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Active cycling

If uranium is internally cycled in coastal environments or if the riverine delivery of U shows some variability, residence time estimates (regardless of their precision) cannot be sensitive indicators of oceanic uranium reactivity. Based on very precise measurements of dissolved uranium in the open ocean, Chen et alJ concluded that uranium may be somewhat more reactive in marine environments than previously inferred. Furthermore, recent studies in high-energy coastal environments " indicate that uranium may be actively cycled and repartitioned (non-conservative) from one phase to the next. [Pg.45]

All mature blood cells arise from primitive hematopoietic cells in the bone marrow, the pluripotent stem cells. Approximately 0.1% of the nucleated cells of the bone marrow are pluripotent stem cells and approximately 5% of these cells may be actively cycling at any one time. The stem cell pool maintains itself through a process of asymmetrical cell division when a stem cell divides, one daughter cell remains a stem cell and the other becomes a committed colony-forming cell (CFC). The proliferation and differentiation of CFCs are controlled by hematopoietic growth factors. The hematopoietic growth factors stimulate cell division, differentiation and maturation, and convert the dividing cells into a population of terminally differentiated functional cells. [Pg.579]

The ATRP experiment is usually commenced with all of the catalyst in its lower oxidation state. The number of propagation events per activation cycle is... [Pg.490]

The transfer constant governs the number of propagation steps per activation cycle and should be small for a narrow molecular weight distribution. Rearrangement of eq. 17 to eq. 18 suggests a method of estimating transfer constants on the basis of measurements of the conversion, molecular weight and dispersity.2j... [Pg.500]

The process of inhibition becomes somewhat more complex if no restriction is made with respect to the concentration of modulators. As seen in Fig. 20.13, compounds with a low affinity to the transporter (EUh < 2) are able to activate if applied at low concentrations. However, if these compounds are applied at high concentration, ATP hydrolysis slows down (low V2 values) and they act as inhibitors (cf. Fig. 20.9). Compounds with EUh < 2 seem not to be transported (see Fig. 20.11). This may lead to an obstruction of the transport route and thus to a slow down of the activation cycle. Examples of this type of inhibitor include pro-... [Pg.483]

Parts a c of Fig. 5 show 3-D plots of the changes in the 14.5 nm layer line and equatorial reflections measured during an activation cycle at 100 ms time resolution, and are to be compared with the tension transient shown in Fig. 5 b. Clearly active tension production is associated with a large depression of the intensity of the 14.5 nm... [Pg.17]

Similar experiments have been performed more recently using rabbit psoas muscle fibres (Poole et al., 1987a b), where the equatorial intensities are known to be sensitive to the number of actively cycling bridges bound (Brenner Yu, 1983). [Pg.23]

Hastings Taking all the data together, we can make a strong prediction. Presumably there is a crippled liver oscillator, but because there is now a functional SCN giving a functional activity cycle on a daily basis, you will get that single pulse per day which the crippled liver can use. So those animals will... [Pg.69]

Hastings I suspect not, but in the motor cortex and striatum of these grafted mice we will probably see a cycle of gene expression there as a consequence of the activity cycle. [Pg.70]

Hastings Your reference point is the activity cycle, and then we are measuring gene expression in peripheral tissue relative to that onset. [Pg.180]

If the model for the oscillator is correct. Per and Cry expression will define solar/ circadian time, driving the activity—rest cycle rather than just being a passive reflection of the activity cycle. Therefore, their expression patterns should exhibit the same phase in the SCN of nocturnal and diurnal species. This is confirmed by examination of Per expression in the SCN of the diurnally active ground squirrel, Spermophilus (Mrosovsky et al 2001). The rhythm of Per1 and Per2 expression in... [Pg.208]

Fig. 1. 55. The function of eIF-2 in eucaryotic translation. eIF-2, the initiator protein for the translation is a regulatory GTPase that occurs in an active GTP-form and in an inactive GDP form (see ch. 5). The active eIF-2 GTP forms a complex with the initiator-tRNA, fMet-tRNA "" and the 40S subunit of the ribosome. This complex binds to the cap structure of mRNA to initiate the scanning process. eIF-2 undergoes an activation cycle typical for regulatory GTPases the inactive eIF-2 GDP fom is activated with the assistance of the eIF-2B protein into the active elF-2 GTP form. eIF-2B acts as a G-nucleotide exchange factor in the cycle (see ch. 5). Fig. 1. 55. The function of eIF-2 in eucaryotic translation. eIF-2, the initiator protein for the translation is a regulatory GTPase that occurs in an active GTP-form and in an inactive GDP form (see ch. 5). The active eIF-2 GTP forms a complex with the initiator-tRNA, fMet-tRNA "" and the 40S subunit of the ribosome. This complex binds to the cap structure of mRNA to initiate the scanning process. eIF-2 undergoes an activation cycle typical for regulatory GTPases the inactive eIF-2 GDP fom is activated with the assistance of the eIF-2B protein into the active elF-2 GTP form. eIF-2B acts as a G-nucleotide exchange factor in the cycle (see ch. 5).
The question of the structural basis and explanation of the dissociation of the activated receptor from the Py-complex is little imderstood. Equally open is the question of the structure of the nucleotide-free heterotrimeric state, postulated as a short-lived intermediate form in the activation cycle of the G-protein. [Pg.202]

Figure 10.11 Voltammetry of 0.45 mM catechol in 0.1 M H2S04 at polished GC (a) after polishing (b) after first, second, fourth, and seventh activation cycles (cycled to 1.78 V vs. Ag QRE at 0.2 V/s) (c) dashed voltammogram was obtained 35 min after activation. [Adapted from Ref. 44.]... Figure 10.11 Voltammetry of 0.45 mM catechol in 0.1 M H2S04 at polished GC (a) after polishing (b) after first, second, fourth, and seventh activation cycles (cycled to 1.78 V vs. Ag QRE at 0.2 V/s) (c) dashed voltammogram was obtained 35 min after activation. [Adapted from Ref. 44.]...

See other pages where Active cycling is mentioned: [Pg.459]    [Pg.49]    [Pg.186]    [Pg.774]    [Pg.838]    [Pg.63]    [Pg.133]    [Pg.97]    [Pg.114]    [Pg.123]    [Pg.125]    [Pg.21]    [Pg.96]    [Pg.97]    [Pg.128]    [Pg.210]    [Pg.282]    [Pg.35]    [Pg.48]    [Pg.391]    [Pg.128]    [Pg.159]    [Pg.134]    [Pg.21]    [Pg.192]   
See also in sourсe #XX -- [ Pg.371 ]




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Acetylcholine receptor activation cycle

Activated methyl cycle

Activities of the Urea Cycle Enzymes

Amino acid synthesis activated methyl cycle

And the circadian rest-activity cycle

Apparent activation energy catalytic cycle

Catalytically active sites catalytic cycle

Cell cycle activity

Circadian rest-activity cycle

Enamine activation catalytic cycle

Factors Affecting Activities of the Urea Cycle Enzymes

Iminium activation catalytic cycle

Life-cycle safety activities

Nitrogen cycle enzyme activity

Nitrogen cycle human activities, effect

Oxidative activation catalytic cycle

Photochemical activation catalytic cycle

Software life cycle activities

Transfer Mechanism, Geochemical Cycle and the Influence of Human Activity

Urea cycle activities

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