Attempts have been made to develop animal models of sequestration (Refs 210, 211); however, their relevance to human disease mechanisms is unclear and unproven.
In this paper, a multiphase flow model of CO2 sequestration into deep ocean sediments was designed associated with the formation of CO2 hydrates.
HUVEC expresses ICAM-1 on TNF stimulation but not CD36 and is used widely as a model of brain sequestration in vitro [21], [36], [59], [89].
Taken together these results show that the loss-of-signal model utilizes sequestration of CLV3 in the clv1-1 mutant in order to generate a stronger phenotype than the clv1-11 null mutant.
Synthesis of the PG-modified LPS (LPS*) requires ready access to the small PG precursor pool but does not weaken cell wall integrity, challenging models of precursor sequestration at PG assembly machinery.
Partial uncoupling of σF activation from cell division by stabilizing SpoIIE is consistent with our model that sequestration of SpoIIE at the divisome prohibits premature oligomerization of SpoIIE and activation of σF.
A carrier model requiring sequestration of both water and its driving ligands within intramembranous compartments is inconsistent with an unbroken continuously transmitting pathway, as is required for electrical current or osmotic pressure driven water flows.
Employing a novel in vivo model of human infected erythrocyte sequestration, immunized animals were challenged with the FCR3S1.2 clone and cross-protection in terms of reduction in lung sequestration amounting to approximately 50% was demonstrated.
Herein we report that an epistatic effect of the apoptosome components apaf- 1 and caspase- 9 on chlamydial infection and its host apoptosis regulation; that is, caspase-9 functions as in the sequestration model of pro-apoptotic factors for the regulation of host apoptosis, and Apaf-1 restricts chlamydial infection.
In conclusion, our model predicts sequestration primarily of PIP2 lipids by the adsorbing basic peptide, and very weak sequestration of PS lipids.
