6,916 research outputs found
Late-time expansion in the semiclassical theory of the Hawking radiation
We give a detailed treatment of the back-reaction effects on the Hawking
spectrum in the late-time expansion within the semiclassical approach to the
Hawking radiation. We find that the boundary value problem defining the action
of the modes which are regular at the horizon admits in general the presence of
caustics. We show that for radii less that a certain critical value no
caustic occurs for all values of the wave number and time and we give a
rigorous lower bound on such a critical value. We solve the exact system of non
linear equations defining the motion, by an iterative procedure rigorously
convergent at late times. The first two terms of such an expansion give the
correction to the Hawking spectrum.Comment: 17 pages, 1 figure, LaTex, typos corrected, one intermediate formula
adde
A lattice Boltzmann formulation to the analysis of radiative heat transfer problems in a participating medium
HyBIS: Windows Guest Protection through Advanced Memory Introspection
Effectively protecting the Windows OS is a challenging task, since most
implementation details are not publicly known. Windows has always been the main
target of malwares that have exploited numerous bugs and vulnerabilities.
Recent trusted boot and additional integrity checks have rendered the Windows
OS less vulnerable to kernel-level rootkits. Nevertheless, guest Windows
Virtual Machines are becoming an increasingly interesting attack target. In
this work we introduce and analyze a novel Hypervisor-Based Introspection
System (HyBIS) we developed for protecting Windows OSes from malware and
rootkits. The HyBIS architecture is motivated and detailed, while targeted
experimental results show its effectiveness. Comparison with related work
highlights main HyBIS advantages such as: effective semantic introspection,
support for 64-bit architectures and for latest Windows (8.x and 10), advanced
malware disabling capabilities. We believe the research effort reported here
will pave the way to further advances in the security of Windows OSes
Thermal stability and aggregation of sulfolobus solfataricus b-glycosidase are dependent upon the N-e-methylation of specific lysyl residues: critical role of in vivo post-translational modifications.
Methylation in vivo is a post-translational modification observed in several organisms belonging to eucarya, bacteria, and archaea. Although important implications of this modification have been demonstrated in several eucaryotes, its biological role in hyperthermophilic archaea is far from being understood. The aim of this work is to clarify some effects of methylation on the properties of ÎČ-glycosidase from Sulfolobus solfataricus, by a structural comparison between the native, methylated protein and its unmethylated counterpart, recombinantly expressed in Escherichia coli. Analysis by Fourier transform infrared spectroscopy indicated similar secondary structure contents for the two forms of the protein. However, the study of temperature perturbation by Fourier transform infrared spectroscopy and turbidimetry evidenced denaturation and aggregation events more pronounced in recombinant than in native ÎČ-glycosidase. Red Nile fluorescence analysis revealed significant differences of surface hydrophobicity between the two forms of the protein. Unlike the native enzyme, which dissociated into SDS-resistant dimers upon exposure to the detergent, the recombinant enzyme partially dissociated into monomers. By electrospray mapping, the methylation sites of the native protein were identified. A computational analysis of ÎČ-glycosidase three-dimensional structure and comparisons with other proteins from S. solfataricus revealed analogies in the localization of methylation sites in terms of secondary structural elements and overall topology. These observations suggest a role for the methylation of lysyl residues, located in selected domains, in the thermal stabilization of ÎČ-glycosidase from S. solfataricu
Anti-Candida targets and cytotoxicity of casuarinin isolated from Plinia cauliflora leaves in a bioactivity-guided study
Peer reviewedPublisher PD
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation.
Hearing impairment is the second most prevalent clinical feature after optic atrophy in Dominant Optic Atrophy associated with mutations in the OPA1 gene. In this study we characterized the hearing dysfunction in OPA1-linked disorders and provided effective rehabilitative options to improve speech perception.
We studied two groups of OPA1 subjects, one comprising 11 patients (7 males; age range 13-79 years) carrying OPA1 mutations inducing haploinsufficiency, the other, 10 subjects (3 males; age range 5-58 years) carrying OPA1 missense mutations. Both groups underwent audiometric assessment with pure tone and speech perception evaluation, and otoacoustic emissions and auditory brainstem response recording. Cochlear potentials were recorded through transtympanic electrocochleography from the group of patients harboring OPA1 missense mutations and were compared to recordings obtained from 20 normally-hearing controls and from 19 subjects with cochlear hearing loss. Eight patients carrying OPA1 missense mutations underwent cochlear implantation. Speech perception measures and electrically-evoked auditory nerve and brainstem responses were obtained after one year of cochlear implant use.
