin-associated glycoprotein complex at the synapse
GSK Pilgram, S Potikanond, RA Baines… - Molecular …, 2010 - Springer
Duchenne muscular dystrophy is caused by mutations in the dystrophin gene and is
characterized by progressive muscle wasting. A number of Duchenne patients also present …
characterized by progressive muscle wasting. A number of Duchenne patients also present …
Dystrophin is required for appropriate retrograde control of neurotransmitter release at the Drosophila neuromuscular junction
MC van der Plas, GSK Pilgram, JJ Plomp… - Journal of …, 2006 - Soc Neuroscience
Mutations in the human dystrophin gene cause the Duchenne and Becker muscular
dystrophies. The Dystrophin protein provides a structural link between the muscle …
dystrophies. The Dystrophin protein provides a structural link between the muscle …
[HTML][HTML] Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin–glycoprotein complex
RM Grady, H Zhou, JM Cunningham, MD Henry… - Neuron, 2000 - cell.com
The dystrophin–glycoprotein complex (DGC) links the cytoskeleton of muscle fibers to their
extracellular matrix. Using knockout mice, we show that a cytoplasmic DGC component, α …
extracellular matrix. Using knockout mice, we show that a cytoplasmic DGC component, α …
The molecular cross talk of the dystrophin–glycoprotein complex
M Gawor, TJ Prószyński - Annals of the New York Academy of …, 2018 - Wiley Online Library
The proper function of skeletal muscles relies on their ability to process signals derived from
motor neurons, transmit stimuli along the muscle fibers, contract, and regenerate efficiently …
motor neurons, transmit stimuli along the muscle fibers, contract, and regenerate efficiently …
Diversity of the brain dystrophin‐glycoprotein complex
K Culligan, K Ohlendieck - BioMed Research International, 2002 - Wiley Online Library
Duchenne muscular dystrophy (DMD), the most common inherited neuromuscular disorder,
is characterized by progressive muscle wasting and weakness. One third of Duchenne …
is characterized by progressive muscle wasting and weakness. One third of Duchenne …
[HTML][HTML] Synaptic alterations as a neurodevelopmental trait of Duchenne muscular dystrophy
ME De Stefano, V Ferretti, C Mozzetta - Neurobiology of Disease, 2022 - Elsevier
Dystrophinopaties, eg, Duchenne muscular dystrophy (DMD), Becker muscular dystrophy
and X-linked dilated cardiomyopathy are inherited neuromuscular diseases, characterized …
and X-linked dilated cardiomyopathy are inherited neuromuscular diseases, characterized …
Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models
EM van der Pijl, M van Putten, EH Niks… - European Journal of …, 2016 - Wiley Online Library
Duchenne muscular dystrophy (DMD) is an X‐linked myopathy caused by dystrophin
deficiency. Dystrophin is present intracellularly at the sarcolemma, connecting actin to the …
deficiency. Dystrophin is present intracellularly at the sarcolemma, connecting actin to the …
The role of the dystrophin glycoprotein complex on the neuromuscular system
DC Belhasan, M Akaaboune - Neuroscience letters, 2020 - Elsevier
Abstract The Dystrophin Glycoprotein Complex (DGC) is a large multi-protein complex that
links cytoskeleton actin to the extracellular matrix. This complex is critical in maintaining the …
links cytoskeleton actin to the extracellular matrix. This complex is critical in maintaining the …
Dystroglycan contributes to the formation of multiple dystrophin‐like complexes in brain
H Moukhles, S Carbonetto - Journal of neurochemistry, 2001 - Wiley Online Library
In muscle, dystrophin anchors a complex of proteins at the cell surface which includes α‐
dystroglycan, β‐dystroglycan, syntrophins and dystrobrevins. Mutations in the dystrophin …
dystroglycan, β‐dystroglycan, syntrophins and dystrobrevins. Mutations in the dystrophin …
[HTML][HTML] Muscle Dystroglycan Organizes the Postsynapse and Regulates Presynaptic Neurotransmitter Release at the Drosophila Neuromuscular Junction
L Bogdanik, B Framery, A Frölich, B Franco, D Mornet… - PLoS …, 2008 - journals.plos.org
Background The Dystrophin-glycoprotein complex (DGC) comprises dystrophin,
dystroglycan, sarcoglycan, dystrobrevin and syntrophin subunits. In muscle fibers, it is …
dystroglycan, sarcoglycan, dystrobrevin and syntrophin subunits. In muscle fibers, it is …