1,352 research outputs found

    The maximum principle and sign changing solutions of the hyperbolic equation with the Higgs potential

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    In this article we discuss the maximum principle for the linear equation and the sign changing solutions of the semilinear equation with the Higgs potential. Numerical simulations indicate that the bubbles for the semilinear Klein-Gordon equation in the de Sitter spacetime are created and apparently exist for all times

    Three-dimensional coherent X-ray diffraction imaging of a ceramic nanofoam: determination of structural deformation mechanisms

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    Ultra-low density polymers, metals, and ceramic nanofoams are valued for their high strength-to-weight ratio, high surface area and insulating properties ascribed to their structural geometry. We obtain the labrynthine internal structure of a tantalum oxide nanofoam by X-ray diffractive imaging. Finite element analysis from the structure reveals mechanical properties consistent with bulk samples and with a diffusion limited cluster aggregation model, while excess mass on the nodes discounts the dangling fragments hypothesis of percolation theory.Comment: 8 pages, 5 figures, 30 reference

    The price of tumor control: an analysis of rare side effects of anti-CTLA-4 therapy in metastatic melanoma from the ipilimumab network

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    Background: Ipilimumab, a cytotoxic T-lymphocyte antigen-4 (CTLA-4) blocking antibody, has been approved for the treatment of metastatic melanoma and induces adverse events (AE) in up to 64% of patients. Treatment algorithms for the management of common ipilimumab-induced AEs have lead to a reduction of morbidity, e.g. due to bowel perforations. However, the spectrum of less common AEs is expanding as ipilimumab is increasingly applied. Stringent recognition and management of AEs will reduce drug-induced morbidity and costs, and thus, positively impact the cost-benefit ratio of the drug. To facilitate timely identification and adequate management data on rare AEs were analyzed at 19 skin cancer centers. Methods and Findings: Patient files (n = 752) were screened for rare ipilimumab-associated AEs. A total of 120 AEs, some of which were life-threatening or even fatal, were reported and summarized by organ system describing the most instructive cases in detail. Previously unreported AEs like drug rash with eosinophilia and systemic symptoms (DRESS), granulomatous inflammation of the central nervous system, and aseptic meningitis, were documented. Obstacles included patientś delay in reporting symptoms and the differentiation of steroid-induced from ipilimumab-induced AEs under steroid treatment. Importantly, response rate was high in this patient population with tumor regression in 30.9% and a tumor control rate of 61.8% in stage IV melanoma patients despite the fact that some patients received only two of four recommended ipilimumab infusions. This suggests that ipilimumab-induced antitumor responses can have an early onset and that severe autoimmune reactions may reflect overtreatment. Conclusion: The wide spectrum of ipilimumab-induced AEs demands doctor and patient awareness to reduce morbidity and treatment costs and true ipilimumab success is dictated by both objective tumor responses and controlling severe side effects

    High BMI is significantly associated with positive progesterone receptor status and clinico-pathological markers for non-aggressive disease in endometrial cancer

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    Background: Endometrial cancer incidence is increasing in industrialised countries. High body mass index (BMI, kg m−2) is associated with higher risk for disease. We wanted to investigate if BMI is related to clinico-pathological characteristics, hormone receptor status in primary tumour, and disease outcome in endometrial cancer. Patients and methods: In total, 1129 women primarily treated for endometrial carcinoma at Haukeland University Hospital during 1981–2009 were studied. Body mass index was available for 949 patients and related to comprehensive clinical and histopathological data, hormone receptor status in tumour, treatment, and follow-up. Results: High BMI was significantly associated with low International Federation of Gynaecology and Obstetrics (FIGO) stage, endometrioid histology, low/intermediate grade, and high level of progesterone receptor (PR) mRNA by qPCR (n=150; P=0.02) and protein expression by immunohistochemistry (n=433; P=0.003). In contrast, oestrogen receptor (ERα) status was not associated with BMI. Overweight/obese women had significantly better disease-specific survival (DSS) than normal/underweight women in univariate analysis (P=0.035). In multivariate analysis of DSS adjusting for age, FIGO stage, histological subtype, and grade, BMI showed no independent prognostic impact. Conclusion: High BMI was significantly associated with markers of non-aggressive disease and positive PR status in a large population-based study of endometrial carcinoma. Women with high BMI had significantly better prognosis in univariate analysis of DSS, an effect that disappeared in multivariate analysis adjusting for established prognostic markers. The role of PR in endometrial carcinogenesis needs to be further studied

