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91.
Andrew JG Simpson 《Genome biology》2000,1(1):reports411.1-reports4112
A meeting report of the sessions on human, eukaryotic and bacterial genome sequencing at the American Society for Microbiology and Institut Pasteur joint conference: Genomes 2000 International Conference on Microbial and Model Genomes, Paris, April 11-15, 2000 相似文献
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Mechanisms of cryoprotection in freezing tolerant animal systems 总被引:1,自引:0,他引:1
J G Baust 《Cryobiology》1973,10(3):197-205
The theoretical mechanisms of freezing protection afforded by the natural occurrence of glycerol in an adult, freezing-tolerant insect have been considered in light of recent findings. While unequivocal identification of the specific site or sites of action of glycerol is yet obscured in a maze of interactions, it is apparent that a multicellular system (organism) that naturally possesses glycerol in high, nonlethal concentrations, that can maintain activity in the presence of tissue ice, that can survive frequent and prolonged freeze-thaw encounters, and finally, that can regulate cryoprotectant levels in the presence of changing environmental conditions should be a major focus of future studies.The carabid beetle, Pterostichus brevicornis has been found to regulate glycerol levels in response to fluctuating ambient temperatures even while frozen. Hemolymph freezing points and whole-body supercooling points correlated well with changes in glycerol. Freezing and supercooling points decreased 0.9 ° C per 4 g/100 ml increase in glycerol.An interpretation of the data accumulated on insect studies and integrated with data from other multicellular systems supports the theory that a single site of freezing concept as applied to considerations of cryoprotection and cryoinjury may not be realistic. Each level of events occurring during the freezing process in glycerolated and nonglycerolated animal systems has been discussed. There appears little room for speculative separation and isolation of the site of action for the events of freezing (and thawing) represent a continuum with changes in each parameter directly dependent upon the entire sequence. 相似文献
94.
Characterization and cloning of a Tenebrio molitor hemolymph protein with sequence similarity to insect odorant-binding proteins 总被引:2,自引:0,他引:2
Graham LA Tang W Baust JG Liou YC Reid TS Davies PL 《Insect biochemistry and molecular biology》2001,31(6-7):691-702
The yellow mealworm beetle, Tenebrio molitor, produces a number of moderately abundant low molecular weight hemolymph proteins ( approximately 12 kDa) which behave in a similar manner during purification and share antigenic epitopes. The cDNA sequence of the major component (THP12) was determined and the deduced protein sequence was found to be similar to those of insect odorant-binding proteins. Southern blot analysis suggests that at least some of the diversity in this family of proteins is encoded at the gene level. Both northern and western blot analysis indicate that THP12 is present in a variety of developmental stages and both sexes. THP12 was originally classified as an antifreeze protein, but the lack of antifreeze activity in the recombinant protein, as well as the clear separation of the antifreeze activity from THP12 following HPLC purification, has ruled out this function. The abundance of THP12, the similarity of THP12 to insect odorant-binding proteins, and the presence of hydrophobic cavities inside the protein (Rothemund et al., A new class of hexahelical insect proteins revealed as putative carriers of small hydrophobic ligands. Structure, 7 (1999) 1325-1332.) suggest that THP12 may function to carry non-water soluble compounds in the hemolymph. THP12 is also similar, particularly in structurally important regions, to other insect proteins from non-sensory tissues, suggesting the existence of a large family of carrier proteins which may perform diverse functions throughout the insect. 相似文献
95.
Chromosomal DNA from 23 closely related, pathogenic strains of Escherichia
coli was digested and probed for the insertion sequences IS1, IS2, IS4,
IS5, and IS30. Under the assumption that elements residing in DNA
restriction fragments of the same apparent length are identical by descent,
parsimony analysis of these characters yielded a unique phylogenetic tree.
This analysis not only distinguished among bacterial strains that were
otherwise identical in their biochemical characteristics and enzyme
electrophoretic mobilities, but certain aspects of the topology of the tree
were consistent across several unrelated insertion elements. The
distribution of IS elements was then reexamined in light of the inferred
phylogenetic relationships to investigate the biological properties of the
elements, such as rates of insertion and deletion, and to discover apparent
recombinational events. The analysis shows that the pattern of distribution
of insertion elements in the bacterial genome is sufficiently stable for
epidemiological studies. Although the rate of recombination by conjugation
has been postulated to be low, at least two such events appear to have
taken place.
相似文献
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97.
Homologues of glucosephosphate isomerase (GPI, EC 5.3.1.9) were purified to
homogeneity and kinetically characterized from Mytilus edulis and Isognomon
alatus, two bivalve molluscs experiencing contrasting thermal environments.
The enzyme isolated from I. alatus functions at warmer temperatures (25-35
C) than GPI from M. edulis, a species that inhabits colder marine littoral
habitats (5-20 C). The former exhibits apparent first-order (with respect
to substrate) catalytic rate constants (Vmax/KM) in vitro that become
progressively greater than the mussel enzyme as the assay temperature is
raised. Apparent zero-order catalytic rate constants (Vmax) are relatively
less differentiated. Catalytic efficiency, defined as the rate at which a
catalytic event occurs in either reaction direction for reference standard
states (substrate concentrations), is greater for the enzyme from the
tropical species (I. alatus) at all realistic combinations of temperature
and substrate concentration except for the lowest temperatures and highest
substrate concentrations, where the GPI from the boreal/temperate M. edulis
is more efficient. This pattern of catalytic divergence appears to be due
primarily to differentiation in Vmax/KM. These results and other published
data are reviewed and shown to be inconsistent with claims that adaptation
of enzymes to higher cell temperatures requires a loss in catalytic
efficiency.
相似文献
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