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101.
Further progress towards a catalogue of all Arabidopsis genes: analysis of a set of 5000 non-redundant ESTs 总被引:9,自引:1,他引:8
Richard Cooke Monique Raynal Michele Laudi Franoise Grellet Michel Delseny Peter-Christian Morris Danile Guerrier Jrme Giraudat Franoise Quigley Grard Clabault You-Fang Li Rgis Mache Micheline Krivitzky Isabelle Jean-Jacques Gy Martin Kreis Alain Lecharny Yves Parmentier Jacqueline Marbach Jacqueline Fleck Bernadette Clment Gabriel Philipps Christine Herv Claude Bardet Dominique Tremousaygue Bernard Lescure Christophe Lacomme Dominique Roby Marie-Franoise Jourjon Patrick Chabrier Jean-Louis Charpenteau Thierry Desprez Joelle Amselem Helen Chiapello Herman Hfte 《The Plant journal : for cell and molecular biology》1996,9(1):101-124
Nearly 7000 Arabidopsis thaliana -expressed sequence tags (ESTs) from 10 cDNA libraries have been sequenced, of which almost 5000 non-redundant tags have been submitted to the EMBL data bank. The quality of the cDNA libraries used is analysed. Similarity searches in international protein data banks have allowed the detection of significant similarities to a wide range of proteins from many organisms. Alignment with ESTs from the rice systematic sequencing project has allowed the detection of amino acid motifs which are conserved between the two organisms, thus identifying tags to genes encoding highly conserved proteins. These genes are candidates for a common framework in genome mapping projects in different plants. 相似文献
102.
Adle Martial Isabelle Gaillard Jean-Marc Engasser Annie Marc 《Enzyme and microbial technology》1995,17(12):1062-1066
A homemade serum-free medium containing a low protein level under 0.1 g l−1 has been proved to support long-term cultures of VO 208 hybridoma cells successfully up to 50 days. The low protein level was achieved by supplying the lipids through liposomes containing cholesterol, oleic acid,
- dipalmitoyl phosphatidylcholine, and bovine serum albumin. The influence of the liposome content in the feeding medium was studied in a continuous culture performed with step variations of the liposomes level, from 7.5 to 30 ml l−1. The cell density decreased at the highest liposomes content while it became higher with 7.5 or 12 ml l−1 of liposomes. For each step variation appeared a transitory activation of the specific rates of nutrient consumption, metabolite production and antibody secretion, as well as a transitory decrease of the specific cell growth rate. The overall structure of the antibodies was not affected during the culture. 相似文献
103.
Assessment of microinjection for introducing DNA into uninuclear microspores of rapeseed 总被引:3,自引:0,他引:3
Elizabeth Jones-Villeneuve Bin Huang Isabelle Prudhomme Sharon Bird Roger Kemble Jiro Hattori Brian Miki 《Plant Cell, Tissue and Organ Culture》1995,40(1):97-100
Approximately 2,000 embryogenic uninuclear microspores of rapeseed (Brassica napus) cv. Topas were intranuclearly injected with a chimaeric -glucuronidase (Escherichia coli Uid A) gene. Stable integration had not occurred among 55 plants that were regenerated. Coinjection of the dye Lucifer Yellow and detection of injected DNA by the polymerase chain reaction revealed high frequencies of transfer. However, the amount of DNA injected was less than 20 copies, which may have been insufficient for stable transformation of microspores.Abbreviations PCR
polymerase chain reaction
- GUS
-glucuronidase 相似文献
104.
Prof. Dr. Dietrich Schumann 《Facies》1995,32(1):189-202
Summary Rudist and stromatoporid associations of the Campanian from Central Oman are nearly monospecific. They are dominated byDurania aff.nicholasi, Vaccinites vesiculosus, Torreites milanovici or phaceloid and massive stromatoporids. Several other rudist genera play a secondary role. The thickness of the associations
is rarely more than one metre. Solitary corals do not occur in the associations. Colonial corals are less common, although
they are up to 1 m high and show considerable diversity. There are no binders. The reef structure indicates variable hydrodynamic
conditions. They are always associated with very shallow water. The pureDurania aff.nicholasi patches with large colonial corals andTorreites milanovici are presumably the most rigid structures. The near monospecific associations ofVaccinites vesiculosus are widely distributed. Although mostly preserved in situ, strong currents, presumably caused by tropical storms, have repeatedly
impaired and interrupted growth. The specific growth characteristics of the shell of some rudists, especially the radiolitids,
enable an estimation of the individual lifespan. Frameworks of approximately 1 metre thickness probably developed in ±100
years. The sediments of the complete sections are predominantly bioclastic. 相似文献
105.
