120 research outputs found

    Estimating the Security of Lattice-based Cryptosystems

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    Encryption and signature schemes based on worst-case lattice problems are promising candidates for the post-quantum era, where classic number-theoretic assumptions are rendered false. Although there have been many important results and breakthroughs in lattice cryptography, the questions of how to systematically evaluate their security in practice and how to choose secure parameters are still open. This is mainly due to the fact that most security proofs are essentially asymptotic statements. In addition, the hardness of the underlying complexity assumption is controlled by several interdependent parameters rather than just a simple bit length as in many classic schemes. With our work, we close this gap by providing a framework that (1) distills a hardness estimate out of a given parameter set and (2) relates the complexity of practical lattice-based attacks to symmetric bit security for the first time. Our approach takes various security levels, or attacker types, into account. Moreover, we use it to predict long-term security in a similar fashion as the results that are collected on www.keylength.com. In contrast to the experiments by Gama and Nguyen (Eurocrypt 2008), our estimates are based on precisely the family of lattices that is relevant in modern lattice-based cryptography. Our framework can be applied in two ways: Firstly, to assess the hardness of the (few) proposed parameter sets so far and secondly, to propose secure parameters in the first place. Our methodology is applicable to essentially all lattice-based schemes that are based on the learning with errors problem (LWE) or the small integer solution problem (SIS) and it allows us to compare efficiency and security across different schemes and even across different types of cryptographic primitives

    Security of Verifiably Encrypted Signatures

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    In a verifiably encrypted signature scheme, signers encrypt their signature under the public key of a trusted third party and prove that they did so correctly. The security properties are unforgeability and opacity. Unforgeability states that a malicious signer should not be able to forge verifiably encrypted signatures and opacity prevents extraction from an encrypted signature. This paper proposes two novel fundamental requirements for verifiably encrypted signatures, called \emph{extractability} and \emph{abuse-freeness}, and analyze its effects on the security model of Boneh et al. Extractability ensures that the trusted third party is always able to extract a valid signature from a valid verifiably encrypted signature and abuse-freeness guarantees that a malicious signer, who cooperates with the trusted party, is not able to forge a verifiably encrypted signature. We further show that both properties are not covered by the model of Boneh et al., introduced at Eurocrypt 2003

    On the Security of the Winternitz One-Time Signature Scheme

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    We show that the Winternitz one-time signature scheme is existentially unforgeable under adaptive chosen message attacks when instantiated with a family of pseudo random functions. Compared to previous results, which require a collision resistant hash function, our result provides significantly smaller signatures at the same security level. We also consider security in the strong sense and show that the Winternitz one-time signature scheme is strongly unforgeable assuming additional properties of the pseudo random function. In this context we formally define several key-based security notions for function families and investigate their relation to pseudorandomness. All our reductions are exact and in the standard model and can directly be used to estimate the output length of the hash function required to meet a certain security level

    High Quality de Novo Transcriptome Assembly of Croton tiglium

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    Haak M, Vinke S, Keller W, et al. High Quality de Novo Transcriptome Assembly of Croton tiglium. Frontiers in Molecular Biosciences. 2018;5: 62

    Lack of association between proton pump inhibitor use and brain aging: a cross-sectional study

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    PURPOSE Due to conflicting scientific evidence for an increased risk of dementia by intake of proton pump inhibitors (PPIs), this study investigates associations between PPI use and brain volumes, estimated brain age, and cognitive function in the general population. METHODS Two surveys of the population-based Study of Health in Pomerania (SHIP) conducted in Northeast Germany were used. In total, 2653 participants underwent brain magnetic resonance imaging (MRI) and were included in the primary analysis. They were divided into two groups according to their PPI intake and compared with regard to their brain volumes (gray matter, white matter, total brain, and hippocampus) and estimated brain age. Multiple regression was used to adjust for confounding factors. Cognitive function was evaluated by the Verbal Learning and Memory Test (VLMT) and the Nuremberg Age Inventory (NAI) and put in relation to PPI use. RESULTS No association was found between PPI use and brain volumes or the estimated brain age. The VLMT score was 1.11 lower (95% confidence interval: - 2.06 to - 0.16) in immediate recall, and 0.72 lower (95% CI: - 1.22 to - 0.22) in delayed recall in PPI users than in non-users. PPI use was unrelated to the NAI score. CONCLUSIONS The present study does not support a relationship between PPI use and brain aging

    Detailed in vitro analyses of the impact of multimodal cancer therapy with hyperthermia and radiotherapy on the immune phenotype of human glioblastoma cells

