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391.
392.
Edna Correia José Pedro Granadeiro Bárbara Santos Vanessa A. Mata Emanuel Dias Aissa Regalla Teresa Catry 《Journal of fish biology》2024,104(1):324-328
We present the first assessment of the diet of the blackchin guitarfish Glaucostegus cemiculus (Geoffroy Saint-Hilaire, 1817) for West Africa using DNA metabarcoding on stomach contents of individuals captured in the Bijagós Archipelago, Guinea-Bissau. The diet was dominated by crustaceans, particularly caramote prawn Penaeus kerathurus (frequency of occurrence [FO] = 74%, numerical frequency [NF] = 54%) and fiddler crab Afruca tangeri (FO = 74%, NF = 12%). Bony fishes were present in 30% of the stomachs. We highlight the importance of conservation action for intertidal habitats and their associated benthic invertebrates for the survival of the critically endangered blackchin guitarfish. 相似文献
393.
Meir Lahav Isabelle Weissbuch Edna Shavit Clarissa Reiner Graeme J. Nicholson Volker Schurig 《Origins of life and evolution of the biosphere》2006,36(2):151-170
The present article challenges reports claiming to have demonstrated the Parity Violating Energetic Difference (PVED) between enantiomorphous D- and L-crystals. Apart from PVED, the presence of minute quantities and differing profiles of impurities incorporated during their different history of preparation will affect the physical properties of D- and L-crystals. These impurities are anticipated to play a much greater role in affecting crystallization behavior than PVED. The effect of impurities on the growth and dissolution of enantiomorphous crystals is illustrated with some representative examples.Shinitzky et al. (2002) reported recently dramatic differences in the growth and dissolution properties of the D- and L-crystals of tyrosine. We have repeated these experiments using commercial samples from different sources and employing a validated enantioselective gas chromatographic technique. We attribute Shinitzky's findings either to the use of inappropriate analytical techniques for the determination of enantiomeric composition and/or to the presence of unidentified contaminants in the commercial tyrosine samples. Related caveats hold also for the recently published claims by Shinitzky (2006) and Scolnik et al. (2006) to have observed experimentally PVED between enantiomeric helices of poly-glutamic acid composed of 24 repeating units.We maintain the term enantiomorphous crystals despite the fact that D- and L crystals differ by PVED 相似文献
394.
The circadian variation in the labelling indices of epidermal basal and sebaceous gland cells in murine pinna is a well documented phenomenon. This, however, observes only the incorporated label and takes no account of any rhythmic changes in the precursor pool. It is reported here that, using a liquid scintillation counting method, there is a diurnal change in the level of unincorporated radio-labelled thymidine, which is apparently not related to the rhythm of thymidine incorporation. The implications of this phenomenon and its relationship to DNA synthesis are discussed. 相似文献
395.
Edna C. Hardeman Akira Endo Robert D. Simoni 《Archives of biochemistry and biophysics》1984,232(2):549-561
A cell line, C100, resistant to 225 μm compactin, has been isolated which overproduces 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase approximately 100-fold compared to the parental cell line [E. Hardeman, H. Jenke and R. Simoni (1983) Proc. Natl. Acad. Sci. U.S.A.80, 1516–1520]. It is demonstrated that the overproduction of HMG-CoA reductase in these cells is the result of increased enzyme synthesis due to elevated levels of translatable mRNA. Furthermore, the apparent molecular weight of the in vitro translation product is 94,000, which agrees with the molecular weight of the in vivo synthesized HMG-CoA reductase protomer in C100 cells. However, a comparison of the Staphylococcus aureus V8 proteolysis patterns between the in vitro and in vivo translation products reveals structural differences which suggests in vivo posttranslation modification(s). It is also demonstrated unequivocally, by comparing proteolytic cleavage patterns and pulse-chase experiments, that the previously reported 63,000-, 52,000-, and 38,000-Da polypeptides recognized by HMG-CoA reductase antiserum derive from the 94,000-Da protomer as a result of nonphysiological proteolysis. Finally, the types of regulatory mechanisms involved in both the induction and repression of the enzyme in the presence or absence of compactin were determined. Four biochemical parameters of HMG-CoA reductase were examined in variant and parental cells grown in the presence and absence of compactin: enzymatic activity, degradation rate, synthesis rate, and concentration of translatable mRNA. These studies revealed that changes in cellular HMG-CoA reductase content are a function of concurrent changes in the rates of enzyme degradation and synthesis. Changes in enzyme synthesis are due to alterations in the level of translatable mRNA. 相似文献
396.
