Flightless flies: Drosophila models of neuromuscular disease

TE Lloyd, JP Taylor - Annals of the New York Academy of …, 2010 - Wiley Online Library
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 …

[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 …

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 …

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 …

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 …

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 …

Functional diversity of dystroglycan

M Bozzi, S Morlacchi, MG Bigotti, F Sciandra… - Matrix Biology, 2009 - Elsevier
During the last 15 years, following its identification and first detailed molecular
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 …

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 …

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 …