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141.
142.
143.
M. C. Léglise P. Darodes de Tailly J. L. Vignot M. A. Le Bot A.-M. Le Roux C. Riché 《Cell biology and toxicology》1996,12(1):39-53
A cellular model of hematopoiesis which would be more convenient than bone marrow (BM) progenitors and directly relevant to human pathology is needed in order to investigate xenobiotic toxicity. Human umbilical cord blood (HCB), previously shown to be able to repopulate BM, provides a powerful in vitro model of normal human hematopoiesis. In order to validate the use of normal HCB progenitors as targets for dose-related myelosuppression, we used clonogenic assays and expansion in a liquid culture of progenitor-enriched cell suspensions from HCB. A series of 8 reference molecules, doxorubicin, cytosine-arabinoside, 5-fluorouracil, 3-azido-3-deoxythymidine, acetylsalicyclic acid, sodium valproate and two cephalosporin antibiotics, were tested. In vitro 50% inhibition concentrations (IC50) were compared to those observed or reported with BM progenitors, and to the values of plasma concentrations from treated patients. HCB progenitors as in vitro targets for cytotoxic molecules were easy to access and handle, and their use was sensitive, specific and reproducible. They gave results similar to BM progenitors and allowed a qualitative approach to cellular metabolism and toxicity using morphological, flow cytometric and chromatographic methods.Abbreviations ARA-CC
cytosine arabinoside
- AS
acetylsalicylic acid
- AZTT
3-azido-3-deoxythymidine
- BFUU
burst-forming units
- BM
bone marrow
- CFU
colony-forming units
- DOXX
doxorubicin
- FU
5-fluorouracil
- glyAA
glyAcophorin A
- HCB
human umbilical cord blood
- IU
international units
- PCMEM
human placenta-conditioned medium
- VA
sodium valproate 相似文献
144.
A. Le Ralec 《BioControl》1995,40(1):87-93
Using transmission electron microscopy, egg content is studied in 10 parasitoid species, which either feed on host hemolymph or do not. As expected, hydropic eggs were found to contain little yolk which is only lipoid. In host-feeding species, the yolk contains a great number of typical protein bodies whereas in species that do not host-feed and which produce large eggs, the yolk contain very different bodies. 相似文献
145.
146.
147.
C. Kevers B. Bisbis F. Le Dily J. P. Billard C. Huault Th. Gaspar 《In vitro cellular & developmental biology. Plant》1995,31(2):122-126
The transfer of light-cultured green normal (N) and white habituated (HNO) sugarbeet callus to darkness reduced the growth
of N callus and improved growth and delayed necrosis in the HNO callus. The decrease of dry matter of N callus under darkness
was accompanied by a reduced content of carotenoids and by decreased CO2 fixation, which was compensated by an increased dependency on externally supplied sucrose. The levels of some organic nitrogen
compounds such as glutamate, proline, and free polyamines were not affected by transfer to darkness of N or HNO callus. Darkness
decreased ethylene emissions in both callus types. In the HNO callus, the sucrose growth dependency and the CO2 fixation were unaffected by darkness. Chlorophylls were absent both in light and darkness, whereas some carotenoids were
accumulated in the HNO callus only in dark conditions. In another connection, a significant increase of peroxidase activity,
which did not occur in the N callus, was induced by darkness in the HNO callus. A decreased content of thio-barbituric acid
(TBA)-reactive substances was measured in the HNO callus transferred to darkness, whereas an increase was noticed in the N
callus placed in the same conditions. These metabolic changes and the reduction of cellular damage in darkness revealed light-induced
stress reactions leading to necrosis and to reduced growth of HNO callus. It appeared that darkness allowed the HNO callus
to avoid the photooxidation stress. Therefore, the favorable effect of darkness on HNO growth might be explained by the suppression
of photooxidative damage due to the absence of carotenoids. The higher peroxidase activity in the HNO callus maintained in
darkness raised the problem of heme synthesis in this heterotrophic callus. 相似文献
148.
