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71.
C. Owen Lovejoy Albert H. Burstein Kingsbury G. Heiple 《American journal of physical anthropology》1976,44(3):489-505
Traditional methods of bone analysis (both metric and topographic) are restricted to external characters. Spacial distribution of material is, however, equally critical to an understanding of a bone's function. Dynamic testing to determine whole bone strength can only be performed on fresh specimens. Methods for the calculation of both bending and torsional strength of other specimens (such as preserved or fossil bones) are developed in this paper. In order to illustrate the methods, the functional significance of tibial shaft cross sectional variation is investigated. 相似文献
72.
A quantitative approach to the analysis of long-bone fractures in skeletal populations is presented. These kinds of data are shown to be valuable in interpreting various behavioral aspects of the population. An example of application is provided for the Libben population. Data from this group show that the overall fracture rate was high (there is a 45% chance of a long-bone fracture in any single individual) but lower than the rates observed in nonhuman primates by almost an order of magnitude when data are adjusted for years of risk. The data for Libben also suggest that traumatic child abuse was not practiced, that most fractures occur as a consequence of accident, that fracture risk was highest in the 10–25 and 45 + age categories, that care of patients was enlightened and skillful in this group, and that chance of fracture is largely determined by accumulated years of risk in the population (r = 0.97). 相似文献
73.
Genetic control of scrapie and Creutzfeldt-Jakob disease in mice 总被引:10,自引:0,他引:10
D T Kingsbury K C Kasper D P Stites J D Watson R N Hogan S B Prusiner 《Journal of immunology (Baltimore, Md. : 1950)》1983,131(1):491-496
Genetic control of experimental scrapie and Creutzfeldt-Jakob disease (CJD) was studied in inbred strains of mice by measuring the times from intracerebral inoculation with the agents to the onset of neurological dysfunction. Every strain of mice examined was susceptible to infection; however, a wide range of incubation times was found for both scrapie and CJD. New Zealand (NZ) mice, which eventually develop an autoimmune disorder, were inoculated intracerebrally with 10(6) ID50 units of the scrapie agent in a Chandler isolate. NZW mice showed incubation periods of less than 95 days; this is the shortest period recorded for any murine host with scrapie. In NZB and NZB X W F1 mice, the incubation periods were approximately 130 days and were similar to those in BALB/c and C57BL mice. Male and female NZ mice exhibited scrapie incubation periods of the same length. Similar results were obtained when B10.Q and C57BL/6J mice were inoculated intracerebrally with 10(4) ID50 units of the CJD agent in a K.Fu. isolate. These observations define a genetic locus or loci controlling the length of scrapie and CJD incubation periods; alleles coding for longer incubation times appear to be autosomal dominant. When congenic mice with a C57BL/10J background differing only in their H-2 haplotypes were studied, the results showed that the D subregion of the H-2 complex played a central role in controlling the length of the CJD incubation period. The q allele at the D subregion resulted in shorter incubation times, whereas the d allele resulted in long incubation times. The p, s, b, and k alleles gave intermediate incubation times. We propose the symbol PID-1 for designating this genetic locus which is located within the D subregion of the major histocompatibility (H-2) complex on murine chromosome 17. In addition, observations on congenic mice provide evidence for the influence of sex on CJD incubation periods. In some strains of inbred mice, males showed significantly shorter incubation periods compared with those for females with experimental CJD. These studies with inbred mice have defined previously unrecognized genes that control the length of scrapie and CJD incubation periods. 相似文献
74.
Newcastle disease virus RNA. I. Isolation and preliminary characterization of RNA from virus particles 总被引:23,自引:0,他引:23
D W Kingsbury 《Journal of molecular biology》1966,18(1):195-203
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Differences in soil characteristics between field and forest may influence the distribution of an invasive earthworm
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In northern North America, invasive earthworms (including the nightcrawler Lumbricus terrestris) have been dispersing from points of introduction and dramatically affecting soil structure, soil food webs, and forest floor dynamics. However, little is known about the factors influencing the local distribution of invasive earthworms south of the Wisconsinan glaciation. Earthworms were sampled at suspected sites of introduction near Mountain Lake Biological Field Station, Virginia, USA. The density of invasive earthworms decreased as distance from suspected sites of introduction increased; native earthworms displayed the opposite relationship. However, the distance that L. terrestris was found into the forest was less than expected given dispersal rates calculated from more northern invasions. We also found correlations among population densities of L. terrestris and physical–chemical properties of the soil, and differences between field and forest soils in terms of temperature, moisture, and soil chemical properties. We conducted two experiments to analyze some factors possibly responsible for the observed distribution: (1) temperature and moisture, and (2) soil type (field vs. forest) and food resources. Our results suggest that L. terrestris may not disperse as far into forested habitats of the Southern Appalachians compared to northern forests due to local physical‐chemical soil characteristics. 相似文献
79.
Krueger AC Madigan DL Beno DW Betebenner DA Carrick R Green BE He W Liu D Maring CJ McDaniel KF Mo H Molla A Motter CE Pilot-Matias TJ Tufano MD Kempf DJ 《Bioorganic & medicinal chemistry letters》2012,22(6):2212-2215
The synthesis of several pyrido[2,3-d]pyrimidine and pyrimido[4,5-d]pyrimidine analogs is described with one such analog possessing subnanomolar potency in both genotype 1a and 1b cell culture HCV replicon assays. 相似文献
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