304 research outputs found

    Creating commons: PhotoVoice philosophy in a third space

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    Teach Toledo is a program that the authors co-coordinate using community assets to create a third space to confront systemic racism’s impact on teacher education programs and facilitate hybridity (Bhaba, 1994). Diverse student cohort members use their lived experience as the base for their individual and shared urban educational philosophies, coordinated in a first-year horizontally and vertically integrated curriculum including written compositions and a PhotoVoice project. “Creating commons” refers not only to provision of a third space as a common space where private experiences can be combined to create a hybrid, new understanding, but also to the creative act of fashioning and communicating a common purpose, i.e., a common philosophy of education. In this paper the authors ask: How can faculty and students develop a shared philosophy of possibility for urban education? What value can be gained from grounding teacher education in shared philosophy

    The Role of WRN Helicase/Exonuclease in DNA Replication

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    Coordination of Nucleases and Helicases during DNA Replication and Double-strand Break Repair

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    Nucleases and helicases are involved in numerous steps in DNA replication and repair. Nucleases act on intermediates in DNA replication created by DNA polymerases (Chapter 4) and helicases (Chapter 3). They can create substrates for repair as in Okazaki fragment processing (OFP) and homologous recombination. They can also create substrates for activation of a checkpoint response, or participate in downregulation of checkpoints. In the special case of telomere replication, they are also involved in essential processing steps (Chapter 8). Nucleases known to act during DNA replication include Dna2, Rad27, Mre11, Sae2, Exo1, RNaseH, Yen1 andMus81/Mms4. Of these, Dna2, Exo1 and Mre11 are of particular interest because they have been identified as crucial activities that initiate repair of double-strand breaks (DSBs) by homologous recombination and thus form an intrinsic link between DNA replication and repair of DSBs derived from replication fork failure. The action of the nucleases is coordinated with those of a number of helicases and is discussed here in the context of a network of their interactions that combine to maintain genome integrity during DNA replication

    Coordination of Nucleases and Helicases during DNA Replication and Double-strand Break Repair

    Get PDF
    Nucleases and helicases are involved in numerous steps in DNA replication and repair. Nucleases act on intermediates in DNA replication created by DNA polymerases (Chapter 4) and helicases (Chapter 3). They can create substrates for repair as in Okazaki fragment processing (OFP) and homologous recombination. They can also create substrates for activation of a checkpoint response, or participate in downregulation of checkpoints. In the special case of telomere replication, they are also involved in essential processing steps (Chapter 8). Nucleases known to act during DNA replication include Dna2, Rad27, Mre11, Sae2, Exo1, RNaseH, Yen1 andMus81/Mms4. Of these, Dna2, Exo1 and Mre11 are of particular interest because they have been identified as crucial activities that initiate repair of double-strand breaks (DSBs) by homologous recombination and thus form an intrinsic link between DNA replication and repair of DSBs derived from replication fork failure. The action of the nucleases is coordinated with those of a number of helicases and is discussed here in the context of a network of their interactions that combine to maintain genome integrity during DNA replication

    Managing resources in later life: older people's experience of change and continuity

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    This report explores the changing lives of older people and shows how resources are used to manage change and maintain stability. An ageing population continues to be of policy concern, in relation to meeting the needs of older people now, and for future welfare provision. This research explores how older people plan, use and value the different resources available to them. Resources are broadly defined, to explore the relative value of different structural, social and individual resources and how they interlink. This holistic overview highlights the complexity of older people’s lives, the variety of resources that people draw on to help manage change and the work involved in maintaining continuity and preventing change. In-depth interviews with people (aged 65–84 at the first interview) were conducted two years apart to explore their changing needs and resources as they move through later life

    Strategies for thiazole/oxazole-modified microcin discovery

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    Natural products continue to be an important source of therapeutically-relevant compounds. With the advent of inexpensive genome sequencing it has become apparent that bacteria produce a larger array of natural products than was previously believed. This new wealth in sequence data has potential to be helpful for the discovery of novel compounds by using genome mining. Although strategies of genome mining have become more efficient and capable of identifying novel biosynthetic gene clusters, it remains difficult to correlate gene clusters with natural products. In this dissertation I discuss limitations with the current methods of genome mining and correlating individual natural products with gene clusters. Furthermore, I characterize a rapidly growing family of natural products, the thiazole/oxazole-modified microcins (TOMMs), and discuss novel methods used to correlate the gene clusters to natural products from this family of metabolites. In chapter 2, I establish the sequence diversity and structural capability of bacteria and archaea to produce TOMM natural products. This genome mining characterization was used to identify nine novel classes of TOMMs, including one class from archaeal producers. In chapter 3, I discuss the utilization of genetic techniques to identify and isolate the TOMM natural product from the archaeal species Sulfolobus acidocaldarius. I demonstrate that although genetic manipulation has been previously used for the identification of natural products, comparative metabolomics is difficult to use for routine identification of low-abundance natural products such as the TOMM from S. acidocaldarius. Very few methods have been created to identify natural products from particular gene clusters. Therefore, in chapter 4, I discuss the creation of a novel method for the rapid identification of natural products following bioinformatics prioritization of antibiotic producing strains. This method utilizes the combination of genome mining and the chemical reactivity of natural products to discover new compounds. Dehydrated amino acids are modified residues commonly found in natural products such as TOMMs. I utilize the mild electrophilic chemical reactivity of dehydrated amino acids to label these natural products using a soft nucleophilic probe. These labeled natural products were easily detected using comparative mass spectrometry. Bacterial strains were prioritized by the genome mining established in chapter 2 to reduce the screening time to find a novel natural product. This dissertation presents the addition of novel genome mining and natural product discovery techniques to increase the discovery and production of therapeutically-relevant compounds

    Use of Drawings to Explore US Women's Perspectives on Why People Might Decline HIV Testing

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    The purpose of this research is to explore through drawings and verbal descriptions women's perspectives about reasons why persons might decline human immunodeficiency virus (HIV) testing. We asked 30 participants to draw a person that would NOT get tested for HIV and then explain drawings. Using qualitative content analysis, we extracted seven themes. We found apprehension about knowing the result of an HIV test to be the most commonly identified theme in women's explanations of those who would not get tested. This technique was well received and its use is extended to HIV issues
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