Special biconformal changes of K\"ahler surface metrics

The term "special biconformal change" refers, basically, to the situation where a given nontrivial real-holomorphic vector field on a complex manifold is a gradient relative to two K\"ahler metrics, and, simultaneously, an eigenvector of one of the metrics treated, with the aid of the other, as an endomorphism of the tangent bundle. A special biconformal change is called nontrivial if the two metrics are not each other's constant multiples. For instance, according to a 1995 result of LeBrun, a nontrivial special biconformal change exists for the conformally-Einstein K\"ahler metric on the two-point blow-up of the complex projective plane, recently discovered by Chen, LeBrun and Weber; the real-holomorphic vector field involved is the gradient of its scalar curvature. The present paper establishes the existence of nontrivial special biconformal changes for some canonical metrics on Del Pezzo surfaces, viz. K\"ahler-Einstein metrics (when a nontrivial holomorphic vector field exists), non-Einstein K\"ahler-Ricci solitons, and K\"ahler metrics admitting nonconstant Killing potentials with geodesic gradients.Comment: 16 page

LEÏOMYOSARCOME UTERIN DE PRESENTATION INHABITUELLE

Utérin Leiomyosarcoma is rare [1.5]. It is likely conjunctiva and developed at the expense of mesenchymal elements of the myometrium. The uterus bicornis united cervical represents 39% of all uterine malformations [8]. The prevalence of these abnormalities is estimated at 0.5%. The association leïomyosarcoma and uterine malformation still very exceptional. The purpose of our work is to study the unique combination from the clinical, paraclinical, pathological, and evolving therapeutic.Le léiomyosarcome utérin est une tumeur maligne, rare [1,5].Elle est de nature conjonctive et développée aux dépens des éléments mésenchymateux du myomètre. L’utérus bicorne uni cervical représente 39% de l’ensemble des malformations utérines [8]. La prévalence de ces malformations est estimée à 0,5%. L’association leïomyosarcome utérin et malformation utérine reste très exceptionnelle et ce du fait que la malformation utérine est de diagnostic précoce à un âge jeune contrairement au leiomyosarcome utérin qui survient chez des femmes d’âge avancé. Le but de notre travail est d’étudier à partir de notre observation cette association exceptionnelle sur le plan clinique, paraclinique, anatomopathologique, thérapeutique et évolutif

Neuronal activity moves protein palmitoylation into the synapse

Many neuronal proteins undergo lipid modification that regulates their function and subcellular localization. One such modification is palmitoylation, which is mediated by a large class of protein palmitoyl acyltransferases (PATs). Now, a paper in this issue (Noritake et al. 2009. J. Cell Biol. doi:10.1083/jcb.200903101) demonstrates that the localization of the PAT DHHC2 is regulated by neuronal activity and thereby selectively controls the palmitoylation and subsequent accumulation of specific proteins in the synapse

Une cause rare d’exophtalmie

Une enfant de 3 ans, issue d’un mariage non consanguin, deuxième d’une fratrie de 3, et sans antécédents pathologiques particuliers. Le début de la symptomatologie remonte à un mois par la constatation par la maman d’une exophtalmie de l’œil gauche qui augmentait rapidement de volume sans autres signes associés. A l’examen clinique, on notait la présence d’une importante exophtalmie de l’œil gauche avec bombement du cavum sans déficits neurologiques, le fond d’œil a objectivé une atrophie optique temporale. Une tomodensitométrie orbitaire a objectivé un processus énorme intra-orbitaire iso dense infiltrant la base du crâne, le sinus caverneux, le sinus sphénoïdal gauche  avec extension vers le cavum sur une étendue de 40 mm

Search based software engineering: Trends, techniques and applications

© ACM, 2012. This is the author's version of the work. It is posted here by permission of ACM for your personal use. Not for redistribution. The definitive version is available from the link below.In the past five years there has been a dramatic increase in work on Search-Based Software Engineering (SBSE), an approach to Software Engineering (SE) in which Search-Based Optimization (SBO) algorithms are used to address problems in SE. SBSE has been applied to problems throughout the SE lifecycle, from requirements and project planning to maintenance and reengineering. The approach is attractive because it offers a suite of adaptive automated and semiautomated solutions in situations typified by large complex problem spaces with multiple competing and conflicting objectives. This article provides a review and classification of literature on SBSE. The work identifies research trends and relationships between the techniques applied and the applications to which they have been applied and highlights gaps in the literature and avenues for further research.EPSRC and E

