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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 …
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
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 …
from mild to severe dystrophin-associated muscular dystrophies. Duchenne (DMD) and …
Single-nucleus cross-tissue molecular reference maps toward understanding disease gene function
Understanding gene function and regulation in homeostasis and disease requires
knowledge of the cellular and tissue contexts in which genes are expressed. Here, we …
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 …
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
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 …
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; …
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 …
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 …
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 …
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
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 …
is known about the underlying signalling mechanisms. The Arabidopsis root radial pattern is …