全文获取类型
收费全文 | 25351篇 |
免费 | 1660篇 |
国内免费 | 1892篇 |
出版年
2024年 | 61篇 |
2023年 | 287篇 |
2022年 | 453篇 |
2021年 | 586篇 |
2020年 | 693篇 |
2019年 | 905篇 |
2018年 | 748篇 |
2017年 | 665篇 |
2016年 | 659篇 |
2015年 | 736篇 |
2014年 | 1150篇 |
2013年 | 1423篇 |
2012年 | 822篇 |
2011年 | 1093篇 |
2010年 | 846篇 |
2009年 | 1142篇 |
2008年 | 1198篇 |
2007年 | 1295篇 |
2006年 | 1167篇 |
2005年 | 1095篇 |
2004年 | 933篇 |
2003年 | 883篇 |
2002年 | 848篇 |
2001年 | 721篇 |
2000年 | 675篇 |
1999年 | 649篇 |
1998年 | 630篇 |
1997年 | 551篇 |
1996年 | 589篇 |
1995年 | 503篇 |
1994年 | 485篇 |
1993年 | 511篇 |
1992年 | 438篇 |
1991年 | 438篇 |
1990年 | 359篇 |
1989年 | 294篇 |
1988年 | 295篇 |
1987年 | 258篇 |
1986年 | 223篇 |
1985年 | 263篇 |
1984年 | 280篇 |
1983年 | 158篇 |
1982年 | 204篇 |
1981年 | 171篇 |
1980年 | 144篇 |
1979年 | 98篇 |
1978年 | 92篇 |
1977年 | 50篇 |
1976年 | 47篇 |
1975年 | 25篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
231.
Mortimer M. Civan Stephen R. Williams David G. Gadian Enrique Rozengurt 《The Journal of membrane biology》1986,94(1):55-64
Summary Swiss mouse 3T3 cells grown on microcarrier beads were superfused with electrolyte solution during continuous NMR analysis. Conventional31P and19F probes of intracellular pH (pH
c
) were found to be impracticable. Cells were therefore superfused with 1 to 4mm 2-deoxyglucose, producing a large intracellular, pH-sensitive signal of 2-deoxyglucose phosphate (2DGP). The intracellular incorporation of 2DGP inhibited the Embden-Meyerhof pathway. However, intracellular ATP was at least in part retained and the cellular responsivity to changes in extracellular ionic composition and to the application of growth factors proved intact. Transient replacement of external Na+ with choline or K+ reversibly acidified the intracellular fluids. Quiescent cells and mitogenically stimulated cells displayed the same dependence of shifts in pH
c
on external Na+ concentration (c
Na
o
). pH
c
also depended on intracellular Na+ concentration (c
Na
o
). Increasingc
Na
c
by withdrawing external K+ (thereby inhibiting the Na,K-pump) caused reversible intracellular acidification; subsequently reducingc
Na
o
produced a larger acid shift in pH
c
than with external K+ present. Comparison of separate preparations indicated that pH
c
was higher in stimulated than in quiescent cells. Transient administration of mitogens also reversibly alkalinized quiescent cells studied continuously. This study documents the feasibility of monitoring pH
c
of Swiss mouse 3T3 cells using31P NMR analysis of 2DGP. The results support the concept of a Na/H antiport operative in these cells, both in quiescence and after mitogenic stimulation. The data document by an independent technique that cytoplasmic alkalinization is an early event in mitogenesis, and that full activity of the Embden-Meyerhof pathway is not required for the expression of this event. 相似文献
232.
Mechanisms of regulation of the Na+/H+ exchanger 总被引:30,自引:0,他引:30
233.
234.
235.
Elly P. H. Best 《Physiologia plantarum》1986,68(3):502-510
The photosynthetic and growth characteristics of Ceratophyllum demersum L. were investigated under laboratory conditions which simulated those encountered in the plants' normal environment. The carbon fixation rate of C. demersum measured with 14 C at light and carbon saturation at pH 8.0 was 4.48 mg C (g ash-free dry weight)−1 h−1 . It was lower at pH 6.5 than at pH 8.0. The light use efficiencies in quiescent plants and actively growing plants were 6.3 and 8.7 × 10−9 kg CO2 J−1 , respectively, with corresponding maximum photosynthetic rates of 2.67 and 4.36 mg C (g ash-free dry weight)−1 h−1 . Photorespiration in actively growing plants consumed 24% of the carbon fixed. Incubation with DCMU demonstrated that about one-third was refixed. The optimum temperature for carbon fixation was 25°C. The C3 -photosynthetic pathway was the main operational route as indicated by the early photosynthetic products (largely C3 -acids) and the absence of Krantz anatomy and the chlorophyll a:b ratio (2.7). The maximum relative growth rates ranged from 0.025 to 0.041 g ash-free dry weight (g ash-free dry weight)−1 day−1 in the field (Lake Vechten, 1 to 3 m depth classes). 相似文献
236.
