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N-type signals

N-type signals, the desired coherence orders are +1 and —1 at these points and thus the phase encoding induced hy each gradient may he represented using shorthand notation as... [Pg.155]

Figure 2 Coherence-transfer pathway diagrams for COSY, illustrating gradient selection of (A) the F =0 artefacts only, [0 0--1] (B) N-type signals, [0 -> +1 -1] and (C) P-type signals, [0 -1 -1]. Figure 2 Coherence-transfer pathway diagrams for COSY, illustrating gradient selection of (A) the F =0 artefacts only, [0 0--1] (B) N-type signals, [0 -> +1 -1] and (C) P-type signals, [0 -1 -1].
Otherwise, the effect of electrode potential and kinetic parameters as contained in the relevant expression for the PMC signal (21), which controls the lifetime of PMC transients (40), may lead to an erroneous interpretation of kinetic mechanisms. The fact that lifetime measurements of PMC transients largely match the pattern of PMC-potential curves, showing peaks in accumulation and depletion of the semiconductor electrode and a minimum at the flatband potential [Figs. 13, 16-18, 34, and 36(b)], demonstrates that kinetic constants are accessible via PMC transient measurements, as indicated by the simplified relation (40) derived for the depletion layer of an n-type electrode. [Pg.504]

Figure 45. (a) Schematic of PMC signal behavior in accumulation region (i), flatband region (ii), and depletion region (iii) with (b) visualization of energy band situation of an n-type semiconductor. [Pg.518]

Endou M, Poli E> Levi R Histamine H3 receptor signaling in the heart possible involvement of Gj/Go proteins and N-type Ca channels. J Pharmacol Exp Ther 1994 269 221. bS... [Pg.109]

Figure 2.16 Sensor signals, the voltage over the diodes at 0.6 mA, for (a) p-type and (b) n-type Schottky diodes while exposed to alternating 2% Oj/Nj or 2% H2/N2 ambient at 300°C. Figure 2.16 Sensor signals, the voltage over the diodes at 0.6 mA, for (a) p-type and (b) n-type Schottky diodes while exposed to alternating 2% Oj/Nj or 2% H2/N2 ambient at 300°C.
The biological effects of histamine (Table 15.1) are mediated via three receptor subtypes, HI, H2 and H3 that are linked to G protein but activate different cell-signalling systems. The histamine HI receptor is associated with the phospholipase C-catalysed formation of inositol 1,4,5-triphosphate (IP3) and 1,2-diacylglycerol (DAG). The H2-receptor is coupled to adenylyl cyclase, increasing the production of cAMP. The cellular messenger system involved in H3-receptor activation has not been fully defined, but it may couple to N-type Ca2+-channels. The genes encoding for HI and H2 receptors have been cloned. A mutation of the human H2 receptor has been linked to schizophrenia. [Pg.239]

First, let us consider the problem of getting electrical signals into and out of a semiconductor device through metallic contacts. If the contact is with an n-type semiconductor, and if the work function of the metal is smaller than... [Pg.419]


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See also in sourсe #XX -- [ Pg.273 ]




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