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3.
6-Azauracil at a concentration of 1 μmole/ml inhibits by 50% the outgrowth of germinated spores of a strain ofBacillus cereus, concentration of 1.5 μmole/ml resulting in 100% inhibition. Two distinct maxima of sensitivity to 6-azauracil are observed during postgerminative development of spores. The first occurs during early stages of development (immediately after depolymerization period) and the second after about 60 min of cultivation (late stage of swelling). Uracil reverses the inhibition of the outgrowth of spores caused by 6-azauracil when added during 0–30 min of the spore development. The addition of uracil after 30 min of the germination does not bring about the reversion of the effect of 6-azauracil. An important role of pyrimidine pathway via orotidine 5′-phosphate in germinating spores was proved, suggesting a possible use of 6-azauracil in synchronization of the postgerminative development of spores. 相似文献
4.
5.
6.
Myrtus communis L. (myrtle), a typical Mediterranean plant species belonging to the family Myrtaceae, was shown to form arbuscular mycorrhizal
symbioses in nature. Many different spore types were isolated from its rhizosphere and grown in pot cultures; six of them
were identified as Glomus species. In the laboratory, the myrtle root system was colonized by indigenous endophytes as well as by an Italian isolate
of Glomus intraradices. In greenhouse experiments, mycorrhizal inoculation reduced transplant stress in 60-day-old myrtle seedlings; their growth
was renewed immediately after transplanting, whereas non-mycorrhizal plants stopped development. Significantly larger growth
responses were obtained using indigenous fungi than the Italian isolate of Glomus intraradices.
Accepted: 16 January 1997 相似文献
7.
Sujay K. Singh Edward K. Wakeland Ivica Vučak Zoltan A. Nagy Jan Klein 《Immunogenetics》1981,14(3-4):273-281
The B10.STA62 strain carries the H-2
w27 haplotype derived from a wild mouse captured in the vicinity of Ann Arbor, Michigan. Products of two class II loci composing this haplotype, A
and A
, are serologically, biochemically (by tryptic peptide mapping), and functionally indistinguishable from products controlled by the A
b
and A
/b
genes of the B10.A(5R) strain. In contrast, the polypeptide chain controlled by the third class II locus, E
, is different from that controlled by the E
/b
gene. This E
/w27
chain lacks an antigenic determinant present on the Eb molecule and carries determinants lacking on the Eb molecule, the E
/b
and E
/w27
peptide maps differ in at least six peptides, and cytotoxic T cells specific for the E
b
chains do not react with B10.STA62 target cells. This great difference between the E
/b
and E
/w27
chains suggests that the corresponding genes have not been derived from one another by a direct mutational conversion; instead, H-2
w27 appears to be a recombinant haplotype derived by crossing-over between the A
A
duplex and the E
locus. This is the first recombinant discovered separating these class II loci. 相似文献
8.
J. T. P. Albrechtová J. Ullmann J. Krekule A. Blažková I. Machžčková Z. Vondráková J. Blažková S. Procházka V. Borkovec D. A. Baker F. Didehvar Z. Tesařová V. Czaková M. Zima K. Doležal T. Doleželová V. Psota M. Dundelová V. Reinöhl S. Prochàzka J. Mikulík M. Dvořěk J. Černohorskě O. Auxtová B. Cholvadová D. Lišková M. Kubačková S. Karácsonyi L. Bilisics 《Biologia Plantarum》1992,34(1):569-587
9.
Cell-mediated lymphocytotoxicity was generated in four strain combinations differing only by the cell-surface expression of the class II E molecule controlled by the H-2 complex. The four combinations were: B10.D2(R107) anti-B10.A(3R), B10.A(4R) anti-B10.A(2R), B10.GD anti-B10.D2(R101), and B10.S(7R) anti-B10.S(9R). In all four of these combinations, the stimulator expresses E molecules on the cell surface, while the responder does not. The cytolytic T lymphocytes generated in the B10.D2(R107) anti-B10.A(3R) and B10.A(4R) anti-B10.A(2R) combinations reacted not only with the stimulator but also with strains that do not express cell-surface E molecules, in particular, strains carrying the H-2
f
and H-2
q
haplotypes. The cross-reactivity with E-negative strains could be blocked by monoclonal antibodies specific for the Af or Aq molecules but not by antibodies recognizing determinants on E or class I (K) molecules. The anti-H-2f cross-reactivity could be inhibited by H-2
q
cold targets and, reciprocally, the anti-H-2q reactivity could be blocked by H-2
f
cold targets. These findings are interpreted as indicating that the cytolytic T lymphocytes stimulated by E molecules can recognize and lyse cells lacking E molecules but expressing A molecules. The observed E-A cross-reactivity supports the notion of structural and functional relatedness between the A and E molecules and suggests a common evolutionary origin of the A- and E-encoding loci. 相似文献
10.