全文获取类型
收费全文 | 10365篇 |
免费 | 899篇 |
国内免费 | 1篇 |
专业分类
11265篇 |
出版年
2024年 | 12篇 |
2023年 | 42篇 |
2022年 | 116篇 |
2021年 | 250篇 |
2020年 | 121篇 |
2019年 | 163篇 |
2018年 | 197篇 |
2017年 | 167篇 |
2016年 | 313篇 |
2015年 | 503篇 |
2014年 | 552篇 |
2013年 | 599篇 |
2012年 | 855篇 |
2011年 | 828篇 |
2010年 | 499篇 |
2009年 | 473篇 |
2008年 | 622篇 |
2007年 | 632篇 |
2006年 | 609篇 |
2005年 | 587篇 |
2004年 | 540篇 |
2003年 | 492篇 |
2002年 | 477篇 |
2001年 | 123篇 |
2000年 | 94篇 |
1999年 | 148篇 |
1998年 | 134篇 |
1997年 | 91篇 |
1996年 | 73篇 |
1995年 | 78篇 |
1994年 | 71篇 |
1993年 | 60篇 |
1992年 | 79篇 |
1991年 | 67篇 |
1990年 | 64篇 |
1989年 | 54篇 |
1988年 | 47篇 |
1987年 | 37篇 |
1986年 | 42篇 |
1985年 | 41篇 |
1984年 | 43篇 |
1983年 | 28篇 |
1982年 | 20篇 |
1981年 | 26篇 |
1979年 | 25篇 |
1978年 | 20篇 |
1977年 | 16篇 |
1976年 | 18篇 |
1974年 | 19篇 |
1972年 | 11篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
101.
A receptor for protein import into potato mitochondria 总被引:3,自引:0,他引:3
Five potential surface receptors for protein import into plant mitochondria were identified by gentle trypsin treatment of intact mitochondria from potato tubers and subsequent preparation of outer mitochondrial membranes. One of them, a 23 kDa protein, was purified to homogeneity and analysed by direct protein sequencing. Copy DNA clones encoding the corresponding polypeptide were isolated with labelled oligonucleotides derived from the amino acid data. The 23 kDa protein shares significant sequence similarity with protein import receptors from fungal mitochondria and contains one of their typical tetratricopeptide motifs. Its integration into the outer membrane is independent of protease accessible surface receptors and not accompanied by proteolytic processing. Monospecific antibodies against the 23 kDa protein significantly reduce import capacity of isolated mitochondria indicating that this component is indeed involved in the recognition or import of precursor proteins. As in fungi, immunological inhibition of protein import with IgGs against a single receptor is incomplete suggesting the existence of other receptors in the outer mitochondrial membrane of plant mitochondria. 相似文献
102.
Summary Techniques for the isolation of ahhighly pure population of viable osteoclasts are limited. For this reason, we developed
an isolation procedure that results in a high yield of osteoclast-like cells, up to 92% pure, from 3-wk-old chicken tibias.
The unique feature of the method is the migration of cells from marrow-free endosteal surfaces to vitronectin-coated plates.
The cells retain the osteoclast phenotype and remain viable in culture for a minimum of 1 wk. The cells were characterized
and compared to two populations of authentic avian osteoclasts, which were isolated on the basis of association with fibronectin-coated
plates. The cells contained substantial amounts of tartrate-resistant acid phosphatase. Alkaline phosphatase levels were negligible,
suggesting little contamination by osteoblasts. Response to parathyroid hormone, dibutyryl cyclic adenosine monophosphate,
calcitonin, acetazolamide, 17β-estradiol, and prostaglandin E2 was evident, as detected by measuring acid production. The vitronectin-associating cells contained numerous mitochondria,
had the ability to resorb bone in anin vitro bone slice assay, and specifically bound biotinylated vitronectin. At 5 d of culture, the cells demonstrated marginal multinuclearity,
having two to three nuclei. A large number (∼1×106 cells/tibia) of viable cells that exhibit characteristics of authentic osteoclasts can be obtained by the method described.
Potentially, this method could be applied to other species. 相似文献
103.