Accelerated expansion from structure formation

We discuss the physics of backreaction-driven accelerated expansion. Using the exact equations for the behaviour of averages in dust universes, we explain how large-scale smoothness does not imply that the effect of inhomogeneity and anisotropy on the expansion rate is small. We demonstrate with an analytical toy model how gravitational collapse can lead to acceleration. We find that the conjecture of the accelerated expansion being due to structure formation is in agreement with the general observational picture of structures in the universe, and more quantitative work is needed to make a detailed comparison.Comment: 44 pages, 1 figure. Expanded treatment of topics from the Gravity Research Foundation contest essay astro-ph/0605632. v2: Added references, clarified wordings. v3: Published version. Minor changes and corrections, added a referenc

α5β1 Integrin-Mediated Adhesion to Fibronectin Is Required for Axis Elongation and Somitogenesis in Mice

The arginine-glycine-aspartate (RGD) motif in fibronectin (FN) represents the major binding site for α5β1 and αvβ3 integrins. Mice lacking a functional RGD motif in FN (FNRGE/RGE) or α5 integrin develop identical phenotypes characterized by embryonic lethality and a severely shortened posterior trunk with kinked neural tubes. Here we show that the FNRGE/RGE embryos arrest both segmentation and axis elongation. The arrest is evident at about E9.0, corresponding to a stage when gastrulation ceases and the tail bud-derived presomitic mesoderm (PSM) induces α5 integrin expression and assumes axis elongation. At this stage cells of the posterior part of the PSM in wild type embryos are tightly coordinated, express somitic oscillator and cyclic genes required for segmentation, and form a tapered tail bud that extends caudally. In contrast, the posterior PSM cells in FNRGE/RGE embryos lost their tight associations, formed a blunt tail bud unable to extend the body axis, failed to induce the synchronised expression of Notch1 and cyclic genes and cease the formation of new somites. Mechanistically, the interaction of PSM cells with the RGD motif of FN is required for dynamic formation of lamellipodia allowing motility and cell-cell contact formation, as these processes fail when wild type PSM cells are seeded into a FN matrix derived from FNRGE/RGE fibroblasts. Thus, α5β1-mediated adhesion to FN in the PSM regulates the dynamics of membrane protrusions and cell-to-cell communication essential for elongation and segmentation of the body axis

Low Levels of Human HIP14 Are Sufficient to Rescue Neuropathological, Behavioural, and Enzymatic Defects Due to Loss of Murine HIP14 in Hip14−/− Mice

Huntingtin Interacting Protein 14 (HIP14) is a palmitoyl acyl transferase (PAT) that was first identified due to altered interaction with mutant huntingtin, the protein responsible for Huntington Disease (HD). HIP14 palmitoylates a specific set of neuronal substrates critical at the synapse, and downregulation of HIP14 by siRNA in vitro results in increased cell death in neurons. We previously reported that mice lacking murine Hip14 (Hip14−/−) share features of HD. In the current study, we have generated human HIP14 BAC transgenic mice and crossed them to the Hip14−/− model in order to confirm that the defects seen in Hip14−/− mice are in fact due to loss of Hip14. In addition, we sought to determine whether human HIP14 can provide functional compensation for loss of murine Hip14. We demonstrate that despite a relative low level of expression, as assessed via Western blot, BAC-derived human HIP14 compensates for deficits in neuropathology, behavior, and PAT enzyme function seen in the Hip14−/− model. Our findings yield important insights into HIP14 function in vivo

Frequency and clinical patterns of stroke in Iran - Systematic and critical review

<p>Abstract</p> <p>Background</p> <p>Cerebrovascular disease is the second commonest cause of death, and over a third of stroke deaths occur in developing countries. To fulfil the current gap on data, this systematic review is focused on the frequency of stroke, risk factors, stroke types and mortality in Iran.</p> <p>Methods</p> <p>Thirteen relevant articles were identified by keyword searching of PubMed, Iranmedex, Iranian University index Libraries and the official national data on burden of diseases.</p> <p>Results</p> <p>The publication dates ranged from 1990 to 2008. The annual stroke incidence of various ages ranged from 23 to 103 per 100,000 population. This is comparable to the figures from Arab Countries, higher than sub-Saharan Africa, but lower than developed countries, India, the Caribbean, Latin America, and China. Similarly to other countries, ischaemic stroke was the commonest subtype. Likewise, the most common related risk factor is hypertension in adults, but cardiac causes in young stroke. The 28-day case fatality rate is reported at 19-31%.</p> <p>Conclusions</p> <p>Data on the epidemiology of stroke, its pattern and risk factors from Iran is scarce, but the available data highlights relatively low incidence of stroke. This may reflect a similarity towards the neighbouring nations, and a contrast with the West.</p