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1.
Two-Dimensional Diffusion Limited System For Cell Growth 总被引:1,自引:0,他引:1
Abstract. A new cell system, designed to supplement multicellular spheroids as tumour analogues, was analysed theoretically and experimentally. This 'sandwich' system is a single layer of cells, subject to self-created gradients of nutrients and metabolic products. Due to these gradients the sandwich system develops a border of viable cells and an inner region of necrotic cells corresponding to the viable rim and the necrotic center of a spheroid. However, sandwiches differ from spheroids in several ways. All the cells in the sandwich can be microscopically viewed during the entire experiment. In sandwiches there is no three-dimensional cell to cell contact. Also, the gradients are less steep in our sandwich system, so the width of the viable region in a sandwich is about 10 times as large as the width of the viable rim in a spheroid. Indeed, in sandwiches the experimenter has some control over the steepness of the gradients and thus can vary the width of this viable border. We used DNA labelling studies and flow cytometry along with visual observation to analyse the system. Our experiments show that the observed cell necrosis, similar to that found in spheroids, is due to diffusion limitations. the results are consistent with the idea that oxygen deprivation stops cell cycling and, when extreme and prolonged, leads to necrosis. the possibility that substances other than oxygen are involved is not excluded by the data. the data also suggests that in the final, near-equilibrium state the average overall oxygen consumption rate for the viable sandwich population may be about one-quarter of that for an exponentially growing population of the same cell line. 相似文献
2.
Michael J Stobart Debra Parchaliuk Sharon LR Simon Jillian LeMaistre Jozef Lazar Richard Rubenstein J David Knox 《Molecular neurodegeneration》2007,2(1):1-13
Background
Alzheimer's disease (AD) is characterized by a decline in cognitive function and accumulation of amyloid-β peptide (Aβ) in extracellular plaques. Mutations in amyloid precursor protein (APP) and presenilins alter APP metabolism resulting in accumulation of Aβ42, a peptide essential for the formation of amyloid deposits and proposed to initiate the cascade leading to AD. However, the role of Aβ40, the more prevalent Aβ peptide secreted by cells and a major component of cerebral Aβ deposits, is less clear. In this study, virally-mediated gene transfer was used to selectively increase hippocampal levels of human Aβ42 and Aβ40 in adult Wistar rats, allowing examination of the contribution of each to the cognitive deficits and pathology seen in AD.Results
Adeno-associated viral (AAV) vectors encoding BRI-Aβ cDNAs were generated resulting in high-level hippocampal expression and secretion of the specific encoded Aβ peptide. As a comparison the effect of AAV-mediated overexpression of APPsw was also examined. Animals were tested for development of learning and memory deficits (open field, Morris water maze, passive avoidance, novel object recognition) three months after infusion of AAV. A range of impairments was found, with the most pronounced deficits observed in animals co-injected with both AAV-BRI-Aβ40 and AAV-BRI-Aβ42. Brain tissue was analyzed by ELISA and immunohistochemistry to quantify levels of detergent soluble and insoluble Aβ peptides. BRI-Aβ42 and the combination of BRI-Aβ40+42 overexpression resulted in elevated levels of detergent-insoluble Aβ. No significant increase in detergent-insoluble Aβ was seen in the rats expressing APPsw or BRI-Aβ40. No pathological features were noted in any rats, except the AAV-BRI-Aβ42 rats which showed focal, amorphous, Thioflavin-negative Aβ42 deposits.Conclusion
The results show that AAV-mediated gene transfer is a valuable tool to model aspects of AD pathology in vivo, and demonstrate that whilst expression of Aβ42 alone is sufficient to initiate Aβ deposition, both Aβ40 and Aβ42 may contribute to cognitive deficits. 相似文献3.
