OPE for Super Loops

We extend the Operator Product Expansion for Null Polygon Wilson loops to the Mason-Skinner-Caron-Huot super loop, dual to non MHV gluon amplitudes. We explain how the known tree level amplitudes can be promoted into an infinite amount of data at any loop order in the OPE picture. As an application, we re-derive all one loop NMHV six gluon amplitudes by promoting their tree level expressions. We also present some new all loops predictions for these amplitudes.Comment: 16 pages + appendices; 5 figure

From Polygon Wilson Loops to Spin Chains and Back

Null Polygon Wilson Loops (WL) in N=4 SYM can be computed using the Operator Product Expansion in terms of a transition amplitude on top of a color flux tube (FT). That picture is valid at any value of the 't Hooft coupling. So far it has been efficiently used at weak coupling (WC) in cases where only a single particle is flowing. At any finite value of the coupling however, an infinite number of particles are flowing on top of the color FT. A major open problem in this approach was how to deal with generic multi-particle states at WC. In this paper we study the propagation of any number of FT excitations at WC. We do this by first mapping the WL into a sum of two point functions of local operators. This map allows us to translate the integrability techniques developed for the spectrum problem back to the WL. E.g., the FT Hamiltonian can be represented as a simple kernel acting on the loop. Having an explicit representation for the FT Hamiltonian allows us to treat any number of particles on an equal footing. We use it to bootstrap some simple cases where two particles are flowing, dual to N2MHV amplitudes. The FT is integrable and therefore has other (infinite set of) conserved charges. The generating function of conserved charges is constructed from the monodromy (M) matrix between sides of the polygon. We compute it for some simple examples at leading order at WC. At strong coupling (SC), these Ms were the main ingredients of the Y-system solution. To connect the WC and SC computations, we study a case where an infinite number of particles are propagating already at leading order at WC. We obtain a precise match between the WC and SC Ms. That match is the WL analogue of the well known Frolov-Tseytlin limit where the WC and SC descriptions become identical. Hopefully, putting the WC and SC descriptions on the same footing is the first step in understanding the all loop structure.Comment: 52 pages, 14 figures, the abstract in the pdf is not encrypted and is slightly more detaile

Tailoring Three-Point Functions and Integrability II. Weak/strong coupling match

We compute three-point functions of single trace operators in planar N=4 SYM. We consider the limit where one of the operators is much smaller than the other two. We find a precise match between weak and strong coupling in the Frolov-Tseytlin classical limit for a very general class of classical solutions. To achieve this match we clarify the issue of back-reaction and identify precisely which three-point functions are captured by a classical computation.Comment: 36 pages. v2: figure added, references adde

Osteoinduction in human fat derived stem cells by recombinant human bone morphogenetic protein-2 produced in Escherichia coli

Bioactive recombinant human bone morphogenetic protein-2 (rhBMP-2) was obtained using Escherichia coli pET-25b expression system: 55 mg purified rhBMP-2 were achieved per g cell dry wt, with up to 95% purity. In murine C2C12 cell line, rhBMP-2 induced an increase in the transcription of Smads and of osteogenic markers Runx2/Cbfa1 and Osterix, measured by semi-quantitative RT-PCR. Bioassays performed in human fat-derived stem cells showed an increased activity of the early osteogenic marker, alkaline phosphatase, and the absence of cytotoxicity

Minor and Unsystematic Cortical Topographic Changes of Attention Correlates between Modalities

In this study we analyzed the topography of induced cortical oscillations in 20 healthy individuals performing simple attention tasks. We were interested in qualitatively replicating our recent findings on the localization of attention-induced beta bands during a visual task [1], and verifying whether significant topographic changes would follow the change of attention to the auditory modality. We computed corrected latency averaging of each induced frequency bands, and modeled their generators by current density reconstruction with Lp-norm minimization. We quantified topographic similarity between conditions by an analysis of correlations, whereas the inter-modality significant differences in attention correlates were illustrated in each individual case. We replicated the qualitative result of highly idiosyncratic topography of attention-related activity to individuals, manifested both in the beta bands, and previously studied slow potential distributions [2]. Visual inspection of both scalp potentials and distribution of cortical currents showed minor changes in attention-related bands with respect to modality, as compared to the theta and delta bands, known to be major contributors to the sensory-related potentials. Quantitative results agreed with visual inspection, supporting to the conclusion that attention-related activity does not change much between modalities, and whatever individual changes do occur, they are not systematic in cortical localization across subjects. We discuss our results, combined with results from other studies that present individual data, with respect to the function of cortical association areas

Current challenges in software solutions for mass spectrometry-based quantitative proteomics

This work was in part supported by the PRIME-XS project, grant agreement number 262067, funded by the European Union seventh Framework Programme; The Netherlands Proteomics Centre, embedded in The Netherlands Genomics Initiative; The Netherlands Bioinformatics Centre; and the Centre for Biomedical Genetics (to S.C., B.B. and A.J.R.H); by NIH grants NCRR RR001614 and RR019934 (to the UCSF Mass Spectrometry Facility, director: A.L. Burlingame, P.B.); and by grants from the MRC, CR-UK, BBSRC and Barts and the London Charity (to P.C.