Cold Atom Clock Test of Lorentz Invariance in the Matter Sector

We report on a new experiment that tests for a violation of Lorentz invariance (LI), by searching for a dependence of atomic transition frequencies on the orientation of the spin of the involved states (Hughes-Drever type experiment). The atomic frequencies are measured using a laser cooled $^{133}$Cs atomic fountain clock, operating on a particular combination of Zeeman substates. We analyze the results within the framework of the Lorentz violating standard model extension (SME), where our experiment is sensitive to a largely unexplored region of the SME parameter space, corresponding to first measurements of four proton parameters and improvements by 11 and 13 orders of magnitude on the determination of four others. In spite of the attained uncertainties, and of having extended the search into a new region of the SME, we still find no indication of LI violation.Comment: 4 pages, accepted for Physical Review Letter

Tests of relativity using a microwave resonator

The frequencies of a cryogenic sapphire oscillator and a hydrogen maser are compared to set new constraints on a possible violation of Lorentz invariance. We determine the variation of the oscillator frequency as a function of its orientation (Michelson-Morley test) and of its velocity (Kennedy-Thorndike test) with respect to a preferred frame candidate. We constrain the corresponding parameters of the Mansouri and Sexl test theory to $\delta - \beta + 1/2 = (1.5\pm 4.2) \times 10^{-9}$ and $\beta - \alpha - 1 = (-3.1\pm 6.9) \times 10^{-7}$ which is equivalent to the best previous result for the former and represents a 30 fold improvement for the latter.Comment: 8 pages, 2 figures, submitted to Physical Review Letters (October 3, 2002

Non-reactive scattering of rotational quantum state selected molecular beams

Non-reactive scattering of rotational quantum state selected molecular beams of symmetric top molecules has been investigated using electrostatic methods. Cross-sections for the defocusing of upper Stark-state molecules in a hexapole electric field have been measured for neat and seeded beams of CH3F with a range of polar and non-polar quencher gases. Calculations of the hexapole focusing voltages for specific rotational states facilitated the assignment of the defocusing cross-sections to individual rotational states in the beam. The technique of Molecular Beam Electric Resonance (MBER) spectrometry has been employed to detect and study individual rotational states, resulting in a dramatic improvement in quantum state resolution over the use of a single hexapole filter. Cross-sections have been measured for the relaxation of selected upper Stark states in beams of methyl halides with a range of polar and non-polar scattering gases. The application of MBER spectrometry to rotational state identification in beams of symmetric to molecules has been explored in this study. Information on the velocity, temperature, and rotational state distribution of the beam can be easily obtained from experimentation using this arrangement. It has also provided insight into the focusing properties of hexapole electric filters. Individual rotational quantum states in a beam of symmetric top molecules could be tagged using an MBER spectrometer for studies of rotational state dependent properties, such as the effect of rotational states in scattering studies. The collisional relaxation of upper Stark-state molecules in a beam could occur through several mechanisms. Cross-sections measured using the technique of MBER have been largely attributed to an Mᴊ changing process. The effects of the long-range attractive van der Waals interaction potential, the relative velocity dependence of the collision partners and the electric field dependence of the Stark energy have been considered in order to account for the magnitude of the relaxation cross-sections measured in this study

Artificial Intelligence, Machine Learning and Modeling for Understanding the Oceans and Climate Change

International audienceThe ongoing transformation of climate and biodiversity will have a drastic impact on almost all forms of life in the ocean with further consequences on food security, ecosystem services in coastal and inland communities. Despite these impacts, scientific data and infrastructures are still lacking to understand and quantify the consequences of these perturbations on the marine ecosystem. Understanding this phenomenon is not only an urgent but also a scientifically demanding task. Consequently, it is a problem that must be addressed with a tific cohort approach, where multi-disciplinary teams collaborate to bring the best of different scientific areas. In this proposal paper, we describe our newly launched four-years project focusedon developing new artificial intelligence, machine learning, and mathematical modeling tools to contribute to the understanding of the structure, functioning, and underlying mechanisms and dynamics of the global ocean symbiome and its relation with climate change. These actions should enable the understanding of our oceans and predict and mitigate the consequences of climate and biodiversity changes

