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991.
Ion conduction pore is conserved among potassium channels. 总被引:15,自引:0,他引:15
Potassium channels, a group of specialized membrane proteins, enable K+ ions to flow selectively across cell membranes. Transmembrane K+ currents underlie electrical signalling in neurons and other excitable cells. The atomic structure of a bacterial K+ channel pore has been solved by means of X-ray crystallography. To the extent that the prokaryotic pore is representative of other K+ channels, this landmark achievement has profound implications for our general understanding of K+ channels. But serious doubts have been raised concerning whether the prokaryotic K+ channel pore does actually represent those of eukaryotes. Here we have addressed this fundamental issue by substituting the prokaryotic pore into eukaryotic voltage-gated and inward-rectifier K+ channels. The resulting chimaeras retain the respective functional hallmarks of the eukaryotic channels, which indicates that the ion conduction pore is indeed conserved among K+ channels. 相似文献
992.
GPS定位和陀螺定向在大型贯通测量中的应用 总被引:1,自引:0,他引:1
详述了GPS定位和陀螺定向在大型贯通测量中的应用,并总结了煤矿测量的成功经验。 相似文献
993.
994.
Dopamine-beta-hydroxylase (DBH) activity was higher in the serum, the mesenteric artery and the cerebral cortex of 4-week-old stroke-prone spontaneously hypertensive rats (SHRSP), and lower in the nucleus tractus solitarii than it was in spontaneously hypertensive rats (SHR). 相似文献
995.
996.
997.
The mitochondrial deoxyribonucleotide (dNTP) pool is separated from the cytosolic pool because the mitochondria inner membrane is impermeable to charged molecules. The mitochondrial pool is maintained by either import of cytosolic dNTPs through dedicated transporters or by salvaging deoxynucleosides within the mitochondria; apparently, enzymes of the de novo dNTP synthesis pathway are not present in the mitochondria. In non-replicating cells, where cytosolic dNTP synthesis is down-regulated, mtDNA synthesis depends solely on the mitochondrial salvage pathway enzymes, the deoxyribonucleosides kinases. Two of the four human deoxyribonucleoside kinases, deoxyguanosine kinase (dGK) and thymidine kinase-2 (TK2), are expressed in mitochondria. Human dGK efficiently phosphorylates deoxyguanosine and deoxyadenosine, whereas TK2 phosphorylates deoxythymidine, deoxycytidine and deoxyuridine. Here we identify two mutations in TK2, histidine 90 to asparagine and isoleucine 181 to asparagine, in four individuals who developed devastating myopathy and depletion of muscular mitochondrial DNA in infancy. In these individuals, the activity of TK2 in muscle mitochondria is reduced to 14-45% of the mean value in healthy control individuals. Mutations in TK2 represent a new etiology for mitochondrial DNA depletion, underscoring the importance of the mitochondrial dNTP pool in the pathogenesis of mitochondrial depletion. 相似文献
998.
H. Kitamura S. Okamoto Y. Shimamoto M. Morimatsu A. Terao M. Saito 《Cellular and molecular life sciences : CMLS》1998,54(3):282-287
Centrally given interleukin (IL)-1 is known to induce a rapid rises in blood IL-6. To extend this and to examine the mechanism
by which this occurs, the effects of intracerebroventricular (icv) injection of human recombinant IL-1β on mRNA expression of IL-6 and tumour necrosis factor (TNF) in the spleen and liver were examined in rats. Icv injection
of IL-1 produced a rapid rise of the tissue mRNA levels of IL-6 and TNF in both organs, prior to and/or in parallel with an
increase in their serum levels. Pretreatment with chlorisondamine, a ganglionic blocking agent, inhibited the IL-6 responses,
while it had little influence on the TNF responses. The results suggest that brain IL-1 induces peripheral production of IL-6,
but not of TNF, through autonomic nervous system activation.
Received 27 October 1997; received after revision 15 December 1997; accepted 12 January 1998 相似文献
999.
Shrinkage Properties of Wool and Acrylic/Wool Plain Knitted Fabrics Treated with DC109 总被引:1,自引:0,他引:1
This paper examines the effects of shrink - resist treatment, washing cycle and fabric tightness on the shrinkage properties of plain knitted fabrics made from 100% wool, acrylic/wool (50/50) and acrylic/wool (70/30). It was found that shrinkages of both treated and untreated wool fabrics were negatively correlated to fabric tightness and exceeded the IWS shrinkage limits (5% in length and 8 % in area) after 2 - 5A washing cycle. The effect of tightness was not as obvious with acrylic/wool (A/W) fabrics, but the shrinkage was seen to increase with stages of washing cycle for untreated A/W fabrics with some exceeding IWS standard. By applying the DC 109 shrink - resist solvent treatment, it was identified that by with higher percentage of acrylic fibre blended with wool, shrinkage could be reduced considerably and within acceptable limits. 相似文献
1000.
S Kitao A Shimamoto M Goto R W Miller W A Smithson N M Lindor Y Furuichi 《Nature genetics》1999,22(1):82-84
Rothmund-Thomson syndrome (RTS; also known as poikiloderma congenitale) is a rare, autosomal recessive genetic disorder characterized by abnormalities in skin and skeleton, juvenile cataracts, premature ageing and a predisposition to neoplasia. Cytogenetic studies indicate that cells from affected patients show genomic instability often associated with chromosomal rearrangements causing an acquired somatic mosaicism. The gene(s) responsible for RTS remains unknown. The genes responsible for Werner and Bloom syndromes (WRN and BLM, respectively) have been identified as homologues of Escherichia coli RecQ, which encodes a DNA helicase that unwinds double-stranded DNA into single-stranded DNAs. Other eukaryotic homologues thus far identified are human RECQL, Saccharomyces cerevisiae SGS1 and Schizosaccharomyces pombe rqh1. We recently cloned two new human helicase genes, RECQL4 at 8q24.3 and RECQL5 at 17q25, which encode members of the RecQ helicase family. Here, we report that three RTS patients carried two types of compound heterozygous mutations in RECQL4. The fact that the mutated alleles were inherited from the parents in one affected family and were not found in ethnically matched controls suggests that mutation of RECQL4 at human chromosome 8q24.3 is responsible for at least some cases of RTS. 相似文献