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Carcinogenesis and cancer progression are often modeled using population dynamics equations for a diverse somatic cell population
undergoing mutations or other alterations that alter the fitness of a cell and its progeny. Usually it is then assumed, paralleling
standard mathematical approaches to evolution, that such alterations are slow compared to selection, i.e., compared to subpopulation
frequency changes induced by unequal subpopulation proliferation rates. However, the alterations can be rapid in some cases.
For example, results in our lab on in vitro analogues of transformation and progression in carcinogenesis suggest there could
be periods where rapid alterations triggered by horizontal intercellular transfer of genetic material occur and quickly result
in marked changes of cell population structure.
We here initiate a mathematical study of situations where alterations are rapid compared to selection. A classic selection-mutation
formalism is generalized to obtain a “proliferation-alteration” system of ordinary differential equations, which we analyze
using a rapid-alteration approximation. A system-theoretical estimate of the total-population net growth rate emerges. This
rate characterizes the diverse, interacting cell population acting as a single system; it is a weighted average of subpopulation
rates, the weights being components of the Perron–Frobenius eigenvector for an ergodic Markov-process matrix that describes
alterations by themselves. We give a detailed numerical example to illustrate the rapid-alteration approximation, suggest
a possible interpretation of the fact that average aneuploidy during cancer progression often appears to be comparatively
stable in time, and briefly discuss possible generalizations as well as weaknesses of our approach. 相似文献
6.
Claudia G Petersen Fabiana C Massaro Ana L Mauri Joao BA Oliveira Ricardo LR Baruffi Jose G FrancoJr 《Reproductive biology and endocrinology : RB&E》2010,8(1):149
Background
The present study aimed to evaluate the efficacy of the hyaluronic acid (HA) binding assay in the selection of motile spermatozoa with normal morphology at high magnification (8400x). 相似文献7.
Ponomarev AL Belli M Hahnfeldt PJ Hlatky L Sachs RK Cucinotta FA 《Radiation and environmental biophysics》2007,46(2):155-160
The non-random distribution of DNA breakage in pulsed-field gel electrophoresis (PFGE) experiments poses a problem of proper subtraction of the background damage to obtain a fragment-size distribution due to radiation only. As been pointed out by various authors, a naive bin-to-bin subtraction of the background signal will not result in the right DNA mass distribution histogram, and may even result in negative values. Previous more systematic subtraction methods have been based mainly on random breakage, appropriate for low-LET radiation but problematic for high LET. Moreover, an investigation is needed whether the background breakage itself is random or non-random. Previously a new generalized formalism based on stochastic processes for the subtraction of the background damage in PFGE experiments for any LET and any background was proposed, and as now applied it to a set of PFGE data for Fe ions. We developed a Monte Carlo algorithm to compare the naïve subtraction procedure in artificial data sets to the result produced by the new formalism. The simulated data corresponded to various cases, involving non-random (high-LET) or random radiation breakage and random or non-random background breakage. The formalism systematically gives better results than naïve bin-by-bin subtraction in all these artificial data sets. 相似文献
8.
Ponomarev AL Belli M Hahnfeldt PJ Hlatky L Sachs RK Cucinotta FA 《Radiation research》2006,166(6):908-916
The non-random distribution of DNA breakage in PFGE (pulsed-field gel electrophoresis) experiments poses a problem of proper subtraction of the background DNA damage to obtain a fragment-size distribution due to radiation only. A naive bin-to-bin subtraction of the background signal will not result in the right DNA mass distribution histogram. This problem could become more pronounced for high-LET (linear energy transfer) radiation, because the fragment-size distribution manifests a higher frequency of smaller fragments. Previous systematic subtraction methods have been based on random breakage, appropriate for low-LET radiation. Moreover, an investigation is needed to determine whether the background breakage is itself random or non-random. We consider two limiting cases: (1) the background damage is present in all cells, and (2) it is present in only a small subset of cells, while other cells are not contributing to the background DNA fragmentation. We give a generalized formalism based on stochastic processes for the subtraction of the background damage in PFGE experiments for any LET and apply it to two sets of PFGE data for iron ions. 相似文献
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