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91.
Joseph W. Mayo William M. Wallace Leroy W. Matthews Don M. Carlson 《Archives of biochemistry and biophysics》1976,175(2):507-513
Submandibular secretions collected from children with cystic fibrosis (CF) showed increased protein concentration (milligrams/milliliter) and increased amylase specific activity (units/milligram of protein) relative to normal secretions. These differences between normal (N) and CF secretions were as follows: protein, 1.25 ± 0.51 (N), 1.75 ± 0.35 (CF) (P < 0.02); and amylase, 58 ± 18 (N), 80 ± 19 (CF) (P < 0.001). To determine the basis for elevated protein in CF saliva, several major proteins resolved by polyacrylamide disc gel electrophoresis were quantitated by densitometry. These included four phosphoproteins (PP), serum albumin, an acid phosphatase-containing fraction, amylase, and an unidentified protein referred to as PI-7.1. Together, these proteins comprise greater than 75% of the total protein in the secretion. Differences in individual protein concentrations (milligrams/milliliter) resolved from normal and CF secretions, respectively, were as follows: PP2, 0.02 ± 0.01, 0.03 ± 0.02 (NS, not significant); PP3, 0.06 ± 0.04, 0.05 ± 0.03 (NS); acid phosphatase fraction, 0.06 ± 0.04, 0.12 ± 0.07 (P < 0.05); amylase, 0.09 ± 0.04, 0.27 ± 0.16 (P < 0.01); and pI-7.1, 0.04 ± 0.02, 0.13 ± 0.08 (P < 0.02). Amylase, the most significant contributor to the elevated protein, comprised 26% of the total protein of normal secretions and 38% of the total protein of CF secretions. Thus, our results do not support the concept of a generalized increase in all organic components in CF submandibular secretions but, rather, increases in specific proteins, namely amylase, component pI-7.1, and an acid phosphatase-containing fraction. 相似文献
92.
Ross H. Hall 《In vitro cellular & developmental biology. Plant》1976,12(3):216-224
Summary Cells possess extraordinary powers to organize their molecular processes not only to maintain a cell in a given steady state
but also to recognize that state during differentiation. Regulation of these organizational forces appears to be under the
control of chemical factors, and a hormonal concept of regulation has evolved. Hormones have been considered to act by reacting
with a specific target site. This may be part of their mode of action, but I would like to suggest that a hormone enters and
becomes part of a total molecular resonance system. In so doing, the entire molecular system of the cell is modified.
Of the known plant hormones, the cytokinins, because of their role in experimentally induced cell division and differentiation,
serve as a probe of hormonal involvement in differentiation. Cultured somatic cells of tobacco plants can be induced to undergo
differentiation by addition of cytokinin and auxin to the medium. Studies of the cytokinin hormones show a series of diverse
molecular involvements. The archetype cytokinin, N6-(Δ2-isopentenyl) adenosine (i6Ado), occurs in some molecular species of tRNA where it plays a vital role in the codon-anticodon interaction of tRNA and
m-RNA. i6Ado under-goes extensive metabolism in the tobacco tissue. It is either degraded to adenosine or converted to derivatives
that possess biological activity. It is perhaps, therefore, more correct to consider the hormone function as being derived
from this total metabolic web.
The normal somatic cells of tobacco cultures spontaneously change occasionally into an autonomous form that requires no external
growth factors. This line of cells synthesizes i6Ado. The metabolic web of the hormone-dependent strain can be perturbed by added auxin but such is not the case in the autonomous
strain. These data provide some insight into the altered state of cytokinin activity in which a cell line changes into an
autonomous form. Curiously, in become independent of the requirement for exogenous cytokinin, the autonomous tissue becomes
sensitive to added cytokinin. i6Ado also inhibits the growth of lines of mammalian cancer cells grown in culture.
Presented in the formal symposium on Information Transfer in Eukaryotic Cells, at the 26th Annual Meeting of the Tissue Culture
Association, Montreal, Quebec, June 2–5, 1975. 相似文献
93.
The arterio--alveolar nitrogen difference (aADN2) has been associated in 27 normal adult subjects aged 20--60 years. As it may be assumed that venous and arterial PN2 are identical, we have used a sample of venous blood. There is a significant positive correlation between aADN2 and age. As the increase of aADN2 with age resembles that found in the literature for AaDO2, we concluded that the latter may be explained by increasing VA/Qc inequality within the lung. 相似文献
94.
