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排序方式: 共有3253条查询结果,搜索用时 15 毫秒
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Jorge Duitama Juan Camilo Quintero Daniel Felipe Cruz Constanza Quintero Georg Hubmann Maria R. Foulquié-Moreno Kevin J. Verstrepen Johan M. Thevelein Joe Tohme 《Nucleic acids research》2014,42(6):e44
Recent advances in high-throughput sequencing (HTS) technologies and computing capacity have produced unprecedented amounts of genomic data that have unraveled the genetics of phenotypic variability in several species. However, operating and integrating current software tools for data analysis still require important investments in highly skilled personnel. Developing accurate, efficient and user-friendly software packages for HTS data analysis will lead to a more rapid discovery of genomic elements relevant to medical, agricultural and industrial applications. We therefore developed Next-Generation Sequencing Eclipse Plug-in (NGSEP), a new software tool for integrated, efficient and user-friendly detection of single nucleotide variants (SNVs), indels and copy number variants (CNVs). NGSEP includes modules for read alignment, sorting, merging, functional annotation of variants, filtering and quality statistics. Analysis of sequencing experiments in yeast, rice and human samples shows that NGSEP has superior accuracy and efficiency, compared with currently available packages for variants detection. We also show that only a comprehensive and accurate identification of repeat regions and CNVs allows researchers to properly separate SNVs from differences between copies of repeat elements. We expect that NGSEP will become a strong support tool to empower the analysis of sequencing data in a wide range of research projects on different species. 相似文献
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Ronald T. Riley Douglas E. Goeger William P. Norred Richard J. Cole Joe W. Dorner 《Journal of biochemical and molecular toxicology》1987,2(3):251-264
In a previous study (1) we demonstrated that increased tetraphenylphosphonium (TPP) uptake by renal epithelial cells (LLC-PK1) exposed to the fungal metabolite cyclopiazonic acid (CPA) was not a result of hyperpolarization across the plasma membrane even though CPA-potentiated TPP uptake could be totally inhibited by the depolarizing agent carbonylcyanide-m-chlorophenylhydrazone (CCCP). We now demonstrate that CPA potentiates TPP accumulation by proliferating skeletal muscle (L6) and LLC-PK1 cells but not by nonproliferating primary rat hepatocytes. In LLC-PK1 cells, CPA-potentiated TPP accumulation is observed in cells at all ages. In s cells, CPA-potentiated TPP accumulation is maximal soon after subculturing, and as the cells age they become less sensitive to CPA until TPP accumulation by CPA-treated cells approaches that of untreated cells. The temporal change in sensitivity of L6 cells to CPA may be related to biochemical and/or metabolic changes which occur as the cells age in culture. Hepatocytes, LLC-PK1 cells, and L6 cells permeabilized by freeze-thaw lysis, all exhibit CPA-potentiated TPP partitioning, even in the presence of CCCP. This result indicates that both TPP and CPA must have access to the intracellular space in order for potentiated TPP partitioning to be observed. We hypothesize that the site of interaction between CPA and TPP is intracellular and probably associated with the cytoplasmic side of the plasma membrane and possibly the mitochondria. 相似文献
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Burt V. Bronk Joe D. Patton David N. Mellard 《Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression》1982,697(3):278-285
Chick embryo fibroblasts were treated with the monofunctional alkylating agent methylmethane sulfonate at various concentrations for 1 h at 42°C, rinsed and then incubated post-treatment at various temperatures at which the kinetics of alkali-labile bond disappearance was followed. Growth experiments showed that these cells grew similarly at temperatures of either 37°C or 42°C. Repair as assessed by removal of alkali-labile bond was also similar for postincubation in the temperature range 37–42°C for damage due to methylmethane sulfonate treatment at concentrations less than 1.5 mM. When the postincubation temperature was raised higher than 42.5–43°C, this type of repair was stopped. The normal internal body temperature of adult chickens is about 41.6°C. Hence the present finding indicates that chick cells are much more severely restricted in DNA repair at temperatures above normal than are mammalian cells, which can function in this respect for several deg. C above 37°C. 相似文献
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Joe T. Ritchie 《Plant and Soil》1981,58(1-3):81-96
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N G Link B N Nathwani K Preston 《Analytical and quantitative cytology and histology / the International Academy of Cytology [and] American Society of Cytology》1989,11(2):119-130
Non-Hodgkin's lymphomas with a follicular pattern are subdivided on the basis of morphologic criteria into four subtypes. Each subtype has a distinctive natural history, response to therapy and survival, and precise histologic diagnosis is essential for optimal treatment. However, recent studies by a panel of seven expert hematopathologists showed that there was a 20% to 40% likelihood of disagreement in subtyping non-Hodgkin's follicular lymphomas; thus, the likelihood of a patient receiving inappropriate treatment is high. To resolve some of the problems relating to subjective morphologic diagnosis, we have continued to investigate the possibility of using computerized image analysis to perform automated subtyping of follicular lymphomas. In the portion of the study reported herein, a total of 37 cases were selected from the set subtyped by the panel of expert hematopathologists, and digitized images of slides from each case were processed by computer. The computer-generated subtypes were compared with those arrived at by the panel. For the cases analyzed, the computer subtyping was at least as good as, and in some instances superior to, that of most of the expert panelists. 相似文献
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Cloning and mapping of the chloroplast DNA sequences for two messenger RNAs from mustard (Sinapis alba L.). 总被引:7,自引:3,他引:4 下载免费PDF全文
G Link 《Nucleic acids research》1981,9(15):3681-3694