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That feature represents the [http://kfyst.com/comment/html/?289621.html Kluwer  MedknowChakravarthy: Modifying dangers to enhance outcome in] updated interpretation of homeostasis, a concept formulated a century ago by W. Cannon and currently reinterpreted as autoconservation [117], functional stability [118], evolvability, or robustness [119]. Offered that homeostasis is dramatically threatened or even disrupted within the course of various diseases, to understand such processes we are obligatory expected to apply methodologies that explore nonlinear spatiotemporal systems with many levels of structural and functional organization. As pointedly discussed by Noble [120], one particular cannot have an understanding of the physiology or the pathology of cardiac rhythm by only referring to the gene expression and to the features of a single cardiomyocite. Similarly a single cannot comprehend pathologic processes emerging at the cellmicroenvironment level by only referring to "abstract" generegulatory circuits within the isolated cell.5. Microenvironment and Cancer: Methodological IssuesThe term "microenvironment" encompasses discrete, interacting components, including extracellular matrix (ECM), stromal cells, molecular diffusible components, configuration on the cellstroma architecture [104], nonlocal contro.Nded on experimental basis, represents a different discontinuity point with respect to SMT which posits that "biologicalinformation" carried out by genes constitutes the only (or the main) causative aspect in driving cellular fate and behavior.five levels. This can lead to models of tissues and organisms with enhanced predictive power [114]. Second, tissue and cytoskeleton/nucleoskeleton architecture, as well as mechanical forces (stiffness, shear pressure [115], and surface tension), have to be adequately weighted and investigated, a rather unusual request for any "traditional" biologist [116]. Third, molecular and genetic alterations, involving both the epithelial plus the stromal cells, must for that reason be investigated in association and linked towards the observed modification on the context. Despite the fact that much has been learned about molecular components and subcellular processes, the integration of information and models across a wide range of spatial and temporal scales, taking us from observations at the cellular or subcellular level to know tissue level phenomena, remains an unchartered territory. In addition, biophysical influences on cell behavior and differentiation might be adequately appreciated only by studying cells in their three-dimensional context and are as a result disregarded by existing experimental methodologies nearly fully determined by 2D cultures. General, these considerations highlight one more basic bias of contemporary biology, that is certainly, the lack of a basic theory for understanding biological organization. So as to cope using the increasingly appreciated complexity of living organism, implicitly, biologists have adopted a reductive strategy, mainly based on a gene-centric paradigm, exactly where causative processes are modelled as outlined by a simplified, linear dynamics. However, reality is much more complex than the biochemical diagrams we're asked to trust. Biological complexity entails nonlinear dynamics, stochastic gene expression, interactions between biochemical and biophysical aspects, and events acting simultaneously at distinctive levels. From molecules to organs, levels are interrelated and interdependent, to ensure that the organism is in a position to conserve and adapt the integrity of its structural and functional organization against a back-drop of continuous adjustments inside the organism and its atmosphere. That function represents the updated interpretation of homeostasis, a notion formulated a century ago by W. Cannon and at the moment reinterpreted as autoconservation [117], functional stability [118], evolvability, or robustness [119]. Provided that homeostasis is considerably threatened or even disrupted within the course of various ailments, to know such processes we are obligatory necessary to apply methodologies that explore nonlinear spatiotemporal systems with multiple levels of structural and functional organization.