An RNA pseudoknot is an essential structural element of the internal ribosome entry site located within the hepatitis C virus 5' noncoding region. 总被引:8,自引:2,他引:6 下载免费PDF全文
Translation of the human hepatitis C virus (HCV) RNA genome occurs by a mechanism known as "internal ribosome entry." This unusual strategy of translation is employed by naturally uncapped picornaviral genomic RNAs and several cellular mRNAs. A common feature of these RNAs is a relatively long 5' noncoding region (NCR) that folds into a complex secondary structure harboring an internal ribosome entry site (IRES). Evidence derived from the use of dicistronic expression systems, combined with an extensive mutational analysis, demonstrated the presence of an IRES within the HCV 5'NCR. The results of our continued mutational analysis to map the critical structural elements of the HCV IRES has led to the identification of a pseudoknot structure upstream of the initiator AUG. The evidence presented in this study is based upon the mutational analysis of the putative pseudoknot structure. This is further substantiated by biochemical and enzymatic probing of the wild-type and mutant 5'NCR. Further, the thermodynamic calculations, based upon a modified RNAKNOT program, are consistent with the presence of a pseudoknot structure located upstream of the initiator AUG. Maintenance of this structural element is critical for internal initiation of translation. The pseudoknot structure in the 5'NCR represents a highly conserved feature of all HCV subtypes and members of the pestivirus family, including hog cholera virus and bovine viral diarrhea virus. 相似文献
149.
B. Canguilhem A. Malan M. Masson-Pévet P. Nobelis R. Kirsch P. Pévet J. Le Minor 《Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology》1994,163(8):690-698
Temporal patterns of hibernation were studied by continuous monitoring of body temperature by radiotelemetry over 6 months in European hamsters, Cricetus cricetus, at constant temperature and photoperiod. Entrances into hibernation occurred mostly at the end of the night (0000–0800 hours), while arousals were randomly distributed between day and night. This is at variance with a control of bout duration by a clock with a period of 24 h. Consequently, the timing of entrances implies a phase-resetting of the circadian clock on each arousal. Persistence of circadian rhythmicity with a period different from 24 h during deep hibernation was investigated examining whether the durations of torpor bouts were integer multiples of a constant period. A non-parametric version of the classical contingency test of periodicity was developed for this purpose. Periods ranging from 21 to 29 h were tested. Nine animals out of ten showed at least one significant period in this range (P<0.01), either below 24 h (21.8±0.5 h, n=4) or above (27.3±0.5 h, n=7). However, we have found a theoretical model of bout durations for which the contingency test of periodicity sometimes gives false significant results. This indicates that the power of the test is weak. With this reservation our results suggest that a circadian oscillator controls the duration of a bout of hibernation, which would occur after an integer, but variable and possibly temperature-dependent number of cycles.Abbreviations b
a contingency test (see Appendix)
- SCN
suprachiasmatic nuclei
-
period
-
T
b
body temperature 相似文献
150.
G. Ferretti M. V. Narici T. Binzoni L. Gariod J. F. Le Bas H. Reutenauer P. Cerretelli 《European journal of applied physiology and occupational physiology》1994,68(2):111-115
The relationships between absolute peak muscle power (W
peak), muscle cross sectional area (CSAtot, i.e. the sum of both thigh and calf CSA) and muscle high energy phosphate concentration (adenosine 5-triphosphate [ATP] and phosphocreatine concentrations [PC]) were studied in 47 subjects classified into five groups: A, 10 sedentary (S) subjects aged 20–35 years; B, 9 S aged 35–50 years; C, 9 S aged more than 50 years; D, 13 children aged 8–13 years; and E, 6 athletes (top level volleyball players) aged 24 (SD 3) years. The W
peak was measured during a maximal vertical high jump off both feet on a force platform. The CSAtot was measured anthropometrically. The [ATP] and [PC] were determined by 31Phosphorus nuclear magnetic resonance spectroscopy. The W
peak decreased with age, was 65% lower in D than in A, and 43% higher in E than in A. The CSAtot did not vary with age, was 45% smaller in D than in A, and 15% greater in E than in A. The [ATP] and [PC] were essentially the same in all groups. The changes observed in W
peak were only partially accounted for by changes in CSAtot. Therefore, in addition to the variables investigated, other factors appear to have been involved in the determination of W
peak with increasing age and training. An important role may be played by hormonal, particularly at puberty, and neural factors. 相似文献