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1 tic expression of the Ca(2+) binding protein frequenin.
2                                              Frequenin, a Ca(2+)-binding protein, has previously been
3 ave examined the effect of overexpression of frequenin, a modulator of phosphatidylinositol 4-kinase
4                                              Frequenin, also known as neuronal calcium sensor-1 (NCS-
5                       The Drosophila protein frequenin and its mammalian homolog neuronal Ca2+ sensor
6 munohistochemical analysis demonstrates that frequenin and Kv4.2 channel proteins are coexpressed in
7                             We conclude that frequenin, and by inference, phosphatidylinositol 4-kina
8 in expression, occluded by overexpression of frequenin, and is selective to N-type Ca(2+) channels.
9  determined that the differential effects of frequenin are mediated by means of the Kv4 N terminus.
10  proteins (e.g. recoverin, neurocalcins, and frequenin) are expressed at highest levels in excitable
11 n Pik1 is a hydrophobic alpha-helix and that frequenins bind to one side of this alpha-helix.
12                Frq1 belongs to the recoverin/frequenin branch of the EF-hand superfamily and regulate
13                            Overexpression of frequenin did not affect postendocytic trafficking steps
14 ficity for Kv4 currents is suggested because frequenin does not modulate Kv1.4 or Kv3.4 currents.
15  frequenin in motoneurons, and inhibition of frequenin expression or activity prevents the synaptic a
16  Ca(2+) currents is blocked by inhibition of frequenin expression, occluded by overexpression of freq
17 onservation between Saccharomyces cerevisiae frequenin (Frq1) and human NCS-1 is also reflected at th
18                                        Yeast frequenin (Frq1), a small N-myristoylated EF-hand protei
19        Adenoviral-mediated overexpression of frequenin had no effect on early Golgi transport of memb
20                                              Frequenin has negligible effects on Kv4.1 current inacti
21              GDNF enhances the expression of frequenin in motoneurons, and inhibition of frequenin ex
22 at of Frq1 in S. cerevisiae and, hence, that frequenins in general may serve as regulators of certain
23 CS-1 (neuronal calcium sensor-1, also termed frequenin) in 3T3L1 adipocytes strongly inhibited insuli
24                                              Frequenin increases Kv4.2 current amplitudes (partly by
25        Here, we provide direct evidence that frequenin is a potent and specific modulator of Kv4 chan
26  provide strong support for the concept that frequenin may be an important Ca(2+)-sensitive regulator
27                                              Frequenin/NCS-1 has been shown to enhance exocytotic act
28 kly expressed in human PFs, whereas DPP6 and frequenin (neuronal calcium sensor-1) were enriched.
29                                        Frq1 (frequenin orthologue) also is essential for viability an
30                                   Endogenous frequenin was identified in these cells by polymerase ch
31 s severely inhibited in cells overexpressing frequenin, whereas basolateral delivery of the polymeric

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