8p22 MTUS1 Gene Product ATIP3 Is a Novel Anti-Mitotic Protein Underexpressed in Invasive Breast Carcinoma of Poor Prognosis

BACKGROUND: Breast cancer is a heterogeneous disease that is not totally eradicated by current therapies. The classification of breast tumors into distinct molecular subtypes by gene profiling and immunodetection of surrogate markers has proven useful for tumor prognosis and prediction of effective targeted treatments. The challenge now is to identify molecular biomarkers that may be of functional relevance for personalized therapy of breast tumors with poor outcome that do not respond to available treatments. The Mitochondrial Tumor Suppressor (MTUS1) gene is an interesting candidate whose expression is reduced in colon, pancreas, ovary and oral cancers. The present study investigates the expression and functional effects of MTUS1 gene products in breast cancer. METHODS AND FINDINGS: By means of gene array analysis, real-time RT-PCR and immunohistochemistry, we show here that MTUS1/ATIP3 is significantly down-regulated in a series of 151 infiltrating breast cancer carcinomas as compared to normal breast tissue. Low levels of ATIP3 correlate with high grade of the tumor and the occurrence of distant metastasis. ATIP3 levels are also significantly reduced in triple negative (ER- PR- HER2-) breast carcinomas, a subgroup of highly proliferative tumors with poor outcome and no available targeted therapy. Functional studies indicate that silencing ATIP3 expression by siRNA increases breast cancer cell proliferation. Conversely, restoring endogenous levels of ATIP3 expression leads to reduced cancer cell proliferation, clonogenicity, anchorage-independent growth, and reduces the incidence and size of xenografts grown in vivo. We provide evidence that ATIP3 associates with the microtubule cytoskeleton and localizes at the centrosomes, mitotic spindle and intercellular bridge during cell division. Accordingly, live cell imaging indicates that ATIP3 expression alters the progression of cell division by promoting prolonged metaphase, thereby leading to a reduced number of cells ungergoing active mitosis. CONCLUSIONS: Our results identify for the first time ATIP3 as a novel microtubule-associated protein whose expression is significantly reduced in highly proliferative breast carcinomas of poor clinical outcome. ATIP3 re-expression limits tumor cell proliferation in vitro and in vivo, suggesting that this protein may represent a novel useful biomarker and an interesting candidate for future targeted therapies of aggressive breast cancer

Stoma-free survival after anastomotic leak following rectal cancer resection : worldwide cohort of 2470 patients

Funding Information: The TENTACLE-Rectum study was funded by Medtronic External Research Program. The authors declare no other conflict of interest.Peer reviewedPublisher PD

Identification of a novel polyfluorinated compound as a lead to inhibit human enzymes aldose reductase and AKR1B10 : structure determination of both ternary complexes and implications for drug design

Aldo-keto reductases (AKRs) are mostly monomeric enzymes which fold into a highly conserved ([alpha]/[beta])8 barrel, while their substrate specificity and inhibitor selectivity are determined by interaction with residues located in three highly variable external loops. The closely related human enzymes aldose reductase (AR or AKR1B1) and AKR1B10 are of biomedical interest because of their involvement in secondary diabetic complications (AR) and in cancer, e.g. hepatocellular carcinoma and smoking-related lung cancer (AKR1B10). After characterization of the IC50 values of both AKRs with a series of polyhalogenated compounds, 2,2',3,3',5,5',6,6'-octafluoro-4,4'-biphenyldiol (JF0064) was identified as a lead inhibitor of both enzymes with a new scaffold (a 1,1'-biphenyl-4,4'-diol). An ultrahigh-resolution X-ray structure of the AR-­NADP+-JF0064 complex has been determined at 0.85 Å resolution, allowing it to be observed that JF0064 interacts with the catalytic residue Tyr48 through a negatively charged hydroxyl group (i.e. the acidic phenol). The non-competitive inhibition pattern observed for JF0064 with both enzymes suggests that this acidic hydroxyl group is also present in the case of AKR1B10. Moreover, the combination of surface lysine methylation and the introduction of K125R and V301L mutations enabled the determination of the X-ray crystallo­graphic structure of the corresponding AKR1B10-NADP+-JF0064 complex. Comparison of the two structures has unveiled some important hints for subsequent structure-based drug-design efforts