Search Results Heading

MBRLSearchResults

mbrl.module.common.modules.added.book.to.shelf
Title added to your shelf!
View what I already have on My Shelf.
Oops! Something went wrong.
Oops! Something went wrong.
While trying to add the title to your shelf something went wrong :( Kindly try again later!
Are you sure you want to remove the book from the shelf?
Oops! Something went wrong.
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
    Done
    Filters
    Reset
  • Language
      Language
      Clear All
      Language
  • Subject
      Subject
      Clear All
      Subject
  • Item Type
      Item Type
      Clear All
      Item Type
  • Discipline
      Discipline
      Clear All
      Discipline
  • Year
      Year
      Clear All
      From:
      -
      To:
  • More Filters
13 result(s) for "Lancaster, M. (Mike)"
Sort by:
Green Chemistry
Sustainable development, the circular economy and environmental issues are at the forefront of public and Government concern. The field of green chemistry aims to provide environmentally benign products from sustainable resources, using processes that do not harm people or the environment at the same time as helping solve key societal problems such as climate change. Updated throughout, this third edition features an expanded section on legislation, a revised chapter on measurement, and a completely re-written chapter on renewable resources, bringing readers the latest developments in this quickly-growing area. Case studies now include more recent examples of real-world applications from industry to demonstrate how the techniques of green chemistry work in practice. This fascinating textbook is suitable for undergraduate and postgraduate courses covering green chemistry, and it encourages new ways of thinking about how products and processes are developed.
Green chemistry
The challenge for today's new chemistry graduates is to meet society's demand for new products that have increased benefits, but without detrimental effects on the environment. Green Chemistry: An Introductory Text outlines the basic concepts of the subject in simple language, looking at the role of catalysts and solvents, waste minimisation, feedstocks, green metrics and the design of safer, more efficient, processes. The inclusion of industrially relevant examples throughout demonstrates the importance of green chemistry in many industry sectors. Intended primarily for use by students and lecturers, this book will also appeal to industrial chemists, engineers, managers or anyone wishing to know more about green chemistry.
Clean technology for the manufacture of speciality chemicals
Producing large quantities of waste is not only environmentally unacceptable, it is also not viable in economic terms. The chemical industry, particularly the speciality and pharmaceuticals sectors, is becoming increasingly aware of the advantages associated with clean technology, particularly in terms of competitive advantage and environmental benefits. Bringing together an understanding of the concepts and values of clean technology by using case studies from some leading European countries, this book provides an insight into subjects such as catalysis; process intensification; and how to measure the \"green\" value of a process. It also highlights the role played by both the chemical and chemical engineering disciplines in the development of cleaner processes. Clean Technology for the Manufacture of Speciality Chemicals will prove valuable reading for process development chemists and engineers, particularly those in the specialities and pharmaceuticals sectors, and will also be an important source of teaching material for the growing number of clean technology chemistry courses.
Green Chemistry
Updated throughout, this fourth edition is suitable for undergraduate and postgraduate courses covering green chemistry, exploring the provision of environmentally benign products from sustainable resources.
Oncogenic pathway signatures in human cancers as a guide to targeted therapies
Tumour profiling advances Molecular tumour profiling is one way in which effective targeted cancer treatment regimes might be developed. Two groups report significant developments in this direction. Bild et al . studied gene expression patterns that reflect the activation of various oncogenic (cancer-causing) signal transduction pathways. Using combinations of these pathway signatures, they predict which patients with breast, lung or ovarian cancer have a particularly poor prognosis. The ability to identify molecular pathways that are deregulated in a particular cancer in this way might be used to predict its sensitivity to specific therapeutic drugs. Solit et al . studied tumour cells with mutations in the RAS and BRAF genes, thought to cause cancer at least in part by activating the MEK/ERK signalling pathway. They show that tumours with the BRAF mutation, but not RAS, are highly sensitive to PD0325901, an MEK inhibitor that is in early-stage clinical trials in patients with melanoma, colon, breast and lung cancers. So by testing for the presence of BRAF mutations it may be possible to identify those patients most likely to benefit from this type of drug. The development of an oncogenic state is a complex process involving the accumulation of multiple independent mutations that lead to deregulation of cell signalling pathways central to the control of cell growth and cell fate 1 , 2 , 3 . The ability to define cancer subtypes, recurrence of disease and response to specific therapies using DNA microarray-based gene expression signatures has been demonstrated in multiple studies 4 . Various studies have also demonstrated the potential for using gene expression profiles for the analysis of oncogenic pathways 5 , 6 , 7 , 8 , 9 , 10 , 11 . Here we show that gene expression signatures can be identified that reflect the activation status of several oncogenic pathways. When evaluated in several large collections of human cancers, these gene expression signatures identify patterns of pathway deregulation in tumours and clinically relevant associations with disease outcomes. Combining signature-based predictions across several pathways identifies coordinated patterns of pathway deregulation that distinguish between specific cancers and tumour subtypes. Clustering tumours based on pathway signatures further defines prognosis in respective patient subsets, demonstrating that patterns of oncogenic pathway deregulation underlie the development of the oncogenic phenotype and reflect the biology and outcome of specific cancers. Predictions of pathway deregulation in cancer cell lines are also shown to predict the sensitivity to therapeutic agents that target components of the pathway. Linking pathway deregulation with sensitivity to therapeutics that target components of the pathway provides an opportunity to make use of these oncogenic pathway signatures to guide the use of targeted therapeutics.
