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121.
It is known that low root zone temperatures (RZT) have moreeffect on infection and early nodule development than on nitrogenfixation by soybean [Glycine max (L.) Merr.]. However, therehave been no studies regarding how the low RZT inhibit the infectionstages of soybean. Two controlled environment experiments wereconducted to examine the effect of low RZT on bacterial attachmentto, and infection thread penetration of, soybean root hairs.The experimental designs were (1) plants maintained at 25, 17.5or 15C RZT, or transferred from 25 or 17.5 to 15C RZT at either0.5, 1, 2, or 7d after inoculation (DAI), (2) early symbioticestablishment between soybean and Bradyrhizobium japonicum wasexamined microscopically under three RZT (15, 17.5 and 25C).These results indicated that (1) keeping plants at 25C only0.5 DAI prior to transfer to a 15C RZT accelerates the onsetof N2 fixation at 15C RZT by 6 d, (2) at RZT between 25 and17.5C the infection processes were progressively delayed astemperature declined, (3) RZT less than 17C strongly inhibitedinfection steps, such that when RZT dropped 8.5C from 25 to17.5C infection initiation was delayed 1 d, while when RZTdropped only 2.5C from 17.5 to 15C, infection initiation wasdelayed another 2 d. Key words: Bradyrhizobium japonicum, low temperature, nodulation, soybean 相似文献
122.
Insect resistance of transgenic plants that express modified Bacillus thuringiensis cryIA(b) and cryIC genes: a resistance management strategy 总被引:7,自引:0,他引:7
123.
Expression of mouse metallothionein-I gene confers cadmium resistance in transgenic tobacco plants 总被引:8,自引:0,他引:8
Aihua Pan Meizhu Yang Feng Tie Lingyua Li Zhangliang Chen Biggen Ru 《Plant molecular biology》1994,24(2):341-351
Transgenic tobacco plants containing a mouse metallothionein-I (MT-I) gene fused to the cauliflower mosaic virus 35S (CaMV 35S) promoter and nopaline synthase (nos) polyadenylation site were obtained by transforming tobacco leaf discs with an Agrobacterium tumefaciens strain carrying the chimaeric gene. Transformants were directly selected and rooted on medium containing cadmium and kanamycin. A total of 49 individual transgenic tobacco plants were regenerated. Among them 20% showed a very high expression level and their growth was unaffected by up to 200 M cadmium, whereas the growth of control plants was severely affected leaf chlorosis occurred on medium containing only 10 M cadmium. The concentration of MT-I in leaves of control and transgenic tobacco was determined with Cd/haemoglobin saturation assay, a polarographic method and western blotting. In addition, seeds from self-fertilized transgenic plants were germinated on medium containing toxic levels of cadmium and scored for tolerance/susceptibility to this heavy metal. The ratio of tolerant to susceptible plants was 3:1 indicating that the metallothionein gene is inherited as a single locus. 相似文献
124.
Expression of the BnmNAP subfamily of napin genes coincides with the induction of Brassica microspore embryogenesis 总被引:3,自引:0,他引:3
Kim A. Boutilier María-Jesús Ginés Janice M. DeMoor Bin Huang Chris L. Baszczynski V. N. Iyer Brian L. Miki 《Plant molecular biology》1994,26(6):1711-1723
Brassica napus cv. Topas microspores can be diverted from pollen development toward haploid embryo formation in culture by subjecting them to a heat stress treatment. We show that this switch in developmental pathways is accompanied by the induction of high levels of napin seed storage protein gene expression. Changes in the plant growth or microspore culture conditions were not by themselves sufficient to induce napin gene expression. Specific members of the napin multigene family were cloned from a cDNA library prepared from microspores that had been induced to undergo embryogenesis. The majority of napin clones represented three members (BnmNAP2, BnmNAP3 and BnmNAP4) that, along with a previously isolated napin genomic clone (BngNAP1), constitute the highly conserved BnmNAP subfamily of napin genes. Both RNA gel blot analysis, using a subfamily-specific probe, and histochemical analysis of transgenic plants expressing a BngNAP1 promoter--glucuronidase gene fusion demonstrated that the BnmNAP subfamily is expressed in embryogenic microspores as well as during subsequent stages of microsporic embryo development. 相似文献
125.
