全文获取类型
收费全文 | 15024篇 |
免费 | 588篇 |
国内免费 | 878篇 |
专业分类
16490篇 |
出版年
2023年 | 126篇 |
2022年 | 174篇 |
2021年 | 222篇 |
2020年 | 201篇 |
2019年 | 286篇 |
2018年 | 262篇 |
2017年 | 251篇 |
2016年 | 276篇 |
2015年 | 267篇 |
2014年 | 422篇 |
2013年 | 648篇 |
2012年 | 369篇 |
2011年 | 432篇 |
2010年 | 377篇 |
2009年 | 520篇 |
2008年 | 588篇 |
2007年 | 657篇 |
2006年 | 628篇 |
2005年 | 590篇 |
2004年 | 523篇 |
2003年 | 543篇 |
2002年 | 486篇 |
2001年 | 459篇 |
2000年 | 410篇 |
1999年 | 424篇 |
1998年 | 414篇 |
1997年 | 368篇 |
1996年 | 366篇 |
1995年 | 371篇 |
1994年 | 434篇 |
1993年 | 397篇 |
1992年 | 403篇 |
1991年 | 441篇 |
1990年 | 371篇 |
1989年 | 318篇 |
1988年 | 305篇 |
1987年 | 274篇 |
1986年 | 216篇 |
1985年 | 260篇 |
1984年 | 246篇 |
1983年 | 110篇 |
1982年 | 159篇 |
1981年 | 184篇 |
1980年 | 154篇 |
1979年 | 121篇 |
1978年 | 94篇 |
1977年 | 96篇 |
1976年 | 110篇 |
1974年 | 25篇 |
1973年 | 30篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
1.
Frank J. Turano Kenneth Glade Wilson 《In vitro cellular & developmental biology. Plant》1985,21(3):135-139
Summary The feasibility of using plant cell culture to measure toxicity was determined by investigating the toxicological effects
of three chemical compounds, allyl alcohol, propargylglycine, and cadmium chloride, on cell cultures ofCatharanthus roseus G. Don (Madagascar periwinkle). Suspension cultures ofC. roseus were maintained in modified B5 medium and transferred every 5 d. Five-day-old cell cultures were exposed to various concentrations
(10,3,1,0.3,0.1,0.03,0.01,0.003,0.001,0.0003,0.0001, 0.00003, and 0.0 mM) of the toxicants in both acute and chronic toxicity tests.
In the acute test, cells were exposed to the toxicant for 24 h, washed three times with sterile medium, and plated in petri
plates with an equal volume of 1.4% agar medium. Cells in the chronic test were plated with an equal volume of 1.4% agar medium
containing various concentrations of the toxicant. Cells were incubated 28 d at 30°C in the dark. The colonies were counted
and the results plotted as percent survival versus toxicant concentration. The results indicate, at the concentrations tested,
thatC. roseus assay may be feasible in that it fulfills the criteria for a practical assay (e.g., rapid, simple, quantifiable, and reproducible).
This work was submitted to the faculty of Miami University in partial fulfillment of the requirements for the degree of Master
of Environmental Science, Institute of Environmental Sciences. 相似文献
2.
Ciliated tracheal epithelia cell cultures were investigated immunocytochemically with anti-tubulin and colloidal gold. When rabbit tracheal cultures were fixed in paraformaldehyde, treated with acetone, anti-tubulin and a second antibody coupled to FITC, fluorescence was associated with cytoskeletal and axonemal microtubules. Cilia covering the apical surface of the ciliated tracheal cells fluoresced very brightly thus facilitating identification of this cell type. Electron microscopy of tracheal cultures fixed as above, treated with Triton-X 100 and incubated in anti-tubulin and protein A coupled to colloidal gold resulted in the highly specific localization of tubulin in ciliary axonemes and basal bodies. Omission of primary or secondary antibody resulted in extremely low levels of fluorescence while no colloidal gold particles could be detected in cultures at the electron microscopy level when rabbit anti-tubulin was omitted. 相似文献
3.
4.
Haploid plants were regenerated in vitro from unpollinated ovules of niger (Guizotia abyssinica (L. f.) (Cass.) on Murashige and Skoog nutrient medium (MS) supplemented with 10 μM naphthaleneacetic acid or 10 μM NAA +
1.5 μM kinetin and 30 g/l sucrose. Gamborg (B5) medium was the best for plant regeneration (in comparison with MS, Nitsch
and Nitsch (NN), and Chu (N6) media) from cultured ovules, and 6.66 and 7.33 ovules of JNC-6 and Ootacamund cultivars were
involved in direct plant regeneration on this medium. Matured ovules (ovules collected one day before anthesis or on the day
of anthesis) only responded to cultural regimes and involved in direct plantlet development. Cytological preparation of root
tips and chloroplast counts in the guard cells of leaf stomata of regenerated plants confirmed their haploid nature.
