3,367 research outputs found

    Double Standards?

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    Double Standards?

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    Somatomedin C in dairy cows related to energy and protein supply and to milk production

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    Somatomedin C and other hormones, as well as blood metabolites, were measured during the dry period and during lactation in dairy cows, given different amounts of energy and protein, to study metabolic and endocrine adaptations. Somatomedin C, specifically measured by radioimmunoassay after separation from its binding protein, did not exhibit typical diurnal variations, in contrast to somatotropin and insulin, which increased particularly after concentrate intake. Somatomedin C markedly decreased at parturition and reached lowest values around the peak of lactation, while levels of somatotropin, nonesterified fatty acids and ketone bodies were high and those of glucose, insulin, thyroxine and triiodothyronine were low. Thereafter somatomedin C values slowly increased up to the 12th week of lactation and remained elevated. Low energy and protein balances were characterized by particularly low somatomedin C concentrations. An additional protein deficit at peak lactation, when cows were already provided with low amounts of energy, did not further decrease somatomedin C levels. However, when high amounts of energy were given in the form of starch or crystalline fat, somatomedin C increased. Overall, there was a positive correlation of somatomedin C primarily with energy, but also with protein balances and a negative correlation with milk yield. Conversely, somatotropin increased markedly after parturition and was positively correlated with milk production and negatively with protein and energy balances. Thus, somatomedin C levels were paradoxically low in the presence of high circulating somatotropin. Insulin most closely paralleled somatomedin C levels. Therefore the anabolic state of metabolism at the end of pregnancy was characterized by high somatomedin C and insulin and relatively low somatotropin, whereas the catabolic state of early lactation was characterized by high somatotropin, low somatomedin C, insulin and thyroid hormone

    p34cdc2-mediated phosphorylation at T124 inhibits nuclear import of SV-40 T antigen proteins

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    The nuclear import of transcription regulatory proteins appears to be used by the cell to trigger transitions in cell cycle, morphogenesis, and transformation. We have previously observed that the rate at which SV-40 T antigen fusion proteins containing a functional nuclear localization sequence (NLS; residues 126-132) are imported into the nucleus is enhanced in the presence of the casein kinase II (CK-II) site S111/112. In this study purified p34cdc2 kinase was used to phosphorylate T antigen proteins specifically at T124 and kinetic measurements at the single-cell level performed to assess its effect on nuclear protein import. T124 phosphorylation, which could be functionally simulated by a T-to-D124 substitution, was found to reduce the maximal extent of nuclear accumulation whilst negligibly affecting the import rate. The inhibition of nuclear import depended on the stoichiometry of phosphorylation. T124 and S111/112 could be phosphorylated independently of one another. Two alterative mechanisms were considered to explain the inhibition of nuclear import by T124 phosphorylation: inactivation of the NLS and cytoplasmic retention, respectively. Furthermore, we speculate that in vivo T124 phosphorylation may regulate the small but functionally significant amount of cytoplasmic SV-40 T antigen. A sequence comparison showed that many transcription regulatory proteins contain domains comprising potential CK-II-sites, cdc2-sites, and NLS. This raises the possibility that the three elements represent a functional unit regulating nuclear protein import

    Direction of light propagation to order G^2 in static, spherically symmetric spacetimes: a new derivation

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    A procedure avoiding any integration of the null geodesic equations is used to derive the direction of light propagation in a three-parameter family of static, spherically symmetric spacetimes within the post-post-Minkowskian approximation. Quasi-Cartesian isotropic coordinates adapted to the symmetries of spacetime are systematically used. It is found that the expression of the angle formed by two light rays as measured by a static observer staying at a given point is remarkably simple in these coordinates. The attention is mainly focused on the null geodesic paths that we call the "quasi-Minkowskian light rays". The vector-like functions characterizing the direction of propagation of such light rays at their points of emission and reception are firstly obtained in the generic case where these points are both located at a finite distance from the centre of symmetry. The direction of propagation of the quasi-Minkowskian light rays emitted at infinity is then straightforwardly deduced. An intrinsic definition of the gravitational deflection angle relative to a static observer located at a finite distance is proposed for these rays. The expression inferred from this definition extends the formula currently used in VLBI astrometry up to the second order in the gravitational constant G.Comment: 19 pages; revised introduction; added references for introduction; corrected typos; published in Class. Quantum Gra

    A computational analysis of lower bounds for big bucket production planning problems

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    In this paper, we analyze a variety of approaches to obtain lower bounds for multi-level production planning problems with big bucket capacities, i.e., problems in which multiple items compete for the same resources. We give an extensive survey of both known and new methods, and also establish relationships between some of these methods that, to our knowledge, have not been presented before. As will be highlighted, understanding the substructures of difficult problems provide crucial insights on why these problems are hard to solve, and this is addressed by a thorough analysis in the paper. We conclude with computational results on a variety of widely used test sets, and a discussion of future research
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