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91.
To study the reliabiliity of formulas for calculating mean skin temperature (T
sk), values were computed by 18 different techniques and were compared with the mean of 10,841 skin temperatures measured by
infrared thermography. One hundred whole-body infrared thermograms were scanned in ten resting males while changing the air
temperature from 40° C to 4° C. Local, regional average and mean skin temperatures were obtained using an image processing
system. The agreement frequency, defined as the percentage of the calculated T
sk values which agreed with the corresponding infrared thermographic T
sk within ±0.2° C, ranged for with the various formulas from 7% to 80%. In many sites, the local skin temperature did not coincide
with the regional average skin temperature. When the local skin temperatures which showed the highest percentage similarity
to the regional average skin temperature within ±0.4° C were applied to the formula, the agreement frequency was markedly
improved for all formulas. However, the agreement frequency was not affected by changing the weighting factors from specific
constants to individually measured values of regional surface area. By applying the physiologically reliable accuracy range
of ±0.2° C in the moderate and ±0.4° C in the cool condition, agreement frequencies of at least 95% were observed in formulas
involving seven or more skin temperature measurement sites, including the hand and foot. We conclude that calculation of a
reliable mean skin temperature must involve more than seven skin temperature measurement sites regardless of ambient temperature.
Optimal sites for skin temperature measurement are proposed for various formulas.
Received: 2 December 1996 / Accepted: 25 June 1997 相似文献
92.
93.
应用标志-释放-回收技术研究小皱蝽成虫的主要种群特征,结果如下:(1)成虫扩散的偏离度Ku=2.4,为一阶峻开曲线;(2)分别用Peterson和Jackson方法对种群蜜度进行了估计,结果表明,Jackson的方法较好;(3)雄虫平均寿命40-45,虫平均寿命120-130。天。 相似文献
94.
P. H. M. Balm Y. Iger P. Prunet T. G. Pottinger S. E. Wendelaar Bonga 《Cell and tissue research》1995,279(2):351-358
The present study describes the effects of 14 days exposure to acidified (pH 4.0) soft water in the absence of aluminium, on the ultrastructure of the skin in rainbow trout (Oncorhynchus mykiss). Compared to control fish, there was a moderate increase in the incidence of necrosis in the filament cells of the fish exposed to pH 4.0, but since the integrity of the tissue appeared to be maintained, most of the ultrastructural changes observed may be considered to be adaptive. There was an increase in epidermal thickness, a higher frequency of electrondense vesicles in filament cells, an increase in the undulation of the basal lamina, and the penetration of the epidermis by cytoplasmatic processes of melanocytes in acid-exposed specimens. An infiltration of leucocytes into the epidermis, and the appearance of serous mucous cells, was also evident. Whether these events were under the control of prolactin and/or -MSH, was also investigated, but no indication for activation or inhibition of either prolactin or -MSH producing cells was obtained. Since a previous study (Balm and Pottinger 1993) had demonstrated that plasma cortisol levels were also identical in control and low pH treated trout throughout a 14 day experimental period, it is concluded that under conditions of environmental acidification, the integument autonomically maintains the adjustments necessary for successful acclimation, presumably via paracrine regulatory circuits. 相似文献
95.
Ex situ conservation of plant germplasm using biotechnology 总被引:6,自引:0,他引:6
Conservation of plant genetic resources attracts more and more public interest as the only way to guarantee adequate food supplies for future human generations. However, the conservation and subsequent use of such resources are complicated by cultural, economical, technical and political issues. Over the last 30 years, there have been significant increases in the number of plant collections and in accessions in ex situ storage centres throughout the World. The present review is of these ex situ collections and the contribution biotechnology has made and can make to conservation of plant germplasm. The applications and limitations of the new, molecular approaches to germplasm characterization are discussed.
In vitro slow growth is used routinely for conserving germplasm of plants such as banana, plantain, cassava and potato. More recently, cryopreservation procedures have become more accessible for long-term storage. New cryopreservation techniques, such as encapsulation-dehydration, vitrification and desiccation, lengthen the list of plant species that can not only tolerate low temperatures but also give normal growth on recovery. Extensive research is still needed if these techniques are to be fully exploited.V.M. Villalobos is with the Food and Agriculture Organization of the United Nations, Viale delle Terme di Caracalia, 00100 Rome, Italy. F. Engelmann is with the International Plant Genetic Resources Institute (IPGRI), Via delle Sette Chiese 142, 00145 Rome, Italy. 相似文献
96.
N. J. H. CAMPBELL F. C. HARRISS M. S. ELPHINSTONE P. R. BAVERSTOCK 《Molecular ecology》1995,4(4):407-418
The ability of DNA screening techniques such as Temperature Gradient Gel Electrophoresis (TGGE) and Heteroduplex Analysis to provide resolution approaching that provided by DNA sequencing for a fraction of the time, effort and expense point to them as the logical successor to allozyme electrophoresis for population genetics. Here we present a novel alternative to the standard TGGE/Heteroduplex Analysis protocol - Outgroup Heteroduplex Analysis (OHA). We assess this technique's sensitivity in comparison to previous screening approaches using a known hierarchy of sequence differences. Our data show that Outgroup Heteroduplex Analysis has greatly increased sensitivity for screening DNA variants from that of TGGE used alone and is easily applicable to large numbers of samples. Using this technique we can consistently detect differences of as small as one base change in a 433-base-pair fragment of Control Region mitochondrial DNA from Melomys cerbinipes (an Australian rodent). The approach should easily be extendable to nuclear loci and is not necessarily dependent on the use of a denaturing gradient When combined with a targeted sequencing effort, OHA provides a sensitive and simple means of obtaining allele/haplotype frequencies and their phylogenies for population and phylogeographic studies in molecular ecology. 相似文献
97.
