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1.
Inbreeding is defined as mating between individuals related by common ancestry. Thus, the degree to which a particular mating is inbred depends on how far back in a pedigree one begins counting common ancestors. In general practice, the term inbreeding is used to describe mating between close relatives (first cousins or closer). Animal breeders have known for centuries that inbreeding causes a loss of constitutional vigor and fertility in domestic livestock. A growing literature now demonstrates that the offspring of matings between close relatives in species of undomesticated birds and mammals are less fit than outbred offspring. The deleterious consequences of inbreeding suggest the possibility that many species have evolved behaviors that lower the frequency of inbreeding. 相似文献
2.
The in vitro activity of several new imidazoles, cloconazole, sulconazole, butoconazole, isoconazole and fenticonazole, were compared with those of amphothericin B, flucytosine, and three azoles: econazole, miconazole and ketoconazole against isolates of pathogenic Candida. A total of 186 clinical isolates of 10 species of the genus Candida and two culture collection strains were tested by an agar-dilution technique. Isoconazole was the most active azole, followed by butoconazole and sulconazole. Differences between some of the species in their susceptibility to the antifungal agents were noted. Sulconazole and cloconazole had the highest activity in vitro against 106 isolates of C. albicans. Butoconazole and isoconazole were also very active against isolates of C. albicans, and were the most active azole compounds against 80 isolates of Candida spp. 相似文献
3.
Marie-Laure Yaspo Nathalie Crété Zoubida Chettouh Jean-Louis Blouin Zohra Rahmani Dominique Stehelin Pierre-Marie Sinet Nicole Créau-Goldberg Jean-Maurice Delabar 《Human genetics》1992,90(4):427-434
To generate new chromosome 21 markers in a region that is critical for the pathogenesis of Down syndrome (D21S55-MX1), we used pulsed field gel electrophoresis (PFGE) to isolate a 600-kb NruI DNA fragment from the WA17 hybrid cell line, which has retained chromosome 21 as the only human material. This fragment, which contains the oncogene ETS2, was used to construct a partial genomic library. Among the 14 unique sequences that were isolated, 3 were polymorphic markers and contained sequences that are conserved in mammals. Five of these markers mapped on the ETS2-containing NruI fragment and allowed us to define an 800-kb high-resolution PFGE map. 相似文献
4.
A novel experimental method was developed which allows the determination of the threshold concentration of sucrose by use of a linear sucrose gradient in water. With this method a continuous tasting of the test-liquid is possible. A panel of 15 persons experienced in taste-testing was used. Three gradients of different steepness were applied: 0 to 1.5% (w/w) sucrose in 2 min (I), 3 min (II) and 4 min (III). The results of the new method were compared with those of the standard method (DIN). With gradients I and II we found values which were significantly higher than those of the standard method (I: 0.49% (w/w); II: 0.46% (w/w); DIN: 0.31% (w/w)), whereas with gradient III the same threshold value was found as with the DIN-Method (III: 0.32% (w/w)). 相似文献
5.
Characterization of In Vivo Reporter Systems for Gene Expression and Biosensor Applications Based on luxAB Luciferase Genes 总被引:2,自引:1,他引:1 下载免费PDF全文
Advances in genetic engineering methods have allowed the development of an increasing number of practical and scientific applications for bioluminescence with lux genes cloned from a variety of organisms. Bioluminescence derived from the shortened lux operon (luxAB genes) is a complex process, and applications seem to be proliferating in advance of an understanding of the underlying biochemical processes. In this report, we describe a two-phase kinetic behavior of the light emission which must be properly taken into account in any quantitative measurements of the bioluminescence signal. By using strains of Escherichia coli and Caulobacter crescentus, this behavior was characterized and interpreted in terms of the biochemistry underlying the bacterial luciferase mechanism. We show that the intensity profile of each of the two phases of the luminescence signal is responsive (and exhibits different sensitivities) to the concentration of added decanal and other components of the assay mix, as well as to the order of mixing and incubation times. This study illustrates the importance of appropriate protocol design, and specific recommendations for using the luxAB system as a molecular reporter are presented, along with versatile assay protocols that yield meaningful and reproducible signals. 相似文献
6.
