全文获取类型
收费全文 | 10961篇 |
免费 | 846篇 |
国内免费 | 4篇 |
出版年
2021年 | 115篇 |
2020年 | 49篇 |
2019年 | 83篇 |
2018年 | 117篇 |
2017年 | 121篇 |
2016年 | 172篇 |
2015年 | 262篇 |
2014年 | 339篇 |
2013年 | 612篇 |
2012年 | 511篇 |
2011年 | 498篇 |
2010年 | 329篇 |
2009年 | 320篇 |
2008年 | 522篇 |
2007年 | 554篇 |
2006年 | 513篇 |
2005年 | 542篇 |
2004年 | 537篇 |
2003年 | 529篇 |
2002年 | 455篇 |
2001年 | 386篇 |
2000年 | 400篇 |
1999年 | 344篇 |
1998年 | 125篇 |
1997年 | 134篇 |
1996年 | 113篇 |
1995年 | 130篇 |
1994年 | 107篇 |
1993年 | 116篇 |
1992年 | 250篇 |
1991年 | 231篇 |
1990年 | 242篇 |
1989年 | 204篇 |
1988年 | 187篇 |
1987年 | 174篇 |
1986年 | 158篇 |
1985年 | 148篇 |
1984年 | 125篇 |
1983年 | 111篇 |
1982年 | 87篇 |
1981年 | 73篇 |
1980年 | 57篇 |
1979年 | 90篇 |
1978年 | 83篇 |
1977年 | 69篇 |
1976年 | 46篇 |
1975年 | 40篇 |
1974年 | 49篇 |
1973年 | 41篇 |
1972年 | 49篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
61.
Mamoru Koketsu Lekh Raj Juneja Hiroshi Kawanami Mujo Kim Takehiko Yamamoto 《Glycoconjugate journal》1992,9(2):70-74
Egg yolk, a large proportion of the egg, was studied for the preparation ofN-acetylneuraminic acid (Neu5Ac). The delipidated hen egg yolk (DEY; 500 kg containing 0.2% w/w, Neu5Ac) was hydrolysed with HCl (pH 1.4) at 80 °C and neutralized with NaOH (pH 6.0). The mixture was filtered and electrodialysed until the conductivity was 240 µS cm–1. The filtrate was applied on a column of Dowex HCR-W2 (20–50 mesh), followed by a column of Dowex 1-X8 (200–400 mesh). The latter column was washed with water, and then eluted with a linear gradient of HCO2H (0–2m). The eluates containing Neu5Ac were concentrated using a reverse osmosis membrane and, finally, rotary evaporated at 40 °C. The residue was then lyophilized to yield 500 g Neu5Ac. The purity of Neu5Ac was >98% (TBA method). HPLC, NMR spectroscopy and TLC chromatography of the product obtained from the DEY showed that Neu5Ac was the sole derivative present in egg yolk. The DEY, a byproduct from egg processing plants, was found to be an excellent source for the large-scale preparation of Neu5Ac.Abbreviations Neu5Ac
N-acetylneuraminic acid
- Neu5Gc
N-glycolylneuraminic acid
- DEY
delipidated egg yolk
- HPLC
high performance liquid chromatography
- TLC
thin layer chromatography
- NMR
nuclear magnetic resonance
- IR
infrared spectroscopy
Presented at the 11th International Symposium on Glycoconjugates, Toronto, Canada. 相似文献
62.
