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241.
V Vegesna H R Withers H D Thames K Mason 《International journal of radiation biology and related studies in physics, chemistry, and medicine》1985,47(4):413-422
The response of mouse lung to repeated doses of 60Co gamma-rays of as low as 115 cGy per fraction was measured using death from pneumonitis between 80 and 120 days after irradiation as the endpoint. A fractionation interval of 3 h was maintained for most regimens but in the longer experiments some 12 h intervals were introduced for logistic reasons. The longest overall duration (for a 43 fraction regimen) was 8 days. The total doses required to produce 50 per cent mortality increased continuously as dose/fraction was decreased, even from 160 to 115 cGy per fraction. Of clinical relevance, the steepness of the isoeffect curve over the dose range 115-500 cGy indicates that the lung shows greater sparing from dose fractionation than is characteristic of more rapidly-responding normal tissues, resembling, in this respect, other more slowly-responding tissues such as spinal cord. The plot of the reciprocal of the LD50 values as a function of dose per fraction was non-linear, suggesting that a linear quadratic dose response model may not be appropriate or that repair of cellular injury in lung is not complete in 3 h, or both. 相似文献
242.
K van Oers A W Santure I De Cauwer N EM van Bers R PMA Crooijmans B C Sheldon M E Visser J Slate M AM Groenen 《Heredity》2014,112(3):307-316
Linking variation in quantitative traits to variation in the genome is an important, but
challenging task in the study of life-history evolution. Linkage maps provide a valuable
tool for the unravelling of such trait−gene associations. Moreover, they give
insight into recombination landscapes and between-species karyotype evolution. Here we
used genotype data, generated from a 10k single-nucleotide polymorphism (SNP) chip, of
over 2000 individuals to produce high-density linkage maps of the great tit (Parus
major), a passerine bird that serves as a model species for ecological and
evolutionary questions. We created independent maps from two distinct populations: a
captive F2-cross from The Netherlands (NL) and a wild population from the United Kingdom
(UK). The two maps contained 6554 SNPs in 32 linkage groups, spanning 2010 cM and
1917 cM for the NL and UK populations, respectively, and were similar in size and
marker order. Subtle levels of heterochiasmy within and between chromosomes were
remarkably consistent between the populations, suggesting that the local departures from
sex-equal recombination rates have evolved. This key and surprising result would have been
impossible to detect if only one population was mapped. A comparison with zebra finch
Taeniopygia guttata, chicken Gallus gallus and the green anole lizard
Anolis carolinensis genomes provided further insight into the evolution of
avian karyotypes. 相似文献
243.
A discrete time state vector model (the Hahn model) has been used to simulate many experiments in cell kinetics. In the first paper in this series the authors described a new method to define the parameters of the Hahn model suitable for use in automatic fitting of fraction of labelled mitoses (FLM) experiments. In this paper it is shown how to compute the first three moments of the transit time distribution which arises from a Hahn model. These moments are compared analytically and numerically to the corresponding moments of the distribution the authors used to define the Hahn model. Finally, the problems involved in estimating the moments of the transit time distribution observed in fitting FLM data using a Hahn model are discussed. 相似文献
244.
245.
In this paper the elements of the matrix of the Hahn cell-cycle model are identified with the infinitesimal transition probabilities of a Markov process, and as a limiting process a differential equation analogue is derived. The probability density function of the discrete time model is derived and used to obtain the density function for transit times of the continuous time model. It is shown that the mean transit time remains constant and that the variances of the discrete and continuous time models are the same to the order of the time increment. Finally, it is shown how to derive the Takahashi model from the continuous time Hahn model. 相似文献
246.
247.
248.
Background
Pelodera (Rhabditis) strongyloides is a small saprophytic nematode that lives in decaying organic matter. On rare occasions, it can invade the mammalian skin, causing a pruritic, erythematous, alopecic and crusting dermatitis on skin sites that come into contact with the ground. Diagnosis of the disease is based on case history (a dog living outdoors on damp straw bedding) with characteristic skin lesions and on the demonstration of typical larvae in skin scrapings or biopsy. Pelodera (rhabditic) dermatitis cases have been reported mainly from Central European countries and the United States. 相似文献249.
250.
In this paper we study the Hahn model of the cell cycle from the point of view that a cell population's age distribution is more relevant to labeled mitoses data than is the distribution of its transit times.Closed-form relationships are derived between the transition probabilities of the Hahn model and the transit time of the mean of a cohort of labeled cells (with the variance of their transit time through mitosis). Constraints result which define the acceptable values for the number of ages in the state vector and the length of the time step (rarely does the dimension of the state vector equal the number of time steps in the generation time).A generalization to distinct probabilities for G1, S and G2M is presented, and the automatic fitting of fraction-labeled mitoses (FLM) data is described. The doubling time of the population is used to define the daughter factor, via the largest eigenvalue of the state transition matrix. The performance of the generalized Hahn model is compared to that of other commonly used fitting methods using two sets of FLM data from the literature. The synthesis of continuous labeling curves is discussed as an independent check of the parametrization. Based on the stable age distribution resulting from fits to experimental FLM data, it is shown that a nonlinear relationship exists between biological age and time. 相似文献