Flightless flies: Drosophila models of neuromuscular disease
The fruit fly, Drosophila melanogaster, has a long and rich history as an important model
organism for biologists. In particular, study of the fruit fly has been essential to much of our …
organism for biologists. In particular, study of the fruit fly has been essential to much of our …
[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 …
Molecular and cell biology of the sarcoglycan complex
E Ozawa, Y Mizuno, Y Hagiwara, T Sasaoka… - Muscle & …, 2005 - Wiley Online Library
The original sarcoglycan (SG) complex has four subunits and comprises a subcomplex of
the dystrophin–dystrophin‐associated protein complex. Each SG gene has been shown to …
the dystrophin–dystrophin‐associated protein complex. Each SG gene has been shown to …
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
HR Shcherbata, AS Yatsenko, L Patterson… - The EMBO …, 2007 - embopress.org
Perturbation in the Dystroglycan (Dg)–Dystrophin (Dys) complex results in muscular
dystrophies and brain abnormalities in human. Here we report that Drosophila is an …
dystrophies and brain abnormalities in human. Here we report that Drosophila is an …
Dystrophin deficiency in Drosophila reduces lifespan and causes a dilated cardiomyopathy phenotype
O Taghli‐Lamallem, T Akasaka, G Hogg, U Nudel… - Aging cell, 2008 - Wiley Online Library
A number of studies have been conducted recently on the model organism Drosophila to
determine the function of genes involved in human disease, including those implicated in …
determine the function of genes involved in human disease, including those implicated in …
Extracellular matrix and its receptors in drosophila neural development
K Broadie, S Baumgartner… - Developmental …, 2011 - Wiley Online Library
Extracellular matrix (ECM) and matrix receptors are intimately involved in most biological
processes. The ECM plays fundamental developmental and physiological roles in health …
processes. The ECM plays fundamental developmental and physiological roles in health …
Functional diversity of dystroglycan
During the last 15 years, following its identification and first detailed molecular
characterization, the dystroglycan (DG) complex has taken centre stage in biology and …
characterization, the dystroglycan (DG) complex has taken centre stage in biology and …
C. elegans dystroglycan DGN-1 functions in epithelia and neurons, but not muscle, and independently of dystrophin
RP Johnson, SH Kang, JM Kramer - 2006 - journals.biologists.com
The C. elegans dystroglycan (DG) homolog DGN-1 is expressed in epithelia and neurons,
and localizes to basement membrane (BM) surfaces. Unlike vertebrate DG, DGN-1 is not …
and localizes to basement membrane (BM) surfaces. Unlike vertebrate DG, DGN-1 is not …
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 …
Drosophila melanogaster as a model of muscle degeneration disorders
RE Kreipke, YV Kwon, HR Shcherbata… - Current topics in …, 2017 - Elsevier
Drosophila melanogaster provides a powerful platform with which researchers can dissect
complex genetic questions and biochemical pathways relevant to a vast array of human …
complex genetic questions and biochemical pathways relevant to a vast array of human …