    Fragile DNA Repair Mechanism Reduces Ageing in Multicellular Model

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    DNA damages, as well as mutations, increase with age. It is believed that these result from increased genotoxic stress and decreased capacity for DNA repair. The two causes are not independent, DNA damage can, for example, through mutations, compromise the capacity for DNA repair, which in turn increases the amount of unrepaired DNA damage. Despite this vicious circle, we ask, can cells maintain a high DNA repair capacity for some time or is repair capacity bound to continuously decline with age? We here present a simple mathematical model for ageing in multicellular systems where cells subjected to DNA damage can undergo full repair, go apoptotic, or accumulate mutations thus reducing DNA repair capacity. Our model predicts that at the tissue level repair rate does not continuously decline with age, but instead has a characteristic extended period of high and non-declining DNA repair capacity, followed by a rapid decline. Furthermore, the time of high functionality increases, and consequently slows down the ageing process, if the DNA repair mechanism itself is vulnerable to DNA damages. Although counterintuitive at first glance, a fragile repair mechanism allows for a faster removal of compromised cells, thus freeing the space for healthy peers. This finding might be a first step toward understanding why a mutation in single DNA repair protein (e.g. Wrn or Blm) is not buffered by other repair proteins and therefore, leads to severe ageing disorders

    Evolutionary Emergence of microRNAs in Human Embryonic Stem Cells

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    Human embryonic stem (hES) cells have unique abilities to divide indefinitely without differentiating and potential to differentiate into more than 200 cell types. These properties make hES cells an ideal model system for understanding early human development and for regenerative medicine. Molecular mechanisms including cellular signaling and transcriptional regulation play important roles in hES cell differentiation. However, very little information is available on posttranscriptional regulation of hES cell pluripotency, self-renewal, and early decisions about cell fate. microRNAs (miRNAs), 22-nt long non-coding small RNAs found in plants and animals, regulate gene expression by targeting mRNAs for cleavage or translation repression. In hES cells we found that 276 miRNAs were expressed; of these, a set of 30 miRNAs had significantly changed expression during differentiation. Using a representative example, miR-302b, we show that miRNAs in human ES cells assemble into a bona fide RISC that contains Ago2 and can specifically cleave perfectly matched target RNA. Our results demonstrate that human ES cell differentiation is accompanied by changes in the expression of a unique set of miRNAs, providing a glimpse of a new molecular circuitry that may regulate early development in humans. Chromosomes 19 and X contained 98 and 40 miRNA genes, respectively, indicating that majority of miRNA genes in hES cells were expressed from these two chromosomes. Strikingly, distribution analysis of miRNA gene loci across six species including dog, rat, mouse, rhesus, chimpanzee, and human showed that miRNA genes encoded in chromosome 19 were drastically increased in chimpanzees and humans while miRNA gene loci on other chrosmomes were decreased as compared with dog, rat, and mouse. Comparative genomic studies showed 99% conservation of chromosome 19 miRNA genes between chimpanzees and humans. Together, these findings reveal the evolutionary emergence, ∼5 million years ago, of miRNAs involved in regulating early human development. One could imagine that this burst of miRNA gene clusters at specific chromosomes was part of an evolutionary event during species divergence

    ETISEQ – an algorithm for automated elution time ion sequencing of concurrently fragmented peptides for mass spectrometry-based proteomics

