6,083 research outputs found

    Performance of the resurfaced hip. Part 1: the influence of the prosthesis size and positioning on the remodelling and fracture of the femoral neck

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    Hip resurfacing is an established treatment for osteoarthritis in young active patients. Failure modes include femoral neck fracture and prosthesis loosening, which may be associated with medium-term bone adaptation, including femoral neck narrowing and densification around the prosthesis stem.Finite element modelling was used to indicate the effects of prosthesis sizing and positioning on the bone remodelling and fracture strength under a range of normal and traumatic loads, with the aim of understanding these failure modes better.The simulations predicted increased superior femoral neck stress shielding in young patients with small prostheses, which required shortening of the femoral neck to give an acceptable implant–bone interface. However, with a larger prosthesis, natural femoral head centre recreation in the implanted state was possible; therefore stress shielding was restricted to the prosthesis interior, and its extent was less sensitive to prosthesis orientation. With valgus orientation, the implanted neck strength was, at worst, within 3 per cent of its intact strength.The study suggests that femoral neck narrowing may be linked to a reduction in the horizontal femoral offset, occurring if the prosthesis is excessively undersized. As such, hip resurfacing should aim to reproduce the natural femoral head centre, and, for valgus prosthesis orientation, to avoid femoral neck fracture

    Unexpected evolutionary proximity of eukaryotic and cyanobacterial enzymes responsible for biosynthesis of retinoic acid and its oxidation

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    Biosynthesis of retinoic acid from retinaldehyde (retinal) is catalysed by an aldehyde dehydrogenase (ALDH) and its oxidation by cytochrome P450 enzymes (CYPs). Herein we show by phylogenetic analysis that the ALDHs and CYPs in the retinoic acid pathway in animals are much closer in evolutionary terms to cyanobacterial orthologs than would be expected from the standard models of evolution

    Scotland’s beginnings: Scotland through time.

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    Did you know that Scotland began under an iceberg-laden sea near the South Pole hundreds of millions of years ago? The journey north of the land we now call Scotland is an astounding tale of great mountains, subtropical rainforests, coral reefs, howling deserts, ammonite-inhabited seas, high lava plateaus and scouring ice caps. The evidence for this journey is recorded in rocks, peat-bogs and lake muds. When the glaciers withdrew the new land was colonised by animals and plants but when hunters and farmers moved in mass extinction began. This beautifully illustrated guide, full of drawings, paintings and photographs, is an excellent introduction to Scotland’s earliest history

    Torsional Monopoles and Torqued Geometries in Gravity and Condensed Matter

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    Torsional degrees of freedom play an important role in modern gravity theories as well as in condensed matter systems where they can be modeled by defects in solids. Here we isolate a class of torsion models that support torsion configurations with a localized, conserved charge that adopts integer values. The charge is topological in nature and the torsional configurations can be thought of as torsional `monopole' solutions. We explore some of the properties of these configurations in gravity models with non-vanishing curvature, and discuss the possible existence of such monopoles in condensed matter systems. To conclude, we show how the monopoles can be thought of as a natural generalization of the Cartan spiral staircase.Comment: 4+epsilon, 1 figur

    Selective proteolysis of the wheat Em polypeptide Identification of an endopeptidase activity in germinating wheat embryos

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    AbstractThe ‘Em’ polypeptide is the most abundant cytosolic polypeptide in mature wheat embryos. It is selectively and completely degraded within the first 24 h of germination. Extracts from germinated embryos contain endopeptidase activities which degrade the Em polypeptide. These are separable into a major and minor component by ion-exchange chromatography and the use of inhibitors shows the major component to be a cysteine proteinase. This activity shows a strong preference for the Em polypeptide as a substrate, being inactive against polypeptides which are not developmentally regulated and showing only low activity towards developmentally related, but otherwise nonhomologous ‘dehydrin’ polypeptides
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