Walking in the high-rise city: a Health Enhancement and Pedometer-determined Ambulatory (HEPA) program in Hong Kong
Due to the lack of good infrastructure in the public estates, many older adults in urban areas are sedentary. The Health Enhancement and Pedometer-Determined Ambulatory (HEPA) program was developed to assist older adults with diabetes and/or hypertension to acquire walking exercise habits and to build social support, while engaged in regular physical activity. This study aimed to describe the HEPA program and to report changes in participants' walking capacity and body strength after 10-week walking sessions. A pre- and postintervention design was used. Pedometers were used to measure the number of steps taken per day before and after the 10-week intervention. Upper and lower body strength, lower body flexibility, and quality of life were assessed. A total of 205 older adults completed the program and all health assessments. After the 10-week intervention, the average number of steps per day increased by 36%, from 6,591 to 8,934. Lower body strength, upper body strength, and aerobic fitness increased significantly after 10 weeks, along with improvement in the 12-item Short Form Health Survey (SF™-12) physical and mental health component summary scores. A social support network was built in the neighborhood, and the local environment was utilized to make walking possible and enjoyable.
Impact of differing protein sources and a creatine containing nutritional formula after 12 weeks of resistance training
We evaluated whether colostrum (Col) or an isocaloric and isonitrogenous blend of whey and casein in addition to creatine (Cr) affects body composition, muscular strength and endurance, and anaerobic performance during resistance training. Forty-nine resistance-trained subjects participated in a standardized 12-wk total body resistance training program. In a double-blind and randomized manner, subjects supplemented their diet with a protein control (Pro), Pro/Col, Pro/Cr, or Col/Cr. Supplements were isocaloric and isonitrogenous and provided 60 g/d of casein/whey (Pro) or Col as the protein source. At 0, 8, and 12 wk of supplementation, subjects were weighed, had body composition determined using dual-energy X-ray absorptiometry (DXA), performed one-repetition maximum (1RM) and 80% of 1RM tests on the bench press and leg press, and 30-s anaerobic sprint capacity tests. Data (mean ± SD) were analyzed by repeated measures analysis of variance and reported as raw data in all tables and as changes from baseline for all figures for the Pro, Pro/Col, Pro/Cr, and Col/Cr groups, respectively. Resistance training increased 1RM strength, muscular endurance, and anaerobic sprint capacity equally in all groups. Significant main and interaction effects ( P < 0.05) were found for body mass, DXA total scanned mass, and fat-free mass (FFM; lean plus bone), whereas no changes ( P > 0.05) were noted for fat mass, percent fat, or bone content. Post hoc analysis showed that, compared with Pro, subjects ingesting Pro/Col, Pro/Cr, and Col/Cr showed greater gains in body mass and DXA total scanned mass. Subjects ingesting Pro/Cr and Col/Cr had greater increases in FFM during training in comparison with Pro/Col. In conjunction with 12 wk of resistance training, ingestion of Col or a blend of whey and casein protein with a vitamin/mineral supplement containing Cr resulted in greater improvements in FFM in comparison with Pro and Pro/Col.