Ultrastructural localization of Na, K-ATPase alpha-subunit along rat nephron segments was investigated quantitatively by immunogold electron microscopy on LR-White ultrathin sections using affinity-purified antibody against alpha-subunit of the enzyme. Ultrathin sections were incubated with the antibody at a saturation level and the number of gold particles bound per micron of the plasma membrane (particle density) of the tubular epithelial cells from the proximal tubule to the collecting duct was determined. In all the tubular epithelial cells, gold particles were located exclusively on the basolateral surface, and no significant binding of gold particles to the apical surface was observed. Distribution of gold particles on the basolateral membranes was quite heterogeneous; lateral membranes and infolded basal membranes were highly labeled, whereas the basal membranes which are in direct contact with the basal lamina were scarcely labeled. The average particle density on the basal surface was highest in the distal straight tubule cells (11.4 units), very high in the distal convoluted tubule cells (9.8 units), intermediate in the proximal tubule cells (3.3 units), in the connecting tubule cells (4.3 units), and in the principal cells of the collecting duct (5.6-3.8 units), low in the thin limb of Henle's loop (1.0 unit), and at the control level in the intercalated cells in the connecting and collecting duct. The relative number of gold particles/mm nephron segment and the relative number of gold particles in the various nephron segments were calculated using quantitative morphological data. The estimated distribution profile of the former was in good agreement with the Na, K-ATPase activity profile in rat nephron, which was determined biochemically with a microenzymatic method. 相似文献
63.
64.
Kenji Kato Su-wan Oh Hiroyuki Yamamoto Takayuki Hanazato Ikuko Yasuda Akira Otuki Masayuki Takahashi 《Ecological Research》1992,7(3):267-276
In order to understand the control mechanisms of a large, stable bacterial standing stock, enclosure experiments were conducted
in a eutrophic lake, where both bacterial productivity and grazing pressure were very high. Total bacterial number in the
different enclosures ranged from 1.2 to 2.7×107 cells mL−1 throughout the experiment. The average bacterial cell production rate estimated from a grazer eliminating experiment was
6.3×105 cells mL−1 h−1. Difference in the bacterial cell production rate between shaded and unshaded enclosures was not apparent. Bacteria showed
a reduction in standing stock of only about 25–30% even after the supply of light was cut to 1%. Bacteria in the shaded enclosures
then recovered their production rate in the first 12 days of perturbation. Grazing pressure in the shaded enclosures was not
less than that for the control. Thus, it was considered a control mechanism of bacterial stable standing stock that the bacteria
shifted their organic substrate from extracellular dissolved organic carbon freshly released from phytoplankton to that already
stocked in the water column, though it is not known whether the dominant bacteria were the same. 相似文献
65.
A novel and efficient method for enzymatic synthesis of high purity maltose using moranoline (1-deoxynojirimycin). 总被引:1,自引:0,他引:1
S Maruo H Yamashita K Miyazaki H Yamamoto Y Kyotani H Ogawa M Kojima Y Ezure 《Bioscience, biotechnology, and biochemistry》1992,56(9):1406-1409
A transglycosylation reaction with moranoline (1-deoxynojirimycin) was done with soluble starch as the glucosyl donor and Bacillus macerans amylase as a cyclodextrin glycosyltransferase [EC 2.4.1.19]. The resultant transglycosylation products with moranoline, obtained by treating the reaction mixture with a strong cation exchange resin, were hydrolyzed by beta-amylase [EC 3.2.1.2] from sweet potatoes. The hydrolysate was treated with a strong cation exchange resin, and high purity maltose was obtained. 相似文献
66.
The gap theory in forest dynamics 总被引:4,自引:0,他引:4
Shin-Ichi Yamamoto 《Journal of plant research》1992,105(2):375-383
Since the late 1970s, ecologists interested in forest dynamics have focused their attention to the responses of individuals,
populations and communities to “gaps” which are openings created in the forest canopy. This review intended to introduce some
collective knowledge on major subjects of the gap theory in forest dynamics, in relation to gap-disturbance regimes, tree
regeneration behaviour and community structure. 相似文献
67.
