Suchergebnisse

1. Opposition to wars and interventions -- 2. From the early republic to the Spanish-American War -- 3. The Great War and World War II -- 4. Arguments in the Cold War and Post-Cold War eras -- 5. Ron Paul : the importance of natural order -- 6. Noam Chomsky : hegemony and manufactured consent -- 7. Chalmers Johnson : the military empire -- 8. Comparisons, analysis and conclusions.

From introduction: "Alasdair MacIntyre is a key figure in the Liberalism-Communitarianism debate, one of the most important and fruitful in the field of Moral and Political Philosophy in the second half of the 20th century. In spite of his resistance to being labeled as a 'communitarianist', MacIntyre has been considered one of the most important representatives (with others like Walzer, Sandel, Taylor, Etzioni, et al.) of this current, one that developed to a great extent as a response to Rawls' Liberalism in his book A Theory of Justice (1971). One of the most important points of Communitarianism is its critique of the liberal view of the self and Ethics and Politics, that is to say, a critique of an individualistic view of the human being (an idea maintained by MacIntyre throughout his intellectual evolution). MacIntyre's thought has been studied from many points of view, but there is no research on his global critique and alternative to Individualism. For that reason, the aim of this paper is to study and analyze such an alternative. The questions that we have had to answer are two: 1) Which are the concepts on which MacIntyre bases his alternative to Individualism?, 2) Does this alternative overcome Individualism? "(.)

Julio Plaza-Diaz and Concepcion M. Aguilera are part of the "UGR Plan Propio de Investigacion 2016" and the "Excellence actions: Unit of Excellence on Exercise and Health (UCEES), University of Granada". Julio Plaza-Diaz is supported by a fellowship to postdoctoral researchers at foreign universities and research centers from the "Fundacion Ramon Areces", Madrid, Spain. Francisco Javier Ruiz-Ojeda is supported by a fellowship from Spanish Government "Agencia Estatal de Investigacion-Juan de la Cierva-Incorporacion" program (IJC2020-042739-I). Alvaro TorresMartos is supported by the Project "Transductores Moleculares del Ejercicio Fisico y la Activacion del Tejido Adiposo Pardo: en Busca de Nuevas Dianas Terapeuticas en la Comunicacion Intercelular" funded by "Consejeria de Economia, Conocimiento, Empresas y Universidad (PY18-4455), Junta de Andalucia", Spain. ; Exercise and physical activity induces physiological responses in organisms, and adaptations in skeletal muscle, which is beneficial for maintaining health and preventing and/or treating most chronic diseases. These adaptations are mainly instigated by transcriptional responses that ensue in reaction to each individual exercise, either resistance or endurance. Consequently, changes in key metabolic, regulatory, and myogenic genes in skeletal muscle occur as both an early and late response to exercise, and these epigenetic modifications, which are influenced by environmental and genetic factors, trigger those alterations in the transcriptional responses. DNA methylation and histone modifications are the most significant epigenetic changes described in gene transcription, linked to the skeletal muscle transcriptional response to exercise, and mediating the exercise adaptations. Nevertheless, other alterations in the epigenetics markers, such as epitranscriptomics, modifications mediated by miRNAs, and lactylation as a novel epigenetic modification, are emerging as key events for gene transcription. Here, we provide an overview and update of the impact of exercise on epigenetic modifications, including the well-described DNA methylations and histone modifications, and the emerging modifications in the skeletal muscle. In addition, we describe the effects of exercise on epigenetic markers in other metabolic tissues; also, we provide information about how systemic metabolism or its metabolites influence epigenetic modifications in the skeletal muscle. ; "Fundacion Ramon Areces", Madrid, Spain ; Spanish Government "Agencia Estatal de Investigacion-Juan de la Cierva-Incorporacion" program IJC2020-042739-I ; Project "Transductores Moleculares del Ejercicio Fisico y la Activacion del Tejido Adiposo Pardo: en Busca de Nuevas Dianas Terapeuticas en la Comunicacion Intercelular" - "Consejeria de Economia, Conocimiento, Empresas y Universidad, Junta de Andalucia", PY18-4455

