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P-type signals

Some 2D experiments provide phase modulation directly as N-type and/or P-type signals, as in Eq. 10.13. These signals can also be processed along the lines that we have described. The signals in Eq. 10.13 are separately Fourier transformed with respect to t2 and the imaginary parts discarded. Then sP is added to %, the complex conjugate of sN, to give... [Pg.273]

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].
The broadening of the characteristic peaks of the silicon XRD signal provides information about stress and size of the crystallites. Figure 7.4 shows the diffraction pattern of microporous silicon powders scraped from p-type Si electrodes and of a bulk silicon powder sample. The peak broadening increases with increasing formation current density. For low formation current densities a superposition of... [Pg.131]

Fig. 7.4 XRD signal for powder samples prepared from bulk Si (top) and micro PS films produced on p-type electrodes using different anodization current densities, as indicated in... Fig. 7.4 XRD signal for powder samples prepared from bulk Si (top) and micro PS films produced on p-type electrodes using different anodization current densities, as indicated in...
Fig. 7.20 Luminescence intensity and peak position versus RTO processing temperature for PS samples grown on p-type silicon substrates (A 1 Q cm, B 1 Q cm, C 0.07 12 cm). Note the anti-correlation of the PL intensity and of the ESR signal (taken for sample series A). After [Pel],... Fig. 7.20 Luminescence intensity and peak position versus RTO processing temperature for PS samples grown on p-type silicon substrates (A 1 Q cm, B 1 Q cm, C 0.07 12 cm). Note the anti-correlation of the PL intensity and of the ESR signal (taken for sample series A). After [Pel],...
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 members of the G, subfamily are not modifiable by pertussis toxin or cholera toxin. The signal protein next in the reaction sequence is generally the P-type of phospholipase C. [Pg.195]

At least four types of cytokine receptors can be differentiated on the basis of sequence homology (Fig. 11.2). Many members of the cytokine receptors of type 1 regulate growth and transmit mitogenic signals to the cell nucleus. The cytokine receptors of type 2 include the receptors for the interferons a and p. Type 3 includes the receptors for tiunor necrosis factor TNF and for CD 40 and Fas protein, which are foimd on T lymphocytes. [Pg.359]

Doped semiconductors are essential components in the modern solid-state electronic devices found in radios, television sets, pocket calculators, and computers. Devices such as transistors, which control electrical signals in these products, are made from M-type and p-type semiconductors. In modern integrated circuits, an amazing number of extremely small devices can be packed into a small space, thus decreasing the size and increasing the speed of electrical equipment. For example, computer microprocessors now contain up to 42 million transistors on a silicon chip with a surface area of about 2 cm2 and are able to execute as many as 1.5 billion instructions per second. [Pg.929]

Presynaptic H3 receptors also are uniform in their signal transduction. They couple to Gi/o proteins and decrease the depolarization-induced release of neurotransmitters by inhibiting multiple calcium channels (e.g., Arrang et al. 1985 Schlicker et al. 1994 Endou et al. 1994 Brown and Haas 1999 see Stark et al. 2004). For comparison, the signal transduction of soma-dendritic H3 autoreceptors in histamin-ergic neurons also involves a pertussis toxin-sensitive G-protein with subsequent inhibition of N- and P-type Ca2+ channels (Takeshita et al. 1998). The few exceptions to this signal transduction pathway are discussed in the corresponding subsections below (see Sections 3.1, 3.3, and 3.9). [Pg.306]


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