Nine out of 11 patients carrying OPA1 mutations inducing haploinsufficiency had normal hearing function. In contrast, all but one subject harboring OPA1 missense mutations displayed impaired speech perception, abnormal brainstem responses and presence of otoacoustic emissions consistent with auditory neuropathy. In electrocochleography recordings, cochlear microphonic had enhanced amplitudes while summating potential showed normal latency and peak amplitude consistent with preservation of both outer and inner hair cell activities. After cancelling the cochlear microphonic, the synchronized neural response seen in both normally-hearing controls and subjects with cochlear hearing loss was replaced by a prolonged, low-amplitude negative potential that decreased in both amplitude and duration during rapid stimulation consistent with neural generation. The use of cochlear implant improved speech perception in all but one patient. Brainstem potentials were recorded in response to electrical stimulation in five subjects out of six, whereas no compound action potential was evoked from the auditory nerve through the cochlear implant.
These findings indicate that underlying the hearing impairment in patients carrying OPA1 missense mutations is a disordered synchrony in auditory nerve fiber activity resulting from neural degeneration affecting the terminal dendrites. Cochlear implantation improves speech perception and synchronous activation of auditory pathways by by-passing the site of lesion
Multistep, sequential control of the trafficking and function of the multiple sulfatase deficiency gene product, SUMF1 by PDI, ERGIC-53 and ERp44.
Sulfatase modifying factor 1 (SUMF1) encodes for the formylglicine generating enzyme, which activates sulfatases by modifying a key cysteine residue within their catalytic domains. SUMF1 is mutated in patients affected by multiple sulfatase deficiency, a rare recessive disorder in which all sulfatase activities are impaired. Despite the absence of canonical retention/retrieval signals, SUMF1 is largely retained in the endoplasmic reticulum (ER), where it exerts its enzymatic activity on nascent sulfatases. Part of SUMF1 is secreted and paracrinally taken up by distant cells. Here we show that SUMF1 interacts with protein disulfide isomerase (PDI) and ERp44, two thioredoxin family members residing in the early secretory pathway, and with ERGIC-53, a lectin that shuttles between the ER and the Golgi. Functional assays reveal that these interactions are crucial for controlling SUMF1 traffic and function. PDI couples SUMF1 retention and activation in the ER. ERGIC-53 and ERp44 act downstream, favoring SUMF1 export from and retrieval to the ER, respectively. Silencing ERGIC-53 causes proteasomal degradation of SUMF1, while down-regulating ERp44 promotes its secretion. When over-expressed, each of three interactors favors intracellular accumulation. Our results reveal a multistep control of SUMF1 trafficking, with sequential interactions dynamically determining ER localization, activity and secretion
Local treatment with electrochemotherapy of superficial angiosarcomas: Efficacy and safety results from a multi-institutional retrospective study
Background:
Angiosarcoma is an aggressive vascular neoplasm with a high propensity for local recurrence. Electrochemotherapy is an emerging
skin-directed therapy, exerting prominent cytotoxic activity, and antivascular effects. Its efficacy in angiosarcoma has not been investigated.
Methods:
This multicenter retrospective analysis reviewed patients who underwent electrochemotherapy from 2007 to 2014 for superficial
advanced angiosarcomas. Bleomycin was administered intravenously and delivered within tumors by means of percutaneously applied electric
pulses, according to the European Standard Operating Procedures for Electrochemotherapy. Tumor assessment was performed using RECIST
(version 1.1). Toxicity (CTCAE, v4.0) and local progression-free survival (LPFS) were also evaluated.
Results:
Nineteen patients (13 with locally advanced and 6 with metastatic angiosarcomas) were treated. Tumor sites were: scalp (nŒ5), breast(nŒ8), other skin sites (nŒ3), and soft tissue (nŒ3). Target lesions (nŒ54) ranged in size from 1.5 to 2.5 cm (median, 2 cm). Treatment was well tolerated. After 2 months, an objective response was observed in 12/19 (63%) patients, complete in 8 (42%). One-year LPFS within treatment field was 68%. Local symptom improvement included palliation of bleeding (5/19 patients) and pain relief (6/19 patients).
Conclusions:
Electrochemotherapy may represent a new locoregional treatment for selected patients with superficial angiosarcomas
N=2 supergravity models with stable de Sitter vacua
In the present talk I shall review the construction of N=2 supergravity
models exhibiting stable de Sitter vacua. These solutions represent the first
instance of stable backgrounds with positive cosmological constant in the
framework of extended supergravities (N >=2). After briefly reviewing the role
of de Sitter space--times in inflationary cosmology, I shall describe the main
ingredients which were necessary for the construction of gauged N=2
supergravity models admitting stable solutions of this kind.Comment: Prepared for Workshop on the Quantum Structure of Spacetime and the
Geometric Nature of Fundamental Interactions, Leuven, Belgium, September
13-19 200
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