11 resultados para Mutação

em SAPIENTIA - Universidade do Algarve - Portugal


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Tese de dout., Bioquímica (Biologia Celular e Molecular), Faculdade de Ciências e Tecnologia, Univ. do Algarve, 2010

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Dissertação de mest., Engenharia Biológica, Faculdade de Ciências e Tecnologia, Univ. do Algarve, 2011

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As preocupações médicas com a alimentação e o seu equilíbrio remontam à Antiguidade, mas apenas a partir do século XVII começaram a ser equacionadas numa perspectiva mais científica e de maior rigor. No período seiscentista, esta questão é retomada, por exemplo, por dois médicos de renome originários dos Países Baixos, Luís Nunes (1553 – 1645) e Willem Piso (1611 – 1678), que escreveram em latim, a língua habitual para a difusão do conhecimento e ciência à época, e de quem podemos consultar tratados de importância inquestionável, pertença do Fundo Antigo da Biblioteca Municipal de Tavira. Referimo-nos, especificamente, ao Ichtyophagia (Antuérpia, 1616), único exemplar sinalizado em Portugal, e ao De Indiae utriusque re naturali et medica. Libri quatuordecim (Amesterdão, 1658), de que existe cópia microfilmada na Biblioteca Nacional, e cuja primeira parte, livro terceiro, logo na abertura, refere explicitamente os peixes ad humanos usus producantur (p. 47), i.e., apresentados na perspectiva da sua utilização pelo homem. A apologia de uma alimentação cuja dieta deve compreender o consumo de peixe é, em nosso entender, um dos motivos que atravessam ambos os textos. Esta comunicação pretende contribuir para a divulgação pública do conteúdos algo olvidados, numa época em que nunca se falou tanto da importância da alimentação no contexto duma educação para a saúde, e ao mesmo tempo enfatizar o valor patrimonial das obras referidas, alertando para a necessidade imperiosa de preservar espólios documentais que integram espécimes como os que aqui se referem. A relevância historiográfica destas obras, que inauguram a defesa científica de hábitos alimentares equilibrados, alicerçando um discurso inovador, numa época de profunda mutação histórica e cultural, imposta pelas contacto com as realidades exóticas do Novo Mundo.

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Esta dissertação tem por objectivo aplicar algoritmos evolutivos multiobjectivo a problemas de afectação de recursos, particulamente a problemas de geração de horários de exames e problemas de geração de horários de aulas em Universidades. Estes problemas são normalmente caracterizados pela existência de múltiplos objectivos conflituosos. Neste sentido, uma formalização multiobjectivo para estes problemas é apresentada, com base no conceito de metas e prioridades. Vários aspectos dos algoritmos evolutivos são propostos e analisados para esta classe de problemas, nomeadamente, métodos de selecção e tipo e parâmetros de operadores de mutação. A escolha da representação e dos operadores utilizados é feita tendo em conta a necessidade de não privilegiar demasiadamente certos objectivos em relação a outros ao nível dos mecanismos de exploração. São apresentados estudos comparativos entre os algoritmos propostos por meio de métodos de inferência estatística em problemas reais na Universidade do Algarve. O conceito de função de aproveitamento é utilizado para avaliação de algoritmos evolutivos multiobjectivo. Finalmente, a análise da evolução do custo das soluções encontradas ao longo do tempo de execução através de funções de aproveitamento é apresentada.

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Epithelial tissues are essential during morphogenesis and organogenesis. During development, epithelial tissues undergo several different remodeling processes, from cell intercalation to cell change shape. An epithelial cell has a highly polarized structure, which is important to maintain tissue integrity. The mechanisms that regulate and maintain apicobasal polarity and epithelial integrity are mostly conserved among all species and in different tissues within the same organism. aPKC-PAR complex localizes in the apical domain of polarized cells, and its function is essential for apicobasal polarization and epithelial integrity. In this work we characterized two novel alleles of aPKC: a temperature sensitive allele (aPKCTS), which has a point mutation on a kinase domain, and another allele with a point mutation on a highly conserved amino acid within the PB1 domain of aPKC (aPKCPB1). Analysis of the aPKCTS mutant phenotypes, lead us to propose that during development different epithelial tissues have differential requirements of aPKC activity. More specifically, our work suggests de novo formation of adherens junctions (AJs) is particularly sensitive to sub-optimal levels of apkc activity. Analysis of the aPKCPB1 allele, suggests that aPKC is likely to have an apical structural function mostly independent of its kinase activity. Altogether our work suggests that although loss of aPKC function is associated to similar epithelial phenotypes (e.g., loss of apicobasal polarization and epithelial integrity), the requirements of aPKC activity within these tissues are nevertheless likely to vary.