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    <p>Abstract</p> <p>Background</p> <p>Concurrent peptide fragmentation (i.e. shotgun CID, parallel CID or MS<sup>E</sup>) has emerged as an alternative to data-dependent acquisition in generating peptide fragmentation data in LC-MS/MS proteomics experiments. Concurrent peptide fragmentation data acquisition has been shown to be advantageous over data-dependent acquisition by providing greater detection dynamic range and providing more accurate quantitative information. Nevertheless, concurrent peptide fragmentation data acquisition remains to be widely adopted due to the lack of published algorithms designed specifically to process or interpret such data acquired on any mass spectrometer.</p> <p>Results</p> <p>An algorithm called Elution Time Ion Sequencing (ETISEQ), has been developed to enable automated conversion of concurrent peptide fragmentation data acquisition data to LC-MS/MS data. ETISEQ generates MS/MS-like spectra based on the correlation of precursor and product ion elution profiles. The performance of ETISEQ is demonstrated using concurrent peptide fragmentation data from tryptic digests of standard proteins and whole influenza virus. It is shown that the number of unique peptides identified from the digests is broadly comparable between ETISEQ processed concurrent peptide fragmentation data and the data-dependent acquired LC-MS/MS data.</p> <p>Conclusion</p> <p>The ETISEQ algorithm has been designed for easy integration with existing MS/MS analysis platforms. It is anticipated that it will popularize concurrent peptide fragmentation data acquisition in proteomics laboratories.</p

    High order structure preserving explicit methods for solving linear-quadratic optimal control problems

