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1 tic expression of the Ca(2+) binding protein frequenin.
3 ave examined the effect of overexpression of frequenin, a modulator of phosphatidylinositol 4-kinase
6 munohistochemical analysis demonstrates that frequenin and Kv4.2 channel proteins are coexpressed in
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
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
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
26 provide strong support for the concept that frequenin may be an important Ca(2+)-sensitive regulator
28 kly expressed in human PFs, whereas DPP6 and frequenin (neuronal calcium sensor-1) were enriched.
31 s severely inhibited in cells overexpressing frequenin, whereas basolateral delivery of the polymeric
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