全文获取类型
收费全文 | 2114篇 |
免费 | 73篇 |
国内免费 | 64篇 |
出版年
2023年 | 21篇 |
2022年 | 30篇 |
2021年 | 46篇 |
2020年 | 54篇 |
2019年 | 53篇 |
2018年 | 80篇 |
2017年 | 39篇 |
2016年 | 44篇 |
2015年 | 78篇 |
2014年 | 113篇 |
2013年 | 145篇 |
2012年 | 77篇 |
2011年 | 115篇 |
2010年 | 53篇 |
2009年 | 69篇 |
2008年 | 66篇 |
2007年 | 72篇 |
2006年 | 103篇 |
2005年 | 68篇 |
2004年 | 68篇 |
2003年 | 64篇 |
2002年 | 84篇 |
2001年 | 33篇 |
2000年 | 67篇 |
1999年 | 45篇 |
1998年 | 45篇 |
1997年 | 48篇 |
1996年 | 54篇 |
1995年 | 39篇 |
1994年 | 37篇 |
1993年 | 41篇 |
1992年 | 29篇 |
1991年 | 32篇 |
1990年 | 34篇 |
1989年 | 27篇 |
1988年 | 16篇 |
1987年 | 23篇 |
1986年 | 14篇 |
1985年 | 28篇 |
1984年 | 20篇 |
1983年 | 12篇 |
1982年 | 16篇 |
1981年 | 17篇 |
1980年 | 12篇 |
1979年 | 7篇 |
1978年 | 5篇 |
1977年 | 2篇 |
1976年 | 3篇 |
1974年 | 1篇 |
1967年 | 1篇 |
排序方式: 共有2251条查询结果,搜索用时 296 毫秒
1.
FAB1/PIKfyve是介导PI(3,5)P2 (磷脂酰肌醇3,5-二磷酸)生物合成的磷酸肌醇激酶。在动物和酵母(Saccharomyces cerevisiae)中, PI(3,5)P2参与调控胞内膜运输, 但在植物中的研究较少。该文通过分析拟南芥(Arabidopsis thaliana) FAB1的T-DNA插入突变体的表型解析PI(3,5)P2的生物学功能。拟南芥FAB1基因家族包含FAB1A、FAB1B、FAB1C和FAB1D四个基因。研究发现, fab1a/b呈现雄配子体致死的表型。利用遗传杂交获得fab1b/c/d三突变体, 发现FAB1B、FAB1C和FAB1D功能缺失导致根毛相比野生型变短, 经FAB1特异性抑制剂YM201636处理后的野生型中也观察到相似的短根毛表型。此外, fab1b/c/d三突变体中DR5转录水平降低。同时, 外源施加生长素类似物2,4-D和NAA能部分恢复fab1b/c/d植株短根毛的表型, 但fab1b/c/d突变体对生长素转运抑制剂(1-NOA和TIBA)的敏感性与野生型相似。此外, FAB1B/C/D功能缺失使根毛中ROS的含量减少且影响肌动蛋白的表达。上述结果表明, FAB1B/C/D通过调控生长素分布、ROS含量和肌动蛋白的表达影响拟南芥根毛伸长。 相似文献
2.
Direct somatic embryogenesis from axes of mature peanut embryos 总被引:2,自引:0,他引:2
A. H. McKently 《In vitro cellular & developmental biology. Plant》1991,27(4):197-200
Summary Plant regeneration via somatic embryogenesis was obtained in peanut (Arachis hypogaea L.) from axes of mature zygotic embryos. The area of greatest embryogenic activity was a 2-mm region adjacent to and encircling
the epicotyl. Somatic embryogenesis was evaluated on Murashige and Skoog media supplemented with a variety of auxin treatments.
Maximum production occurred on medium supplemented with 3 mg · liter−1 4-amino-3,5,6-trichloropicolinic acid. Explant cultures were transferred to half-strength medium supplemented with 1 mg ·
liter−1 gibberellic acid for somatic embryo germination and early plantlet growth. Plantlets, transferred to soil, were placed in
a greenhouse and grown to maturity. 相似文献
3.
4.
C. S. Lin M. C. Tseng P. I. Hong W. C. Chang 《In vitro cellular & developmental biology. Plant》2006,42(4):331-335
Summary Inflorescence proliferation is a plant tissue culture technique that, can be used to obtain in vitro inflorescences year-round without the intervening development of vegetative organs. In this study, we used albino mutant
inflorescences of Dendrocalamus latiflorus as the original explant material to investigate, the effect of plant growth regulators on long-term inflorescence proliferation.
The albino inflorescences proliferated on solidified Murashige and Skoog (MS) basal medium supplemented with thidiazuron (TDZ),
and the optimal concentration for successful long-term inflorescence proliferation was 0.45 μM TDZ. A combination of α-naphthaleneacetic acid (NAA) with 0.45 μM TDZ inhibited the inflorescence proliferation. Inflorescences cultured on a TDZ-free medium supplemented with 26.82 μM NAA rooted in 21 d, vegetative shoots formed by 42 d and, in one case, flowering occurred after 63 d. The auxins 2,4-dichlorophenoxyacetic
acid (2,4-D, 4.52 μM) and pieloram (4.14 μM) induced shoot formation. The protocol described can be used to produce large numbers of mutant inflorescences within a relatively
short period of time. 相似文献
5.