Rapid Isolation of the 7S-Nerve Growth Factor Complex and Its Subunits from Murine Submaxillary Glands and Saliva 总被引:5,自引:3,他引:2
7S-Nerve growth factor (NGF) and its alpha, beta-NGF, and gamma subunits have been purified from murine submaxillary glands and saliva by a combination of gel filtration on rigid polyvinyl gels, reversed-phase liquid chromatography on short alkyl chain supports (C4 columns), and ion-exchange chromatography on silica-based carboxymethyl columns. This technique is superior to previously used methods in that it is much more rapid and allows the purification of larger quantities of polypeptide from the same amount of starting material. Beta-NGF prepared with this method elicits the outgrowth of fibers of cells of a pheochromocytoma cell line (PC 12) in vitro, indicating that the biological activity is not impaired by the organic solvents and strong acids utilized for its isolation. 相似文献
237.
Yuzuru Matsuda Nobuo Nakanishi Geneva Dickens Gordon Guroff 《Journal of neurochemistry》1986,47(6):1728-1734
Soluble extracts from nerve growth factor (NGF)-stimulated PC12 cells prepared by alkaline lysis show a two- to 10-fold greater ability to phosphorylate the 40S ribosomal protein S6 than do extracts from control cells. The alkaline lysis method yields a preparation of much higher specific activity than does sonication. Half-maximal incorporation of 32P from [32P]ATP into S6 occurred after 4-7 min of NGF treatment. The partially purified NGF-sensitive S6 kinase has a molecular weight of 45,000. It is not inhibited by NaCl, chlorpromazine, or the specific inhibitor of cyclic AMP (cAMP)-dependent protein kinase, nor is it activated by addition of diolein plus phosphatidylserine. Trypsin treatment of either crude extracts or partially purified S6 kinase from control or NGF-treated cells was without effect. These data suggest that the S6 kinase stimulated by NGF is neither cAMP-dependent protein kinase or protein kinase C nor the result of tryptic activation of an inactive proenzyme. Treatment of intact cells with dibutyryl cAMP or 5'-N-ethylcarboxamideadenosine also increases the subsequent cell-free phosphorylation of S6. This observation suggests that cAMP-dependent protein kinase may be involved in the phosphorylation of S6 kinase. 相似文献
238.
239.
Ieharu Hishinuma Tetsuro Ishii Hiroyuki Watanabe Shiro Bannai 《In vitro cellular & developmental biology. Plant》1986,22(3):127-134
Summary Mouse lymphoma L1210 cells maintained in vitro at a high cell density for a certain time period adapted themselves to the
in vitro environment and were able to grow indefinitely. From these adapted cells, more than 30 clones were isolated. They
all had much higher activity to take up cystine than the original L1210 cells, supporting a previous view that the deficiency
of the cystine uptake limits the survival and growth of L1210 cells in vitro. The cystine uptake of one cloned cell line was
characterized. The enhanced uptake of cystine in these cells was mainly mediated by a Na+-independent, saturable system and was potently inhibited by glutamate and some other anionic amino acids, but less by aspartate.
Such activity of cystine uptake was not observed in the original L1210 cells. The results suggest that, upon adaptation in
vitro, L1210 cells acquire a new cystine transport activity necessary for survival and growth in vitro. 相似文献
240.
Emily L. Germain John W. Littlefield 《In vitro cellular & developmental biology. Plant》1986,22(2):107-112
Summary Stem cells of the embryonal carcinoma cell line called H6 can be induced to differnetiate to endoderm-like cells by retinoic
acid (3×10−6
M). We have detected a diffusible and stable factor which is secreted by H6 endoderm-like cells and stimulates the growth of
H6 stem cells. The stimulation by the endoderm-like cells is considereably greater than that by mouse fibroblasts or H6 stem
cells themselves. No reciprocal stimulation of endoderm-like cells by stem cells occurs. Part but not all of the stimulation
might be due to extracellular matrix proteins or to insulin-like growth factor type 2, each of which also stimulates the growth
of H6 stem cells. Insulin causes no such stimulation.
This work was supported by research rant no. CA-16754 from the National Cancer Institute to J. W. L. E. L. G. was supported
by an American Heart Association Medical Student Research Award.
Editor's Statement This paper presents a good example of cooperativity between undifferentiated teratoma stem cells and differentiated
parietal endoderm-derived countrparts in terms of growth support. It raises the interesting question of the relationship between
factors produced by paprietal and visceral endoderm cells. Gordon H. Sato 相似文献