Investigation about the mechanisms involved in the onset of type 2 diabetes in absence of familiarity is the focus of a research project which has led to the development of a computational model that recapitulates the aetiology of the disease.

Sex dimorphism in cell response to stress has previously been investigated by different research groups. This dimorphism could be at least in part accounted for by sex-biased expression of regulatory elements such as microRNAs (miRs). In order to spot previously unknown miR expression differences we took advantage of prior knowledge on specialized databases to identify X chromosome-encoded miRs potentially escaping X chromosome inactivation (XCI).

In this paper we present a new multi-scale method for reproducing traffic flow which couples a first-order macroscopic model with a second-order microscopic model, avoiding any interface or boundary conditions between them. The multi-scale model is characterized by the fact that microscopic and macroscopic descriptions are not spatially separated. On the contrary, the macro-scale is always active while the micro-scale is activated only if needed by the traffic conditions.

Tor hidden services allow offering and accessing various Internet resources while guaranteeing a high degree of provider and user anonymity. So far, most research work on the Tor network aimed at discovering protocol vulnerabilities to de-anonymize users and services. Other work aimed at estimating the number of available hidden services and classifying them. Something that still remains largely unknown is the structure of the graph defined by the network of Tor services.

In recent years we are witnessing a continuous growth in the amount of data that both public and private organizations collect and profit by. Search engines are the most common tools used to retrieve information, and more recently, clustering techniques showed to be an effective tool in helping users to skim query results.

Predicting the release performance of a drug delivery device is an important challenge in pharmaceutics and biomedical science. In this paper, we consider a multi-layer diffusion model of drug release from a composite spherical microcapsule into an external surrounding medium. Based on this model, we present two approaches for estimating the release time, i.e. the time required for the drug-filled capsule to be depleted.

In recent years, a number of functional inequalities have been derived for Poisson random measures, with a wide range of applications. In this paper, we prove that such inequalities can be extended to the setting of marked temporal point processes, under mild assumptions on their Papangelou conditional intensity. First, we derive a Poincare inequality. Second, we prove two transportation cost inequalities. The first one refers to functionals of marked point processes with a Papangelou conditional intensity and is new even in the setting of Poisson random measures.

In the literature on Network Optimization, k-splittable flows were introduced to enhance modeling accuracy in cases where an upper bound on the number of supporting paths for each commodity needs to be imposed, thus extending the suitability of network flow tools for an increased number of practical applications. Such modeling feature has recently been extended to dynamic flows with the introduction of the novel strongly NP-hard Quickest Multicommodity k-splittable Flow Problem (QMCkFP).

Network-based ranking methods (e.g. centrality analysis) have found extensive use in systems medicine for the prediction of essential proteins, for the prioritization of drug targets candidates in the treatment of several pathologies and in biomarker discovery, and for human disease genes identification. Here we propose to use critical nodes as defined by the Critical Node Problem for the analysis of key physiological and pathophysiological signaling pathways, as target candidates for treatment and management of several cancer types, neurologic and inflammatory dysfunctions, among others.