全文获取类型
收费全文 | 4916篇 |
免费 | 389篇 |
出版年
2021年 | 39篇 |
2020年 | 22篇 |
2019年 | 34篇 |
2018年 | 49篇 |
2017年 | 46篇 |
2016年 | 81篇 |
2015年 | 121篇 |
2014年 | 142篇 |
2013年 | 209篇 |
2012年 | 248篇 |
2011年 | 250篇 |
2010年 | 169篇 |
2009年 | 172篇 |
2008年 | 251篇 |
2007年 | 255篇 |
2006年 | 254篇 |
2005年 | 257篇 |
2004年 | 240篇 |
2003年 | 304篇 |
2002年 | 310篇 |
2001年 | 90篇 |
2000年 | 53篇 |
1999年 | 93篇 |
1998年 | 101篇 |
1997年 | 92篇 |
1996年 | 80篇 |
1995年 | 64篇 |
1994年 | 60篇 |
1993年 | 68篇 |
1992年 | 79篇 |
1991年 | 58篇 |
1990年 | 39篇 |
1989年 | 52篇 |
1988年 | 56篇 |
1987年 | 41篇 |
1986年 | 35篇 |
1985年 | 45篇 |
1984年 | 49篇 |
1983年 | 41篇 |
1982年 | 60篇 |
1981年 | 56篇 |
1980年 | 52篇 |
1979年 | 47篇 |
1978年 | 46篇 |
1977年 | 41篇 |
1976年 | 46篇 |
1975年 | 24篇 |
1974年 | 22篇 |
1973年 | 23篇 |
1972年 | 19篇 |
排序方式: 共有5305条查询结果,搜索用时 672 毫秒
61.
Claude Penel Thomas Gaspar Michèle Crèvecoeur Claire Kevers Hubert Greppin 《Physiologia plantarum》1990,79(2):250-254
Ca2+ and Mn2+ activate the conversion of 1-aminocyclopropane-1-carboxylic acid (ACC) by root microsomes of Vicia lens as they do in other similar systems. The preparation of microsomes in the presence of Mn2+ greatly increases their ability to convert ACC into ethylene, without addition of Mn2+ in the reaction mixture. Ca2+ does not have this property. The effect could not be attributed to Mn2+ entrapping into membrane vesicles (sonication followed by repelleting had no effect) but, possibly, in part to Mn2+ -mediated binding to microsomes of a soluble factor favouring the conversion of ACC to C2 H4 . Although no direct correlation could be established in vitro between ethylene-forming-enzyme (EFE) and peroxidase activities, some soluble peroxidases might be this soluble factor. Mn2+ favoured attachment to membranes of some peroxidase activity from the soluble fraction and from commercial HRP and lipoxygenase. This binding effect of Mn2+ cannot be readily distinguished from its role in the generation of a chain of free radicals and in redox mechanisms. 相似文献
62.
63.
Evidence for interference, coinfections, and intertypic virus enhancement of infection by ovine-caprine lentiviruses. 总被引:2,自引:2,他引:0
下载免费PDF全文
![点击此处可从《Journal of virology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
The ovine-caprine lentiviruses share nucleotide homology and serological properties in their gag-pol genes and gene products but constitute two distinct biological groups represented by ovine visna virus of Icelandic origin and by caprine arthritis-encephalitis and ovine progressive pneumonia viruses of U.S. origin. Two members of each group, visna 1514 and its antigenic variant LV1-1 in the first group and CAEV/CO and S93, a field isolate virus from a local arthritic sheep, in the second group, were examined in the present study in competitive-binding studies in fibroblast and macrophage cell cultures. The cultures were preinoculated with each of the four viruses and then reinoculated with either 1514 virus or CAEV/CO, labeled with [35S]methionine. Both 1514 and CAEV/CO caused homologous interference. LV1-1 and S93 viruses shared the interference patterns of 1514 and CAEV/CO, respectively. 1514 and LV1-1 did not interfere with binding of CAEV/CO. Similarly, CAEV/CO and S93 did not interfere with binding of 1514. Remarkably, certain combinations, such as S93 plus 1514, resulted in enhanced binding of the second virus. Other experiments showed that the enhancement in binding extended to enhancement in replication of the second virus. These latter data suggested that individual cells supported replication of both viruses. Further testing of this phenomenon showed that goats could be doubly infected with two noninterfering viruses, 1514 and CAEV/CO. The ability of noninterfering related lentiviruses to infect the same cell and also the same host animal may be important in the natural history of these viruses in providing ideal conditions for the development of new recombinant viruses. 相似文献
64.
