2-Server PIR with sub-polynomial communication

A 2-server Private Information Retrieval (PIR) scheme allows a user to retrieve the $i$th bit of an $n$-bit database replicated among two servers (which do not communicate) while not revealing any information about $i$ to either server. In this work we construct a 1-round 2-server PIR with total communication cost $n^{O({\sqrt{\log\log n/\log n}})}$. This improves over the currently known 2-server protocols which require $O(n^{1/3})$ communication and matches the communication cost of known 3-server PIR schemes. Our improvement comes from reducing the number of servers in existing protocols, based on Matching Vector Codes, from 3 or 4 servers to 2. This is achieved by viewing these protocols in an algebraic way (using polynomial interpolation) and extending them using partial derivatives

Epilepsy syndrome-associated balance dysfunction assessed by static posturography

AbstractPurposeTo compare subclinical balance dysfunction in patients with various epilepsy syndromes with apparently healthy subjects.MethodsTwenty-seven patients with localization-related epilepsy (LRE), 19 with primary generalized epilepsy (PGE), who had no subjective complaints of impaired balance and no abnormal neurologic findings on examination, and 22 apparently healthy subjects, underwent static posturography using the Posture Scale Analyzer (PSA) system.ResultsSway index was higher in patients compared to healthy subjects in all tests, significant for single leg stance (p=0.005). Patients with PGE had a higher sway index compared to patients with LRE in six of the tests, also significant for single leg stance (p=0.027). This difference was not affected by the type of AED treatment or disease duration.ConclusionPosturography can improve balance function assessment in patients with epilepsy, demonstrate subclinical impairment in seemingly asymptomatic patients, and further characterize balance deficits in different epilepsy syndromes

Tribological behavior of shape-specific microplate-enriched synovial fluids on a linear two-axis tribometer

Nano- and micro-particles are being increasingly used to tune interfacial frictional properties in diverse applications, from friction modifiers in industrial lubrication to enhanced biological fluids in human osteoarthritic joints. Here, we assessed the tribological properties of a simulated synovial fluid enriched with non-spherical, poly lactic-co-glycolic acid (PLGA) microparticles (μPL) that have been previously demonstrated for the pharmacological management of osteoarthritis (OA). Three different μPL configurations were fabricated presenting a 20 μm 20 μm square base and a thickness of 5 μm (thin, 5H μPL), 10 μm (10H μPL), and 20 μm (cubical, 20H μPL). After extensive morphological and physicochemical characterizations, the apparent Young’s modulus of the μPL was quantified under compressive loading returning an average value of 6 kPa, independently of the particle morphology. Then, using a linear two-axis tribometer, the static (μs) and dynamic (μd) friction coefficients of the μPL-enriched simulated synovial fluid were determined in terms of particle configuration and concentration, varying from 0 (fluid only) to 6105 μPL/mL. The particle morphology had a modest influence on friction, possibly because the μPL were fully squeezed between two mating surfaces by a 5.8 N normal load realizing boundary-like lubrication conditions. Differently, friction was observed to depend on the dimensionless parameter , defined as the ratio between the total volume of the μPL enriching the simulated synovial fluid and the volume of the fluid itself. Both coefficients of friction were documented to grow with reaching a plateau of μs 0.4 and μd 0.15, already at  210-3. Future investigations will have to systematically analyze the effect of sliding velocity, normal load, and rigidity of the mating surfaces to elucidate in full the tribological behavior of μPL in the context of osteoarthritis

Network Physiology reveals relations between network topology and physiological function

The human organism is an integrated network where complex physiologic systems, each with its own regulatory mechanisms, continuously interact, and where failure of one system can trigger a breakdown of the entire network. Identifying and quantifying dynamical networks of diverse systems with different types of interactions is a challenge. Here, we develop a framework to probe interactions among diverse systems, and we identify a physiologic network. We find that each physiologic state is characterized by a specific network structure, demonstrating a robust interplay between network topology and function. Across physiologic states the network undergoes topological transitions associated with fast reorganization of physiologic interactions on time scales of a few minutes, indicating high network flexibility in response to perturbations. The proposed system-wide integrative approach may facilitate the development of a new field, Network Physiology.Comment: 12 pages, 9 figure

