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201.
C J Van Noorden W M Frederiks D C Aronson F Marx K Bosch G N Jonges I M Vogels J James 《Virchows Archiv. B, Cell pathology including molecular pathology》1987,52(6):501-511
Extrahepatic cholestasis induced by ligation and transsection of the common bile duct caused a change in the parenchyma/stroma relationship in rat liver. Two weeks after ligation, the periportal zones of the parenchyma were progressively invaded by expanding bile ductules with surrounding connective tissue diverging from the portal areas. Parenchymal disarray developed and small clumps of hepatocytes or isolated hepatocytes were scattered within the expanded portal areas. These cells showed normal activity of lactate, succinate and glutamate dehydrogenase and may, therefore, be considered to be functionally active. After cholestasis the remainder of the liver parenchyma showed adaptational changes with respect to glucose homeostasis, as demonstrated by histochemical means. Glycogen stores disappeared completely whereas glycogen phosphorylase activity increased about ten fold. The increased glycogen phosphorylase activity and glycogen depletion indicate a greater glycogenolytic capacity in liver parenchyma after bile duct ligation to maintain as far as possible a normal plasma glucose concentration. The parenchymal distribution pattern of glucose-6-phosphatase activity did not change significantly after bile duct ligation. The isolated hepatocytes within the expanded portal tracts showed a high activity of this enzyme whereas the pericentral parenchyma was only moderately active. The distribution patterns of glucose-6-phosphate dehydrogenase and lactate dehydrogenase activity in the liver parenchyma were also largely unchanged after bile duct ligation, but the histochemical reaction for glucose-6-phosphate dehydrogenase activity demonstrated infiltration of the remainder of the parenchyma by non-parenchymal cells, possibly Küpffer cells and leucocytes as part of an inflammatory reaction. Under normal conditions the mitochondrial enzymes succinate and glutamate dehydrogenase show an opposite heterogenous distribution pattern in liver parenchyma. Following cholestasis both enzymes became uniformly distributed. The underlying regulatory mechanism for these different changes in distribution patterns of enzyme activities is not yet understood. 相似文献
202.
203.
Synopsis Woundfin, Plagopterus argentissimus, fed predominantly on simuliid larvae during the day, and shifted to the larger Hydropsyche spp. at night. Ephemeropteran larvae were eaten nearly uniformly throughout the 24 hour period. Mean weight of food consumed varied from 20–40 mg per individual (0.7–2.5% body weight) throughout the 24 h period. Our estimated daily ration of about 8% body weight, at temperatures that varied between 15–25°C, is based upon our measure of mean gut contents over a 24h period, combined with intestinal evacuation rates suggested for other cyprinids in the literature. The relatively continuous feeding pattern suggests a foraging strategy that would minimize competition with other species for food during June, a period of minimum annual food abundance in Virgin River. 相似文献
204.
Cyrenius Jone Laurie Erickson James E. Trosko Chia C. Chang 《Cell biology and toxicology》1987,3(1):1-15
Since chemical modulation of gap junctional intercellular communication has been implicated in several toxicological endpoints, a study to examine the ability of several biological toxins to inhibit this process was undertaken. Eight biological toxins were tested for their ability to inhibit metabolic cooperation, a measure of gap-junctional intercellular communication, in the Chinese V79 cell system. Aplysiatoxin, anhydrodebromoaplysiatoxin and debromoaplysiatoxin showed the strongest ability to inhibit metabolic cooperation while T2-toxin and vomitoxin inhibited metabolic cooperation to a lesser degree. Afatoxin B1, afatoxin B2 and palytoxin were inactive in the Chinese V79 system. Palytoxin, which was extremely cytotoxic, might act as a tumor promoter if it induces compensatory hyperplasia in vivo.Abbreviations 6-TG
6-thioguanine
- TPA
12-0-tetradecanoylphorbol-13-acetate 相似文献
205.
The partition of native Escherichia coli -galactosidase and of two different fusion proteins comprised mainly of -galactosidase from E. coli was studied in aqueous two-phase systems composed of polyethylene glycol (PEG) and dextran. These fusions contain an amino-terminal segment from the E. coli outer membrane protein F (OmpF) and a linker peptide. Differences in the partition pattern could be observed for the three enzymes despite their similarity. Decreased polymer concentrations in the phase system increased the partition coefficient for all three -galactosidases. 相似文献
206.
207.
Summary DNA sequence analysis of genetic deletions in bacteriophage T7 has shown that these chromosomal rearrangements frequently
occur between directly repeated DNA sequences. To study this type of spontaneous deletion in more quantitative detail synthetic
fragments of DNA, made by hybridizing two complementary oligonucleotides, were introduced into the non-essential T7 gene 1.3
which codes for T7 DNA ligase. This insert blocked synthesis of functional ligase and made the phage that carried an insert
unable to form plaques on a host strain deficient in bacterial ligase. The sequence of the insert was designed so that after
it is put into the T7 genome the insert is bracketed by direct repeats. Perfect deletion of the insert between the directly
repeated sequences results in a wild-type phage. It was found that these deletion events are highly sensitive to the length
of the direct repeats at their ends. In the case of 5 bp direct repeats excision from the genome occurred at a frequency of
less than 10−10, while this value for an almost identical insert bracketed by 10 bp direct repeats was approximately 10−6. The deletion events were independent of a hostrecA mutation. 相似文献
208.
James M. Mason Nita N. Scobie Akihiko H. Yamamoto 《Molecular & general genetics : MGG》1989,215(2):190-199
Summary The mutagen-sensitive mutant mus(1)104
D1
of Drosophila melanogaster maps to a position on the X chromosome very close to the meiotic mutant mei-41
D5
. Both mutants have been characterized as mutagen-sensitive and defective in post-replication repair. In the present report we show by complementation studies that mus(1)104 and mus(1)103 are allelic with mei-41. In addition, two reported alleles of mus(1)104 lie between the mei-41 alleles A10 and D5. The size of the mei-41 locus is estimated to be about 0.1 centimorgans (cM). Because several alleles of mei-41 have been shown to reduce recombination and increase meiotic chromosome loss and nondisjunction, mus(1)104
D1
females were examined for defects in meiosis. Although there was no evidence for reduced recombination on the second chromosome in homozygous mus(1)104
D1
females, heterozygous mus(1)104
D1
/mei-41
>D5
and mus(1)104
D1
/deficiency females showed reduced levels of recombination. However, there was no evidence of an increase in nondijunction in these females.We dedicate this article to the memory of Larry Sandler, who passed away suddenly on February 7, 1987 相似文献
209.
Dennis L. Welker Arturo De Lozanne James A. Spudich 《Molecular & general genetics : MGG》1989,216(2-3):498-502
Summary A mutation (mhcA1 in strain HMM) created by insertional gene inactivation was used to map the Dictyostelium discoideum myosin heavy chain gene (mhcA) to linkage group IV. Three phenotypic traits associated with this mutation (slow colony growth, inability of the mutant to develop past aggregation, and the presence of five to ten integrated vector copies) cosegregated as expected for the consequences of a single insertional event. This linkage was confirmed using a restriction fragment length polymorphism. The mhcA1 mutation was recessive to wild type and was nonallelic with mutations at the following loci on linkage group IV: aggJ, aggL, couH, minA, phgB and tsgB. This work demonstrates the ability to apply standard techniques developed for D. discoideum parasexual genetic analyses to mutants generated by transformation, which is of particular relevance to analysis of genes for which no classical mutations or restriction fragment length polymorphisms are available. 相似文献
210.