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    Purpose Improvements of heat-delivery systems have led to hyperthermia (HT) being increasingly recognized as an adjunct treatment modality also for brain tumors. But how HT affects the immune phenotype of glioblastoma cells is only scarcely known. Materials and Methods We therefore investigated the effect of in vitro HT, radiotherapy (RT), and the combination of both (RHT) on cell death modalities, immune checkpoint molecule (ICM) expression and release of the danger signal HSP70 of two human glioblastoma cell lines (U87 and U251) by using multicolor flow cytometry and ELISA. Hyperthermia was performed once or twice for 60-minute sessions reaching temperatures of 39 °C, 41 °C, and 44 °C, respectively. RT was administered with 5 x 2 Gy. Results A hyperthermia chamber for cell culture t-flasks regulating the temperature via a contact sensor was developed. While the glioblastoma cells were rather radioresistant, particularly in U251 cells, the combination of RT with HT significantly increased the percentage of apoptotic and necrotic cells for all temperatures examined and for both, single and double HT application. In line with that, an increased release of HSP 70 was seen only in U251 cells, mainly following treatment with HT at temperatures of 44 °C alone or in combination with RT. In contrast, immune suppressive (PD-L1, PD-L2, HVEM) and immune stimulatory (ICOS-L, CD137-L and Ox40-L) ICMs were significantly increased mostly on U87 cells, and particularly after RHT with 41 °C. Conclusions Individual assessment of the glioblastoma immune cell phenotype with regard to the planned treatment is mandatory to optimize multimodal radio-immunotherapy protocols including HT

    Open Surgical versus Minimal Invasive Necrosectomy of the Pancreas-A Retrospective Multicenter Analysis of the German Pancreatitis Study Group

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    Background Necrotising pancreatitis, and particularly infected necrosis, are still associated with high morbidity and mortality. Since 2011, a step-up approach with lower morbidity rates compared to initial open necrosectomy has been established. However, mortality and complication rates of this complex treatment are hardly studied thereafter. Methods The German Pancreatitis Study Group performed a multicenter, retrospective study including 220 patients with necrotising pancreatitis requiring intervention, treated at 10 hospitals in Germany between January 2008 and June 2014. Data were analysed for the primary endpoints "severe complications" and "mortality" as well as secondary endpoints including "length of hospital stay", "follow up", and predisposing or prognostic factors. Results Of all patients 13.6% were treated primarily with surgery and 86.4% underwent a step-up approach. More men (71.8%) required intervention for necrotising pancreatitis. The most frequent etiology was biliary (41.4%) followed by alcohol (29.1%). Compared to open necrosectomy, the step-up approach was associated with a lower number of severe complications (primary composite endpoint including sepsis, persistent multiorgan dysfunction syndrome (MODS) and erosion bleeding: 44.7% vs. 73.3%), lower mortality (10.5% vs. 33.3%) and lower rates of diabetes mellitus type 3c (4.7% vs. 33.3%). Low hematocrit and low blood urea nitrogen at admission as well as a history of acute pancreatitis were prognostic for less complications in necrotising pancreatitis. A combination of drainage with endoscopic necrosectomy resulted in the lowest rate of severe complications. Conclusion A step-up approach starting with minimal invasive drainage techniques and endoscopic necrosectomy results in a significant reduction of morbidity and mortality in necrotising pancreatitis compared to a primarily surgical intervention

    Human alveolar progenitors generate dual lineage bronchioalveolar organoids

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    Mechanisms of epithelial renewal in the alveolar compartment remain incompletely understood. To this end, we aimed to characterize alveolar progenitors. Single-cell RNA-sequencing (scRNA-seq) analysis of the HTII-280+/EpCAM+ population from adult human lung revealed subclusters enriched for adult stem cell signature (ASCS) genes. We found that alveolar progenitors in organoid culture in vitro show phenotypic lineage plasticity as they can yield alveolar or bronchial cell-type progeny. The direction of the differentiation is dependent on the presence of the GSK-3β inhibitor, CHIR99021. By RNA-seq profiling of GSK-3β knockdown organoids we identified additional candidate target genes of the inhibitor, among others FOXM1 and EGF. This gives evidence of Wnt pathway independent regulatory mechanisms of alveolar specification. Following influenza A virus (IAV) infection organoids showed a similar response as lung tissue explants which confirms their suitability for studies of sequelae of pathogen-host interaction

    Flimma: a federated and privacy-aware tool for differential gene expression analysis

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    Abstract Aggregating transcriptomics data across hospitals can increase sensitivity and robustness of differential expression analyses, yielding deeper clinical insights. As data exchange is often restricted by privacy legislation, meta-analyses are frequently employed to pool local results. However, the accuracy might drop if class labels are inhomogeneously distributed among cohorts. Flimma (https://exbio.wzw.tum.de/flimma/) addresses this issue by implementing the state-of-the-art workflow limma voom in a federated manner, i.e., patient data never leaves its source site. Flimma results are identical to those generated by limma voom on aggregated datasets even in imbalanced scenarios where meta-analysis approaches fail
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