全文获取类型
收费全文 | 2122篇 |
免费 | 132篇 |
国内免费 | 1篇 |
专业分类
2255篇 |
出版年
2022年 | 13篇 |
2021年 | 26篇 |
2019年 | 17篇 |
2018年 | 20篇 |
2017年 | 16篇 |
2016年 | 22篇 |
2015年 | 46篇 |
2014年 | 60篇 |
2013年 | 158篇 |
2012年 | 85篇 |
2011年 | 100篇 |
2010年 | 64篇 |
2009年 | 47篇 |
2008年 | 76篇 |
2007年 | 87篇 |
2006年 | 81篇 |
2005年 | 76篇 |
2004年 | 79篇 |
2003年 | 100篇 |
2002年 | 75篇 |
2001年 | 84篇 |
2000年 | 71篇 |
1999年 | 63篇 |
1998年 | 24篇 |
1997年 | 31篇 |
1996年 | 21篇 |
1994年 | 14篇 |
1993年 | 23篇 |
1992年 | 48篇 |
1991年 | 46篇 |
1990年 | 39篇 |
1989年 | 42篇 |
1988年 | 36篇 |
1987年 | 41篇 |
1986年 | 29篇 |
1985年 | 45篇 |
1984年 | 35篇 |
1983年 | 21篇 |
1982年 | 21篇 |
1981年 | 21篇 |
1980年 | 16篇 |
1979年 | 22篇 |
1978年 | 27篇 |
1977年 | 13篇 |
1975年 | 13篇 |
1974年 | 16篇 |
1973年 | 15篇 |
1970年 | 17篇 |
1969年 | 15篇 |
1966年 | 14篇 |
排序方式: 共有2255条查询结果,搜索用时 15 毫秒
31.
32.
Koichi Suzuki Misa Iwata Shigenori Ito Kiyoshi Matsui Atsuko Uchida Yasuhiko Mizoi 《Human genetics》1994,94(2):129-135
The “a” subunit of human coagulation factor XIII (F13A) exhibits genetic polymorphism defined by four common alleles, F13A*1A, *1B, *2A, and *2B. We have previously suggested on the basis of the isoelectric focusing patterns of the four allele products that point mutations at two separate sites and one intragenic crossing over might be involved in the genes of F13A polymorphism. Here, we report nucleotide substitutions associated with F13A polymorphism. A C/T transition of the second nucelotide of codon 564 in exon 12 is responsible for the difference between F13A*1A and *1B and that between F13A*2A and *2B, and a set of two base changes in codons 650 and 651 in exon 14 leads to the differences between F13A*1A and *2A and those between F13A*1B and *2B. The four combinations of the point mutations at the two exons thus correspond to the four alleles, two of which were generated by the point mutations from ancestral monomorphic gene. The results suggest strongly that intragenic crossing over must be involved in the genesis of the fourth allele. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) methods discriminating these base changes in exons 12 and 14 are also presented. 相似文献
33.
The effects of three forms of alginate (free acid, sodium and calcium salts) on ingestion and excretion of cholesterol in
the rat were studied. For two weeks, Male Sprague-Dawley rats were fed a cholesterol-rich diet containing 3% alginate from
the brown alga Ascophyllum nodosum. The food efficiency of the three types of alginate was: Na-alginate > Ca-alginate > alginic acid. A significant increase
in the weight of cecum was also observed in alginate diets. Alginate was not effective in preventing the elevation of serum
total cholesterol levels, although irregularly changing patterns were observed. The cholesterol level of liver showed a tendency
to decrease with alginate feeding, while fecal excretion of cholesterol increased. 相似文献
34.