黄土丘陵沟壑区水平梯田改土培肥增产技术措施体系 总被引:2,自引:0,他引:2
黄土丘陵沟壑区水平梯田改土培肥增产技术措施体系刘东海赵廷宁(宁夏西吉县农业局756200)(北京林业大学水土保持学院100083)赵国杰(宁夏西吉县农业技术推广站756200)TechniquesofSoilImprovementandYieldIn... 相似文献
98.
F. Leboulenger I. Perroteau P. Netchitailo I. Lihrmann P. Leroux C. Delarue D.H. Coy H. Vaudry 《Peptides》1984,5(2):299-303
Vasoactive intestinal peptide (VIP) is located in chromaffin cells of the frog adrenal gland and is able to stimulate corticosteroid secretion in amphibians. In the present study we have investigated the possible involvement of prostaglandins, microfilaments and calcium in the mechanism of action of VIP on frog adrenocortical tissue. Rana ridibunda interrenal dice were perifused with amphibian culture medium for more than 10 hours. Corticosterone and aldosterone concentrations were measured in the effluent perifusate using sensitive and specific radioimmunoassay methods. In the presence of indomethacin (5 μM), a specific blocker of prostaglandin biosynthesis, the spontaneous secretion of corticosteroids was markedly reduced (80%) but the stimulatory effect of VIP was not altered. The administration of the microfilament disrupting agent cytochalasin B (50 μM) inhibited both spontaneous and VIP-induced corticosteroid secretion. In the absence of calcium, the spontaneous level of corticosteroid was reduced to about 60% but VIP was still able to stimulate corticosteroid secretion. From these data we conclude that the integrity of the cytoskeleton is required for the secretory response of adrenocortical cells to VIP, whereas neither prostaglandins nor calcium are involved in VIP-induced adrenocortical stimulation. 相似文献
99.
Michele Yarnall Kathleen J. Reis Elia M. Ayoub Michael D.P. Boyle 《Journal of microbiological methods》1984,3(2):83-93
A rapid semiquantitative procedure that enables bacteria to be screened for surface or secreted receptors for the Fc region of human IgG is described. Surface Fc receptors were detected by direct transfer of bacterial colonies to nitrocellulose by electroblotting and then probing with 125I-labeled human IgG in the presence of a two fold molar excess of unlabeled F(ab′)2fragments. The blots were exposed to X-ray film and the intensity of the resulting autoradiograph was a measure of surface Fc receptors expression. This procedure reliably distinguished Staphylococcus aureus strains which expressed different levels of surface Fc receptors. When applied to the study of group A streptococci, a number of Fc receptor-positive strains were identified. Unlike the homogeneous Fc receptor expression on individual colonies of the staphylococcal strains, a wide variation in the level of Fc receptor expression was observed within a given streptococcal strain. Group A streptococcal substrains which expressed high and low levels of surface Fc receptors could be isolated from replica plates.Secreted Fc receptors were measured by a simple modification of the blotting procedure in which the nitrocellulose was placed on the opposite side of the agar from the bacterial colonies. Secreted Fc receptors was electroblotted through the agar onto nitrocellulose and probed as described above. This approach readily detected nanogram quantities of secreted type I Fc receptor (protein A) from the Staphylococcus aureus Cowan strain. None of the group A streptococcal strains tested were found to secrete detectable quantities of Fc receptors. 相似文献
100.
M. Jose Comez-L Pilar Lopez Jose V. Castell 《In vitro cellular & developmental biology. Plant》1984,20(11):826-832
Summary The present study was undertaken to define the conditions for optimal cryopreservation of hepatocytes. Two different freezing
procedures were analyzed: a slow freezing rate (SFR) (−2° C/min down to −30°C and then quick freezing to −196° C) and a fast
freezing rate (FFR) (direct freezing of tubes to −196° C: −39° C/min). Cells were frozen in fetal bovine serum containing
10% Dimethyl sulfoxide (DMSO). After rapid thawing at 37° C, followed by dilution and removal of the cryoprotectant, cells
were plated and several parameters were followed as criteria for optimal cryopreservation of cells. The FFR cells showed no
apparent ultrastructural damage after 24 h of culture. Plating efficiency and spreading were similar as controls. Gluconeogenesis
from pyruvate and fructose, tyrosine amino transferase induction by glucagon and dexamethasone, urea production, and plasma
protein synthesis of FFR cells were similar to those found in control cultures. The FFR procedure, in comparison to the SFR
method, seemed to render the best preserved hepatocytes.
The financial support for this work was from Fondo de Investigaciones Sanitarias de la Seguridad Social, Grants 41/82 and
48/82. 相似文献