63 research outputs found

    Aspects of growth and metabolism in the musculature of Antarctic fishes : with particular reference to 'Notothenia neglecta' nybelin

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    1. Aspects of the physiology and biochemistry of Antarctic fish muscle have been examined, principally for the nototheniid, Notothenia neglecta Nybelin. 2. Sampling was most successful during the late summer/autumn. The trammel net was the best method for catching fish above 200mm standard length. Smaller fish were best caught by SCUBA divers using hand-nets. 3. The condition factor for fish caught was highest during the summer (high food availability) and remained low during the winter months. Analysis of trunk muscle constituents (water, protein, lipid) indicated no evidence for marked depletion at any time of the year. Seasonal variation in relative gonad size and relative liver size were observed. 4. Metabolically the pectoral abductor muscle of N.neglecta had higher activities of anaerobic and aerobic enzymes than either the red or white trunk muscles. This is in line with the fact that this species normally swims using enlarged pectoral fins, while sprint swimming in short bursts is carried out by the white trunk muscle. 5. Differences in the metabolic profiles of the trunk muscles of 3 Antarctic species (N.neglecta, Notothenia gibberifrons and Trematomus newnesi) are related to their different lifestyles, particularily feeding behaviours. 6. Muscle growth in N.neglecta is probably both by hypertrophy, and recruitment of myosatellite cells. Both the fibres and capillaries in Antarctic species are much larger in cross-sectional area than for temperate species. 7. Lactate dehydrogenase isozymes in the trunk and cardiac muscles of N.neqlecta are electrophoretically and kinetically similar. This, along with its high activities of anaerobic enzymes indicates that the cardiac muscle is adapted to utilise fuels anaerobically if necessary. 8. The majority of physiological and cellular adaptations can be explained on the basis of physiological/ecological constraints rather than cold temperature per se

    Prospectus, May 24, 2000

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    https://spark.parkland.edu/prospectus_2000/1016/thumbnail.jp

    The supportive care needs of parents caring for a child with a rare disease : a scoping review

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    Background: Parents caring for a child with a rare disease report unmet needs, the origins of which are varied and complex. Few studies have systematically attempted to identify the supportive care needs of parents with a child with a rare disease comprehensively. We have used the widely accepted Supportive Care Needs Framework (SCNF) as the structure for this review. Objective: The purpose of the current review was to identify the supportive care needs of parents with a child with a rare disease, irrespective of condition. Methods: We conducted a scoping study review comprising 29 studies (1990–2014) to identify and examine the research literature related to the supportive care needs of parents, and to compare these needs with the seven domains outlined in the SCNF. Results: Most common needs cited were social needs (72% of papers), followed by informational needs (65% of papers) and emotional needs (62% of papers), with the most common parental needs overall being information about their child's disease, emotional stress, guilt and uncertainty about their child's future health care needs, parents own caring responsibilities and the need for more general support. Conclusion: A paucity of studies exists that explore the supportive care needs of parents of a child with a rare disease. The SCNF only partially reflects the breadth and type of needs of these parents, and a preliminary revised framework has been suggested. Further research is required in this area, particularly empirical research to amend or confirm the suggested new framework

    Severe asthma exists despite suppressed tissue inflammation: findings of the U-BIOPRED study

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    The U-BIOPRED study is a multicentre European study aimed at a better understanding of severe asthma. It included three steroid-treated adult asthma groups (severe nonsmokers (SAn group), severe current/ex-smokers (SAs/ex group) and those with mild–moderate disease (MMA group)) and healthy controls (HC group). The aim of this cross-sectional, bronchoscopy substudy was to compare bronchial immunopathology between these groups. In 158 participants, bronchial biopsies and bronchial epithelial brushings were collected for immunopathologic and transcriptomic analysis. Immunohistochemical analysis of glycol methacrylate resin-embedded biopsies showed there were more mast cells in submucosa of the HC group (33.6 mm⁻ ²) compared with both severe asthma groups (SAn: 17.4 mm⁻ ², p<0.001; SAs/ex: 22.2 mm⁻ ², p=0.01) and with the MMA group (21.2 mm⁻ ², p=0.01). The number of CD4+ lymphocytes was decreased in the SAs/ex group (4.7 mm⁻ ²) compared with the SAn (11.6 mm⁻ ², p=0.002), MMA (10.1 mm⁻ ², p=0.008) and HC (10.6 mm⁻ ², p<0.001) groups. No other differences were observed. Affymetrix microarray analysis identified seven probe sets in the bronchial brushing samples that had a positive relationship with submucosal eosinophils. These mapped to COX-2 (cyclo-oxygenase-2), ADAM-7 (disintegrin and metalloproteinase domain-containing protein 7), SLCO1A2 (solute carrier organic anion transporter family member 1A2), TMEFF2 (transmembrane protein with epidermal growth factor like and two follistatin like domains 2) and TRPM-1 (transient receptor potential cation channel subfamily M member 1); the remaining two are unnamed. We conclude that in nonsmoking and smoking patients on currently recommended therapy, severe asthma exists despite suppressed tissue inflammation within the proximal airway wall

    Epithelial dysregulation in obese severe asthmatics with gastro-oesophageal reflux

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    Finishing the euchromatic sequence of the human genome

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    The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

    2021 roadmap on lithium sulfur batteries

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    Abstract: Batteries that extend performance beyond the intrinsic limits of Li-ion batteries are among the most important developments required to continue the revolution promised by electrochemical devices. Of these next-generation batteries, lithium sulfur (Li–S) chemistry is among the most commercially mature, with cells offering a substantial increase in gravimetric energy density, reduced costs and improved safety prospects. However, there remain outstanding issues to advance the commercial prospects of the technology and benefit from the economies of scale felt by Li-ion cells, including improving both the rate performance and longevity of cells. To address these challenges, the Faraday Institution, the UK’s independent institute for electrochemical energy storage science and technology, launched the Lithium Sulfur Technology Accelerator (LiSTAR) programme in October 2019. This Roadmap, authored by researchers and partners of the LiSTAR programme, is intended to highlight the outstanding issues that must be addressed and provide an insight into the pathways towards solving them adopted by the LiSTAR consortium. In compiling this Roadmap we hope to aid the development of the wider Li–S research community, providing a guide for academia, industry, government and funding agencies in this important and rapidly developing research space

    The Collaborative Process as Research

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    A critical reflection on a collaboration between Fabrice Fitch and Neil Heyde as composer and performer, respectively. This dialogue traces the genesis of a composition by Fabrice Fitch for speaking cellist, "Per Serafino Calbarsi II: Le Songe de Panurge", written in 2002-3 and premiered at the BMIC's Cutting Edge series in October 2006. The collaboration first evolved as a constant exchange of ideas in which concept, technique and realization were held in fine balance. The session begins with a performance of the piece. The video accompanies the article '"Recercar' - The Collaborative Process as Invention' in twentieth-century music, 4/1 (2007), 71-85 doi:10.1017/S1478572207/00053
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