879 research outputs found

    A New Cryptosystem Based On Hidden Order Groups

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    Let G1G_1 be a cyclic multiplicative group of order nn. It is known that the Diffie-Hellman problem is random self-reducible in G1G_1 with respect to a fixed generator gg if ϕ(n)\phi(n) is known. That is, given g,gxG1g, g^x\in G_1 and having oracle access to a `Diffie-Hellman Problem' solver with fixed generator gg, it is possible to compute g1/xG1g^{1/x} \in G_1 in polynomial time (see theorem 3.2). On the other hand, it is not known if such a reduction exists when ϕ(n)\phi(n) is unknown (see conjuncture 3.1). We exploit this ``gap'' to construct a cryptosystem based on hidden order groups and present a practical implementation of a novel cryptographic primitive called an \emph{Oracle Strong Associative One-Way Function} (O-SAOWF). O-SAOWFs have applications in multiparty protocols. We demonstrate this by presenting a key agreement protocol for dynamic ad-hoc groups.Comment: removed examples for multiparty key agreement and join protocols, since they are redundan

    Antifungal activity of essential oils and their volatile constituents against respiratory tract pathogens causing Aspergilloma and Aspergillosis by gaseous contact

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    Aspergillosis is an acute chronic and rapidly fatal disease which is not contagious. Invasive Aspergillosis is often found in severely immuno-suppressed patients, and is characterized by invasion of blood vessels which can result into dissemination to other organs. Aspergilloma is a fungal ball that develops in previous cavitary lung lesions. Essential oils and their volatile constituents have been used as antifungal, anti-infectious and antimicrobial agents. Inhalation of vapours of the essential oils kill invaders attached to the inner respiratory lining and worksynergistically with the body defences. In this study, 16 essential oils were used against Aspergillus niger and A. fumigatus of which about 14 oils proved to be effective. Results showed that the most effective oils against both Aspergillus species were found to be of Cinnamomum zeylanicum (Cinnamon), Syzygium aromaticum (Clove), Carum carvi (Caraway), Cymbopogon citrates (Lemongrass), Foeniculum vulgare (Fennel) and Myristica fragrans (Nutmeg). Moderately effective oils were of Gaultheria procumbens (Wintergreen), Pinus palustris (Turpentine), Sesamum indicum (Sesame), Trachyspermum ammi (Ajowain) and Origanum vulgare (Oregano). The oils of Lavandula augustifolia (Lavender), Elletaria cardamomum (Cardamon) and Cymbopogon nardus (Citronella) showed minimum activity. Azadirachta indica (Neem) and Linum usitatissimum (Linseed) showed no activity giving no inhibition zones

    Bypassing Non-Outsourceable Proof-of-Work Schemes Using Collateralized Smart Contracts

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    Centralized pools and renting of mining power are considered as sources of possible censorship threats and even 51% attacks for decentralized cryptocurrencies. Non-outsourceable Proof-of-Work schemes have been proposed to tackle these issues. However, tenets in the folklore say that such schemes could potentially be bypassed by using escrow mechanisms. In this work, we propose a concrete example of such a mechanism which is using collateralized smart contracts. Our approach allows miners to bypass non-outsourceable Proof-of-Work schemes if the underlying blockchain platform supports smart contracts in a sufficiently advanced language. In particular, the language should allow access to the PoW solution. At a high level, our approach requires the miner to lock collateral covering the reward amount and protected by a smart contract that acts as an escrow. The smart contract has logic that allows the pool to collect the collateral as soon as the miner collects any block reward. We propose two variants of the approach depending on when the collateral is bound to the block solution. Using this, we show how to bypass previously proposed non-outsourceable Proof-of-Work schemes (with the notable exception for strong non-outsourceable schemes) and show how to build mining pools for such schemes

    White-Box Cryptography: Formal Notions and (Im)possibility Results

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    A key research question in computer security is whether one can implement software that offers some protection against software attacks from its execution platform. While code obfuscation attempts to hide certain characteristics of a program P, white-box cryptography specifically focusses on software implementations of cryptographic primitives (such as encryption schemes); the goal of a white-box implementation is to offer a certain level of robustness against an adversary who has full access to and control over the implementation of the primitive. Several formal models for obfuscation have been presented before, but it is not clear if any of these definitions can capture the concept of white-box cryptography. In this paper, we discuss the relation between obfuscation and white-box cryptography, and formalize the notion of white-box cryptography by capturing the security requirement using a \u27White-Box Property\u27 (WBP). In the second part, we present positive and negative results on white-box cryptography. We show that for interesting programs (such as encryption schemes, and digital signature schemes), there are security notions that cannot be satisfied when adversaries have white-box access, while the notion is satisfied when the adversary has black-box access to its functionality. On the positive side, we show that there exists an obfuscator for a symmetric encryption scheme for which a useful security notion (such as CPA security) remains satisfied when an adversary has access to its white-box implementation

    Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.