Abrogation of the Fc gamma receptor IIA-mediated phagocytic signal by stem-loop Syk antisense oligonucleotides. 总被引:4,自引:0,他引:4
下载免费PDF全文
![点击此处可从《Molecular biology of the cell》网站下载免费的PDF全文](/ch/ext_images/free.gif)
M Matsuda J G Park D C Wang S Hunter P Chien A D Schreiber 《Molecular biology of the cell》1996,7(7):1095-1106
The role of Syk kinase in Fc gamma receptor (Fc gamma R) IIA-mediated phagocytosis was examined with two forms of antisense oligodeoxynucleotides (ODNs) designed to hybridize to human Syk mRNA. Monocytes were incubated with linear and stem-loop antisense ODNs targeted to Syk mRNA. When complexed with cationic liposomes, stem-loop Syk antisense ODN with phosphorothioate modification exhibited stability in fetal bovine and human serum. The stem-loop Syk antisense ODN at a concentration of 0.2 microM inhibited Fc gamma RIIA-mediated phagocytosis by 90% and completely eliminated Syk mRNA and protein in monocytes, whereas scrambled-control ODNs had no effect. The Syk antisense ODNs did not change beta-actin mRNA levels and Fc gamma RII cell-surface expression. In addition, stem-loop Syk antisense ODN inhibited Fc gamma RI and Fc gamma RIIIA-mediated phagocytosis. These data indicate the efficacy of stem-loop Syk antisense ODN for targeting and degrading Syk mRNA and protein and the importance of Syk kinase in Fc gamma receptor-mediated phagocytosis. Immunoblotting assay demonstrated that Fc gamma RII tyrosine phosphorylation after Fc gamma RII cross-linking did not change in the absence of Syk protein. These results indicate that Syk kinase is required for Fc gamma RIIA-mediated phagocytic signaling and that Fc gamma RII cross-linking leads to tyrosine phosphorylation of Fc gamma RII independent of Syk kinase. 相似文献
104.
The fluid dynamics of sperm motility near both rigid and elastic walls is studied using the immersed boundary method. Simulations
of both single and interacting organisms are presented. In particular, we find that nearby organisms originally undulating
with a 90° phase shift may adjust their relative swimming velocities and phase-lock. Comparisons with previous analytical
results are also discussed. The tendency of a near-wall to attract organisms is demonstrated. 相似文献
105.
106.
Thylakoids from mesophyll cells of maize showed a high rateof the ferredoxin (Fd)-dependent and antimycin A (AntiA)-sensitivecyclic electron flow as determined by the quenching of 9-aminoacridinefluorescence which indicates the formation of 相似文献
107.
Suppression of Quantum Yield of Photosystem II by Hyperosmotic Stress in Chlamydomonas reinhardtii 总被引:1,自引:0,他引:1
Addition of ethylene glycol (EG) or NaCl to cells of Chlamydomonasreinhardtii induced transient non-photochemical quenching ofChl fluorescence correlated with the inhibition of photosyntheticoxygen evolution. The induction of the quenching and subsequentrecovery proceeded not only in the light but also in the dark.The quenching was almost unaffected by the protonophore nigericin,suggesting the involvement of a type of non-photochemical quenchingattributable to a state 2 transition. Higher concentrationsof EG or NaCl caused a delay of the recovery of the maximumfluorescence yield (Fm'). Dark reduction rate of P700+ afterthe application of a flash light in the presence of DCMU wasenhanced by the hyperosmotic shock, suggesting a stimulatedreduction of the intersystem electron carriers. It is proposedthat the osmotic stress stimulates electron donation from stromalcomponents via the NAD(P)H dehydrogenase, which results in thereduction of the intersystem chain and triggering of a state2 transition leading to stimulated cyclic PSI activity. (Received May 16, 1995; Accepted July 26, 1995) 相似文献
108.
In order to better understand the biochemical mechanisms of DNA metabolism in chloroplasts, repair of UV induced plastome damage in vivo was determined by exposure of soybean suspension cells to UV light and subsequent quantitation of the damage remaining in nuclear and chloroplast encoded genes with time by quantitative polymerase chain reaction (QPCR). The kinetics of damage rapir in the nuclear rbcS gene suggest that photoreactivation and dark mechanisms are active, while for the plastome encoded psbA gene only a light-dependent repair process was detected which is considerably slower than would be expected for photolyase-mediated photoreactivation. 相似文献
109.
110.
Andrea Manni Rita Wechter Lisa Wei Daniel Heitjan Laurence Demers 《Journal of cellular physiology》1995,163(1):129-136
Polyamines (PA) have been shown to be critical mediators of estradiol-induced breast cancer cell proliferation. This finding suggests that constitutive activation of the PA pathway may promote tumor progression, possibly leading to hormone independence. To test this hypothesis, we transfected hormone-responsive MCF-7 breast cancer cells with a complementary DNA coding for ornithine-decarboxylase (ODC), the first rate-limiting enzyme in PA biosynthesis. Marked ODC over-expression observed in stably transfected clones was associated with a selective increase in cellular putrescine content, while spermidine and spermine levels were not altered. ODC-overexpressing MCF-7 cells were resistant to the antiproliferative effects of low but not high concentrations of the enzyme inhibitor, α-difluoromethylornithine. In agreement with our hypothesis, sensitivity to the growth-promoting action of estradiol was reduced by approximately one third (P < 0.001) in ODC-overexpressing MCF-7 cells compared with vector-only transfected clones. Basal growth under anchorage-dependent conditions was only marginally increased by ODC overexpression (P = 0.048), while clonogenicity in soft agar was actually reduced. These data suggest that activation of PA biosynthesis may contribute in part to the acquisition of estrogen independence by breast cancer cells. Since only putrescine content was increased as a result of ODC overexpression, these data may underestimate the overall influence of the PA pathway on breast cancer phenotype. © 1995 Wiley-Liss, Inc. 相似文献