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C. Rossi A. Cuesta-Marcos I. Vales L. Gomez-Pando G. Orjeda R. Wise K. Sato K. Hori F. Capettini H. Vivar X. Chen P. Hayes 《Molecular breeding : new strategies in plant improvement》2006,18(4):355-366
We used a well-characterized barley mapping population (BCD 47 × Baronesse) to determine if barley stripe rust (BSR) resistance quantitative trait loci (QTL) mapped in Mexico and the USA were effective against a reported new race in Peru. Essentially the same resistance QTL were detected using data from each of the three environments, indicating that these resistance alleles are effective against the spectrum of naturally occurring races at these sites. In addition to the mapping population, we evaluated a germplasm array consisting of lines with different numbers of mapped BSR resistance alleles. A higher BSR disease severity on CI10587, which has a single qualitative resistance gene, in Peru versus Mexico suggests there are differences in pathogen virulence between the two locations. Confirmation of a new race in Peru will require characterization using a standard set of differentials, an experiment that is underway. The highest levels of resistance in Peru were observed when the qualitative resistance gene was pyramided with quantitative resistance alleles. We also used the mapping population to locate QTL conferring resistance to barley leaf rust and barley powdery mildew. For mildew, we identified resistance QTL under field conditions in Peru that are distinct from the Mla resistance that we mapped using specific isolates under controlled conditions. These results demonstrate the long-term utility of a reference mapping population and a well-characterized germplasm array for locating and validating genes conferring quantitative and qualitative resistance to multiple pathogens. 相似文献
3.
Cytological mechanism of pollen abortion resulting from allelic interaction of F1 pollen sterility locus in rice (Oryza sativa L.) 总被引:5,自引:0,他引:5
Pollen abortion is one of the major reasons causing the inter-subspecific F1 hybrid sterility in rice and is due to allelic interaction of F1 pollen sterility genes. The microsporogenesis and microgametogenesis of Taichung 65 and its three F1 hybrids were comparatively studied by using techniques of differential interference contrast microscopy, semi-thin section
light microscopy, epifluorescence microscopy and TEM. The results showed that there were differences among the cytological
mechanisms of pollen abortion due to allelic interaction at the three F1 pollen sterility loci. The allelic interaction at S-a locus resulted in microspores unable to extend the protoplasm membrane with the enlargement of the microspore at the middle
microspore stage and finally producing empty abortive pollen. The allelic interaction at S-b locus caused asynchronous development of microspores at the middle microspore stage producing stainable abortive pollen.
The allelic interaction at S-c locus mainly led to the non-dissolution of the generative cell wall and finally caused the hybrid F1 mainly producing stainable abortive pollen. Genotypic identification indicated that the abortive pollen were those with S
j
allele. 相似文献
4.
Electrophoretic variation characterized by the presence (ES-5B+) or absence (ES-5B–) of esterase-5B in the plasma of the house mouse has been observed. It is suggested that the expression of esterase-5B is controlled by an autosomal locus, Esr, linked to Ldr-1 on chromosome 6, in addition to the presumptive structural locus Es-5, which is located on chromosome 8. A gene order of Lyt-3-Esr-Ldr-1 was determined by two crosses.Supported by the Deutsche Forschungsgemeinschaft (SFB 46).This is communication No. 33 of a research program devoted to the investigation of cellular distribution and genetics of nonspecific esterases. 相似文献
5.
6.
Ekman J Kosonen M Jokela S Kolari M Korhonen P Salkinoja-Salonen M 《Journal of industrial microbiology & biotechnology》2007,34(3):203-211
Colored biofilms cause problems in paper industry. In this work we used real-time PCR to detect and to quantitate members
of the genus Meiothermus from the process samples and end products from 24 machines manufacturing pulp, paper and board in four countries. The results
obtained from 200 samples showed the importance of members of the genus Meiothermus as ubiquitous biofoulers in paper machines. This genus was the dominant biofouler in some mills. From ≤104 to 1011 copies of Meiothermus 16S rRNA genes were found per gram of process deposit (wet weight). Meiothermus spp. were found in paper and board products with colored defects and connection between deposit-forming microbes and end-product
spots was shown. 16S rRNA gene sequences of 29 biofilm producing bacterial isolates from different mills were determined.
Based on sequence data, 25 of the isolates were assigned to the genus Meiothermus, with Meiothermus silvanus and M. ruber as the most frequent species. 相似文献
7.