This text was submitted by the authors in English. 相似文献
5.
Cell division in cell suspension cultures can be completely blocked by the growth retardant tetcyclacis at a concentration of 10-4 mol l-1. In rice cells it has been demonstrated that the growth inhibition can be completely overcome by application of cholesterol independent of the duration of pretreatment with tetcyclacis. In suspension cultures of maize and soybean, too, the effect of tetcyclacis on cell division was neutralized by adding cholesterol. Other plant sterols, stigmasterol, campesterol and sitosterol were active in a decreasing order. Modifications in the cholesterol perhydro-cyclopentanophenanthrene-ring system indicate that the hydroxyl group at C-3 and the double bond between C-5 and C-6 in ring B are required for the activity. In contrast, gibberellic acid as well as ent-kaurenoic acid could not compensate retardant effects. Likewise, tetcyclasis did not change the level of gibberellins in rice cells as shown by radioimmunoassay. Thus, it is concluded that in cell suspension cultures sterols play a more important role in cell division than gibberellins.Abbreviation GAx
gibberelin Ax 相似文献
6.
7.
Dov Borovsky 《Archives of insect biochemistry and physiology》1985,2(4):333-349
Oostatic hormone, the hormone that inhibits vitellogenesis in mosquitoes, was purified 7,000-fold with a recovery of 70% from the ovaries of the mosquito Aedes aegypti. The purification procedure included heat treatment and chromatography on ion exchange and gel filtration columns. The hormone is a small peptidelike molecule of molecular weight 2,200 at pH 4.5, which aggregates into larger molecular species of trimer and octamer at pH 7.0 as determined by gel filtration. The hormone is positively charged at pH 7.8 and has a low Rf at pH 9.4 on disc gel electrophoresis. Injection of purified oostatic hormone (9 ng) into female mosquitoes inhibited yolk deposition and vitellogenin synthesis. Activity of the oostatic hormone in the mosquito ovary increased rapidly following blood feeding and reached a maximum after 48 h. Oostatic hormone of A. aegypti injected into autogenous Aedes taeniorhynchus inhibited egg development. Repeated injections of dilute oostatic hormone at 24 h intervals partially arrested egg development, resulting in 60% reduction in the number of eggs laid. This hormone does not block release of egg development neurosecretory hormone (EDNH) from the mosquito brain but rather appears to act on the ovary. 相似文献
8.
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
9.
Compelling evidence suggests the limitation and shortcomings of the current and well established cell culture method using multi-well plates, flasks and Petri dishes. These are particularly important when cell functions are sensitive to the local microenvironment, cell–cell and cell–extracellular matrix interactions. There is a clear need for advanced cell culture systems which mimic in vivo and more physiological conditions. This review summarises and analyses recent progress in three dimensional (3D) cell culture with perfusion as the next generation cell culture tools, while excluding engineered tissue culture where three dimensional scaffold has to be used for structural support and perfusion for overcoming mass transfer control. Apart from research activities in academic community, product development in industry is also included in this review. 相似文献
10.
Role of Thidiazuron (TDZ) in inducing adventitious organogenesis in Pongamia was studied. TDZ at different concentrations (0, 0.45, 2.27, 4.54, 6.71, 9.08, 11.35, 13.12 and 22.71 μM) were used for induction
of caulogenic bud formation in deembryonated cotyledon explants. Each cotyledon was cut into three segments and identified
as proximal, middle and distal. Duration of TDZ exposure, influence of the segment and orientation of the explant were studied.
TDZ at 11.35 μM concentration was optimum for the induction of shoots and rapid elongation. Shoots induced at higher concentration
elongated after several passages in growth regulator free medium, thereby extending the period of differentiation. Exposure
of the explant for 20 days yielded more number of buds than 10 days. Proximal segment of the cotyledon was more responsive.
Contact of abaxial surface in the medium was more effective and generated more buds than the adaxial side. Buds differentiated
and elongated on transfer to MS basal medium for 8–12 passages of 15 days each. Rooting and elongation of shoots was achieved
in charcoal supplemented half-strength MS medium. Rooted plantlets survived on transfer to sand soil mixture. The plants were
hardened and transferred to green house. This is the first report on in vitro regeneration of Pongamia pinnata via adventitious organogenesis using TDZ. This protocol may find application in studies in genetic transformation, isolation
of somaclonal variants and in induction of mutants. It also provides a system to study the inhibitory role of TDZ on shoot
differentiation. 相似文献