65.
Valérie Maxime Marguerite Peyraud-Waitzenergger Guy Claireaux Claude Peyraud 《Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology》1990,160(1):31-39
Summary Oxygen consumption, gill ventilation, blood acid-base/ionic status and haemoglobin oxygen affinity were studied in seawater-adapted adult salmon (Salmo salar) during five weeks after transfer into fresh water. Freshwater exposure induced the following changes: Standard oxygen consumption (
) and ventilatory flow (
) decreased markedly during the first days after transfer, then decreased more gradually until a new steady-state was achieved at which
and
were about 80% and 56% of the control values, respectively. The marked increase in oxygen extraction coefficient (Ew
O
2) and the marked decrease in the oxygen convection requirement (
) were associated with a reduction in the partial pressure of carbon dioxide in arterial blood (Pa
CO
2), in spite of a decrease of both ventilatory flow and water CO2 capacitance. These results suggested that transfer into fresh water induced an increase in branchial diffusive conductance. A biphasic pattern was observed in the time-course of the changes in both plasma ion concentration and acid-base status. During the first 10 days, plasma Na+, K+, and Cl– concentrations fell abruptly, then more gradually. [Cl–] decreased more than [Na+] resulting in a progressive increase in the [Na+]/[Cl–] ratio. During the second phase of acclimation to fresh water plasma Na+, K+, and Cl– concentrations progressively increased. [Cl–] increased more than [Na+], so that [Na+]/[Cl–] ratio decreased. Transfer into fresh water did not significantly change plasma lactate concentration. Upon exposure to fresh water, blood pH increased from 7.94±0.04 to 8.43±0.06 at day 10 and then decreased to 8.08±0.03 at day 34. The increase in blood pH induced by transfer to fresh water initially represented a mixed metabolic/respiratory alkalosis. However, after 15 days Pa
CO
2 had returned to pretransfer values and the alkalosis was purely metabolic. The metabolic component of the alkalosis was associated with appropriate changes in the plasma strong ion difference (S.I.D.). Blood alkalosis moved the oxygen dissociation curve to the left, so that P50 was decreased by 30% below the value in seawater for the maximal increase in blood pH. This rise in haemoglobin affinity for O2, associated with a marked increase in blood buffer capacity, are regarded as adaptative processes allowing the salmon to cope with the markedly increased energy expenditure required for upstream migration. 相似文献
66.
67.
I M Fearnley J E Walker R D Martinus R D Jolly K B Kirkland G J Shaw D N Palmer 《The Biochemical journal》1990,268(3):751-758
The ceroid lipofuscinoses are a group of neurodegenerative lysosomal storage diseases of children and animals that are recessively inherited. In diseased individuals fluorescent storage bodies accumulate in a wide variety of cells, including neurons. Previous studies of these bodies isolated from tissues of affected sheep confirmed that the storage occurs in lysosomes, and showed that the storage body is mostly made of a single protein with an apparent molecular mass of 3500 Da with an N-terminal amino acid sequence that is the same as residues 1-40 of the c-subunit (or dicyclohexylcarbodi-imide-reactive proteolipid) of mitochondrial ATP synthase. In the present work we have shown by direct analysis that the stored protein is identical in sequence with the entire c-subunit of mitochondrial ATP synthase, a very hydrophobic protein of 75 amino acid residues. As far as can be detected by the Edman degradation, the stored protein appears not to have been subject to any post-translational modification other than the correct removal of the mitochondrial import sequences that have been shown in other experiments to be present at the N-terminal of its two different precursors. No other protein accumulates in the storage bodies to any significant extent. Taken with studies of the cDNAs for the c-subunit in normal and diseased sheep, these results indicate that the material that is stored in lysosomes of diseased animals has probably entered mitochondria and has been subjected to the proteolytic processing that is associated with mitochondrial import. This implies that the defect that leads to the lysosomal accumulation concerns the degradative pathway of the c-subunit of ATP synthase. An alternative, but less likely, hypothesis is that for some unknown reason the precursors of subunit c are being directly mis-targeted to lysosomes, where they become processed to yield a protein identical with the protein that is normally found in the mitochondrial ATP synthase assembly, and which then accumulates. 相似文献
68.