Adventitious root formation in vitro in 1-mm stem slices cut from microshoots of apple cv. Jork 9 was studied using light
and electron microscopy. When indole-3-butyric acid (IBA) had been added to the medium, starch grains accumulated during the
first 24 h of culture in cells of the cambial region and in cells in the vicinity of vascular tissue and in the primary rays.
This accumulation occurred only in the basal part of explants. After that, the nuclei in these cells were activated, and the
density of the cytoplasm and the number of cell organelles increased, whereas starch was broken down. Cambium cells started
to divide transversely and at 96 h, after several divisions, a continuous ring of isodiametric cytoplasmic cells had appeared
around the xylem near the basal cutting surface. The cells in this ring were rich in cell structures, and did not contain
large starch grains and a central vacuole. Root meristemoids regenerated from the portions of the ring that were localized
in the primary rays. From the other cells in the ring, callus developed. The meristemoids did not grow into the direction
of the epidermis as in shoots, but along the vascular bundles. After emergence from the cutting surface, the meristemoids
were transformed into small, dome-like primordia. They developed a typical root apex with root cap, root ground meristem and
tracheid connection with shoot vascular tissue.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
6.
Aqueous extracts of smoke, derived from Themeda triandra, a fire-climax grass, and Passerina vulgaris, a fynbos plant, stimulated the growth of primary root sections of tomato roots in suspension culture. The optimal dilution for both extracts was 1:2000. Several of the fractions obtained from TLC separation of the Themeda and the Passerina extracts significantly promoted primary root growth. The auxins naphthaleneacetic acid (NAA), indolebutyric acid (IBA) and indoleacetic acid (IAA) were found to stimulate the growth of the primary root axis, with IAA and NAA significantly promoting lateral root number. Similarly, the naturally occurring cytokinins, zeatin and its derivatives (zeatin-O-glucoside; dihydrozeatin and zeatin riboside) stimulated primary root length. Zeatin and dihydrozeatin promoted secondary root growth, but only at very low concentrations. 相似文献
7.
《Bioorganic & medicinal chemistry letters》2014,24(1):382-385
The chiral isomers of the two potent simplified RTX-based vanilloids, compounds 2 and 3, were synthesized employing highly enantioselective PTC alkylation and evaluated as hTRPV1 ligands. The analysis indicated that the R-isomer was the eutomer in binding affinity and functional activity. The agonism of compound 2R was comparable to that of RTX. Docking analysis of the chiral isomers of 3 suggested the basis for its stereospecific activity and the binding mode of 3R. 相似文献
8.
Auxin-induced mRNA species in tobacco cell cultures 总被引:6,自引:0,他引:6
E. J. van der Zaal J. Memelink A. M. Mennes A. Quint K. R. Libbenga 《Plant molecular biology》1987,10(2):145-157
9.
Four new auxin-responsive RNAs from soybean (Glycine max (L.) Merr., var. Wayne) are described. The RNAs were identified by hybridization to three cDNA probes obtained from a library enriched for sequences which increase in abundance within 60 min after 2,4-D (2,4-dichlorophenoxyacetic acid) treatment. These RNAs appear to define a new class of small (i.e. approximately 550 nucleotides) RNAs that respond extremely rapidly to application of exogenous auxin. In excised elongating hypocotyl sections, an increase in the abundance of these RNAs can be detected 2 to 5 min after treatment with 50 M 2,4-D. This response is half maximal after 10 min and reaches steady state in 60 min. RNA blot analysis shows that these RNAs are expressed differentially in various parts of the seedling. The degree of inducibility by auxin is also organ-specific, with the elongating hypocotyl being the most responsive of the organs tested. The RNAs display identical response specificities with one exception. Accumulation of one RNA, designated 10A, is completely abolished by simultaneous addition of cycloheximide and 2,4-D. This RNA also displays a different 2,4-D dose response than other RNAs examined. These results suggest that more than one mechanism is involved in rapid modulation of gene expression by auxin. 相似文献
10.
Gas chromatography-mass spectrometric analyses of purified extracts from cultures of Rhizobium phaseoli wild-type strain 8002, grown in a non-tryptophan-supplemented liquid medium, demonstrated the presence of indole-3-acetic acid (IAA), indole-3-ethanol (IEt), indole-3-aldehyde and indole-3-methanol (IM). In metabolism studies with 3H-, 14C- and 2H-labelled substrates the bacterium was shown to convert tryptophan to IEt, IAA and IM; IEt to IAA and IM; and IAA to IM. Indole-3-acetamide (IAAm) could not be detected as either an endogenous constituent or a metabolite of [3H]tryptophan nor did cultures convert [14C]IAAm to IAA. Biosynthesis of IAA in R. phaseoli, thus, involves a different pathway from that operating in Pseudomonas savastanio and Agrobacterium tumefaciens-induced crown-gall tumours.Abbreviations IAA
indole-3-acetic acid
- IAld
indole-3-aldehyde
- IAAm
indole-3-acetamide
- IEt
indole-3-ethanol
- IM
indole-3-methanol
- HPLC-RC
high-performance liquid chromatography-radio counting
- GC-MS
gas chromatography-mass spectrometry 相似文献