全文获取类型
收费全文 | 2239篇 |
免费 | 99篇 |
国内免费 | 1篇 |
出版年
2022年 | 6篇 |
2021年 | 26篇 |
2020年 | 10篇 |
2019年 | 12篇 |
2018年 | 22篇 |
2017年 | 25篇 |
2016年 | 39篇 |
2015年 | 63篇 |
2014年 | 51篇 |
2013年 | 157篇 |
2012年 | 114篇 |
2011年 | 112篇 |
2010年 | 74篇 |
2009年 | 72篇 |
2008年 | 108篇 |
2007年 | 124篇 |
2006年 | 129篇 |
2005年 | 124篇 |
2004年 | 133篇 |
2003年 | 126篇 |
2002年 | 95篇 |
2001年 | 61篇 |
2000年 | 54篇 |
1999年 | 58篇 |
1998年 | 45篇 |
1997年 | 39篇 |
1996年 | 41篇 |
1995年 | 25篇 |
1994年 | 24篇 |
1993年 | 18篇 |
1992年 | 35篇 |
1991年 | 25篇 |
1990年 | 24篇 |
1989年 | 26篇 |
1988年 | 22篇 |
1987年 | 27篇 |
1986年 | 23篇 |
1985年 | 14篇 |
1984年 | 18篇 |
1983年 | 11篇 |
1982年 | 16篇 |
1981年 | 8篇 |
1980年 | 14篇 |
1979年 | 12篇 |
1978年 | 10篇 |
1977年 | 10篇 |
1976年 | 6篇 |
1975年 | 12篇 |
1974年 | 11篇 |
1968年 | 8篇 |
排序方式: 共有2339条查询结果,搜索用时 843 毫秒
41.
42.
The human S1-5 gene (fibrillin-like; FBNL) was originally isolated from a subtractively enriched cDNA library established from a subject with Werner syndrome (WS). We isolated genomic clones containing the entire S1-5 gene and determined its genomic structure including the exon–intron organization. The gene spanned approximately 18 kb of genomic DNA and consisted of 12 exons. Its expression was abundant in all tissues examined except brain and peripheral leukocytes, where it was undetectable. In addition, we have mapped S1-5 by fluorescencein situhybridization to chromosome 2p16, a position that excludes it as a candidate for WS. Our data should facilitate an understanding of the function and regulation of S1-5 in human tissues. 相似文献
43.
44.
The carboxy-terminal region of mammalian HSP90 is required for its dimerization and function in vivo. 总被引:1,自引:0,他引:1
下载免费PDF全文
![点击此处可从《Molecular and cellular biology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
The majority of mouse HSP90 exists as alpha-alpha and beta-beta homodimers. Truncation of the 15-kDa carboxy-terminal region of mouse HSP90 by digestion with the Ca(2+)-dependent protease m-calpain caused dissociation of the dimer. When expressed in a reticulocyte lysate, the full-length human HSP90 alpha formed a dimeric form. A plasmid harboring human HSP90 alpha cDNA was constructed so that the carboxy-terminal 49 amino acid residues were removed when translated in vitro. This carboxy-terminally truncated human HSP90 alpha was found to exist as a monomer. In contrast, loss of the 118 amino acid residues from the amino terminus of human HSP90 alpha did not affect its in vitro dimerization. Introduction of an expression plasmid harboring the full-length human HSP90 alpha complements the lethality caused by the double mutations of two HSP90-related genes, hsp82 and hsc82, in a haploid strain of Saccharomyces cerevisiae. The carboxy-terminally truncated human HSP90 alpha neither formed dimers in yeast cells nor rescued the lethal double mutant. 相似文献
45.
Evidence for a critical role for the cytoplasmic region of the interleukin 2 (IL-2) receptor gamma chain in IL-2, IL-4, and IL-7 signalling. 总被引:9,自引:0,他引:9
下载免费PDF全文
![点击此处可从《Molecular and cellular biology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
The high-affinity interleukin 2 receptor (IL-2R) consists of at least three distinct subunits: the IL-2R alpha chain (IL-2R alpha), beta chain (IL-2R beta), and gamma chain (IL-2R gamma). It has been shown that the cytoplasmic region of IL-2R beta, but not of IL-2R alpha, is essential for IL-2 signalling to the cell interior. In the present study, we examined the functional role of the IL-2R gamma cytoplasmic region in the IL-3-dependent mouse hematopoietic cell line BAF-B03, which expresses the endogenous IL-2R alpha and IL-2R gamma, or its subline F7, which additionally expresses human IL-2R beta cDNA. We show that overexpression of a mutant IL-2R gamma, lacking all but 7 amino acids of its cytoplasmic region, results in the selective inhibition of IL-2-induced c-fos gene activation and cellular proliferation in F7 cells. When two chimeric receptor molecules in which the cytoplasmic regions of IL-2R beta and IL-2R gamma had been swapped with each other (IL-2R beta/gamma and IL-2R gamma/beta) were coexpressed in BAF-B03, the cells responded to IL-2. These results indicate the critical importance of the IL-2-induced functional cooperation of the two cytoplasmic regions. Finally, we provide evidence that the IL-2R gamma cytoplasmic region is also critical for the IL-4 and IL-7-induced growth signal transduction in BAF-B03. 相似文献
46.