Jin Feng Kunitoshi Yamanaka Hironori Niki Teru Ogura Sota Hiraga 《Molecular & general genetics : MGG》1994,243(2):136-147
The nucleotide sequence was determined of the region upstream of the mukB gene of Escherichia coli. Two new genes were found, designated kicA and kicB (killing of cell); the gene order is kicB-kicA-mukB. Promoter activities were detected in the regions immediately upstream of kicB and kicA, but not in front of mukB. Gene disruption experiments revealed that the kicA disruptant was nonviable, but the kicB-disrupted mutant and the mutant lacking both the kicB and kicA genes were able to grow. When kicA disruptant cells bearing a temperature-sensitive replication plasmid carrying the kicA
+ gene were grown at 30° C and then transferred to 42° C, the mutant cells gradually lost colony-forming ability, even in the presence of a mukB
+ plasmid. Rates of protein synthesis, but not of RNA or DNA synthesis, fell dramatically during incubation at 42° C. These results suggested that the kicB gene encodes a killing factor and the kicA gene codes for a protein that suppresses the killing function of the kicB gene product. It was also demonstrated that KicA and KicB can function as a post-segregational killing system, when the genes are transferred from the E. coli chromosome onto a plasmid. 相似文献
126.
河南叶县下寒武统辛集组单板类和腹足类化石的研究 总被引:8,自引:3,他引:5
本文描述和讨论了河南叶县杨寺庄下寒武统辛集组单板类13种,腹足类2种,未定类1种。其中包括2新属6新种:Repenoconus xinjiensis gen.nov.,Scenella pycna sp.nov.,Securiconus vulgaris sp.nov.,Obtusocnus grossicostus sp.nov.,Igorellina proboscis sp.nov.,Gal 相似文献
127.
植物细胞离析酶的制备和应用 总被引:2,自引:0,他引:2
用 Aspergillus sp.A-19菌经固体发酵研制成一种新的植物细胞离析酶(SeparatasezA—P)。其离析单细胞的酶活力平均为70 767u/g,有效作用的pH在3.0—7.0,温度为20—45℃。发酵培养基配方是麸皮:桔皮粉:(NH4)2SO4(w/w)为100:100:O.63,料水比为1 :2.0,培养适宜条件为25℃、60小时。 相似文献
128.
卡拉胶固定粘质赛氏菌产碱性蛋白酶的研究 总被引:4,自引:0,他引:4
将粘质赛氏菌(Seratia marcescens)包埋于卡拉胶中,发现2.5%的卡拉胶适于固定该菌产碱性蛋白酶。固定化细胞在其较适宜产酶培养基中发酵,酶活力一般可达400u/ml,在卡拉胶中添加3%玉米粉和1%豆饼粉或2%砂子制备固定化细胞,其产酶能力分别提高了25%和23.9%;固定化细胞颗粒越小,其产酶能力越高。采用摇瓶半连续发酵。其产酶半衰期为14次(24小时为一个周期);而用环流器进行半连续发酵,其产酶半衰期为52次(12小时为一个周期),产酶效率分别比游离细胞摇瓶发酵的产酶效率高11.8%和45.07%,而环流器半连续发酵的产酶效率比摇瓶半连续发酵高29.7%。 相似文献
129.
130.
Largepterosaurwithamaximumwingspanofmorethan5metres.Theskullislowerandlonger,withoutmiddlecrestorsupraoccipita1crest.ThenasaIandpre-orbita1fenestraareconfluentcompletely,andoccupyaboutha1foftheskulI1ength.Thetoothlessbeakisslenderandpointed.The1ongneckiscomposedbyse-venslendercervicalvertebrae.Thenotariumconsistsofsixco-ossifiedanteriordorsalvertebrae-ThetaiIisextremlyshort.lthassixpairsof"A"shapegastralia.Theanteriorlimbsarestrong;thehumerusarethickandshort;thewing-metacarpalbonearelongert… 相似文献