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    Indians undergoing socioeconomic and lifestyle transitions will be maximally affected by epidemic of type 2 diabetes (T2D). We conducted a two-stage genome-wide association study of T2D in 12,535 Indians, a less explored but high-risk group. We identified a new type 2 diabetes-associated locus at 2q21, with the lead signal being rs6723108 (odds ratio 1.31; P = 3.32 × 10⁻⁹). Imputation analysis refined the signal to rs998451 (odds ratio 1.56; P = 6.3 × 10⁻¹²) within TMEM163 that encodes a probable vesicular transporter in nerve terminals. TMEM163 variants also showed association with decreased fasting plasma insulin and homeostatic model assessment of insulin resistance, indicating a plausible effect through impaired insulin secretion. The 2q21 region also harbors RAB3GAP1 and ACMSD; those are involved in neurologic disorders. Forty-nine of 56 previously reported signals showed consistency in direction with similar effect sizes in Indians and previous studies, and 25 of them were also associated (P < 0.05). Known loci and the newly identified 2q21 locus altogether explained 7.65% variance in the risk of T2D in Indians. Our study suggests that common susceptibility variants for T2D are largely the same across populations, but also reveals a population-specific locus and provides further insights into genetic architecture and etiology of T2D

    A Prospective Multicenter Study Evaluating Learning Curves and Competence in Endoscopic Ultrasound and Endoscopic Retrograde Cholangiopancreatography Among Advanced Endoscopy Trainees: The Rapid Assessment of Trainee Endoscopy Skills (RATES) Study

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    Background and aims Based on the Next Accreditation System, trainee assessment should occur on a continuous basis with individualized feedback. We aimed to validate endoscopic ultrasound (EUS) and endoscopic retrograde cholangiopancreatography (ERCP) learning curves among advanced endoscopy trainees (AETs) using a large national sample of training programs and to develop a centralized database that allows assessment of performance in relation to peers. Methods ASGE recognized training programs were invited to participate and AETs were graded on ERCP and EUS exams using a validated competency assessment tool that assesses technical and cognitive competence in a continuous fashion. Grading for each skill was done using a 4-point scoring system and a comprehensive data collection and reporting system was built to create learning curves using cumulative sum analysis. Individual results and benchmarking to peers were shared with AETs and trainers quarterly. Results Of the 62 programs invited, 20 programs and 22 AETs participated in this study. At the end of training, median number of EUS and ERCP performed/AET was 300 (range 155-650) and 350 (125-500). Overall, 3786 exams were graded (EUS:1137; ERCP–biliary 2280, pancreatic 369). Learning curves for individual endpoints, and overall technical/cognitive aspects in EUS and ERCP demonstrated substantial variability and were successfully shared with all programs. The majority of trainees achieved overall technical (EUS: 82%; ERCP: 60%) and cognitive (EUS: 76%; ERCP: 100%) competence at conclusion of training. Conclusions These results demonstrate the feasibility of establishing a centralized database to report individualized learning curves and confirm the substantial variability in time to achieve competence among AETs in EUS and ERCP

    Common variants in CLDN2 and MORC4 genes confer disease susceptibility in patients with chronic pancreatitis

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    A recent Genome-wide Association Study (GWAS) identified association with variants in X-linked CLDN2 and MORC4 and PRSS1-PRSS2 loci with Chronic Pancreatitis (CP) in North American patients of European ancestry. We selected 9 variants from the reported GWAS and replicated the association with CP in Indian patients by genotyping 1807 unrelated Indians of Indo-European ethnicity, including 519 patients with CP and 1288 controls. The etiology of CP was idiopathic in 83.62% and alcoholic in 16.38% of 519 patients. Our study confirmed a significant association of 2 variants in CLDN2 gene (rs4409525—OR 1.71, P = 1.38 x 10-09; rs12008279—OR 1.56, P = 1.53 x 10-04) and 2 variants in MORC4 gene (rs12688220—OR 1.72, P = 9.20 x 10-09; rs6622126—OR 1.75, P = 4.04x10-05) in Indian patients with CP. We also found significant association at PRSS1-PRSS2 locus (OR 0.60; P = 9.92 x 10-06) and SAMD12-TNFRSF11B (OR 0.49, 95% CI [0.31–0.78], P = 0.0027). A variant in the gene MORC4 (rs12688220) showed significant interaction with alcohol (OR for homozygous and heterozygous risk allele -14.62 and 1.51 respectively, P = 0.0068) suggesting gene-environment interaction. A combined analysis of the genes CLDN2 and MORC4 based on an effective risk allele score revealed a higher percentage of individuals homozygous for the risk allele in CP cases with 5.09 fold enhanced risk in individuals with 7 or more effective risk alleles compared with individuals with 3 or less risk alleles (P = 1.88 x 10-14). Genetic variants in CLDN2 and MORC4 genes were associated with CP in Indian patients

    Differential cross section measurements for the production of a W boson in association with jets in proton–proton collisions at √s = 7 TeV

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    Measurements are reported of differential cross sections for the production of a W boson, which decays into a muon and a neutrino, in association with jets, as a function of several variables, including the transverse momenta (pT) and pseudorapidities of the four leading jets, the scalar sum of jet transverse momenta (HT), and the difference in azimuthal angle between the directions of each jet and the muon. The data sample of pp collisions at a centre-of-mass energy of 7 TeV was collected with the CMS detector at the LHC and corresponds to an integrated luminosity of 5.0 fb[superscript −1]. The measured cross sections are compared to predictions from Monte Carlo generators, MadGraph + pythia and sherpa, and to next-to-leading-order calculations from BlackHat + sherpa. The differential cross sections are found to be in agreement with the predictions, apart from the pT distributions of the leading jets at high pT values, the distributions of the HT at high-HT and low jet multiplicity, and the distribution of the difference in azimuthal angle between the leading jet and the muon at low values.United States. Dept. of EnergyNational Science Foundation (U.S.)Alfred P. Sloan Foundatio
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