Purification and characterization of Clostridium perfringens 120-kilodalton collagenase and nucleotide sequence of the corresponding gene. 总被引:7,自引:3,他引:4
下载免费PDF全文
![点击此处可从《Journal of bacteriology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Clostridium perfringens type C NCIB 10662 produced various gelatinolytic enzymes with molecular masses ranging from approximately 120 to approximately 80 kDa. A 120-kDa gelatinolytic enzyme was present in the largest quantity in the culture supernatant, and this enzyme was purified to homogeneity on the basis of sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The purified enzyme was identified as the major collagenase of the organism, and it cleaved typical collagenase substrates such as azocoll, a synthetic substrate (4-phenylazobenzyloxy-carbonyl-Pro-Leu-Gly-Pro-D-Arg [Pz peptide]), and a type I collagen fibril. In addition, a gene (colA) encoding a 120-kDa collagenase was cloned in Escherichia coli. Nested deletions were used to define the coding region of colA, and this region was sequenced; from the nucleotide sequence, this gene encodes a protein of 1,104 amino acids (M(r), 125,966). Furthermore, from the N-terminal amino acid sequence of the purified enzyme which was found in this reading frame, the molecular mass of the mature enzyme was calculated to be 116,339 Da. Analysis of the primary structure of the gene product showed that the enzyme was produced with a stretch of 86 amino acids containing a putative signal sequence. Within this stretch was found PLGP, the amino acid sequence constituting the Pz peptide. This sequence may be implicated in self-processing of the collagenase. A consensus zinc-binding sequence (HEXXH) suggested for vertebrate Zn collagenases is present in this bacterial collagenase. Vibrio alginolyticus collagenase and Achromobacter lyticus protease I showed significant homology with the 120-kDa collagenase of C. perfringens, suggesting that these three enzymes are evolutionarily related. 相似文献
47.
Summary Using an ethanol solution of nile blue, we have developed an efficient method to detect the colonies of poly(3-hydroxyalkanoic
acids) (PHA) producing bacteria on the agar plate. When the bacterial colonies with PHA granules were stained with nile blue,
the stained colonies fluoresced bright orange on the irradiation of UV light. In the fluoresce emission spectra, fluorescence
intensity increased with an increase in the PHA content of bacterial cells.Alcaligenes eutrophus andA.latus colonies with poly(3-hydroxybutyric acid) (PHB) homopolymer exhibited an emission maximum at 580nm on the excitation at 490nm.
On the other hand,Pseudomonas oleovorans andP.putida with medium-chain-length (mcl-) PHA copolymers of C6, C8 and C10 units exhibited an emission maximum at 570nm. 相似文献
48.
Tomonari Tsutsumi Tetsuyuki Kobayashi Hiroshi Ueda Emiko Yamauchi Shiro Watanabe Harumi Okuyama 《Neurochemical research》1994,19(4):399-406
A membrane preparation from rat brain catalyzed the hydrolysis of [2-3H]glycerol-labeled lysophosphatidylinositol (lysoPI) to yield monoacylglycerol (MG) and inositolphosphates. This phospholipase C activity had an optimal pH of 8.2. The membrane preparation did not require the addition of Ca2+ for its maximum activity, but the activity was inhibited by addition of 0.1 mM EDTA to the assay mixture and was restored by simultaneous addition of 0.2 mM Ca2+. The activity was found to be localized in synaptic plasma membranes prepared by Ficoll and Percoll density gradients. The phospholipase C was highly specific for lysoPI; diacylglycerol formation from phosphatidylinositol, and MG formation from lysophosphatidylcholine, lysophosphatidylethanolamine, and lysophosphatidylserine were below 5% of that observed with lysoPI under the conditions used. We concluded that there is a pathway for phosphatidylinositol metabolism in brain synaptic membranes which is different from the well-characterized phosphoinositide-specific phospholipase C pathway.Abbreviations PI
phosphatidylinositol
- lysoPI
lysophosphatidylinositol
- lysoPI-PLC
lysophosphoinositide-specific phospholipase C
- PI-PLC
phosphoinositide-specific phospholipase C
- MG
monoacylglycerol
- PLC
phospholipase C
To whom to address reprint requests. 相似文献
49.
Connections among species-abundance (i-m
i
), species-frequency (i-F
i
), and species-sample size (S
n
-n) relationships were examined on the basis of the mapping data of a natural forest in Thailand. The spatial distribution of
individual trees without any discrimination of species was nearly random. Provided that the spatial distribution of each species
was random, thei-m
i
and thei-F
i
relationship was reconstructed from each other in terms of the total number of species (S) and the total number of individuals (N) in the data. The number of species (S
n
) in a subsample consisting ofn individuals was then obtained from thei-F
i
relationship. Logarithm ofS
n
increased with logn and showed a convex curve through the origin. The values of diversity indices based onN andS(orn andS
n
) were affected by sample size. These trends were further examined on the basis of 944 data sets of biotic communities and
three mathematical models of anS-N relationship. The properties of species-area relation were discussed in the light of these results. 相似文献
50.
Shiro Higashi Akinori Nakashima Hideki Ozaki Mikiko Abe Toshiki Uchiumi 《Journal of plant research》1993,106(1):47-54
The process of digestion of captured feeds in a pitcher, an insect-trapping organ, ofNepenthes was studied. Changes in bacterial population, pH and NH4
+ concentrations in pitcher juice were examined. Strong activities of both acid- and alkaline phosphatase, phosphoamidase,
esterase C4 and esterase C8 were found in the pitcher juice. Optimum pH of proteases in the juice and those secreted from
bacteria showed pH 3.0 and pH 8.0–9.0, respectively. Twenty six strains of bacteria were isolated from 4 pitchers: 10 strains
were gram positive, 16 strains were gram negative (10 strains had casein hydrolase activity). A proton excretion was induced
by NH4
+ released from the added solutions, and accordingly, the pH of the solutions fell. As a simulation model of the digestion
process of feeds in pitcher juice and polypeptone solution was added into the washed pitcher. A good correlation was found
among the NH4
+ concentration, pH and bacterial cell titer. 相似文献