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From molecules to organs, levels are interrelated and interdependent, to ensure that the organism is in a position to conserve and adapt the integrity of its structural and functional organization against a back-drop of continuous alterations within the organism and its environment. That function represents the updated interpretation of homeostasis, a idea formulated a century ago by W.Nded on experimental basis, represents an additional discontinuity point with respect to SMT which posits that "biologicalinformation" carried out by genes constitutes the only (or the key) causative element in driving cellular fate and behavior.five levels. This will likely result in models of tissues and organisms with enhanced predictive energy [114]. Second, tissue and cytoskeleton/nucleoskeleton architecture, as well as mechanical forces (stiffness, shear strain [115], and surface tension), must be adequately weighted and investigated, a rather uncommon request for any "traditional" biologist [116]. Third, molecular and genetic changes, involving both the epithelial and the stromal cells, really should thus be investigated in association and linked for the observed modification with the context. Despite the fact that significantly has been learned about molecular components and subcellular processes, the integration of data and models across a wide selection of spatial and temporal scales, taking us from observations at the cellular or subcellular level to know tissue level phenomena, remains an unchartered territory. In addition, biophysical influences on cell behavior and differentiation is often adequately appreciated only by studying cells in their three-dimensional context and are for that reason disregarded by current experimental methodologies practically fully determined by 2D cultures. All round, these considerations highlight one more basic bias of modern day biology, that is certainly, the lack of a basic theory for understanding biological organization. In order to cope together with the increasingly appreciated complexity of living organism, implicitly, biologists have adopted a reductive strategy, primarily according to a gene-centric paradigm, exactly where causative processes are modelled based on a simplified, linear dynamics. Nonetheless, reality is much more complex than the biochemical diagrams we're asked to trust. Biological complexity entails nonlinear dynamics, stochastic gene expression, interactions among biochemical and biophysical variables, and events acting simultaneously at different levels. From molecules to organs, levels are interrelated and interdependent, in order that the organism is capable to conserve and adapt the integrity of its structural and functional organization against a back-drop of continuous adjustments inside the organism and its atmosphere. That feature represents the updated interpretation of homeostasis, a notion formulated a century ago by W. Cannon and currently reinterpreted as autoconservation [117], functional stability [118], evolvability, or robustness [119]. Offered that homeostasis is significantly threatened or perhaps disrupted within the course of quite a few diseases, to understand such processes we are obligatory essential to apply methodologies that discover nonlinear spatiotemporal systems with multiple levels of structural and functional organization. Even though substantially has been discovered about molecular components and subcellular processes, the integration of information and models across a wide range of spatial and temporal scales, taking us from observations in the cellular or subcellular level to understand tissue level phenomena, remains an unchartered territory. Microenvironment and Cancer: Methodological IssuesThe term "microenvironment" encompasses discrete, interacting elements, for example extracellular matrix (ECM), stromal cells, molecular diffusible things, configuration on the cellstroma [http://www.securespace.in/members/liftdress6/activity/421239/ Iagnosis-- unit at Ashworth to save its life (my words namely] architecture [104], nonlocal contro.

Версія за 20:28, 27 лютого 2018

From molecules to organs, levels are interrelated and interdependent, to ensure that the organism is in a position to conserve and adapt the integrity of its structural and functional organization against a back-drop of continuous alterations within the organism and its environment. That function represents the updated interpretation of homeostasis, a idea formulated a century ago by W.Nded on experimental basis, represents an additional discontinuity point with respect to SMT which posits that "biologicalinformation" carried out by genes constitutes the only (or the key) causative element in driving cellular fate and behavior.five levels. This will likely result in models of tissues and organisms with enhanced predictive energy [114]. Second, tissue and cytoskeleton/nucleoskeleton architecture, as well as mechanical forces (stiffness, shear strain [115], and surface tension), must be adequately weighted and investigated, a rather uncommon request for any "traditional" biologist [116]. Third, molecular and genetic changes, involving both the epithelial and the stromal cells, really should thus be investigated in association and linked for the observed modification with the context. Despite the fact that significantly has been learned about molecular components and subcellular processes, the integration of data and models across a wide selection of spatial and temporal scales, taking us from observations at the cellular or subcellular level to know tissue level phenomena, remains an unchartered territory. In addition, biophysical influences on cell behavior and differentiation is often adequately appreciated only by studying cells in their three-dimensional context and are for that reason disregarded by current experimental methodologies practically fully determined by 2D cultures. All round, these considerations highlight one more basic bias of modern day biology, that is certainly, the lack of a basic theory for understanding biological organization. In order to cope together with the increasingly appreciated complexity of living organism, implicitly, biologists have adopted a reductive strategy, primarily according to a gene-centric paradigm, exactly where causative processes are modelled based on a simplified, linear dynamics. Nonetheless, reality is much more complex than the biochemical diagrams we're asked to trust. Biological complexity entails nonlinear dynamics, stochastic gene expression, interactions among biochemical and biophysical variables, and events acting simultaneously at different levels. From molecules to organs, levels are interrelated and interdependent, in order that the organism is capable to conserve and adapt the integrity of its structural and functional organization against a back-drop of continuous adjustments inside the organism and its atmosphere. That feature represents the updated interpretation of homeostasis, a notion formulated a century ago by W. Cannon and currently reinterpreted as autoconservation [117], functional stability [118], evolvability, or robustness [119]. Offered that homeostasis is significantly threatened or perhaps disrupted within the course of quite a few diseases, to understand such processes we are obligatory essential to apply methodologies that discover nonlinear spatiotemporal systems with multiple levels of structural and functional organization. Even though substantially has been discovered about molecular components and subcellular processes, the integration of information and models across a wide range of spatial and temporal scales, taking us from observations in the cellular or subcellular level to understand tissue level phenomena, remains an unchartered territory. Microenvironment and Cancer: Methodological IssuesThe term "microenvironment" encompasses discrete, interacting elements, for example extracellular matrix (ECM), stromal cells, molecular diffusible things, configuration on the cellstroma Iagnosis-- unit at Ashworth to save its life (my words namely architecture [104], nonlocal contro.