Focal adhesions, contractility, and signaling

K Burridge… - Annual review of cell and …, 1996 - annualreviews.org
▪ Abstract Focal adhesions are sites of tight adhesion to the underlying extracellular matrix
developed by cells in culture. They provide a structural link between the actin cytoskeleton …

Global prevalence of Duchenne and Becker muscular dystrophy: a systematic review and meta-analysis

N Salari, B Fatahi, E Valipour, M Kazeminia… - Journal of orthopaedic …, 2022 - Springer
Background A variety of mutations in the largest human gene, dystrophin, cause a spectrum
from mild to severe dystrophin-associated muscular dystrophies. Duchenne (DMD) and …

Single-nucleus cross-tissue molecular reference maps toward understanding disease gene function

G Eraslan, E Drokhlyansky, S Anand, E Fiskin… - Science, 2022 - science.org
Understanding gene function and regulation in homeostasis and disease requires
knowledge of the cellular and tissue contexts in which genes are expressed. Here, we …

Dystrophin protects the sarcolemma from stresses developed during muscle contraction.

BJ Petrof, JB Shrager, HH Stedman, AM Kelly… - Proceedings of the …, 1993 - pnas.org
The protein dystrophin, normally found on the cytoplasmic surface of skeletal muscle cell
membranes, is absent in patients with Duchenne muscular dystrophy as well as mdx (X …

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin

JM Ervasti, KP Campbell - The Journal of cell biology, 1993 - rupress.org
The dystrophin-glycoprotein complex was tested for interaction with several components of
the extracellular matrix as well as actin. The 156-kD dystrophin-associated glycoprotein (156 …

Function and genetics of dystrophin and dystrophin-related proteins in muscle

DJ Blake, A Weir, SE Newey… - Physiological …, 2002 - journals.physiology.org
The X-linked muscle-wasting disease Duchenne muscular dystrophy is caused by mutations
in the gene encoding dystrophin. There is currently no effective treatment for the disease; …

The Dystrophin Complex: structure, function and implications for therapy

Q Gao, EM McNally - Comprehensive physiology, 2015 - pmc.ncbi.nlm.nih.gov
The dystrophin complex stabilizes the plasma membrane of striated muscle cells. Loss of
function mutations in the genes encoding dystrophin, or the associated proteins, triggers …

The neuromuscular junction in health and disease: molecular mechanisms governing synaptic formation and homeostasis

PM Rodríguez Cruz, J Cossins, D Beeson… - Frontiers in molecular …, 2020 - frontiersin.org
The neuromuscular junction (NMJ) is a highly specialized synapse between a motor neuron
nerve terminal and its muscle fiber that are responsible for converting electrical impulses …

[HTML][HTML] Mechanisms regulating neuromuscular junction development and function and causes of muscle wasting

LA Tintignac, HR Brenner… - Physiological …, 2015 - journals.physiology.org
The neuromuscular junction is the chemical synapse between motor neurons and skeletal
muscle fibers. It is designed to reliably convert the action potential from the presynaptic …

Intercellular movement of the putative transcription factor SHR in root patterning

K Nakajima, G Sena, T Nawy, PN Benfey - Nature, 2001 - nature.com
Positional information is pivotal for establishing developmental patterning in plants,,, but little
is known about the underlying signalling mechanisms. The Arabidopsis root radial pattern is …