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561.
对虾的慢适应和快适应感受器的放电型式可因环境中 Mg~( )浓度的改变而发生转变:在用蔗糖代替全部 Mg~( )的海水(无镁海水)中,当感受器肌肉受到持续性牵拉时,两种感受器都发出持续性节律放电,即快感受器也给出了慢适应型放电;反之,在 Mg~( )浓度加倍的海水(高镁海水)中,两者都只在感受器肌肉受到牵拉的瞬时给出短暂的放电,即慢感受器也给出了快适应型放电。这种放电型式的转变只有当无镁或高镁海水接触感受器细胞体时才出现。在正常海水中,10~(-3)M 的γ-氨基丁酸(GABA)即可完全抑制由牵拉引起的对虾牵张感受器的放电,但在无镁海水中,必需10~(-2)M GABA 方能达到同样的抑制效果。若在无镁亦无钙海水中,即使用1M 的 GABA 亦不能抑制感受器的牵拉放电。不仅如此,在这种海水中抑制神经对感受器细胞放电的抑制作用也消失。 相似文献
562.
Adaptive evolution of G-protein coupled receptor genes 总被引:2,自引:0,他引:2
The phylogeny and patterns of nucleotide substitutions in the visual
pigment genes, adrenergic receptor genes, muscarinic receptor genes, and in
the human mas oncogene were studied by comparing their DNA sequences. The
evolutionary tree obtained shows that the visual pigment genes and mas
oncogene form one cluster and that the receptor genes form another. In the
evolution of rhodopsin genes, synonymous substitutions outnumber
nonsynonymous substitutions. This is consistent with the neutral theory of
molecular evolution. However, the early evolutionary stages of alpha- and
beta-adrenergic and muscarinic receptors are notable for significantly more
nonsynonymous substitutions than synonymous substitutions, suggesting the
acquisition of novel functional adaptations. Variable rates of
nonsynonymous changes in different domains of these proteins reveal DNA
segments that might have been important in their functional adaptations.
相似文献
563.
Differences in the poly(ADP-ribosyl)ation patterns of ICP4, the herpes simplex virus major regulatory protein, in infected cells and in isolated nuclei.
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J A Blaho N Michael V Kang N Aboul-Ela M E Smulson M K Jacobson B Roizman 《Journal of virology》1992,66(11):6398-6407
Infected-cell protein 4 (ICP4), the major regulatory protein in herpes simplex viruses 1 and 2, was previously reported to accept 32P from [32P]NAD in isolated nuclei. This modification was attributed to poly(ADP-ribosyl)ation (C. M. Preston and E. L. Notarianni, Virology 131:492-501, 1983). We determined that an antibody specific for poly(ADP-ribose) reacts with ICP4 extracted from infected cells, electrophoretically separated in denaturing gels, and electrically transferred to nitrocellulose. Our results indicate that all forms of ICP4 observed in one-dimensional gel electrophoresis are poly(ADP-ribosyl)ated. Poly(ADP-ribose) on ICP4 extracted from infected cells was resistant to cleavage by purified poly(ADP-ribose) glycohydrolase unless ICP4 was in a denatured state. Poly(ADP-ribose) added to ICP4 in isolated nuclei was sensitive to this enzyme. This result indicates that the two processes are distinct and may involve different sites on the ICP4 molecule. 相似文献
564.
Factors affecting nest-site choice and reproductive success of Curlews Numenius arquata on farmland 总被引:2,自引:1,他引:1
Nest-site choice and reproductive success of Curlews Numenius arquata in different habitats were studied at a mixed farmland site (grasslands and flooded tilled fields relatively common) and at an arable farmland site (dry tilled fields more dominant than at the mixed site) in central Sweden. At both sites Curlews preferred to nest on grassland and fallow fields, where hatching success was higher than on tillage fields. Nests were also situated further away from forest edges than random sites, but hatching success did not vary with distance to the forest edge. Only 35.6% of the pairs were estimated to hatch young. The main cause of nest loss was predation and the second most important factor was destruction by farming practices, which was an important factor in tillage early in season. Surprisingly, nest survival was higher at the arable than at the mixed farmland site, probably being an effect of the increased proportion of fallowing during recent years. Mortality of chicks was 79.7% before fledgling age (both sites combined) and, surprisingly, chick survival was lower on meadows than on arable fields and leys. The mean production of young was only 0.25 fledglings per pair, which is lower than in areas less affected by farming practice. The low production of young is probably an important factor in the decline of Curlew populations on Swedish farmland. On bogs 1.4 fledglings per pair were produced, indicating that reproductive success of Curlews is higher in more natural habitats. 相似文献
565.
566.
台湾铗蠓吸血和生殖的观察 总被引:1,自引:0,他引:1
实验室条件下,台湾铗蠓[Forcipomyia (Lasiohelea)taiwana]吸食小鸡、小白鼠乳鼠的血液,吸血率为7.07%±1.64和65.70%±5.41.亦能通过人胎盘膜进行离体喂血,吸血率为35.44%±6.91.80对成蠓用人工交配的方法其交配率达到19%,但未授精.雌蠓未交配能吸血、产卵但不孵化.雌蠓饱血一次,发育成熟的卵平均为49.23±21.33个,实际产出的卵平均为35.35±22.38个.关于交配和产卵习性也做了观察. 相似文献
567.
