1,588 research outputs found
Core design for use with precision composite reflectors
A uniformly flexible core, and method for manufacturing the same, is disclosed for use between the face plates of a sandwich structure. The core is made of a plurality of thin corrugated strips, the corrugations being defined by a plurality of peaks and valleys connected to one another by a plurality of diagonal risers. The corrugated strips are orthogonally criss-crossed to form the core. The core is particularly suitable for use with high accuracy spherically curved sandwich structures because undesirable stresses in the curved face plates are minimized due to the uniform flexibility characteristics of the core in both the X and Y directions. The core is self venting because of the open geometry of the corrugations. The core can be made from any suitable composite, metal, or polymer. Thermal expansion problems in sandwich structures may be minimized by making the core from the same composite materials that are selected in the manufacture of the curved face plates because of their low coefficients of thermal expansion. Where the strips are made of a composite material, the core may be constructed by first cutting an already cured corrugated sheet into a plurality of corrugated strips and then secondarily bonding the strips to one another or, alternatively, by lying a plurality of uncured strips orthogonally over one another in a suitable jig and then curing and bonding the entire plurality of strips to one another in a single operation
Design and Validation of a Novel and Cost-Effective Animal Tissue Model for Training Laparoscopic Adhesiolysis and Mesh Repair of an Incisional Hernia
3D mid-air audio-haptic navigation for digital signage
In this workshop we discuss the application of using mid-air haptics to provide directions for navigation to users in large indoor spaces. We propose a feed-forward approach from objects and locations that enable a physical way of thinking, communication and general accessibility
Carbon Free Boston: Transportation Technical Report
Part of a series of reports that includes:
Carbon Free Boston: Summary Report;
Carbon Free Boston: Social Equity Report;
Carbon Free Boston: Technical Summary;
Carbon Free Boston: Buildings Technical Report;
Carbon Free Boston: Waste Technical Report;
Carbon Free Boston: Energy Technical Report;
Carbon Free Boston: Offsets Technical ReportOVERVIEW:
Transportation connects Boston’s workers, residents and tourists to their livelihoods, health care, education,
recreation, culture, and other aspects of life quality. In cities, transit access is a critical factor determining
upward mobility. Yet many urban transportation systems, including Boston’s, underserve some populations
along one or more of those dimensions. Boston has the opportunity and means to expand mobility access to
all residents, and at the same time reduce GHG emissions from transportation. This requires the
transformation of the automobile-centric system that is fueled predominantly by gasoline and diesel fuel.
The near elimination of fossil fuels—combined with more transit, walking, and biking—will curtail air
pollution and crashes, and dramatically reduce the public health impact of transportation. The City embarks
on this transition from a position of strength. Boston is consistently ranked as one of the most walkable and
bikeable cities in the nation, and one in three commuters already take public transportation.
There are three general strategies to reaching a carbon-neutral transportation system:
• Shift trips out of automobiles to transit, biking, and walking;1
• Reduce automobile trips via land use planning that encourages denser development and affordable
housing in transit-rich neighborhoods;
• Shift most automobiles, trucks, buses, and trains to zero-GHG electricity.
Even with Boston’s strong transit foundation, a carbon-neutral transportation system requires a wholesale
change in Boston’s transportation culture. Success depends on the intelligent adoption of new technologies,
influencing behavior with strong, equitable, and clearly articulated planning and investment, and effective
collaboration with state and regional partners.Published versio
Amino acid changes in the spike protein of feline coronavirus correlate with systemic spread of virus from the intestine and not with feline infectious peritonitis
Recent evidence suggests that a mutation in the spike protein gene of feline coronavirus (FCoV), which results in an amino acid change from methionine to leucine at position 1058, may be associated with feline infectious peritonitis (FIP). Tissue and faecal samples collected post mortem from cats diagnosed with or without FIP were subjected to RNA extraction and quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR) to detect FCoV RNA. In cats with FIP, 95% of tissue, and 81% of faecal samples were PCR-positive, as opposed to 22% of tissue, and 60% of faecal samples in cats without FIP. Relative FCoV copy numbers were significantly higher in the cats with FIP, both in tissues (P < 0.001) and faeces (P = 0.02). PCR-positive samples underwent pyrosequencing encompassing position 1058 of the FCoV spike protein. This identified a methionine codon at position 1058, consistent with the shedding of an enteric form of FCoV, in 77% of the faecal samples from cats with FIP, and in 100% of the samples from cats without FIP. In contrast, 91% of the tissue samples from cats with FIP and 89% from cats without FIP had a leucine codon at position 1058, consistent with a systemic form of FCoV. These results suggest that the methionine to leucine substitution at position 1058 in the FCoV spike protein is indicative of systemic spread of FCoV from the intestine, rather than a virus with the potential to cause FIP
Bod1, a novel kinetochore protein required for chromosome biorientation
We have combined the proteomic analysis of Xenopus laevis in vitro–assembled chromosomes with RNA interference and live cell imaging in HeLa cells to identify novel factors required for proper chromosome segregation. The first of these is Bod1, a protein conserved throughout metazoans that associates with a large macromolecular complex and localizes with kinetochores and spindle poles during mitosis. Small interfering RNA depletion of Bod1 in HeLa cells produces elongated mitotic spindles with severe biorientation defects. Bod1-depleted cells form syntelic attachments that can oscillate and generate enough force to separate sister kinetochores, suggesting that microtubule–kinetochore interactions were intact. Releasing Bod1-depleted cells from a monastrol block increases the frequency of syntelic attachments and the number of cells displaying biorientation defects. Bod1 depletion does not affect the activity or localization of Aurora B but does cause mislocalization of the microtubule depolymerase mitotic centromere- associated kinesin and prevents its efficient phosphorylation by Aurora B. Therefore, Bod1 is a novel kinetochore protein that is required for the detection or resolution of syntelic attachments in mitotic spindles
Physicochemical and physiological mechanisms for the effects of food on drug absorption: The role of lipids and pH
Drugs are absorbed after oral administration as a consequence of a complex array of interactions between the drug, its formulation, and the gastrointestinal (GI) tract. The presence of food within the GI tract impacts significantly on transit profiles, pH, and its solubilization capacity. Consequently, food would be expected to affect the absorption of co‐administered drugs when their physicochemical properties are sensitive to these changes. The physicochemical basis by which ingested food/lipids induce changes in the GI tract and influence drug absorption are reviewed. The process of lipid digestion is briefly reviewed and considered in the context of the absorption of poorly water‐soluble drugs. The effect of food on GI pH is reviewed in terms of location (stomach, upper and lower small intestine) and the temporal relationship between pH and drug absorption. Case studies are presented in which postprandial changes in bioavailability are rationalized in terms of the sensitivity of the physicochemical properties of the administered drug to the altered GI environment.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/97269/1/1_ftp.pd
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