首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   2835篇
  免费   462篇
  国内免费   288篇
  3585篇
  2024年   13篇
  2023年   112篇
  2022年   91篇
  2021年   131篇
  2020年   159篇
  2019年   174篇
  2018年   137篇
  2017年   146篇
  2016年   165篇
  2015年   186篇
  2014年   185篇
  2013年   211篇
  2012年   191篇
  2011年   139篇
  2010年   127篇
  2009年   151篇
  2008年   142篇
  2007年   180篇
  2006年   120篇
  2005年   109篇
  2004年   90篇
  2003年   94篇
  2002年   77篇
  2001年   67篇
  2000年   55篇
  1999年   53篇
  1998年   40篇
  1997年   33篇
  1996年   44篇
  1995年   25篇
  1994年   21篇
  1993年   22篇
  1992年   17篇
  1991年   14篇
  1990年   6篇
  1989年   6篇
  1988年   12篇
  1987年   3篇
  1986年   6篇
  1985年   4篇
  1984年   4篇
  1983年   3篇
  1982年   1篇
  1981年   4篇
  1980年   6篇
  1979年   3篇
  1978年   4篇
  1976年   1篇
  1975年   1篇
排序方式: 共有3585条查询结果,搜索用时 0 毫秒
51.
The microsporidian Nosema antheraeae is a pathogen that infects the Chinese oak silkworm, Antheraea pernyi. We sequenced the complete small subunit (SSU) rRNA gene and the internal transcribed spacer (ITS) of N. antheraeae, and compared the SSU rRNA sequences in other microsporidia. The results indicated that Nosema species, including N. antheraeae, formed two distinct clades, consistent with previous observations. Furthermore, N. antheraeae is clustered with N. bombycis with high bootstrap support. The organization of the rRNA gene of N. antheraeae is LSU-ITS1-SSU-ITS2-5S, also following a pattern similar to the Nosema type species, N. bombycis. Thus, N. antheraeae is a Nosema species and has a close relationship to N. bombycis.  相似文献   
52.
黄肉桃种质资源的RAPD分析   总被引:19,自引:0,他引:19  
利用RAPD技术,采用从200个十碱基随机物筛选的22个随机引物对37个黄肉桃品种的基因组DNA进行扩增,通过扩增的180个位点的谱带的聚类,分析供试黄肉桃的系统发育,运用特殊谱带,建立了黄肉桃的分子检索表,并提出了重点保存的黄肉桃种质。  相似文献   
53.
Protein domains are conserved and functionally independent structures that play an important role in interactions among related proteins. Domain-domain inter- actions have been recently used to predict protein-protein interactions (PPI). In general, the interaction probability of a pair of domains is scored using a trained scoring function. Satisfying a threshold, the protein pairs carrying those domains are regarded as "interacting". In this study, the signature contents of proteins were utilized to predict PPI pairs in Saccharomyces cerevisiae, Caenorhabditis ele- gans, and Homo sapiens. Similarity between protein signature patterns was scored and PPI predictions were drawn based on the binary similarity scoring function. Results show that the true positive rate of prediction by the proposed approach is approximately 32% higher than that using the maximum likelihood estimation method when compared with a test set, resulting in 22% increase in the area un- der the receiver operating characteristic (ROC) curve. When proteins containing one or two signatures were removed, the sensitivity of the predicted PPI pairs in- creased significantly. The predicted PPI pairs are on average 11 times more likely to interact than the random selection at a confidence level of 0.95, and on aver- age 4 times better than those predicted by either phylogenetic profiling or gene expression profiling.  相似文献   
54.
An extensive size homoplasy was found at microsatellite locus B11 of the bumblebee, Bombus diversus, in northern to central Honshu, Japan. A total of 16 alleles of different nucleotide sequences in five length morphs was obtained at B11 for this species. Of these alleles, five were 141 base pairs (bp) in length, five were 137 bp and four were 133 bp. Allele diversity in each length morph was high compared with previous studies. It is noteworthy that this extensive size homoplasy was found in a relatively small geographic area, in contrast to results from previous studies. Reconstruction of a median‐joining network revealed the complicated evolutionary process of the locus, involving insertion/deletion and point mutations. Preliminary estimation of the mutation rate of the B11 locus in B. diversus gives a value comparable to those estimated from experimental Drosophila populations. Effects of the extensive size homoplasy in population genetic studies is discussed.  相似文献   
55.