J L Blouin D Avramopoulos C Pangalos S E Antonarakis 《American journal of human genetics》1993,53(5):1074-1078
Uniparental disomy (UPD) involving several different chromosomes has been described in several cases of human pathologies. In order to investigate whether UPD for chromosome 21 is associated with abnormal phenotypes, we analyzed DNA polymorphisms in DNA from a family with de novo Robertsonian translocation t(21q;21q). The proband was a healthy male with 45 dup(21q) who was ascertained through his trisomy 21 offspring. No phenotypic abnormalities were noted in the physical exam, and his past medical history was unremarkable. We obtained genotypes for the proband and his parents' leukocyte DNAs from 17 highly informative short sequence repeat polymorphisms that map in the pericentromeric region and along the entire length of 21q. The order of the markers has been previously determined through the linkage and physical maps of this chromosome. For the nine informative markers there was no maternal allele contribution to the genotype of the proband; in addition, there was always reduction to homozygosity of a paternal allele. These data indicated that there was paternal uniparental isodisomy for chromosome 21 (pUPiD21). We conclude that pUPiD21 is not associated with abnormal phenotypes and that there are probably no imprinted genes on chromosome 21. 相似文献
7.
Michael S. Blouin 《Evolution; international journal of organic evolution》1992,46(3):735-744
It is often proposed that the morphometric shape of animals often evolves as a correlated response to selection on life-history traits such as whole-body growth and differentiation rates. However, there exists little empirical information on whether selection on rates of growth or differentiation in animals could generate correlated response in morphometric shape beyond that owing to the correlation between these rates and body size. In this study genetic correlations were estimated among growth rate, differentiation rate, and body-size-adjusted head width in the green tree frog, Hyla cinerea. Head width was adjusted for size by using the residuals from log-log regressions of head width on snout-vent length. Size-adjusted head width at metamorphosis was positively genetically correlated with larval period length. Thus, size-independent shape might evolve as a correlated response to selection on a larval life-history trait. Larval growth rate was not significantly genetically correlated with size-adjusted head width. An additional morphometric trait, size-adjusted tibiofibula length, had a nonnormal distribution of breeding values, and so was not included in the analysis of genetic correlations (offspring from one sire had unusually short legs). This result is interesting because, although using genetic covariance matrices to predict long-term multivariate response to selection depends on the assumption that all loci follow a multivariate Gaussian distribution of allelic effects, few data are available on the distribution of breeding values for traits in wild populations. Size at metamorphosis was positively genetically correlated with larval period and larval growth rate. Quickly growing larvae that delay metamorphosis therefore emerge at a large size. The genetic correlation between larval growth rate and juvenile (postmetamorphic) growth rate was near zero. Growth rate may therefore be an example of a fitness-related trait that is free to evolve in one stage of a complex life cycle without pleiotropic constraints on the same trait expressed in the other stage. 相似文献
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应用GLC/MS联用仪对室内培养的钝顶螺旋藻(Spirulina platensis (Nordstedt) Geitler)、极大螺旋藻(S.maxima (Stechell & Gardiner) Geitler)和盐泽螺旋藻(S.subsalsa Oerst)的甾醇成分进行了测定。从钝顶螺旋藻和盐泽螺旋藻中共分出11个相同的甾醇组分:胆甾醇、胆甾烷醇、芸苔甾醇、麦角甾醇、海绵甾醇、菜子甾醇、豆甾醇、24-乙基-Δ~(5,7,22)-胆甾醇、β-谷甾醇、异岩藻甾醇和4α,23,24-三甲基Δ~(5,22)-胆甾醇;从极大螺旋藻中只分离出8个甾醇组分。其中胆甾醇含量最高。4α,23,24-三甲基-Δ~(5,22)-胆甾醇为蓝藻中首次报导。 相似文献