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4 (ZT) 0430 and 0530, were incubated, and then tetanized between ZT 1340 and 1930, where ZT=0 denotes l
5 nontetanized dendrite but cannot invade the tetanized dendrite, where recurrent EPSPs and evoked IPS
6 ever, the disrupted electrophysiology of the tetanized dendrites will disable normal information proc
8 weight during a 7 s tetanus, only in muscles tetanized in the presence of 10 mM [Ca2+]o when cytoplas
9 th LTP analyzed at 2 hr post-tetanus, slices tetanized in the presence of APV, and control slices rec
11 e range of velocities (0.1-10 L(0) s(-1)) of tetanized intact rat muscle fibre bundles (L0 approximat
12 ip obtained under steady-state conditions in tetanized muscle was shifted significantly to the left (
13 discontinuous or burst-like property of the tetanizing paradigm, required NMDA-receptor activation a
14 multaneously, BDNF treatment potentiated the tetanized pathway without affecting the synaptic efficac
15 rmed that SCG10 mRNA levels were elevated in tetanized rat hippocampi compared with those of sham con
16 shortening (n) is estimated by imposing, on tetanized single fibres from Rana esculenta (at 4 degree
19 ard trials, comparing the ERPs evoked by the tetanized stimuli (1000 Hz tones: TS+) and untetanized s
21 ted in LTP of the EPSPs elicited in both the tetanized thalamic pathway and the untetanized cortical
22 lls were measured before (control) and after tetanizing the Schaffer/collateral commissural pathway.
23 lts show that untreated control brain slices tetanized with either HFS or TBS gave similar levels of
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