Summary The distribution of Gc types was investigated in an Indian group residing in Cuetzalan, Puebla, and in a Mestizo group from Mexico City. Gc1 and Gc2 gene frequencies were 0.862 and 0.138 in Cuetzalan, and 0.858 and 0.142 in Mexico City. These figures are similar to those obtained by other authors in one Northeastern Mexican City. A literature review showed that there appears to be a pattern of high Gc2-frequency in most Brazilian Indians (above 0.3) in contrast to a low frequency (below 0.2) in most other Amerindian groups studied. 相似文献
397.
Paul E. March Edna Antonian Diane M. Schneider David M. Rothwarf Edward R. Thornton 《Neurochemical research》1987,12(7):635-640
High molecular mass polypeptides (M
r
>100,000) of plain synaptic vesicles from bovine cerebral cortex were separated using porous polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate. Four major bands, ofM
r
262,000, 249,000, 216,000, and 173,000, were resolved. Investigations into the membrane association of theM
r
216,000 and 173,000 proteins by means of solubilization experiments and Sepharose 4B chromatography indicate that the former is a peripheral protein and the latter is more firmly attached, possibly an integral protein. Finally, theM
r
216,000 protein was shown to be highly enriched in synaptic vesicles compared to other brain subfractions. It thus appears to be specifically associated with synaptic vesicles and therefore may have an important role specific to synaptic vesicle function or structure. 相似文献
398.
399.
Strain dependent differences were found in the ability of inbred mice to produce antibodies to a thymus independent synthetic polypeptide, poly (DTyr, DGlu)-polyDPro-polyDLys. These differences were detected after injecting the antigen either in complete Freund's adjuvant or in aqueous solution, and were significant already in the primary response. High- and low-responder mice produced mainly antibodies of the IgG class as deduced from their mercaptoethanol resistance and their elution in the second fraction of a Sephadex G-200 chromatography. Genetic analysis of the immune response potential to poly(DTyr,DGlu)-polyDPro-polyDLys has indicated that responsiveness to this immunogen is controlled by a dominant, quantitative gene(s) which is not linked to either the major histocompatibility complex (H-2) of the mouse or to the heavy chain locus and is not located on the X-chromosome. 相似文献
400.
Median S-phase lengths of pinna epidermis and sebaceous glands, and of epithelia from the oesophagus and under surface of the tongue of Albino Swiss S mice were estimated by the percentage labelled mitoses method (PLM). The 18.4 and 18.8 hr for the median length of S-phase for pinna epidermis and sebaceous glands respectively made it possible for these two tissues to be used experimentally for testing tissue specificity in chalone assay experiments. The 10.0 and 11.5 hr for oesophagus and tongue epithelium respectively made experimental design for chalone assay difficult when pinna epidermis was the target tissue. The results of the Labelling Index measured each hour throughout a 24-hr period showed no distinct single peaked diurnal rhythm for pinna epidermis and sebaceous glands. Instead a circadian rhythm with several small peaks occurred which would be expected if an S-phase of approximately 18 hr was imposed on the diurnal rhythm. This indicates that there may be very little change in the rate of DNA synthesis. The results are given for the assay in vivo of purified epidermal G1 and G2 chalones, and the 72–81% ethanol precipitate of pig skin from which they could be isolated. These experiments were performed over a time period which took into account the diurnal rhythm of activity of the mice as well as the S-phase lengths. Extrapolating the results with time of action of the chalone shows that the G1 chalone acts at the point of entry into DNA synthesis and that the S-phase length was approximately 17 hr for both the pinna epidermis and sebaceous glands. This may be a more correct value since the PLM method overestimates the median S-phase length as it is known that in pinna skin the [3H]TdR is available to the tissues for 2 hr and true flash labelling does not take place. The previous reports that epidermal G1 chalone acts some hours prior to entry into S-phase resulted from experiments on back skin where the S-phase is shorter and there is a pronounceddiurnal rhythm which could mask the chalone effect. The epidermal G, chalone had no effect on DNA synthesis even at different times in the circadian rhythm. Thus the circadian rhythms and S-phase lengths of the test tissues need to be considered when experiments are performed with chalones. Ideally, the target tissues selected for cell line specificity tests should have the same cell kinetics for the easier and more accurate assessment and interpretation of results. When the tissues have markedly different cell kinetics, experimental procedures and results need to be evaluated accordingly. The point of action of G, chalone can only be assessed if the effect is measured over the peak of incorporation of 13H]TdR into DNA. The results of the effects of skin extracts are analysed in relation to changes in the availability of i3H]TdR for the incorporation into DNA and to the possibility of there being two distinct populations of proliferating cells. 相似文献