Prof. Dr. Wolf-Christian Dullo Dr. Marcos Gektidis Prof. Dr. Stjepko Golubic Dr. Georg A. Heiss Dipl. Biol. Heike Kampmann Dr. William Kiene Dipl. Ökol. Dieter K. Kroll Dipl. Biol. Martin L. Kuhrau Dr. Gudrun Radtke Dr. John G. Reijmer Dr. Götz B. Reinicke Prof. Dr. Dietrich Schlichter Prof. Dr. Helmut Schuhmacher Klaus Vogel 《Facies》1995,32(1):145-188
106.
Marie-Jos Navarro-Prigent Isabelle Sguin Pierre Boivin Didier Dhermy 《Biology of the cell / under the auspices of the European Cell Biology Organization》1995,83(1):33-38
Summary— The membrane skeleton, responsible for shape and mechanical properties of the red cell, was purified by the Triton extraction procedure in presence of 5 mM, 150 mM or 600 mM NaCl. The proportion of spectrin, protein 4.1 and actin present in erythrocyte skeletons does not depend on the molarity of NaCl used. In contrast ankyrin, protein band 3 and protein 4.2 are removed from skeletons as the ionic strength increased. Solubilization assays of membrane skeletons were used to study protein interactions inside the skeleton. Solubilization was performed by Tris, a non-selective disruptive reagent, or by p-mercuribenzene sulfonic acid (PMBS), which principally release spectrin and actin. Tris action was assessed by calculation of the percentage of solubilized proteins, which increased proportionally with Tris molarity. PMBS action was kinetically determined as the decrease in skeleton turbidity. With these two reagents, we observed a lower dissociation of skeletons prepared with high ionic strength buffer. Erythrocyte pretreatment with okadaic acid, an inhibitor of serine-threonine phosphatases, revealed a phosphorylation-induced skeleton gelation and a better resistance to Tris-solubilization. 相似文献
107.
Cloning and electrophysiological analysis of KST1, an inward rectifying K+ channel expressed in potato guard cells. 总被引:18,自引:2,他引:16
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B Müller-R?ber J Ellenberg N Provart L Willmitzer H Busch D Becker P Dietrich S Hoth R Hedrich 《The EMBO journal》1995,14(11):2409-2416
Potassium uptake by guard cells represents part of the osmotic motor which drives stomatal opening. Patch-clamp measurements have identified inward rectifying K+ channels capable of mediating K+ uptake in guard cells and various other plant cell types. Here we report the molecular cloning and characterization of a voltage-dependent K+ channel (KST1) from potato (Solanum tuberosum L.) guard cells. In situ hybridization shows expression of kst1 in guard cells. Two-electrode voltage-clamp and patch-clamp studies of the gene product after cRNA injection into Xenopus oocytes identified KST1 as a slowly activating, voltage-dependent, inward rectifying K+ channel. The single channel current voltage curve was linear in the range -160 to +20 mV, with a deduced single channel conductance of 7 pS in symmetrical 100 mM K+. This channel type, modulated by pH changes within the physiological range, required ATP for activation. In line with the properties of a K(+)-selective channel, KST1 was permeable to K+, Rb+ and NH4+ and excluded Na+ and Li+. Cs+ at submillimolar concentrations blocked the channel in a voltage-dependent manner. Related studies on potato guard cell protoplasts confirmed the biophysical characteristics of the kst1 gene product (KST1) in the heterologous expression system. Therefore, KST1 represents a major K+ uptake channel in potato guard cells. 相似文献
108.
Marc Pauly Isabelle Kayser Martine Schmitz Fernand Ries François Hentges Mario Dicato 《Journal of molecular evolution》1995,41(6):974-978
The mdr1 gene, first member of the human multidrug-resistance gene family, is a major gene involved in cellular resistance to several drugs used in anticancer chemotherapy. Its product, the drug-excreting P-glycoprotein, shows a bipartite structure formed by two similar adjacent halves. According to one hypothesis, the fusion of two related ancestral genes during evolution could have resulted in this structure. The DNA sequence analysis of the introns located in the region connecting the two halves of the human mdr1 gene revealed a highly conserved poly(CA) · poly (TG) sequence in intron 15 and repeated sequences of the Alu family in introns 14 and 17. These repeated sequences most likely represent molecular fossils of ancient DNA elements which were involved in such a recombination event.
Correspondence to: M. Pauly 相似文献
109.
Christine Heberden Thierry Mercier Isabelle Gaillard-Sanchez Brigitte Huet Paule Martel 《Experimental cell research》1995,218(2)
We assessed the presence and the role of membrane TGF-α in two rat liver epithelial cell lines, either parental or transfected with c-fos proto-oncogene. c-fos overexpressing cells had more TGF-α-like activity in their membranes. When TGF-α was removed by elastase or neutralized, the growth rates of both cell lines were markedly reduced, but to a higher extent for parental cells. If membrane TGF-α seemed to play a key contribution in normal cell growth, both cell lines were unable to react to the addition of soluble TGF-α, showing that these two forms of growth factors are not equivalent. 相似文献
110.