Resistance of nicotiana benthamiana to phytophthora infestans is mediated by the recognition of the elicitor protein INF1 总被引:11,自引:0,他引:11
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Phytophthora infestans, the agent of potato and tomato late blight disease, produces a 10-kD extracellular protein, INF1 elicitin. INF1 induces a hypersensitive response in a restricted number of plants, particularly those of the genus Nicotiana. In virulence assays with different P. infestans isolates, five Nicotiana species displayed resistance responses. In all of the interactions, after inoculation with P. infestans zoospores, penetration of an epidermal cell was observed, followed by localized necrosis typical of a hypersensitive response. To determine whether INF1 functions as an avirulence factor in these interactions, we adopted a gene-silencing strategy to inhibit INF1 production. Several transformants deficient in inf1 mRNA and INF1 protein were obtained. These strains remained pathogenic on host plants. However, in contrast to the wild-type and control transformant strains, INF1-deficient strains induced disease lesions when inoculated on N. benthamiana. These results demonstrate that the elicitin INF1 functions as an avirulence factor in the interaction between N. benthamiana and P. infestans. 相似文献
568.
The involvement of the microtubule (MT) and actin microfilament (MF) cytoskeletons in establishing nuclear positions during zoosporogenesis in Allomyces macrogynus was assessed using selective cytoskeletal disrupting treatments and documented with light microscopy. These experiments were coupled with low-speed centrifugation studies to determine the degree to which cytoskeletal elements anchor nuclear position. At the onset of zoospore formation, nuclei were positioned only in cortical cytoplasmic regions of the zoosporangia (ZS). Immunofluorescence microscopy revealed that MTs primarily emanated from centrosomal regions into the surrounding cytoplasm at this stage. During delimitation of the cytoplasm into individual uninucleate zoospores, nuclei migrated from cortical regions to become distributed throughout the cytoplasm. Coincident with nuclear migrations, MTs were primarily organized at and emanated from nuclear surfaces, forming extensive perinuclear arrays. Nuclear migrations were suppressed in ZS induced to sporulate in the presence of cytochalasin D, an actin MF inhibiting compound. Disruption of MTs with nocodazole did not block nuclear migrations, although resultant nuclear spacing was irregular. Centrifugation treatments of control and drug-treated ZS demonstrated that nuclear positions were stabilized by perinuclear MT arrays. The results indicate that nuclear motility in ZS of A. macrogynus is the result of an actin-based system while perinuclear MTs arrays function to establish and fix nuclear position during zoospore formation. Copyright 1998 Academic Press. 相似文献
569.
Modified VP22 Localizes to the Cell Nucleus during Synchronized Herpes Simplex Virus Type 1 Infection 总被引:10,自引:0,他引:10
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The UL49 gene product (VP22) of herpes simplex virus types 1 and 2 (HSV-1 and HSV-2) is a virion phosphoprotein which accumulates inside infected cells at late stages of infection. We previously (J. A. Blaho, C. Mitchell, and B. Roizman, J. Biol. Chem. 269:17401-17410, 1994) discovered that the form of VP22 packaged into infectious virions differed from VP22 extracted from infected-cell nuclei in that the virion-associated form had a higher electrophoretic mobility in denaturing gels. Based on these results, we proposed that VP22 in virions was "undermodified" in some way. The goal of this study is to document the biological and biochemical properties of VP22 throughout the entire course of a productive HSV-1 infection. We now report the following. (i) VP22 found in infected cells is distributed in at least three distinct subcellular localizations, which we define as cytoplasmic, diffuse, and nuclear, as measured by indirect immunofluorescence. (ii) Using a synchronized infection system, we determined that VP22 exists predominantly in the cytoplasm early in infection and accumulates in the nucleus late in infection. (iii) While cytoplasmic VP22 colocalizes with the HSV-1 glycoprotein D early in infection, the nuclear form of VP22 is not restricted to replication compartments which accumulate ICP4. (iv) VP22 migrates as at least three unique electrophoretic species in denaturing sodium dodecyl sulfate-DATD-polyacrylamide gels. VP22a, VP22b, and VP22c have high, intermediate, and low mobility, respectively. (v) The relative distribution of the various forms of VP22 derived from infected whole-cell extracts varies during the course of infection such that low-mobility species predominate at early times and high-mobility forms accumulate later. (vi) The highest-mobility forms of VP22 partition with the cytoplasmic fraction of infected cells, while the lowest-mobility forms are associated with the nuclear fraction. (vii) Finally, full-length VP22 which partitions in the nucleus incorporates radiolabel from [32P]orthophosphate whereas cytoplasmic VP22 does not. Based on these results, we conclude that modification of VP22 coincides with its appearance in the nucleus during the course of productive HSV-1 infection. 相似文献
570.