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排序方式: 共有775条查询结果,搜索用时 31 毫秒
1.
We describe the development of DNA markers for the fungal pathogen of Eucalyptus, Cryphonectria cubensis. These markers originated from cloned intershort sequence repeat polymerase chain reactions, which enrich for medium to highly repetitive DNA sequences. In total, 10 markers were isolated, eight of which were polymorphic, and these can subsequently be applied to study populations of C. cubensis. 相似文献
2.
DAVID WEETMAN LORENZ HAUSER PAUL W. SHAW MICHELLE K. BAYES 《Molecular ecology resources》2005,5(2):361-362
Five microsatellite loci are described for the commercially exploited marine gastropod, Buccinum undatum. Levels of polymorphism were variable with three to 19 alleles per locus and expected heterozygosities of 0.26–0.94 in 60 individuals of the population from which the loci were isolated. Homozygote excess at two of the loci might be attributable to null alleles, and these loci should not be used in, for example, parentage analysis. Nevertheless, because null allele frequencies can be estimated and their effects partitioned, all are useful markers for studies of population differentiation. 相似文献
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4.
Universal primers for amplification of three non-coding regions of chloroplast DNA 总被引:90,自引:0,他引:90
Six primers for the amplification of three non-coding regions of chloroplast DNA via the polymerase chain reaction (PCR) have been designed. In order to find out whether these primers were universal, we used them in an attempt to amplify DNA from various plant species. The primers worked for most species tested including algae, bryophytes, pteridophytes, gymnosperms and angiosperms. The fact that they amplify chloroplast DNA non-coding regions over a wide taxonomic range means that these primers may be used to study the population biology (in supplying markers) and evolution (inter- and probably intraspecific phylogenies) of plants. 相似文献
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6.
S. Chao C. Baysdorfer O. Heredia-Diaz T. Musket G. Xu E. H. Coe Jr 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1994,88(6-7):717-721
We report here the results of mapping a set of 92 leaf cDNA clones in maize. The ends of each of these cDNA clones have previously been partially sequenced, and the sequence comparison has revealed the putative function for 28 clones. It is expected that the RFLP map developed using these expressed sequence tags will be of great importance for future maize genome analysis, such as for PCR-based gene mapping or gene function identification.Contribution from the Missouri Agricultural Experiment Station. Journal Series N. 12,019. 相似文献
7.
Jeffrey A. Banas Daniel Simon Lisa K. Williams Joseph J. Ferretti Roy R.B. Russell 《FEMS microbiology letters》1994,123(3):349-354
Abstract A glucosyltransferase (GTF) gene, designated gtfL , from Streptococcus salivarius was cloned and expressed in Escherichia coli and its nucleotide sequence determined. The GTF-L enzyme catalysed the synthesis of water-insoluble glucan in a primer-independent manner. The nucleotide sequence and derived amino acid sequence of GTF-L were similar in size and domain structure to previously sequenced glucosyltransferases. However, a 464-bp region of high variability was identified which could be selectively amplified from strains of S. salivarius by the polymerase chain reaction and could therefore form the basis for species identification. No sequence-specific motifs related to the solubility and linkage of the glucan product or its need for a dextran primer could be ascertained. 相似文献
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A PCR primer-specific to Cylindrocarpon heteronema for detection of the pathogen in apple wood 总被引:1,自引:0,他引:1
Averil E. Brown S. Muthumeenakshi S. Sreenivasaprasad Peter R. Mills Terence R. Swinburne 《FEMS microbiology letters》1993,108(1):117-120
Abstract An oligonucleotide primer (ChInt) was synthesised from the variable internally transcribed spacer (ITS) 1 region of ribosomal DNA (rDNA) of Cylindrocarpon heteronema . PCR with primers ChInt and ITS4 (from a conserved sequence of the rDNA) amplified a 470-bp fragment from several isolates of C. heteronema but not from various apple wood saprophytes. Amplification of this fragment was achieved from 1–2 pg of fungal DNA. These primers amplified a fragment of the same size from DNA extracted from cankered wood but only after impurities were removed from the DNA on a Qiagen tip-5 column. Southern hybridization analysis confirmed the 470-bp fragment from C. heteronema DNA and cankered wood to be identical. 相似文献
10.
Joachim Messing 《Molecular biotechnology》1996,5(1):39-47
DNA sequence and expression analyses have greatly benefited from using M13 and pUC derived cloning vectors and their polycloning
sites. A chronology of the original concepts and experiments is reviewed. 相似文献