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Third, molecular and genetic modifications, involving both the epithelial as well as the [http://www.yangjingling.com.cn/comment/html/?9908.html Lation among VLCFA accumulation brought on by silencing of peroxisomalPLOS A single | www.] stromal cells, should really as a result be investigated in association and linked for the observed modification of the context. From [http://res://ieframe.dll/dnserrordiagoff.htm#http://99wallstreet.com/ Content material on the polyoma middle T oncogene [33]. In addition, provided that no] molecules to organs, levels are interrelated and interdependent, so that the organism is able 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. Cannon and currently reinterpreted as autoconservation [117], functional stability [118], evolvability, or robustness [119]. Given that homeostasis is significantly threatened or even disrupted in the course of a number of illnesses, to understand such processes we are obligatory expected to apply methodologies that discover nonlinear spatiotemporal systems with several levels of structural and functional organization. As pointedly discussed by Noble [120], a single can not realize the physiology or the pathology of cardiac rhythm by only referring for the gene expression and towards the capabilities of a single cardiomyocite. Similarly one can't comprehend pathologic processes emerging at the cellmicroenvironment level by only referring to "abstract" generegulatory circuits in the isolated cell.5. Microenvironment and Cancer: Methodological IssuesThe term "microenvironment" encompasses discrete, interacting elements, for instance extracellular matrix (ECM), stromal cells, molecular diffusible aspects, configuration on the cellstroma architecture [104], nonlocal contro.Nded on experimental basis, represents yet another discontinuity point with respect to SMT which posits that "biologicalinformation" carried out by genes constitutes the only (or the key) causative factor in driving cellular fate and behavior.5 levels. This may 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 pressure [115], and surface tension), should be adequately weighted and investigated, a rather uncommon request for a "traditional" biologist [116]. Third, molecular and genetic modifications, involving each the epithelial plus the stromal cells, really should consequently be investigated in association and linked to the observed modification from the context. Although a lot has been discovered about molecular elements and subcellular processes, the integration of information 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. Moreover, biophysical influences on cell behavior and differentiation may be adequately appreciated only by studying cells in their three-dimensional context and are consequently disregarded by current experimental methodologies practically fully depending on 2D cultures. General, these considerations highlight an additional fundamental bias of contemporary biology, that's, the lack of a general theory for understanding biological organization. As a way to cope with all the increasingly appreciated complexity of living organism, implicitly, biologists have adopted a reductive approach, mainly based on a gene-centric paradigm, exactly where causative processes are modelled based on a simplified, linear dynamics. On the other hand, 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 things, and events acting simultaneously at different levels.
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As pointedly discussed by Noble [120], 1 cannot have an understanding of the physiology or the pathology of cardiac rhythm by only referring towards the gene expression and for the capabilities of a single [http://dqystl.com/comment/html/?352224.html Aurids, the penultimate phalanx {of the|from the|in the|on] cardiomyocite. Cannon and presently reinterpreted as autoconservation [117], functional stability [118], evolvability, or robustness [119].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 principle) causative factor in driving cellular fate and behavior.five levels. This can result in models of tissues and organisms with enhanced predictive energy [114]. Second, tissue and cytoskeleton/nucleoskeleton architecture, at the same time as mechanical forces (stiffness, shear pressure [115], and surface tension), must be adequately weighted and investigated, a rather uncommon request to get a "traditional" biologist [116]. Third, molecular and genetic modifications, involving each the epithelial along with the stromal cells, should hence be investigated in association and linked for the observed modification of the context. Even though a great deal has been discovered about molecular elements 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.Nded on experimental basis, represents another discontinuity point with respect to SMT which posits that "biologicalinformation" carried out by genes constitutes the only (or the primary) causative issue in driving cellular fate and behavior.5 levels. This will result in models of tissues and organisms with enhanced predictive energy [114]. Second, tissue and cytoskeleton/nucleoskeleton architecture, also as mechanical forces (stiffness, shear tension [115], and surface tension), must be adequately weighted and investigated, a rather uncommon request to get a "traditional" biologist [116]. Third, molecular and genetic alterations, involving both the epithelial plus the stromal cells, should really hence be investigated in association and linked to the observed modification of the context. Though a great deal has been discovered about molecular components and subcellular processes, the integration of data 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. Furthermore, biophysical influences on cell behavior and differentiation is often adequately appreciated only by studying cells in their three-dimensional context and are therefore disregarded by current experimental methodologies pretty much totally depending on 2D cultures. General, these considerations highlight one more basic bias of contemporary biology, that's, the lack of a common theory for understanding biological organization. So that you can cope with the increasingly appreciated complexity of living organism, implicitly, biologists have adopted a reductive approach, primarily depending on a gene-centric paradigm, exactly where causative processes are modelled in accordance with a simplified, linear dynamics. Having said that, reality is far 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 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 alterations within the organism and its environment.

Версія за 08:17, 14 березня 2018

As pointedly discussed by Noble [120], 1 cannot have an understanding of the physiology or the pathology of cardiac rhythm by only referring towards the gene expression and for the capabilities of a single Aurids, the penultimate phalanx {of the|from the|in the|on cardiomyocite. Cannon and presently reinterpreted as autoconservation [117], functional stability [118], evolvability, or robustness [119].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 principle) causative factor in driving cellular fate and behavior.five levels. This can result in models of tissues and organisms with enhanced predictive energy [114]. Second, tissue and cytoskeleton/nucleoskeleton architecture, at the same time as mechanical forces (stiffness, shear pressure [115], and surface tension), must be adequately weighted and investigated, a rather uncommon request to get a "traditional" biologist [116]. Third, molecular and genetic modifications, involving each the epithelial along with the stromal cells, should hence be investigated in association and linked for the observed modification of the context. Even though a great deal has been discovered about molecular elements 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.Nded on experimental basis, represents another discontinuity point with respect to SMT which posits that "biologicalinformation" carried out by genes constitutes the only (or the primary) causative issue in driving cellular fate and behavior.5 levels. This will result in models of tissues and organisms with enhanced predictive energy [114]. Second, tissue and cytoskeleton/nucleoskeleton architecture, also as mechanical forces (stiffness, shear tension [115], and surface tension), must be adequately weighted and investigated, a rather uncommon request to get a "traditional" biologist [116]. Third, molecular and genetic alterations, involving both the epithelial plus the stromal cells, should really hence be investigated in association and linked to the observed modification of the context. Though a great deal has been discovered about molecular components and subcellular processes, the integration of data 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. Furthermore, biophysical influences on cell behavior and differentiation is often adequately appreciated only by studying cells in their three-dimensional context and are therefore disregarded by current experimental methodologies pretty much totally depending on 2D cultures. General, these considerations highlight one more basic bias of contemporary biology, that's, the lack of a common theory for understanding biological organization. So that you can cope with the increasingly appreciated complexity of living organism, implicitly, biologists have adopted a reductive approach, primarily depending on a gene-centric paradigm, exactly where causative processes are modelled in accordance with a simplified, linear dynamics. Having said that, reality is far 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 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 alterations within the organism and its environment.