Genetic diversity in spring bread wheat (T.␣aestivum L.) was studied in a total of 69 accessions. For this purpose, 52 microsatellite (SSR) markers were used and a total of 406
alleles were detected, of which 182 (44.8%) occurred at a frequency of <5% (rare alleles). The number of alleles per locus
ranged from 2 to 14 with an average of 7.81. The largest number of alleles per locus occurred in the B genome (8.65) as␣compared
to the A (8.43) and D (5.93) genomes, respectively. The polymorphism index content (PIC) value varied from 0.24 to 0.89 with
an average of 0.68. The highest PIC for all accessions was found in the B␣genome (0.71) as compared to the A (0.68) and D␣genomes
(0.63). Genetic distance-based method (standard UPGMA clustering) and a model-based method (structure analysis) were used for cluster analysis. The two methods led to analogical results. Analysis of molecular variance (AMOVA)
showed that 80.6% of the total variation could be explained by the variance within the geographical groups. In comparison
to the diversity detected for all accessions (H
e
= 0.68), genetic diversity among European spring bread wheats was H
e
= 0.65. A comparatively higher diversity was observed between wheat varieties from Southern European countries (Austria/Switzerland,
Portugal/Spain) corresponding to those from other regions. 相似文献
8.
Y. N. Xiao X. H. Li M. L. George M. S. Li S. H. Zhang Y. L. Zheng 《Plant Molecular Biology Reporter》2005,23(2):155-165
Drought accounts for significant yield losses in crops. Maize (Zea mays L.) is particularly sensitive to water stress at reproductive stages, and breeding to improve drought tolerance has been
a challenge. By use of a linkage map with 121 single sequence repeat (SSR) markers, quantitative trait loci (QTLs) for grain
yield and yield components were characterized in the population of the cross X178×B73 under water-stressed and well-watered
conditions. Under the well-watered regime, 2, 4, 4, 1, 2, 2, and 3 QTLs were identified for grain yield, 100-kernel weight,
kernel number per ear, cob weight per ear, kernel weight per ear, ear weight, and ear number per plant, respectively, whereas
under the water-stressed conditions, 1, 5, 2, 6, 1, 3, and 2 QTLs, respectively, were found. The significant phenotypic correlations
among yield and yield components to some extent were observed under both water conditions, and some overlaps between the corresponding
QTLs were also found. QTLs for grain yield and kernel weight per ear under well-watered conditions and ear weight under both
well-watered and water-stressed conditions over-lapped, and all were located on chromosome 1.03 near marker bnlg176. Two other
noticeable QTL regions were on chromosome 9.05 and 9.07 near markers umc1657 and bnlg1525; the first corresponded to grain
yield, kernel weight per ear, and ear weight under well-watered conditions and kernel number per ear under both water conditions,
and the second to grain yield and cob weight per ear under water-stressed conditions and ear number per plant under both water
conditions. A comparative analysis of the QTLs herein identified with those described in previous studies for yield and yield
components in different maize populations revealed a number of QTLs in common. These QTLs have potential use in molecular
marker-assisted selection. 相似文献
9.
10.
General cognitive ability ( g ), which refers to what cognitive abilities have in common, is an important target for molecular genetic research because multivariate quantitative genetic analyses have shown that the same set of genes affects diverse cognitive abilities as well as learning disabilities. In this first autosomal genome-wide association scan of g , we used a two-stage quantitative trait locus (QTL) design with pooled DNA to screen more than 500 000 single nucleotide polymorphisms (SNPs) on microarrays, selecting from a sample of 7000 7-year-old children. In stage 1, we screened for allele frequency differences between groups pooled for low and high g . In stage 2, 47 SNPs nominated in stage 1 were tested by individually genotyping an independent sample of 3195 individuals, representative of the entire distribution of g scores in the full 7000 7-year-old children. Six SNPs yielded significant associations across the normal distribution of g , although only one SNP remained significant after a false discovery rate of 0.05 was imposed. However, none of these SNPs accounted for more than 0.4% of the variance of g , despite 95% power to detect associations of that size. It is likely that QTL effect sizes, even for highly heritable traits such as cognitive abilities and disabilities, are much smaller than previously assumed. Nonetheless, an aggregated 'SNP set' of the six SNPs correlated 0.11 ( P < 0.00000003) with g . This shows that future SNP sets that will incorporate many more SNPs could be useful for predicting genetic risk and for investigating functional systems of effects from genes to brain to behavior. 相似文献