An algal suspension containing protoplasmic detritus [termed, single cell detritus (SCD)] was prepared from freeze-dried fronds
of Ulva and its dietary value to Artemia nauplii was tested after size fractionation. The dissolved fraction (<0.22 μm) ofthe
Ulva suspension contained ca. 48% of theoriginal protein in the Ulva, but had no dietaryvalue to Artemia, which is a suspension
feeder. In contrast, the fraction passing through a 100-μm meshand containing SCD of 2–14 μm in diameter, contributedto the
survival of Artemia. The fraction remaining on the 100 μm mesh was further incubated with and without the bacterium Pseudoalteromonas
espejiana strain AR06 FERM BP-5024. The bacterium degraded
Ulva forming new SCD over 106 mL -1 level as rapidly as by 16 h of incubation. The dietary
value of Ulva for Artemia growth was elevated over four times by the incubation. The protein content of the SCD
was approximately doubled by the attaching of bacteria, suggesting the enhanced Artemia growth is attributable to
the combined effect of the SCD and the bacteria. Development of a hatchery diet from Ulva , a resource with a low
commercial value, is suggested utilizing the degrading and attaching ability of P. espejiana.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
35.
36.
37.
A new prolyl hydroxylase acting on poly-L-proline, from suspension cultured cells of Vinca rosea 总被引:3,自引:0,他引:3
A new prolyl hydroxylase having a novel substrate specificity was isolated from the suspension-cultured cells of Vinca rosea. This enzyme was solubilized with 0.05 M Tris-HCl buffer (pH 7.4) containing 0.1% Triton X-100, 0.3 M NaCl and 0.5 mM beta-mercaptoethanol from the membrane fractions of the cells, and was partially purified by (NH4)2SO4 fractionation and DEAE-Sephadex A-50 column chromatography. The enzyme preparation was found to require O2, Fe2+, ascorbate, alpha-ketoglutarate and poly-L-proline to attain maximum activity. The plant enzyme does not hydroxylate free proline and di-, tri- and tetra-L-proline, but hydroxylates octa-L-proline and poly-L-proline (Mr greater than 2000). Model peptides of unhydroxylated collagen, (Pro-Pro-Gly)5 and (Pro-Pro-Gly)10 are poor substrates for the plant enzyme. This means that the plant enzyme has a novel substrate specificity in regard to peptidyl substrate, and this differs from vertebrate prolyl hydroxylase, proline,2-oxoglutarate dioxygenase (prolyl-glycyl-peptide, 2-oxoglutarate: oxygen oxidoreductase, EC 1.14.11.2). 相似文献
38.
Erythrocyte ghosts containing a known number of molecules of purified fragment A of diphtheria toxin with a constant amount of FITC-BSA as a fluorescence marker were prepared by dialyzing a mixture of erythrocytes and these substances against hypotonic solution. These substances were then introduced into diphtheria toxin-resistant mouse L cells by virus-mediated cell fusion of the cells with the ghosts, and mononuclear recipients that had fused with only one erythrocyte ghost were separated in a fluorescence-activated cell sorter (FACS) on the basis of their cell size and fluorescence intensity. After separation, the viability of cells containing known numbers of fragment A was examined by measuring colony-forming ability. The results demonstrated that a single molecule of fragment A was sufficient to kill a cell.This fact was confirmed by introduction into cells of fragment A from an immunologically related mutant toxin, CRM 176 (fragment A-176); this has a completely functional fragment B region, but in cell extracts, the enzymic activity of its fragment A is about 10 fold less than that of wild toxin. The cytotoxicity of CRM 176 is about two hundredths of that of the wild-type (Uchida, Pappenheimer and Greany, 1973). As expected, about 100–200 fold excess of fragment A-176 was needed to kill the cells. 相似文献
39.
40.
Eisuke Mekada Kenji Kohno Masahiro Ishiura Tsuyoshi Uchida Yoshio Okada 《Biochemical and biophysical research communications》1982,109(3):792-799
We have measured the specific uptake of 125I-labelled diphtheria toxin in the presence of methylamine by a number of cell lines with different sensitivities to diphtheria toxin. The results show a strong correlation between the toxin sensitivities of the cell lines and the amount of specific uptake. The specific association of labelled toxin with cells was clearly demonstrated even with CHO cells, a cell line with relatively low sensitivity. Thus, CHO cell mutants that are resistant to diphtheria toxin could be classified as toxin-binding or non-binding cells by this method. 相似文献