about
Acetylcholine receptors are required for agrin-induced clustering of postsynaptic proteins.Tyrosine phosphatases such as SHP-2 act in a balance with Src-family kinases in stabilization of postsynaptic clusters of acetylcholine receptors.Association of muscle-specific kinase MuSK with the acetylcholine receptor in mammalian muscle.Src-family kinases stabilize the neuromuscular synapse in vivo via protein interactions, phosphorylation, and cytoskeletal linkage of acetylcholine receptors.Cholesterol and lipid microdomains stabilize the postsynapse at the neuromuscular junction.The postsynaptic submembrane machinery at the neuromuscular junction: requirement for rapsyn and the utrophin/dystrophin-associated complex.PICK1 interacts with alpha7 neuronal nicotinic acetylcholine receptors and controls their clustering.Aminopeptidase N is directly sorted to the apical domain in MDCK cells.Regulation of nicotinic acetylcholine receptors by tyrosine kinases in the peripheral and central nervous system: same players, different roles.Endocytosis by the asialoglycoprotein receptor is independent of cytoplasmic serine residues.Alpha7 neuronal nicotinic acetylcholine receptors are negatively regulated by tyrosine phosphorylation and Src-family kinases.Agrin-induced activation of acetylcholine receptor-bound Src family kinases requires Rapsyn and correlates with acetylcholine receptor clustering.Roles of rapsyn and agrin in interaction of postsynaptic proteins with acetylcholine receptors.Functional interaction of Src family kinases with the acetylcholine receptor in C2 myotubes.Charged residues are major determinants of the transmembrane orientation of a signal-anchor sequence.Related signals for endocytosis and basolateral sorting of the asialoglycoprotein receptor.Dynamic interactions of the asialoglycoprotein receptor subunits with coated pits. Enhanced interactions of H2 following association with H1.Src, Fyn, and Yes are not required for neuromuscular synapse formation but are necessary for stabilization of agrin-induced clusters of acetylcholine receptors.Efficient transfection of DNA or shRNA vectors into neurons using magnetofectionAgrin / MuSK signaling: willing and Abl
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description
researcher ORCID ID = 0000-0001-8216-8883
@en
wetenschapper
@nl
name
Christian Fuhrer
@ast
Christian Fuhrer
@en
Christian Fuhrer
@es
Christian Fuhrer
@nl
type
label
Christian Fuhrer
@ast
Christian Fuhrer
@en
Christian Fuhrer
@es
Christian Fuhrer
@nl
prefLabel
Christian Fuhrer
@ast
Christian Fuhrer
@en
Christian Fuhrer
@es
Christian Fuhrer
@nl
P21
P31
P496
0000-0001-8216-8883