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Gerard Notario,1 Pamela Vo,2 Katherine Gooch,2 Roger Deaton,3 Xionghua Wu,4 Brian Harris,4 Parthiv J Mahadevia,4 Pablo J Sánchez51Clinical Development and Medical Affairs, 2Global Heath Economics and Outcomes Research, 3Statistics, AbbVie Inc., North Chicago, IL, 4MedImmune, LLC, Gaithersburg, MD, 5The Research Institute at Nationwide Children's Hospital, The Ohio State University, Columbus, OH, USABackground: Respiratory syncytial virus (RSV) infections are common during childhood and are a major cause of hospitalization resulting from serious lower respiratory tract infections. Palivizumab is approved for prevention of serious lower respiratory tract disease caused by RSV infection in infants and young children at high risk of RSV disease. Although the previously published IMpact-RSV trial included the overall results for palivizumab prophylaxis in a cohort of premature infants who did not have bronchopulmonary dysplasia (BPD), there is an ongoing demand to understand the efficacy of palivizumab in premature infants without BPD by gestational age group.Methods: This post hoc analysis assesses IMpact-RSV trial data within eleven gestational age groups for the cohort of 724 premature infants who were ≤6 months of age and did not have BPD. RSV-related hospitalization rates along with corresponding 95% exact binomial confidence intervals were determined for these specific gestational age groups. Relative reductions in risk of RSV-related hospitalizations for palivizumab versus placebo with corresponding 95% confidence intervals were also calculated.Results: Analysis of a cohort of premature infants without BPD from the IMpact-RSV trial revealed that palivizumab consistently reduced RSV-related hospitalizations (64.5%–100%) versus placebo in all eleven gestational age groups evaluated. Palivizumab significantly decreased the relative risk of RSV-related hospitalization (73%–82%, P

Presents a study which examined the effect of stress induced by temperature gradients on rapid-thermal oxidation (RTO) of silicon. Effects of the intrinsic stress and viscous flow of the oxide on the oxidation kinetics; Implications of results for rapid thermal processing temperature measurement and RTO process uniformity.

Anayzes arsenic and phosphorus codiffusion. Details on the experiment; Results of the study; Conclusion.

To study electrostatic actuation, researchers commonly use a setup proposed by G. I. Taylor in [Proc. R. Soc. Lond. Ser. A, 306 (1968), pp. 423–434]. It consists of soap film held at a distance h above a rigid plate so that when a voltage difference is applied between the two components, the top film deflects towards the bottom plate. The most striking feature of this system is when the voltage difference exceeds a critical value V*, the electrostatic forces dominate the surface forces and the soap film gets ‘pulled-into’ or collapses onto the bottom plate. This so-called ‘pull-in’ instability is a ubiquitous feature of electrostatic actuation and as a result, has been the subject of many studies. Recently, Siddique et al. [J. Electrostatics, 69 (2011), pp. 1–6] measured the value of V* as a function of the separation distance and found that the standard prediction breaks down as h increases. Here, we continue the work done in [N. D. Brubaker and J. A. Pelesko, European J. Appl. Math., 22 (2011), pp. 455–470] by investigating the cause of this discrepancy. Specifically, we model the effect of gravity on the generalized version of Taylor's model and study whether it provides the proper correction to the predicted value of V*. In doing so, we derive two nonlinear eigenvalue value problems and investigate their solutions sets. [ABSTRACT FROM AUTHOR]

Abstract Background Molecular markers identifying alterations in proliferation and apoptotic pathways could be particularly important in characterizing high-risk normal or pre-neoplastic tissue. We evaluated the following markers: Ki67, Minichromosome Maintenance Protein-2 (Mcm-2), activated caspase-3 (a-casp3) and Bcl-2 to determine if they showed differential expression across progressive degrees of intraepithelial neoplasia and cancer in the prostate. To identify field effects, we also evaluated whether high-risk expression patterns in normal tissue were more common in prostates containing cancer compared to those without cancer (supernormal), and in histologically normal glands adjacent to a cancer focus as opposed to equivalent glands that were more distant. Methods The aforementioned markers were studied in 13 radical prostatectomy (RP) and 6 cystoprostatectomy (CP) specimens. Tissue compartments representing normal, low grade prostatic intraepithelial neoplasia (LGPIN), high grade prostatic intraepithelial neoplasia (HGPIN), as well as different grades of cancer were mapped on H&E slides and adjacent sections were analyzed using immunohistochemistry. Normal glands within 1 mm distance of a tumor focus and glands beyond 5 mm were considered "near" and "far", respectively. Randomly selected nuclei and 40 × fields were scored by a single observer; basal and luminal epithelial layers were scored separately. Results Both Ki-67 and Mcm-2 showed an upward trend from normal tissue through HGPIN and cancer with a shift in proliferation from basal to luminal compartment. Activated caspase-3 showed a significant decrease in HGPIN and cancer compartments. Supernormal glands had significantly lower proliferation indices and higher a-casp3 expression compared to normal glands. "Near" normal glands had higher Mcm-2 indices compared to "far" glands; however, they also had higher a-casp3 expression. Bcl-2, which varied minimally in normal tissue, did not show any trend across compartments or evidence for field effects. Conclusion These results demonstrate that proliferation and apoptosis are altered not only in preneoplastic lesions but also in apparently normal looking epithelium associated with cancer. Luminal cell expression of Mcm-2 appears to be particularly promising as a marker of high-risk normal epithelium. The role of apoptotic markers such as activated caspase-3 is more complex, and might depend on the proliferation status of the tissue in question.

Inspired by self-assembled biological growth, the Circuit Tile Assembly Model (cTAM) was developed to provide insights into signal propagation, information processing, and computation in bioelectric networks. The cTAM is an abstract model that produces a family of circuits of different sizes that is amenable to exact analysis. Here, the cTAM is extended to the Boolean Circuit Tile Assembly Model (bcTAM) that implements a computationally complete set of Boolean gates through self-assembled and self-controlled growth. The proposed model approximates axonal growth in neural networks and thus, investigates the computational capability of dynamic biological networks, for example, in growing networks of axons. Thus, the bcTAM models the effect of electrical activity on growth and shows how that growth might implement Boolean computations. In this sense, given a set of input voltages, the bcTAM is a system that is able to monitor and make decisions about its own growth., Competing Interests: The authors have declared that no competing interests exist., (Copyright: © 2022 Yasmin, Deaton. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)

By guiding cell and chemical migration and coupling with genetic mechanisms, bioelectric networks of potentials influence biological pattern formation and are known to have profound effects on growth processes. An abstract model that is amenable to exact analysis has been proposed in the circuit tile assembly model (cTAM) to understand self-assembled and self-controlled growth as an emergent phenomenon that is capable of complex behaviors, like self-replication. In the cTAM, a voltage source represents a finite supply of energy that drives growth until it is unable to overcome randomizing factors in the environment, represented by a threshold. Here, the cTAM is extended to the axon or alternating cTAM model (acTAM) to include a circuit similar to signal propagation in axons, exhibiting time-varying electric signals and a dependence on frequency of the input voltage. The acTAM produces systems of circuits whose electrical properties are coupled to their length as growth proceeds through self-assembly. The exact response is derived for increasingly complex circuit systems as the assembly proceeds. The model exhibits complicated behaviors that elucidate the interactive role of energy, environment, and noise with electric signals in axon-like circuits during biological growth of complex patterns and function., (© 2022. The Author(s).)