Multiple regeneration from axolotl limb stumps bearing cross-transplanted minced muscle regenerates.
B M Carlson 《Developmental biology》1975,45(1):203-208
Flexor and extensor muscles in the upper arms of axolotls were minced and cross-transplanted. The limbs were amputated 5 and 30 days after mincing. In each experiment a high percentage of the regenerates consisted of multiple limbs. This demonstrates that the morphogenetic information which produces multiple regenerates after the cross-transplantation of limb stump muscle is stable enough to be expressed after both mincing and the subsequent tissue regeneration of the muscle. 相似文献
95.
96.
R P Carlson M L Ogletree A M Lefer 《Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)》1975,150(1):52-56
LIS had no action on the mechanical activity of isolated cat vascular, intestinal smooth, or cardiac muscle. No effect on platelet aggregation was observed, and PGF2alpha activity was absent in LIS preparations. Isolated lysosomal enzyme release was increased significantly when LIS was added to the incubation medium. This action may help to explain the inflammatory action of this naturally occurring material found in the inflamed synovial fluid of the canine knee joint. 相似文献
97.
Structures and immunochemical properties of oligosaccharides isolated from pig submaxillary mucins 总被引:54,自引:0,他引:54
D M Carlson 《The Journal of biological chemistry》1968,243(3):616-626
98.
Brotherton P Endicott P Sanchez JJ Beaumont M Barnett R Austin J Cooper A 《Nucleic acids research》2007,35(17):5717-5728
Ancient DNA (aDNA) research has long depended on the power of PCR to amplify trace amounts of surviving genetic material from preserved specimens. While PCR permits specific loci to be targeted and amplified, in many ways it can be intrinsically unsuited to damaged and degraded aDNA templates. PCR amplification of aDNA can produce highly-skewed distributions with significant contributions from miscoding lesion damage and non-authentic sequence artefacts. As traditional PCR-based approaches have been unable to fully resolve the molecular nature of aDNA damage over many years, we have developed a novel single primer extension (SPEX)-based approach to generate more accurate sequence information. SPEX targets selected template strands at defined loci and can generate a quantifiable redundancy of coverage; providing new insights into the molecular nature of aDNA damage and fragmentation. SPEX sequence data reveals inherent limitations in both traditional and metagenomic PCR-based approaches to aDNA, which can make current damage analyses and correct genotyping of ancient specimens problematic. In contrast to previous aDNA studies, SPEX provides strong quantitative evidence that C > U-type base modifications are the sole cause of authentic endogenous damage-derived miscoding lesions. This new approach could allow ancient specimens to be genotyped with unprecedented accuracy. 相似文献
99.
O'Shea RD Lau CL Farso MC Diwakarla S Zagami CJ Svendsen BB Feeney SJ Callaway JK Jones NM Pow DV Danbolt NC Jarrott B Beart PM 《Neurochemistry international》2006,48(6-7):604-610
Excitatory amino acid transporters (EAATs) are responsible for homeostasis of extracellular L-glutamate, and the glial transporters are functionally dominant. EAAT expression or function is altered in acute and chronic neurological conditions, but little is known about the regulation of EAATs in reactive astroglia found in such neuropathologies. These studies examined the effects of the bacterial endotoxin lipopolysaccharide (LPS) on glial EAATs in vitro. The effects of LPS (1 microg/ml, 24-72 h) on EAAT activity and expression were examined in primary cultures of mouse astrocytes. [(3)H]D-aspartate uptake increased to 129% of control by 72 h treatment with LPS. Saturation analysis revealed that apparent K(m) was unchanged whilst V(max) was significantly increased to 172% of control by 72 h LPS treatment. Biotinylation and Western blotting indicated that cell-surface expression of GLT-1 was significantly elevated (146% control) by LPS treatment whereas GLAST expression was unchanged. Confocal analyses revealed that LPS treatment resulted in cytoskeletal changes and stellation of astrocytes, with rearrangement of F-actin (as shown by phalloidin labelling). Immunocytochemistry revealed clustering of GLAST, and increased expression and redistribution of GLT-1 to the cell-surface following treatment with LPS. Similar experiments were conducted in microglia, where LPS (50 ng/ml) was found to up-regulate expression of GLT-1 at 24 and 72 h in concert with cytoskeletal changes accompanying activation. These findings suggest an association of cytoskeletal changes in glia with EAAT activity, with the predominant adaptation involving up-regulation and redistribution of GLT-1. 相似文献
100.