Results 281 to 290 of about 100,070 (325)

Absence of T-box transcription factor 21 limits neuromuscular junction recovery after nerve injury in <i>T-bet</i>-knockout mice. [PDF]

Front Cell Dev Biol
Jablonka-Shariff A, Broberg C, Snyder-Warwick AK.   +2 more
europepmc   +1 more source

Basal lamina: A novel pH regulator at the neuromuscular junction. [PDF]

Sci Prog
Durbin R, Renden R.
europepmc   +1 more source

Effects of physical exercise on neuromuscular junction degeneration during ageing: A systematic review. [PDF]

J Orthop Translat
Wang Q, Cui C, Zhang N, Lin W, Chai S, Chow SK, Wong RMY, Hu Y, Law SW, Cheung WH.   +9 more
europepmc   +1 more source

Muscle cofilin alters neuromuscular junction postsynaptic development to strengthen functional neurotransmission.

Development
Christophers B, Leahy SN, Soffar DB, von Saucken VE, Broadie K, Baylies MK.   +5 more
europepmc   +1 more source

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Autonomic neuromuscular junctions

Autonomic Neuroscience, 2021
This review traces the history of the discovery and subsequent understanding of smooth muscle cells and their motor innervation. Smooth muscle tissue is made up of thousands of very small, individual, electrically connected, muscle cells. Each axon that enters a smooth muscle tissue branches extensively to form a terminal arbour that comes close to ...
Madeleine R, Di Natale, Martin J, Stebbing, John B, Furness   +2 more
openaire   +2 more sources

Neuromuscular Junction Disorders

PM&R, 2013
AbstractDisorders of the neuromuscular junction, such as myasthenia gravis and Lambert‐Eaton myasthenic syndrome, constitute an important and treatable class of diseases. Both disorders are typically caused by an immunologically mediated attack on discrete components of the neuromuscular junction, compromise the efficacy of neurotransmitter ...
Chiawen Lucy, Liang, Steve, Han
openaire   +2 more sources

Neuromuscular junctional disorders

The Indian Journal of Pediatrics, 2008
Neuromuscular junctional disorders (NMJ) in children are distinct entity. They may be acquired or hereditary. They pose problem in diagnosis because of the higher occurrence of sero negative Myasthenia Gravis (MG) cases in children. The identity of MusK antibody positivity in a good percentage of sero negative cases further adds to problems in ...
A S, Girija, V V, Ashraf
openaire   +2 more sources

Cholinesterases of neuromuscular junction

Neurochemistry International, 1980
The ultrastructural localization of AChE and BuChE was studied in motor endplates of the rat and mouse diaphragms, using the CNS(?) modification of the one-step Cu-thiocholine procedure. AChE activity was observed on pre- and postsynaptic membranes, in the basal lamina and in the Schwann cell-nerve terminal interspace.
M, Brzin, J, Sketelj, Z, Grubi, T, Kiauta   +3 more
openaire   +2 more sources