Adprhl1, a member of the ADP-ribosylhydrolase protein family, is expressed exclusively in the developing heart of all vertebrates. In the amphibian Xenopus laevis, distribution of its mRNA is biased towards actively growing chamber myocardium. Morpholino oligonucleotide-mediated knockdown of all Adprhl1 variants inhibits striated myofibril assembly and prevents outgrowth of the ventricle. The resulting ventricles retain normal electrical conduction and express markers of chamber muscle differentiation but are functionally inert. Using a cardiac-specific Gal4 binary expression system, we show that the abundance of Adprhl1 protein in tadpole hearts is tightly controlled through a negative regulatory mechanism targeting the 5′-coding sequence of Xenopus adprhl1. Over-expression of full length (40 kDa) Adprhl1 variants modified to escape such repression, also disrupts cardiac myofibrillogenesis. Disarrayed myofibrils persist that show extensive branching, with sarcomere division occurring at the actin-Z-disc boundary. Ultimately, Adprhl1-positive cells contain thin actin threads, connected to numerous circular branch points. Recombinant Adprhl1 can localize to stripes adjacent to the Z-disc, suggesting a direct role for Adprhl1 in modifying Z-disc and actin dynamics as heart chambers grow. Modelling the structure of Adprhl1 suggests this cardiac-specific protein is a pseudoenzyme, lacking key residues necessary for ADP-ribosylhydrolase catalytic activity.
Abstract-By changing the way software is delivered to endusers, markets for mobile apps create a false sense of security: apps are downloaded from a market that can potentially be regulated. In practice, this is far from truth and instead, there has been evidence that security is not one of the primary design tenets for the mobile app stores. Recent studies have indicated mobile markets are harboring apps that are either malicious or vulnerable leading to compromises of millions of devices. The key technical obstacle for the organizations overseeing these markets is the lack of practical and automated mechanisms to assess the security of mobile apps, given that thousands of apps are added and updated on a daily basis. In this paper, we provide an overview of a multi-faceted project targeted at automatically testing the security and robustness of Android apps in a scalable manner. We describe an Android-specific program analysis technique capable of generating a large number of test cases for fuzzing an app, as well as a test bed that given the generated test cases, executes them in parallel on numerous emulated Androids running on the cloud.
Babesia bovis (B. bovis) is a major causative agent of bovine babesiosis, with a considerable worldwide impact. The objective of this study was to evaluate the usefulness of PCR assay and microscopical examination (ME) for detection of B. bovis in naturally infected and apparently healthy water buffaloes and crossbred cattle under field circumstances from Sharkia province of Egypt. A total 34 animals (20 crossbred cattle and 14 buffaloes) were clinically and laboratory investigated during the period from March to August 2008. Fifteen animals showed symptoms of bovine babesiosis while 19 animals were apparently healthy. Two blood samples were collected from each animal; one was used for preparation of Giemsa-stained smears for ME while the other sample was used for DNA extraction and PCR testing. Out of 34 cattle and buffaloes, ME identified 13 animals (38.2%) as infected by B. bovis whereas PCR identified 29 (85.3%). B. bovis infected animals showed high fever, anaemia, jaundice, haemoglobinuria, and accelerated heart and respiratory rates. Out of 15 animals clinically infected, PCR identified 14 animals (93.3%) as infected while ME identified only, 8 animals (53.3%). Out of 19 animals apparently healthy, 5 animals (26.3%) were identified as infected by ME meanwhile 15 animals (78.9%) were identified by PCR. In conclusion, our findings demonstrated that water buffalos are likely to have a natural tolerance to B. bovis pathogen and/or more likely to be persistent carriers which were not picked up by microscopy. The severity of clinical symptoms of B. bovis infection on water buffaloes was less than the severity of clinical symptoms appeared on cattle. PCR assay is more sensitive technique than microscopical examination for detection of B. bovis in both clinically infected and apparently health cattle and water buffaloes which suggests its use as a routine technique for diagnosis of bovine babesiosis.
We present an efficient and scalable framework for the generation of guaranteed passive compact dynamical models for multiport structures. The proposed algorithm enforces passivity using frequency independent linear matrix inequalities, as opposed to the existing optimization based algorithms which enforce passivity using computationally expensive frequency dependent constraints. We have tested our algorithm for various multiport structures. An excellent match between the given samples and our passive model was achieved.
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