Although virtually no phylogenetic evidence (in the sense advocated by Hennig, 1966) had been previously presented to support the monophyly of the Characidiinae, and most 'diagnostic' characters used by previous authors were found to be unacceptable in a cladistic classification, i t is still possible to diagnose the Characidiinae in a phylogenetic sense. This study revealed the existence of 13 synapomorphies supporting the monophyly of the group. Several of these synapomorphies, such as the modifications associated with the mesethmoid, the jaw bones, and the ribs of the fifth vertebra, are unique to the Characidiinae, thus providing a solid basis for recognizing the group as a monophyletic unit of characiform fishes. Demonstration of characidiin monophyly provides a solid foundation for further phylogenetic analysis of characidiin interrelationships, and higher level relationships among characiform fishes.  相似文献   
56.
During the survey of two successive years 2012–2013, in nearby places of Gorakhpur districts, Uttar Pradesh, India, Arundo donax plants were found to be exhibiting witches’ broom, excessive branching accompanied with little leaf symptoms with considerable disease incidence. Nested PCR carried out with universal primers pair R16F2n/R16R2 employing the PCR (P1/P7) product as a template DNA (1:20) resulted in expected size positive amplification ~1.2 kb in all symptom-bearing plants suggested the association of phytoplasma with witches’ broom disease of Narkat plants. BLASTn analysis of the 16S rRNA gene sequence showed the highest (99%) sequence identity with Candidatus phytoplasma asteris (16SrI group). In phylogenetic analysis, the sequence data showed close relationships with the members of 16SrI phytoplasma and clustered within a single clade of 16SrI group and closed to B subgroup representatives. This is a first report of 16Sr I-B group phytoplasma associated with witches’ broom accompanied with little leaf disease of Narkat in India.  相似文献   
57.
  • Passiflora edulis f. flavicarpa is the most economically important species in the genus Passiflora. However, the origin of this yellow form of passion fruit remains unclear, being suggested as a hybrid (P. edulis f. edulis × P. ligularis) or wild mutant.
  • Here, the origin and genomic relationships of P. edulis f. flavicarpa with some related species in the genus Passiflora (subgenera Decaloba and Passiflora) were investigated using genomic in situ hybridization (GISH). Genomic DNA of 18 species was used as probe, which was hybridized onto chromosomes of P. edulis f. flavicarpa.
  • Of all genomic DNA probes tested, none allowed us to identify a specific chromosome set in P. edulis f. flavicarpa. Conversely, probes from the subgenus Passiflora, P. edulis f. edulis, P. alata, P. cincinnata, P. coccinea, P. nitida and P. vitifolia, produced intense and uniform hybridizations on all chromosomes of P. edulis f. flavicarpa. Moreover, probes from P. ligularis, P. foetida and P. sublanceolata produced more intense hybridizations in the terminal region of four chromosomes, corresponding to the DNAr 45S locus, and also dispersed, less intense, hybridization across all chromosomes. Probes from the subgenus Decaloba, P. biflora, P. capsularis, P. cervii, P. coriacea, P. micropetala, P. morifolia, P. rubra and P. suberosa, produced hybridizations restricted to the DNAr 45S sites.
  • The hybrid origin of P. edulis f. flavicarpa could not be supported based on the GISH results, and it is suggested that this species is conspecific with P. edulis f. edulis, because the probe with DNA of this form hybridized strongly throughout the target genome. The other putative parent species, P. ligularis, showed only a distant relationship with the target genome. The results also suggest that species of the subgenus Passiflora share many repetitive sequences and that the relationship between subgenera Decaloba and Passiflora is very distant.
  相似文献   
58.
59.
60.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号