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71.
Phytochrome control of maize coleoptile section elongation: the role of cell wall extensibility 总被引:1,自引:0,他引:1 下载免费PDF全文
Maize (Zea mays) coleoptile section cell wall extensibility was found to be stimulated by red light. This stimulation was largely removed by simultaneous or immediately subsequent far-red treatment. Qualitatively similar patterns of response occurred at 0 C and 20 C. Plastic extensibility responded more than elastic extensibility after red light treatment. Red-induced extensibility increases were detectable by 20 minutes after irradiation, and extensibility continued to increase up to at least 1 hour after irradiation. The kinetics of escape from far-red reversibility indicate that the initial events leading to this phenomenon are among the fastest known phytochrome responses. 相似文献
72.
The effects of the calcium antagonists ruthenium red and D-600 and the cation ionophore A23187 on steroidogenesis were investigated. Steroidogenesis triggered by corticotrophin and cyclic AMP was inhibited by each of the agents. Incubation of Y-1 cells with an excess of ethyleneglycol-bis-(beta-amino-ethylether)-N,N'-tetraacetic acid (EGTA) abolished the steroidogenic response to corticotrophin while the response to cyclic AMP was unaffected. The ability of ruthenium red and D-600 (1 . 10(-5) M), and A23187 (6 . 10(-6 M) to inhibit a response which does not require the presence of extracellular calcium (cyclic AMP induced steroidogenesis) suggests that they are altering intracellular calcium. Neither of the calcium antagonists nor the cation ionophore inhibited the steroidogenic response to exogenous pregnenolone, thereby suggesting that the cells were still viable. Only when A23187 was used in the presence of a 15-fold increase in extracellular calcium (4.8 mM) was the response to pregnenolone diminished. The data are interpreted as a further indication that, in intact cells, intracellular calcium plays a role in the steroidogenic pathway. 相似文献
73.
Carol M. Warner Ruth M. Graves Carla M. Tollefson Mary Jo F. Schmerr Thomas J. Stephens Carmen F. Merryman Paul H. Maurer 《Immunogenetics》1976,3(1):337-348
The immune response of allophenic mice of type C57BL/6(A × SJL) F1 to GL administered in complete Freund's adjuvant was tested. Control mice of the three strains C57BL/6, A, and SJL are all nonresponders to this antigen. However, the F1 generations of C57BL/6 × A, C57BL/6 × SJL, and A × SJL were all responders to the antigen, so that the complementarity of at least two genes is confirmed. The allophenic mice showed no further complementation beyond the F1 generation, a result which may argue against the possibility that more than two genes control the response to GL in these mouse strains. Characterization of the allophenic mice over several months showed that they exhibit chimeric drift, both in their coat color and in peripheral white blood cell population. There is no apparent correlation of coat color to the lymphocyte composition of the mice at any one time. The mice are true chimeras, since killing of the two populations of white blood cells with two different anti-H-2 sera produced a 100 percent killing. The immune response of individual allophenic mice to GL showed a good correlation to the number of A × SJL lympho-cytes in the animal.Abbreviations used in this paper are GL
an amino acid polymer of 57 %l-glutamic acid, 38%l-lysine, and 5%l-phenylalanine
- GLT15
an amino acid polymer ofl-glutamic acid,l-lysine, and 15 %l-tyrosine
- (T,G)-A-L
an amino acid polymer having a polylysine backbone with side chains of polyd-l-alanine, terminating in short sequences of tyrosine and glutamic acid
- GAT10
an amino acid polymer of 60%l-glutamic acid, 30%l-alanine, and 10%l-tyrosine
- GLA5
an amino acid polymer of 57%l-glutamic acid, 38%l-lysine, and 5%l-alanine
- DNP
2,4 dinitrophenyl
- BGG
bovine gamma globulin
- FCS
fetal calf serum
- PWBC
peripheral white blood cell
- SWBC
spleen white blood cell
- T cell
thymus-derived lymphocyte
- B cell
bone marrow-derived lymphocyte 相似文献
74.
DNA-dependent RNA polymerase has been measured at various stages of preimplantation development in mouse embryos. The total RNA polymerase activity per embryo increases rapidly from the 8-cell stage to the blastocyst stage. Studies with low α-amanitin concentrations, which inhibit form II RNA polymerase, and high α-amanitin concentrations, which inhibit both form II and III RNA polymerases indicate that the relative proportions of the three forms change significantly during preimplantation development. The changes which occur in the types and levels of RNA polymerase appear to parallel corresponding changes in the synthesis of the major classes of RNA. 相似文献
75.
A marked decrease in the amount of the A2 component of phenol oxidase occurs in the speck locus of Drosophila melanogaster. The amount of A2 in speck is restored to a normal amount in the presence of the suppressor mutant, su(s) 2. 相似文献
76.
Kinetics of cell fusion induced by a syncytia-producing mutant of herpes simplex virus type I. 总被引:2,自引:0,他引:2 下载免费PDF全文
We have isolated a number of plaque-morphology mutants from a strain of herpes simplex virus type I which, unlike the wild type, cause extensive cell fusion during a productive viral infection. After the onset of fusion, there is an exponential decrease in the number of single cells as a function of time after infection. At a multiplicity of infection (MOI) of 3.8 plaque-forming units per cell, fusion begins 5.3 h after infection with the number of single cells decreasing to 10% of the original number 10.2 h after infection. As the MOI is gradually increased from 0.4 to 8, the onset of fusion occurs earlier during infection. However, when the MOI is increased from 8 to 86, the onset of fusion does not occur any earlier. The rate of fusion is independent of the MOI for an MOI greater than 1. The rate of fusion varies linearly with initial cell density up to 3.5 X 10(4) cells/cm2 and is independent of initial cell density at higher cell concentrations. To assay cell fusion we have developed a smiple quantitative assay using a Coulter counter to measure the number of single cells as a function of time after infection. Data obtained using a Coulter counter are similar to those obtained with a microscope assay. 相似文献
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