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1 53924, which causes the substitution R70C in phospholemman.
2 in myocytes lacking the regulatory protein, phospholemman.
3 tion alters the interaction of Na/K-pump and phospholemman.
4 ar to the Na(+),K(+)-ATPase regulator, FXYD1/Phospholemman.
9 y of small membrane proteins, represented by phospholemman and the gamma subunit of Na,K-ATPase, was
10 t (CFP/YFP) fusion proteins of Na/K pump and phospholemman and whether phospholemman phosphorylation
12 pitation and functional studies suggest that phospholemman associates with the Na/K-pump (NKA) and me
13 PKA targets, such as phospholamban at Ser16, phospholemman at Ser68 and cardiac myosin-binding protei
15 Much like phospholamban regulation of SERCA, phospholemman exists as both a sodium pump inhibiting mo
16 not NKA-alpha1 was coupled to a decrease in phospholemman expression and phosphorylation, which woul
21 dies, phospholemman knock-in mice (PLM(3SA); phospholemman [FXYD1] in which the 3 phosphorylation sit
24 hed human genomic databases for mutations in phospholemman in the region of the phosphorylation sites
26 8, and 69 are mutated to alanines), in which phospholemman is rendered unphosphorylatable, were used
29 e-spanning membrane proteins such as cardiac phospholemman, Mat-8 and renal CHIF, large ion conductan
34 without any differences in membrane markers (phospholemman, phosphalamban, dihydropyridine-binding co
36 very close proximity (FRET occurs) and that phospholemman phosphorylation alters the interaction of
40 These studies demonstrate the importance of phospholemman phosphorylation in the regulation of vascu
41 horylatable, were used to assess the role of phospholemman phosphorylation in vitro in aortic and mes
43 f this study was to test the hypothesis that phospholemman phosphorylation regulates vascular tone in
44 an embryonic kidney cells, and its effect on phospholemman phosphorylation was determined using Weste
45 photobleach), and this FRET was enhanced by phospholemman phosphorylation, consistent with phosphole
46 nt experimental approaches demonstrated that phospholemman physically associated with the Na,K-ATPase
51 e NKA-associated small transmembrane protein phospholemman (PLM) mediates beta-adrenergic-induced NKA
60 Previous reports have demonstrated that the phospholemman (PLM), a 72-residue plasma-membrane protei
65 arts) expression of Na/K-ATPase isoforms and phospholemman (PLM), a putative Na/K-ATPase regulatory s
66 eased, the palmitoylated regulatory protein, phospholemman (PLM), and the cardiac Na/Ca exchanger (NC
71 a key modulatory partner is the FXYD protein phospholemman (PLM, FXYD1), but the stoichiometry of the
73 Antibodies against the C-terminal domain of phospholemman reduced Na,K-ATPase activity in vitro with