Amina El Jamali Nadia Rachdaoui Claude Jacquemin Claude Corrèze 《Journal of neurochemistry》1996,67(6):2532-2539
Abstract: Long-term (48-h) forskolin treatment of rat astroglial cells led to a slight decrease (30–40%) in the response to isoproterenol, vasoactive-intestinal peptide, guanyl 5'-(βγ-imido)diphosphate, guanosine 5'- O -(3-thiotriphosphate) [GTP(S)], and AIF4 − in crude membrane fractions. In contrast, the acute stimulatory effect of forskolin was increased by 1.25–1.5-fold. These two opposite effects of forskolin were mediated by a cyclic AMP-dependent mechanism. No changes in Gs α, Gi α, or Gβ protein levels could be determined by immunoblotting using specific antisera. No significant differences were observed in the ability of G proteins extracted from control and forskolin-treated cells to reconstitute a full adenylyl cyclase activity in membranes from S49 cyc− cells, lacking Gs α protein. Gs α proteins were detected in two pools of membranes, one in the heavy sucrose fractions and the other in light sucrose fractions. Forskolin treatment of the cells shifted Gs α protein toward the light-density membranes. We did not find any significant change in the distribution of adenylyl cyclase. In contrast to the decreased stimulation of adenylyl cyclase activity by agonists acting via Gs α, observed in the crude membrane fraction, the responses of adenylyl cyclase to forskolin as well as to GTP(S) were increased in the purified plasma membrane fractions. These results may indicate that sensitization of the catalyst appears to be the dominant component in the astroglial cell response to long-term treatment by forskolin. 相似文献
69.
Elumalai Sivamani Ping Shen Natacha Opalka Roger N. Beachy Claude M. Fauquet 《Plant cell reports》1996,15(5):322-327
The microprojectile bombardment of immature embryos has proven to be effective in transforming many indica rice varieties. One of the drawbacks of using immature embryos is the requirement of a large number of high quality immature embryos, which itself is a tedious and laborious process. To circumvent these problems, we have developed a procedure, using indica variety TN1 as a model that generates highly homogenous populations of embryogenic subcultured calli by selectively propagating a small number of regeneration-proficient calli derived from seeds. Thousands of embryogenic calli were produced from 50 seeds within 10 weeks. Ten to 20 independent R0 transgenic lines were regenerated per 500 embryogenic calli bombarded. The convenience and reliability offered by this transformation system has made transformation of indica rice a routine procedure.Abbreviations 2,4-D
2,4-dichlorophenoxy acetic acid
- NAA
naphthalene acetic acid
- BAP
6-benzylaminopurine
- kb
kilobase
- GUS
-glucuronidase
- X-gluc
5-bromo-4-chloro-3-indolyl--D-glucuronide
- HPH
hygromycin B phosphotransferase 相似文献
70.
Regeneration of fertile transgenic indica (group 1) rice plants following microprojectile transformation of embryogenic suspension culture cells 总被引:8,自引:0,他引:8
Shiping Zhang Lili Chen Rongda Qu Philippe Marmey Roger Beachy Claude Fauquet 《Plant cell reports》1996,15(7):465-469
Regenerable embryogenic suspensions of elite Indica (group 1) rice varieties IR24, IR64, IR72 and an advanced Indica rice breeding line IR57311-95-2-3 were established within 6–8 weeks from 3–4 week old calli derived from mature seeds. Transgenic rice plants were obtained by introducing a plasmid carrying genes encoding hygromycin phosphotransferase (hph, conferring resistance to hygromycin B) and ß-glucuronidase (uidA), both driven by the CaMV 35S promoter, via particle bombardment of embryogenic suspensions. The effect of osmotic conditioning on transformation was evaluated. Regenerated plants were resistant to hygromycin B and expressed the uidA (GUS) gene. The growth of mother plants (R0) was normal and seeds were produced. Southern blot analysis of R0 and R1 plants showed that hygromycin resistant plants contained intact hph genes that were inherited in a Mendelian fashion. A protocol for a simple, efficient, repeatable, genotype- and environment-independent Indica rice transformation system is described.Abbreviations 2,4-D
2,4-dichlorophenoxy acetic acid
- NAA
-naphthalene acetic acid
- kb
kilobase
- GUS
ß-glucuronidase
- hph
hygromycin B phosphotransferase 相似文献