Sub-logarithmic Distributed Oblivious RAM with Small Block Size

Oblivious RAM (ORAM) is a cryptographic primitive that allows a client to securely execute RAM programs over data that is stored in an untrusted server. Distributed Oblivious RAM is a variant of ORAM, where the data is stored in $m>1$ servers. Extensive research over the last few decades have succeeded to reduce the bandwidth overhead of ORAM schemes, both in the single-server and the multi-server setting, from $O(\sqrt{N})$ to $O(1)$. However, all known protocols that achieve a sub-logarithmic overhead either require heavy server-side computation (e.g. homomorphic encryption), or a large block size of at least $\Omega(\log^3 N)$. In this paper, we present a family of distributed ORAM constructions that follow the hierarchical approach of Goldreich and Ostrovsky [GO96]. We enhance known techniques, and develop new ones, to take better advantage of the existence of multiple servers. By plugging efficient known hashing schemes in our constructions, we get the following results: 1. For any $m\geq 2$, we show an $m$-server ORAM scheme with $O(\log N/\log\log N)$ overhead, and block size $\Omega(\log^2 N)$. This scheme is private even against an $(m-1)$-server collusion. 2. A 3-server ORAM construction with $O(\omega(1)\log N/\log\log N)$ overhead and a block size almost logarithmic, i.e. $\Omega(\log^{1+\epsilon}N)$. We also investigate a model where the servers are allowed to perform a linear amount of light local computations, and show that constant overhead is achievable in this model, through a simple four-server ORAM protocol

Do Israelis understand the Hebrew bible?

The Hebrew Bible should be taught like a foreign language in Israel too, argues Ghil'ad Zuckermann, inter alia endorsing Avraham Ahuvia’s recently-launched translation of the Old Testament into what Zuckermann calls high-register 'Israeli'. According to Zuckermann, Tanakh RAM fulfills the mission of 'red 'el ha'am' not only in its Hebrew meaning (Go down to the people) but also – more importantly – in its Yiddish meaning ('red' meaning 'speak!', as opposed to its colorful communist sense). Ahuvia's translation is most useful and dignified. Given its high register, however, Zuckermann predicts that the future promises consequent translations into more colloquial forms of Israeli, a beautifully multi-layered and intricately multi-sourced language, of which to be proud.Ghil'ad Zuckerman

Characterization of gene-activated human acid-β-glucosidase: Crystal structure, glycan composition, and internalization into macrophages

Gaucher disease, the most common lysosomal storage disease, can be treated with enzyme replacement therapy (ERT), in which defective acid-β-glucosidase (GlcCerase) is supplemented by a recombinant, active enzyme. The X-ray structures of recombinant GlcCerase produced in Chinese hamster ovary cells (imiglucerase, Cerezyme®) and in transgenic carrot cells (prGCD) have been previously solved. We now describe the structure and characteristics of a novel form of GlcCerase under investigation for the treatment of Gaucher disease, Gene-ActivatedTM human GlcCerase (velaglucerase alfa). In contrast to imiglucerase and prGCD, velaglucerase alfa contains the native human enzyme sequence. All three GlcCerases consist of three domains, with the active site located in domain III. The distances between the carboxylic oxygens of the catalytic residues, E340 and E235, are consistent with distances proposed for acid–base hydrolysis. Kinetic parameters (Km and Vmax) of velaglucerase alfa and imiglucerase, as well as their specific activities, are similar. However, analysis of glycosylation patterns shows that velaglucerase alfa displays distinctly different structures from imiglucerase and prGCD. The predominant glycan on velaglucerase alfa is a high-mannose type, with nine mannose units, while imiglucerase contains a chitobiose tri-mannosyl core glycan with fucosylation. These differences in glycosylation affect cellular internalization; the rate of velaglucerase alfa internalization into human macrophages is at least 2-fold greater than that of imiglucerase