Effects of chronic trawling disturbance on the production of infaunal communities
Trawling causes widespread physical disturbance in shallow shelf seas. While the impacts of trawling on the biomass and community structure of benthic fauna are well known, no existing studies have quantified the effects of trawling disturbance on the absolute production of small benthic infauna. We investigated the effects of beam trawling disturbance on the production of small benthic infauna (AFDM > 0.78 to 62.5 mg) at 9 sites that were subject to a 17.5-fold range in annual trawling disturbance, using a size-based approach that could be applied to other soft-bottom systems. We developed a generalised additive model to test for relationships between trawling disturbance and infaunal production and size structure, after accounting for differences in sediment characteristics and depth. The statistical power of our analyses to detect linear and non-linear relationships between production and disturbance, including increased production at intermediate levels of disturbance, was high (>90% probability of detecting a 50% change in production across the range of disturbance). The analyses showed that trawling frequencies of 0.35 to 6.14 times yr–1did not have a significant effect on the production of small infauna or polychaetes. This result contrasts with order of magnitude decreases in the production of large infauna, and shows that small polychaetes with fast life histories are less vulnerable to trawling disturbance. Since small infaunal polychaetes are a key source of food for flatfishes, we conclude that beam trawling disturbance does not have a positive or negative effect on their food supply.
Impact of differing protein sources and a creatine containing nutritional formula after 12 weeks of resistance training
We evaluated whether colostrum (Col) or an isocaloric and isonitrogenous blend of whey and casein in addition to creatine (Cr) affects body composition, muscular strength and endurance, and anaerobic performance during resistance training. Forty-nine resistance-trained subjects participated in a standardized 12-wk total body resistance training program. In a double-blind and randomized manner, subjects supplemented their diet with a protein control (Pro), Pro/Col, Pro/Cr, or Col/Cr. Supplements were isocaloric and isonitrogenous and provided 60 g/d of casein/whey (Pro) or Col as the protein source. At 0, 8, and 12 wk of supplementation, subjects were weighed, had body composition determined using dual-energy X-ray absorptiometry (DXA), performed one-repetition maximum (1RM) and 80% of 1RM tests on the bench press and leg press, and 30-s anaerobic sprint capacity tests. Data (mean +/- SD) were analyzed by repeated measures analysis of variance and reported as raw data in all tables and as changes from baseline for all figures for the Pro, Pro/Col, Pro/Cr, and Col/Cr groups, respectively. Resistance training increased 1RM strength, muscular endurance, and anaerobic sprint capacity equally in all groups. Significant main and interaction effects (P < 0.05) were found for body mass, DXA total scanned mass, and fat-free mass (FFM; lean plus bone), whereas no changes (P > 0.05) were noted for fat mass, percent fat, or bone content. Post hoc analysis showed that, compared with Pro, subjects ingesting Pro/Col, Pro/Cr, and Col/Cr showed greater gains in body mass and DXA total scanned mass. Subjects ingesting Pro/Cr and Col/Cr had greater increases in FFM during training in comparison with Pro/Col. In conjunction with 12 wk of resistance training, ingestion of Col or a blend of whey and casein protein with a vitamin/mineral supplement containing Cr resulted in greater improvements in FFM in comparison with Pro and Pro/Col.
Applied nutritional investigation: Impact of differing protein sources and a creatine containing nutritional formula after 12 weeks of resistance training
Objective We evaluated whether colostrum (Col) or an isocaloric and isonitrogenous blend of whey and casein in addition to creatine (Cr) affects body composition, muscular strength and endurance, and anaerobic performance during resistance training. Methods Forty-nine resistance-trained subjects participated in a standardized 12-wk total body resistance training program. In a double-blind and randomized manner, subjects supplemented their diet with a protein control (Pro), Pro/Col, Pro/Cr, or Col/Cr. Supplements were isocaloric and isonitrogenous and provided 60 g/d of casein/whey (Pro) or Col as the protein source. At 0, 8, and 12 wk of supplementation, subjects were weighed, had body composition determined using dual-energy X-ray absorptiometry (DXA), performed one-repetition maximum (1RM) and 80% of 1RM tests on the bench press and leg press, and 30-s anaerobic sprint capacity tests. Data (mean - SD) were analyzed by repeated measures analysis of variance and reported as raw data in all tables and as changes from baseline for all figures for the Pro, Pro/Col, Pro/Cr, and Col/Cr groups, respectively. Results Resistance training increased 1RM strength, muscular endurance, and anaerobic sprint capacity equally in all groups. Significant main and interaction effects (P < 0.05) were found for body mass, DXA total scanned mass, and fat-free mass (FFM; lean plus bone), whereas no changes (P > 0.05) were noted for fat mass, percent fat, or bone content. Post hoc analysis showed that, compared with Pro, subjects ingesting Pro/Col, Pro/Cr, and Col/Cr showed greater gains in body mass and DXA total scanned mass. Subjects ingesting Pro/Cr and Col/Cr had greater increases in FFM during training in comparison with Pro/Col. Conclusion In conjunction with 12 wk of resistance training, ingestion of Col or a blend of whey and casein protein with a vitamin/mineral supplement containing Cr resulted in greater improvements in FFM in comparison with Pro and Pro/Col.