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81.
Inhibition of endoplasmic reticulum (ER)-to-Golgi transport induces relocalization of binding protein (BiP) within the ER to form the BiP bodies. 总被引:11,自引:6,他引:5 下载免费PDF全文
Immunofluorescence staining of yeast cells with anti-binding protein (BiP) antibodies shows uniform staining of the endoplasmic reticulum (ER). We have found that overproduction of Sec12p, an ER membrane protein, causes a change of BiP distribution within the cell. Upon induction of Sec12p by the GAL1 promoter, the staining pattern of BiP turns into bright dots scattering in the cell, whereas the staining of Sec12p remains to be the typical ER figure. Overproduction of other ER membrane proteins, HMG-CoA reductase or Sed4 protein, does not induce such relocalization of BiP. Pulse-chase experiments and electron microscopy have revealed that the overproduction of Sec12p inhibits protein transport from the ER to the Golgi apparatus. When the transport is arrested by one of the sec mutations that block the ER-to-Golgi step at the restrictive temperature, the BiP staining also changes into the punctate pattern. In contrast, the sec mutants that block later or earlier steps of the secretory pathway do not induce such change of BiP localization. These observations indicate that relocalization of BiP is caused by the inhibition of ER-to-Golgi transport. Using immunoelectron microscopy, we have found that the punctate staining is because of the accumulation of BiP in the restricted region of the ER, which we propose to call the "BiP body." This implicates existence of ER subdomains in yeast. A vacuolar protein, proteinase A, appears to colocalize in the BiP body when the ER-to-Golgi transport is blocked, suggesting that the BiP body may have a role as the site of accumulation of cargo molecules before exit from the ER. 相似文献
82.
Heat production, oxygen consumption, and lipolysis in isolated interscapular brown adipocytes from the rat were investigated. Epinephrine, norepinephrine, and isoproterenol increased heat production in a concentration-dependent manner, showing, about 6-, 4-, and 5-fold higher effects than controls, respectively. The concentration of isoproterenol for threshold heat production and glycerol release were 10(-10) M and 10(-9) M, respectively. The fact that 10(-9) M isoproterenol increased heat production by about 3-fold while glycerol release had no effect at all indicates that calorimetry is more appropriate for investigation of brown adipocytes. At least the method is more sensitive than that of measuring glycerol release. 相似文献
83.
Acetyl esterase production was detected in a wood-rotting fungus,Coriolus versicolor, by the formation of a clear zone on a double layer agar plate containing glucose β-d-pentaacetate. Two polysaccharide acetates, carboxymethyl cellulose acetate and xylan acetate, also served as detectable substrates
in place of glucose acetate to form clear zone. In an esterase assay, this fungal esterase showed a higher specificity to
acetylxylan than did porcine liver esterase, indicating that it is an acetylxylan esterase. 相似文献
84.
A Novel Class of Herbicides (Specific Inhibitors of Imidazoleglycerol Phosphate Dehydratase) 总被引:4,自引:2,他引:2 下载免费PDF全文
Mori I Fonne-Pfister R Matsunaga S Tada S Kimura Y Iwasaki G Mano J Hatano M Nakano T Koizumi S Scheidegger A Hayakawa K Ohta D 《Plant physiology》1995,107(3):719-723
A new mode of herbicidal action was established by finding specific inhibitors of imidazoleglycerol phosphate dehydratase, an enzyme of histidine (His) biosynthesis. Three triazole phosphonates inhibited the reaction of the enzyme with Ki values of 40 [plus or minus] 6.5, 10 [plus or minus] 1.6, and 8.5 [plus or minus] 1.4 nM, respectively, and were highly cytotoxic to cultured plant cells. This effect was completely reversed by the addition of His, proving that the cytotoxicity was primarily caused by the inhibition of His biosynthesis. These inhibitors showed wide-spectrum, postemergent herbicidal activity at application rates ranging from 0.05 to 2 kg/ha. 相似文献
85.
86.
Masaru Nakano Keizo Hosokawa Tomo Oomiya Saburo Yamamura 《Plant Cell, Tissue and Organ Culture》1995,41(3):221-227
A protoplast-to-plant system was developed in Gentiana using a gellan gum-embedding culture. Viable protoplasts could be routinely isolated from in vitro-grown plantlets, and they were embedded in 0.2% gellan gum-solidified B5 medium containing 2 mg l-1 NAA, 0.1 mg l-1 TDZ, 0.1 M sucrose and 0.4 M mannitol. Weekly addition of fresh liquid medium was essential for preventing cell browning. Colony growth was promoted by lowering mannitol concentration of the culture media after one month, and visible colonies were produced after 2 months of culture. Shoot regeneration from protoplast-derived calluses was stimulated by 1 to 10 mg l-1 TDZ in combination with 0.1 mg l-1 NAA. Protoplast-derived plants were recovered following rooting of the shoots in plant growth regulator-free medium and they were successfully transferred to soil.Abbreviations BA
benzylaminopurine
- FDA
fluorescein diacetate
- FW
fresh weight
- MES
2-N-morpholinoethane sulfonic acid
- NAA
-naphthaleneacetic acid
- TDZ
N-1,2,3-thiadiazol-5-yl-N-phenylurea (also called thidiazuron) 相似文献
87.
88.
89.
Immunocytochemical localization of thrombomodulin in the aqueous humor passage of the rat eye 总被引:1,自引:1,他引:0
T. Daimon Mutsuyoshi Kazama Yukari Miyajima Masahiko Nakano 《Histochemistry and cell biology》1997,108(2):121-131
This report describes the distribution and localization of thrombomodulin (TM) in the rat eye by light and electron microscopic
immunocytochemistry. In addition to the endothelium of the entire vasculature, TM was found on the non-vascular structures
lining the cavities of the posterior and anterior chambers and the limbus. TM was localized on the basal, lateral, and apical
plasma membranes of the inner and outer ciliary epithelium, and the posterior iris epithelium in which there was no polarized
expression of TM. In the anterior chamber, TM was localized on the luminal surface of the corneal endothelium, but was negative
on the anterior border layer of the iris, which is composed of a discontinuous layer of fibroblasts and collagen fibers. Thus,
TM was present at sites of cell-to-cell contact. TM was also present on the endothelia of the trabecular meshwork and the
Schlemm’s canal in the limbus. TM was localized not only on the luminal plasma membrane, but also on the cytoplasmic giant
vacuoles in the endothelial cells of the Schlemm’s canal. These findings extend the importance of anticoagulant mechanisms
to the systems of secretion, circulation, and drainage of the aqueous humor.
Accepted: 18 March 1997 相似文献
90.