Kunio Nakagawa Norio Omori Kahoko Hashimoto Tetsuya Yamamoto Takashi Tsunoda Tadao Nose 《Biotherapy》1992,4(2):109-115
Thein vitro effect of a combined treatment with lymphokine activated killer (LAK) cell and radiation therapy on rat brain tumor was examined using51Cr release assay. The tumor cell-line used in this experiment was 9L rat brain tumor derived from a Fischer 344 rat. LAK cells were obtained by culturing rat lymphocytes with recombinant human interleukin 2 for at least 3 days. The cytotoxic activity of the LAK cells was examined by51Cr release assay. Irradiation was done by exposing the microtiter plate in which the15Cr labeled 9L cells and LAK cells were cultured to a137Cs gamma cell unit. Without irradiation, there was 18% cytotoxicity in the 1:100 tumor-to-LAK cell ratio specimen after 24 hrs cocultivation. However, if 5 Gy of irradiation was given, followed by 12 hrs incubation, the cytotoxicity was enhanced significantly at the same cell ratio (30%). This enhancement effect was the most prominent when the cell ratio was 1:100 and the irradiation dose was 5 Gy. To generate the enhancement effect, an incubation time of over 8 hrs both before and after irradiation was required. The supernatant of the LAK cells showed 19.8% and 11.4% cytotoxicity with and without irradiation, respectively. This result indicates the participation of a cytotoxic factor released from LAK cells.This work is supported in part by grant from Univeristy of Tsukuba Project Research. 相似文献
68.
Komeda Yoshibumi; Yamashita Hirofumi; Sato Naoki; Tsukaya Hirokazu; Naito Satoshi 《Plant & cell physiology》1991,32(6):737-743
The 5'-upstream region (2.4 kb) of the gene for phytochromeI from Pisum sativum (phyl) was fused to the uidA gene fromEscherichia coli that encodes ß-glucuronidase (GUS).The resulting PHY-GUS fusion was introduced into Petunia hybridaand was used as a reporter of the expression of the phyI genewhich was recognized by GUS activity. The PHY-GUS fusion wasexpressed at a relatively high level when transgenic plantswere grown in the dark, while leaves and stems of light-grownplants showed background activity. Flowers of light-grown plantswere shown to have significant levels of GUS activity but rootsdid not have such activity. When light-grown transgenic plantswere transferred to the dark, they expressed the activity atlevels that corresponded to those of dark-grown plants. Lighttreatment prior to growth in darkness revealed red/far-red reversibilityof recovery of the activity. Thus, the 2.4-kb fragment fromthe 5' region of the phyI gene carries the information necessaryfor the light-repressible autoregulation. (Received March 30, 1991; Accepted May 20, 1991) 相似文献
69.
Shiraishi Tomonori; Araki Miwa; Yoshioka Hirofumi; Kobayashi Issei; Yamada Tetsuji; Ichinose Yuki; Kunoh Hitoshi; Oku Hachiro 《Plant & cell physiology》1991,32(7):1067-1075
A pathogenic fungus of pea, Mycosphaerella pinodes, secretesa so-called "suppressor" in its pycnospore germination fluid.The suppressor blocks the defense responses and induces localsusceptibility (accessibility) in pea plants to agents thatare not pathogenic in pea. The suppressor nonspecifically inhibitsthe ATPase activity in plasma membranes prepared from pea, soybean,kidney bean, cowpea and barley plants. However, cytochemicalstudies by electron microscopy indicate that the suppressorspecifically inhibits the ATPase in pea cell membranes, butnot in those of four other plant species tested. That is, thespecificity of the suppressor appears at the cell and/or tissuelevel, but is not evident in vitro. Furthermore, the inhibitoryeffect of the suppressor is temporary because the ATPase activityrecovers 9 h after the treatment. A similar effect was observedafter inoculation with M. pinodes but not with a nonpathogenof pea, M. ligulicola. The role of the suppressor in host-parasitespecificity is discussed. (Received April 9, 1991; Accepted August 6, 1991) 相似文献
70.
In vitro binding of nuclear proteins from wheat germ to the5'-upstream region of the rolC gene of Ri plasmid was investigated.The specific DNA sequences interacting with proteins were detectedby DNase I footprinting. (Received October 8, 1990; Accepted November 30, 1990) 相似文献