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51.
Analysis of the inducible MEL1 gene of Saccharomyces carlsbergensis and its secreted product, alpha-galactosidase (melibiase) 总被引:8,自引:0,他引:8
We have determined both the nucleotide sequence of the MEL1 gene of Saccharomyces carlsbergensis and the N-terminal amino acid (aa) sequence of its extracellular gene product, alpha-galactosidase (melibiase) (alpha-Gal). The predicted translation product of MEL1 is a pre-alpha-Gal protein containing an 18 aa N-terminal signal sequence for secretion. The purified enzyme is a dimer consisting of two 50-kDal polypeptides, each of which is glycosylated with no more than eight side chains. The 5'-flank of the MEL1 gene contains a region (UASm) having certain areas of sequence homology to similar sites found upstream of the structural genes GAL1, GAL7 and GAL10, which are also regulated by the action of the products of genes GAL4 and GAL80. There are three TATA boxes between UASm and the initiation codon of pre-alpha-Gal, as well as a typical yeast cleavage/polyadenylation sequence in the 3'-flank of the gene. 相似文献
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乙型脑炎病毒减毒株(2-8株)和野毒株(SA14株)在生物学性质上有明显的不同,特别是嗜神经毒力方面,2-8株已丧失了对小白鼠、马,猴等敏感动物的脑内致病力。为了探讨这些生物学性质变化的物质基础,我们开展了乙脑强、弱毒株聚丙烯酰胺凝胶 相似文献
55.
Horizontal starch gel electrophoresis was used to estimate the amount of genetic divergence between Notropis cornutus and N. chrysocephalus. Measures of genetic identity (1) and distance (D) were 0.881 and 0.127 ± 0.055 (s.e.), respectively. These estimates correspond more closely to the sibling species status of these taxa than other previously reported estimates. Notropis cornutus was found to be significantly more variable than N. chrysocephalus electrophoretically and morphologically. Assuming the existence of an electrophoretic clock, the time of divergence was calculated to be roughly 1.9–2.5 million years. This estimate corresponds very closely to a previously hypothesized late Pliocene divergence. 相似文献
56.
The effects of particle concentration and season on the filtration rates of the freshwater clamSphaerium striatinum Lamarck were assessed by measuring clearance rates of small (2.02 μm) latex beads from dilute suspensions. Filtration rates
decreased as particle concentration increased over a range of 2–64 mg 1−1, with rates decreasing in similar proportion for clams of all sizes. For a 1-mg clam, rates decreased from approximately
8.4 to 0.57 ml clam−1 h−1. Seasonal filtration rates for adult clams peaked during periods of greatest reproduction. The patterns for smaller clams
are similar, though proportional changes in filtration rates differ for various sizes of clams.
It is estimated that clams occupying 1 m2 of stream substrate removed about 3.67 gCa−1. This is equivalent to 0.0004% of the carbon that flows past them annually. Filter-feeding provided only 24% of the calculated
energy needs of the population, suggesting that another mode of feeding (e.g. deposit-feeding) may provide an important energy
source for these forms.
Funded in part by a grant-in-aid to D. J. Hornbach from Sigma-Xi, The Research Society.
Funded in part by a grant-in-aid to D. J. Hornbach from Sigma-Xi, The Research Society. 相似文献
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Two species of Anabas Cuvier, 1816 (Osteichthyes: Anabantidae): A. testudineus (Bloch, 1795) and A. oligolepis Bleeker, 1855 are widely distributed in India. Since both species are represented in one habitat — Lake Kolleru, and are very closely related, they were compared using starch gel electrophoresis. Electrophoretic separation of proteins of eye lens, skeletal muscle and heart muscle revealed differences such as i) absence of one protein fraction in one of them, ii) mobility and iii) staining intensity of some of the bands. The esterase (non-specific) patterns of serum, liver, kidney, skeletal muscle, heart muscle and eggs also showed differences. The LDH fraction of eye lens showed a difference in mobility. 相似文献
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Q Q Zhuang S Rosenberg J Lawrence A Stracher 《Biochemical and biophysical research communications》1984,118(2):508-513
Actin binding protein from human blood platelets is shown to exist in the resting platelet as a phosphorylated protein and contains two residues of phosphate per 260,000 kd. Removal of one-half of these residues with E. coli alkaline phosphatase results in the loss of its ability to crosslink F-actin into a low speed sedimentable complex (its cytoskeleton) and to bind to an F-actin affinity column. Thus, phosphorylation-dephosphorylation of ABP may be an important regulatory mechanism by which the platelet regulates its shape via its cytoskeletal structure. 相似文献
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Y Gache F Landon H Touitou A Olomucki 《Biochemical and biophysical research communications》1984,124(3):877-881
Purified alpha-actinin from human platelets was digested with Ca2+-activated protease from muscle. The alpha subunit (Mr = 100 kDa) was degraded into a unique polypeptide b of slightly lower molecular mass. In fresh platelets, only the a subunit was detected by immunoblotting techniques, while in out-dated platelets, both a and b polypeptides were present. Since a similar conversion of a to b occurs in vitro as in whole platelets, it can be assumed that, in platelets, alpha-actinin is cleaved by the endogenous Ca2+-activated protease. 相似文献