In the case where no information is available on the division time distribution, it is shown that the estimation procedure using constant division times yields more reliable results. Numerical results both on observed and simulated data are reported.”
“Background: Soon after birth, all mammals must initiate milk suckling to survive. In rodents, this innate behavior is critically dependent on uncharacterized maternally derived chemosensory ligands. Recently, the first pheromone sufficient to initiate suckling was isolated from the rabbit. Identification of the olfactory LBH589 solubility dmso cues that

trigger first suckling in the mouse would provide the means to determine the neural mechanisms that generate innate behavior.\n\nResults: Here we use behavioral analysis, metabolomics, and MRT67307 in vitro calcium imaging of primary sensory neurons and find no evidence of ligands with intrinsic bioactivity, such as pheromones, acting to promote first suckling in the mouse. Instead, we find that the initiation of suckling is dependent on variable blends of maternal “signature odors” that are learned and recognized prior to first suckling.\n\nConclusions: As observed with pheromone-mediated behavior, the response to signature odors releases innate behavior. However, this mechanism

tolerates variability in both the signaling ligands and sensory neurons, which may maximize the probability that this first essential behavior is successfully Galardin supplier initiated. These results suggest that mammalian species have evolved multiple strategies to ensure the onset of this critical behavior.”
“Two main types of model structures have been proposed for the pharmacokinetics of paclitaxel; an empirical model structure based on total plasma concentrations of paclitaxel, and a mechanism-based model structure derived

from both total and unbound paclitaxel concentrations and concentrations of the formulation vehicle Cremophor EL. The purpose was to compare the two pharmacokinetic model structures when only total paclitaxel concentrations are available. To support the mechanism-based model structure with Cremophor EL concentrations, in silico concentrations were obtained from simulations of a pharmacokinetic model available in the literature. Local algebraic observability was tested on both model structures; the mechanism-based model structure was found, with high probability, not to be algebraically observable if total paclitaxel concentration is considered to be the only model output, and if no kind of prior information is used. Sensitivity analysis was performed to reveal which parameter should be fixed in order to make it locally observable. Parameter estimation was then performed On both model structures using nonlinear mixed effects and data from a clinical study The estimated mechanism-based model turned out to have a somewhat better fit to data than the corresponding empirical model, Delta AIC = -31, where AIC is the Akaike Information Criterion.