Altres ajuts: a PIF PhD fellowship from the Universitat Autònoma de Barcelona (Spain) to CGD, and a Beatriu de Pinós Postdoctoral fellowship by the Commission for Universities and Research of the Ministry of Innovation, Universities and Enterprise of the Autonomous Government of Catalonia and the Cofund programme of the Marie Curie Actions of the FP7 to JILL. ; Despite many years of study into inversions, very little is known about their functional consequences, especially in humans. A common hypothesis is that the selective value of inversions stems in part from their effects on nearby genes, although evidence of this in natural populations is almost nonexistent. Here we present a global analysis of a new 415-kb polymorphic inversion that is among the longest ones found in humans and is the first with clear position effects. This inversion is located in chromosome 19 and has been generated by non-homologous end joining between blocks of transposable elements with low identity. PCR genotyping in 541 individuals from eight different human populations allowed the detection of tag SNPs and inversion genotyping in multiple populations worldwide, showing that the inverted allele is mainly found in East Asia with an average frequency of 4.7%. Interestingly, one of the breakpoints disrupts the transcription factor gene ZNF257, causing a significant reduction in the total expression level of this gene in lymphoblastoid cell lines. RNA-Seq analysis of the effects of this expression change in standard homozygotes and inversion heterozygotes revealed distinct expression patterns that were validated by quantitative RT-PCR. Moreover, we have found a new fusion transcript that is generated exclusively from inverted chromosomes around one of the breakpoints. Finally, by the analysis of the associated nucleotide variation, we have estimated that the inversion was generated ~40,000-50,000 years ago and, while a neutral evolution cannot be ruled out, its current frequencies are more consistent with those expected for a deleterious variant, although no significant association with phenotypic traits has been found so far.

Inversions are one type of structural variants linked to phenotypic differences and adaptation in multiple organisms. However, there is still very little information about polymorphic inversions in the human genome due to the difficulty of their detection. Here, we develop a new high-throughput genotyping method based on probe hybridization and amplification, and we perform a complete study of 45 common human inversions of 0.1-415 kb. Most inversions promoted by homologous recombination occur recurrently in humans and great apes and they are not tagged by SNPs. Furthermore, there is an enrichment of inversions showing signatures of positive or balancing selection, diverse functional effects, such as gene disruption and gene-expression changes, or association with phenotypic traits. Therefore, our results indicate that the genome is more dynamic than previously thought and that human inversions have important functional and evolutionary consequences, making possible to determine for the first time their contribution to complex traits. ; This work was supported by research grants ERC Starting Grant 243212 (INVFEST) from the European Research Council under the European Union Seventh Research Framework Programme (FP7), BFU2013-42649-P and BFU2016-77244-R funded by the Agencia Estatal de Investigación (AEI, Spain) and the European Regional Development Fund (FEDER, EU), and 2014-SGR-1346 and 2017-SGR-1379 from the Generalitat de Catalunya (Spain) to M.C., a PIF PhD fellowship from the Universitat Autònoma de Barcelona (Spain) to C.G.D., a La Caixa Doctoral fellowship to J.L.J., and a FPI PhD fellowship from the Ministerio de Economía y Competitividad (Spain) to M.O. and I.N. M.G.V. was supported in part by POCI-01-0145-FEDER-006821 funded through the Operational Programme for Competitiveness Factors (COMPETE, EU) and UID/BIA/50027/2013 from the Foundation for Science and Technology (FCT, Portugal).

Inversions are one type of structural variants linked to phenotypic differences and adaptation in multiple organisms. However, there is still very little information about polymorphic inversions in the human genome due to the difficulty of their detection. Here, we develop a new high-throughput genotyping method based on probe hybridization and amplification, and we perform a complete study of 45 common human inversions of 0.1-415 kb. Most inversions promoted by homologous recombination occur recurrently in humans and great apes and they are not tagged by SNPs. Furthermore, there is an enrichment of inversions showing signatures of positive or balancing selection, diverse functional effects, such as gene disruption and gene-expression changes, or association with phenotypic traits. Therefore, our results indicate that the genome is more dynamic than previously thought and that human inversions have important functional and evolutionary consequences, making possible to determine for the first time their contribution to complex traits. ; This work was supported by research grants ERC Starting Grant 243212 (INVFEST) from the European Research Council under the European Union Seventh Research Framework Programme (FP7), BFU2013-42649-P and BFU2016-77244-R funded by the Agencia Estatal de Investigación (AEI, Spain) and the European Regional Development Fund (FEDER, EU), and 2014-SGR-1346 and 2017-SGR-1379 from the Generalitat de Catalunya (Spain) to M.C., a PIF PhD fellowship from the Universitat Autònoma de Barcelona (Spain) to C.G.D., a La Caixa Doctoral fellowship to J.L.J., and a FPI PhD fellowship from the Ministerio de Economía y Competitividad (Spain) to M.O. and I.N. M.G.V. was supported in part by POCI-01-0145-FEDER-006821 funded through the Operational Programme for Competitiveness Factors (COMPETE, EU) and UID/BIA/50027/2013 from the Foundation for Science and Technology (FCT, Portugal).