A quantitative fluorescence-imaging technique for studying acetylcholine receptor turnover at neuromuscular junctions in living animals.
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A standard for calibration and shading correction of a fluorescence microscope.Dynamics of the rapsyn scaffolding protein at the neuromuscular junction of live miceNeural agrin controls acetylcholine receptor stability in skeletal muscle fibersCalcium/calmodulin kinase II-dependent acetylcholine receptor cycling at the mammalian neuromuscular junction in vivoPKC and PKA regulate AChR dynamics at the neuromuscular junction of living mice.CLASP2-dependent microtubule capture at the neuromuscular junction membrane requires LL5β and actin for focal delivery of acetylcholine receptor vesicles.An automated protocol for performance benchmarking a widefield fluorescence microscope.The knockdown of αkap alters the postsynaptic apparatus of neuromuscular junctions in living mice.Neuregulin/ErbB regulate neuromuscular junction development by phosphorylation of α-dystrobrevinAcetylcholinesterase mobility and stability at the neuromuscular junction of living miceNicotinic acetylcholine receptor stability at the NMJ deficient in α-syntrophin in vivo.Linker molecules between laminins and dystroglycan ameliorate laminin-alpha2-deficient muscular dystrophy at all disease stagesSubtle neuromuscular defects in utrophin-deficient mice.Viral delivery of C9orf72 hexanucleotide repeat expansions in mice leads to repeat-length-dependent neuropathology and behavioural deficits.Quantification of the surface density of a fluorescent label with the optical microscope.Effects of purified recombinant neural and muscle agrin on skeletal muscle fibers in vivo.Rapid and modifiable neurotransmitter receptor dynamics at a neuronal synapse in vivo.In vivo regulation of acetylcholinesterase insertion at the neuromuscular junction.Acetylcholinesterase dynamics at the neuromuscular junction of live animals.Spatial distribution and molecular dynamics of dystrophin glycoprotein components at the neuromuscular junction in vivo.Quantification of fluorescence in thick specimens, with an application to cyclin B-GFP expression in starfish oocytes.The dynamics of the rapsyn scaffolding protein at individual acetylcholine receptor clusters.A robust diffusion-based gradient generator for dynamic cell assays.
P2860
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P2860
A quantitative fluorescence-imaging technique for studying acetylcholine receptor turnover at neuromuscular junctions in living animals.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
A quantitative fluorescence-im ...... r junctions in living animals.
@ast
A quantitative fluorescence-im ...... r junctions in living animals.
@en
type
label
A quantitative fluorescence-im ...... r junctions in living animals.
@ast
A quantitative fluorescence-im ...... r junctions in living animals.
@en
prefLabel
A quantitative fluorescence-im ...... r junctions in living animals.
@ast
A quantitative fluorescence-im ...... r junctions in living animals.
@en
P1476
A quantitative fluorescence-im ...... r junctions in living animals.
@en
P2093
P304
P356
10.1016/0165-0270(95)00135-2
P577
1996-02-01T00:00:00Z