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Induced pluripotent stem cells (iPSc) have great potential for applications in regenerative medicine, disease modeling and basic research. Several methods have been developed for their derivation. The original method of Takahashi and Yamanaka involved the use of retroviral vectors which result in insertional mutagenesis, presence in the genome of potential oncogenes and effects of residual transgene expression on differentiation bias of each particular iPSc line. Other methods have been developed, using different viral vectors (adenovirus and Sendai virus), transient plasmid transfection, mRNA transduction, protein transduction and use of small molecules. However, these methods suffer from low efficiencies; can be extremely labor intensive, or both. An additional method makes use of the piggybac transposon, which has the advantage of inserting its payload into the host genome and being perfectly excised upon re-expression of the transposon transposase. Briefly, a policistronic cassette expressing Oct4, Sox2, Klf4 and C-Myc flanked by piggybac terminal repeats is delivered to the cells along with a plasmid transiently expressing piggybac transposase. Once reprogramming occurs, the cells are re-transfected with transposase and subclones free of tranposon integrations screened for. The procedure is therefore very labor intensive, requiring multiple manipulations and successive rounds of cloning and screening. The original method for reprogramming with the the PiggyBac transposon was created by Woltjen et al in 2009 (schematized here) and describes a process with which it is possible to obtain insert-free iPSc. Insert-free iPSc enables the establishment of better cellular models of iPS and adds a new level of security to the use of these cells in regenerative medicine. Due to the fact that it was based on several low efficiency steps, the overall efficiency of the method is very low (<1%). Moreover, the stochastic transfection, integration, excision and the inexistence of an active way of selection leaves this method in need of extensive characterization and screening of the final clones. In this work we aime to develop a non-integrative iPSc derivation system in which integration and excision of the transgenes can be controlled by simple media manipulations, avoiding labor intensive and potentially mutagenic procedures. To reach our goal we developed a two vector system which is simultaneously delivered to original population of fibroblasts. The first vector, Remo I, carries the reprogramming cassette and GFP under the regulation of a constitutive promoter (CAG). The second vector, Eneas, carries the piggybac transposase associated with an estrogen receptor fragment (ERT2), regulated in a TET-OFF fashion, and its equivalent reverse trans-activator associated with a positive-negative selection cassette under a constitutive promoter. We tested its functionality in HEK 293T cells. The protocol is divided in two the following steps: 1) Obtaining acceptable transfection efficiency into human fibroblasts. 2) Testing the functionality of the construct 3) Determining the ideal concentration of DOX for repressing mPB-ERT2 expression 4) Determining the ideal concentration of TM for transposition into the genome 5) Determining the ideal Windows of no DOX/TM pulse for transposition into the genome 6) 3, 4 and 5) for transposition out of the genome 7) Determination of the ideal concentration of GCV for negative selection We successfully demonstrated that ENEAS behaved as expected in terms of DOX regulation of the expression of mPB-ERT2. We also demonstrated that by delivering the plasmid into 293T HEK cells and manipulating the levels of DOX and TM in the medium, we could obtain puromycin resistant lines. The number of puromycin resistant colonies obtained was significantly higher when DOX as absent, suggesting that the colonies resulted from transposition events. Presence of TM added an extra layer of regulation, albeit weaker. Our PCR analysis, while not a clean as would be desired, suggested that transposition was indeed occurring, although a background level of random integration could not be ruled out. Finally, our attempt to determine whether we could use GVC to select clones that had successfully mobilized PB out of the genome was unsuccessful. Unexpectedly, 293T HEK cells that had been transfected with ENEAS and selected for puromycin resistance were insensitive to GCV.

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All systems found in nature exhibit, with different degrees, a nonlinear behavior. To emulate this behavior, classical systems identification techniques use, typically, linear models, for mathematical simplicity. Models inspired by biological principles (artificial neural networks) and linguistically motivated (fuzzy systems), due to their universal approximation property, are becoming alternatives to classical mathematical models. In systems identification, the design of this type of models is an iterative process, requiring, among other steps, the need to identify the model structure, as well as the estimation of the model parameters. This thesis addresses the applicability of gradient-basis algorithms for the parameter estimation phase, and the use of evolutionary algorithms for model structure selection, for the design of neuro-fuzzy systems, i.e., models that offer the transparency property found in fuzzy systems, but use, for their design, algorithms introduced in the context of neural networks. A new methodology, based on the minimization of the integral of the error, and exploiting the parameter separability property typically found in neuro-fuzzy systems, is proposed for parameter estimation. A recent evolutionary technique (bacterial algorithms), based on the natural phenomenon of microbial evolution, is combined with genetic programming, and the resulting algorithm, bacterial programming, advocated for structure determination. Different versions of this evolutionary technique are combined with gradient-based algorithms, solving problems found in fuzzy and neuro-fuzzy design, namely incorporation of a-priori knowledge, gradient algorithms initialization and model complexity reduction.

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Dissertação de mestrado, Biologia Molecular e Microbiana, Faculdade de Ciências e Tecnologia, Universidade do Algarve, 2015

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Dissertação de mestrado, Ciências Biomédicas, Departamento de Ciências Biomédicas e Medicina, Universidade do Algarve, 2014

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Dissertação de Mestrado, Ciências Farmacêuticas, Faculdade de Ciências e Tecnologia, Universidade do Algarve, 2014

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Dissertação de mest. em Gestão Empresarial, Faculdade de Economia, Univ. do Algarve, 2004