Homeostatic control of presynaptic neurotransmitter release

GW Davis, M Müller - Annual review of physiology, 2015 - annualreviews.org
It is well established that the active properties of nerve and muscle cells are stabilized by
homeostatic signaling systems. In organisms ranging from Drosophila to humans, neurons …

The neuromuscular junction: roles in aging and neuromuscular disease

SR Iyer, SB Shah, RM Lovering - International journal of molecular …, 2021 - mdpi.com
The neuromuscular junction (NMJ) is a specialized synapse that bridges the motor neuron
and the skeletal muscle fiber and is crucial for conversion of electrical impulses originating …

Muscle-specific kinase myasthenia gravis IgG4 autoantibodies cause severe neuromuscular junction dysfunction in mice

R Klooster, JJ Plomp, MG Huijbers, EH Niks… - Brain, 2012 - academic.oup.com
Myasthenia gravis is a paralytic disorder with autoantibodies against acetylcholine receptors
at the neuromuscular junction. A proportion of patients instead has antibodies against …

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 …

Homeostatic plasticity at the Drosophila neuromuscular junction

CA Frank - Neuropharmacology, 2014 - Elsevier
In biology, homeostasis refers to how cells maintain appropriate levels of activity. This
concept underlies a balancing act in the nervous system. Synapses require flexibility (ie …

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 …

Biology of the striated muscle dystrophin–glycoprotein complex

JM Ervasti, KJ Sonnemann - International review of cytology, 2008 - Elsevier
Since its first description in 1990, the dystrophin–glycoprotein complex has emerged as a
critical nexus for human muscular dystrophies arising from defects in a variety of distinct …

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 …

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 …

The role of neuronal complexes in human X-linked brain diseases

F Laumonnier, PC Cuthbert, SGN Grant - The American Journal of Human …, 2007 - cell.com
Beyond finding individual genes that are involved in medical disorders, an important
challenge is the integration of sets of disease genes with the complexities of basic biological …