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    [EN] We consider the numerical integration of linear-quadratic optimal control problems. This problem requires the solution of a boundary value problem: a non-autonomous matrix Riccati differential equation (RDE) with final conditions coupled with the state vector equation with initial conditions. The RDE has positive definite matrix solution and to numerically preserve this qualitative property we propose first to integrate this equation backward in time with a sufficiently accurate scheme. Then, this problem turns into an initial value problem, and we analyse splitting and Magnus integrators for the forward time integration which preserve the positive definite matrix solutions for the RDE. Duplicating the time as two new coordinates and using appropriate splitting methods, high order methods preserving the desired property can be obtained. The schemes make sequential computations and do not require the storrage of intermediate results, so the storage requirements are minimal. The proposed methods are also adapted for solving linear-quadratic N-player differential games. The performance of the splitting methods can be considerably improved if the system is a perturbation of an exactly solvable problem and the system is properly split. Some numerical examples illustrate the performance of the proposed methods.The author wishes to thank the University of California San Diego for its hospitality where part of this work was done. He also acknowledges the support of the Ministerio de Ciencia e Innovacion (Spain) under the coordinated project MTM2010-18246-C03. The author also acknowledges the suggestions by the referees to improve the presentation of this work.Blanes Zamora, S. (2015). High order structure preserving explicit methods for solving linear-quadratic optimal control problems. Numerical Algorithms. 69:271-290. https://doi.org/10.1007/s11075-014-9894-0S27129069Abou-Kandil, H., Freiling, G., Ionescy, V., Jank, G.: Matrix Riccati equations in control and systems theory. Basel, Burkhäuser Verlag (2003)Al-Mohy, A.H., Higham, N.J.: Computing the Action of the Matrix Exponential, with an Application to Exponential Integrators. SIAM. J. Sci. Comp. 33, 488–511 (2011)Anderson, B.D.O., Moore, J.B.: Optimal control: linear quadratic methods. Dover, New York (1990)Ascher, U.M., Mattheij, R.M., Russell, R.D.: Numerical solutions of boundary value problems for ordinary differential equations. Prentice-Hall, Englewood Cliffs (1988)Bader, P., Blanes, S., Ponsoda, E.: Structure preserving integrators for solving linear quadratic optimal control problems with applications to describe the flight of a quadrotor. J. Comput. Appl. Math. 262, 223–233 (2014)Basar, T., Olsder, G.J.: Dynamic non cooperative game theory, 2nd Ed, SIAM, Philadelphhia (1999)Blanes, S., Casas, F.: On the necessity of negative coefficients for operator splitting schemes of order higher than two. Appl. Num. Math. 54, 23–37 (2005)Blanes, S., Casas, F., Farrés, A., Laskar, J., Makazaga, J., Murua, A.: New families of symplectic splitting methods for numerical integration in dynamical astronomy. Appl. Numer. Math. 68, 58–72 (2013)Blanes, S., Casas, F., Oteo, J.A., Ros, J.: The Magnus expansion and some of its applications. Phys. Rep. 470, 151–238 (2009)Blanes, S., Casas, F., Ros, J.: High order optimized geometric integrators for linear differential equations. BIT 42, 262–284 (2002)Blanes, S., Diele, F., Marangi, C., Ragni, S.: Splitting and composition methods for explicit time dependence in separable dynamical systems. J. Comput. Appl. Math. 235, 646–659 (2010)Blanes, S., Moan, P.C.: Practical symplectic partitioned Runge-Kutta and Runge-Kutta-Nystrm methods. J. Comput. Appl. Math. 142, 313–330 (2002)Blanes, S., Ponsoda, E.: Magnus integrators for solving linear-quadratic differential games. J. Comput. Appl. Math. 236, 3394–3408 (2012)Brif, C., Chakrabarti, R., Rabitz, H.: Control of quantum phenomena: past, present and future. New J. Phys. 12, 075008(68pp) (2010)Cruz, J.B., Chen, C.I.: Series Nash solution of two person non zero sum linear quadratic games. J. Optim. Theory Appl. 7, 240–257 (1971)Dieci, L., Eirola, T.: Positive definitness in the numerical solution of Riccati differential quations. Numer. Math. 67, 303–313 (1994)Engwerda, J.: LQ dynamic optimization and differential games. Wiley (2005)Hairer, E., Lubich, C., Wanner, G.: Geometric Numerical Integration. Structure-Preserving Algorithms for Ordinary Differential Equations (2nd edition). Springer Series in Computational Mathematics, 31. Springer-Verlag (2006)Hochbruck, M., Ostermann, A.: Exponential integrators. Acta Numerica 19, 209–286 (2010)Horn, R.A., Johnson, C.R.: Matrix Analysis. Cambridge University Press, New York (1985)Iserles, A., Munthe-Kaas, H.Z., Nørsett, S.P., Zanna, A.: Lie group methods. Acta Numerica 9, 215–365 (2000)Iserles, A., Nørsett, S.P.: On the solution of linear differential equations in Lie groups. Phil. Trans. R. Soc. Lond. A 357, 983–1019 (1999)Jódar, L., Ponsoda, E.: Non-autonomous Riccati-type matrix differential equations: existence interval, construction of continuous numerical solutions and error bounds. IMA. J. Num. Anal. 15, 61–74 (1995)Jódar, L., Ponsoda, E., Company, R.: Solutions of coupled Riccati equations arising in differential games. Control. Cybern. 24, 117–128 (1995)Kaitala, V, Pohjola, M. In: Carraro, Filar (eds.) : Sustainable international agreement on greenhouse warming. A game theory study. Control and Game Theoretic Models of the Environment, pp 67–87. Birkhauser, Boston (1995)Keller, H.B.: Numerical solution of two point boundary value problems. In: CBMS-NSF Regional Conference Series in Applied Mathematics, Vol. 24. SIAM, Philadelphia (1976)McLachlan, R.I.: Composition methods in the presence of small parameters. BIT 35, 258–268 (1995)McLachlan, R.I., Quispel, R.: Splitting Methods. Acta Numer. 11, 341–434 (2002)Moler, C.B., Van Loan, C.F.: Nineteen Dubious Ways to Compute the Exponential of a Matrix, twenty-five years later. SIAM Rev. 45, 3–49 (2003)Na, T.Y.: Computational methods in engineering boundary value problems. In: Mathematics in Science and Engineering, Vol. 145. Accademic Press, New York (1979)Palao, J.P., Kosloff, R.: Quantum computing by an optimal control algorithm for unitry transformations. Phys. Rev. Lett. 28 (2002)Peirce, A.P., Dahleh, M.A., Rabitz, H.: Optimal control of quantum-mechanical systems: existence, numerical approximation, and applications. Phys. Rev. A 37, 4950–4967 (1988)Reid, W.T.: Riccati Differential Equations. Academic, New York (1972)Sanz-Serna, J.M., Calvo, M.P.: Numerical Hamiltonian Problems. Chapman & Hall, London (1994)Sidje, R.B.: Expokit: a software package for computing matrix exponentials. ACM Trans. Math. Software 24, 130–156 (1998)Speyer, J.L., Jacobson, D.H.: Primer on optimal control theory. SIAM, Philadelphia (2010)Starr, A.W., Ho, Y.C.: Non-zero sum differential games. J. Optim. Theory and Appl 3, 179–197 (1969)Zhu, W., Rabitz, H.: A rapid monotonically convergent iteration algorithm for quantum optimal control ever the expectation value of a positive definite operator. J. Chem. Phys. 109, 385–391 (1998
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