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Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiency. , Ishigaki K., Neuromuscul Disord. March 1, 2003; 13 (3): 236-44.
PRiMA: the membrane anchor of acetylcholinesterase in the brain. , Perrier AL., Neuron. January 17, 2002; 33 (2): 275-85.
Acetylcholinesterase clustering at the neuromuscular junction involves perlecan and dystroglycan. , Peng HB ., J Cell Biol. May 17, 1999; 145 (4): 911-21.
Former neuritic pathways containing endogenous neural agrin have high synaptogenic activity. , Cohen MW ., Dev Biol. February 1, 1995; 167 (2): 458-68.
Cellular and secreted forms of acetylcholinesterase in mouse muscle cultures. , Rubin LL., J Neurochem. December 1, 1985; 45 (6): 1932-40.
Membrane-related specializations associated with acetylcholine receptor aggregates induced by electric fields. , Luther PW ., J Cell Biol. January 1, 1985; 100 (1): 235-44.
Acetylcholine receptor aggregation parallels the deposition of a basal lamina proteoglycan during development of the neuromuscular junction. , Anderson MJ., J Cell Biol. November 1, 1984; 99 (5): 1769-84.
Aggregates of acetylcholine receptors are associated with plaques of a basal lamina heparan sulfate proteoglycan on the surface of skeletal muscle fibers. , Anderson MJ., J Cell Biol. November 1, 1983; 97 (5 Pt 1): 1396-411.