全文获取类型
收费全文 | 797638篇 |
免费 | 82601篇 |
国内免费 | 245篇 |
专业分类
880484篇 |
出版年
2018年 | 7998篇 |
2017年 | 7632篇 |
2016年 | 10721篇 |
2015年 | 13539篇 |
2014年 | 16121篇 |
2013年 | 23247篇 |
2012年 | 26061篇 |
2011年 | 26824篇 |
2010年 | 18340篇 |
2009年 | 16925篇 |
2008年 | 23947篇 |
2007年 | 24919篇 |
2006年 | 23284篇 |
2005年 | 22398篇 |
2004年 | 22172篇 |
2003年 | 21327篇 |
2002年 | 20833篇 |
2001年 | 34746篇 |
2000年 | 34203篇 |
1999年 | 27582篇 |
1998年 | 10177篇 |
1997年 | 10270篇 |
1996年 | 9840篇 |
1995年 | 9062篇 |
1994年 | 8722篇 |
1993年 | 8752篇 |
1992年 | 22337篇 |
1991年 | 21922篇 |
1990年 | 21371篇 |
1989年 | 20814篇 |
1988年 | 19083篇 |
1987年 | 18327篇 |
1986年 | 17094篇 |
1985年 | 16956篇 |
1984年 | 13937篇 |
1983年 | 12188篇 |
1982年 | 9234篇 |
1981年 | 8358篇 |
1980年 | 7756篇 |
1979年 | 12940篇 |
1978年 | 10202篇 |
1977年 | 9194篇 |
1976年 | 8804篇 |
1975年 | 9820篇 |
1974年 | 10487篇 |
1973年 | 10353篇 |
1972年 | 9478篇 |
1971年 | 8460篇 |
1970年 | 7387篇 |
1969年 | 7255篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
111.
A physical domain of herpes simplex virus ICP8 is expressed and active in Escherichia coli.
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)
In this report, we describe a series of procedures to assay the function of fusion genes in Escherichia coli and the specific application to the carboxy-terminal third of the herpes simplex virus type 1 (HSV-1) DNA-binding protein ICP8. E. coli cells containing the cloned HSV-1 BamHI G fragment with the HSV-1 BamHI-G-V site, map unit 0.388, nearest the tet promoter in pBR322 synthesized an active product containing a portion of ICP8. The new product induced phenotypic alterations in recipient hosts that were measurable and stable yet limited to the stability of the plasmid. The corresponding cloned DNA from the characterized HSV-1 DNA-binding protein mutant tsHA1 exhibited a predictable temperature-sensitive phenotype. Screening procedures based on the loss of induction of the parental plasmid-induced phenotype in E. coli cells allowed us to select additional mutations. One of these, which conferred a phenotype different from that of tsHA1, was transferred to the viral genome by marker transfer techniques. We suggest that any mutant could be isolated in any sequence, provided that the wild-type coding sequences induce alterations in E. coli cells. The observed alterations should have relevance in determining the mode of action of the protein in its normal environment. 相似文献
112.
A.M. Ageel K.E.H. El-Tahir A.R. Abu-Jayyb 《Prostaglandins & other lipid mediators》1985,30(3):369-381
The effect of bromocriptine mesylate on cyclic nucleotides and PGI2 release by rat aortic and uterine tissues was investigated. Treatment of rats with bromocriptine (10 mg kg−1 I.P. daily for 14 days) increased PGI2 release by the thoracic aorta from 0.67 ± 0.02 to 1.4 ± 0.03 ng/mg wet tissue (P < 0.001; n = 6). This increase was antagonized by treatment with sulpiride (15 mg kg−1). Incubation of the arterial tissue with bromocriptive (50 ug ml−) in vitro also stimulated PGI2 release. Mepacrine (160 μg ml−) significantly decreased both basal and stimulated PGI2 release. Incubation of myometrial tissue from pregnant rats with bromocriptine (50 μg ml−1) in vitro significantly decreased PGI2 release from 1.25 ± 0.07 to 0.60 ± 0.08 ng/mg wet tissue (P < 0.05, n = 6).It also elevated uterine cAMP from 40 ± 2 to 64 ± 3 pmoles/100 mg wet tissue. Both effects were antagonized by sulpiride. Bromocriptine did not affect uterine cGMP or the cyclic nucleotides in the aorta. It is concluded that the increase in aortic PGI2 was mediated via activation of dopamine D-2 receptors that stimulate phospholipase A2 enzyme. The decrease in myometrial PGI2 release may be related to the increase in uterine cAMP resulting from activation of dopamine D-1 receptors. Previous studies suggested a role for PGI2 in implantation in the rat. The results suggest that the inhibitory effèct on uterine PGI2 may underlie the reported inhibition of bromocriptine on implantation. On broad basis, the decrease in uterine PGI2 together with the reported luteolytic effect of bromocriptine point to a potential role for the compound in postcoital contraception. 相似文献
113.
114.
K N Iarygin A N Kazimirski? G I Kositski? A Iu Rubina V A Vinogradov 《Biulleten' eksperimental'no? biologii i meditsiny》1986,101(6):680-682
The authors studied the anabolic effect of peptide morphogen of the hydra undecapeptide on normal and regenerating rat liver. Ornithine decarboxylase (EC 4.1.1.17) activity served as a marker. Intraperitoneal injection of the peptide into intact animals stimulated ornithine decarboxylase activity in a dose-dependent manner. In partially hepatectomized rats the peptide stimulated ornithine decarboxylase activity in the dose of 20 micrograms/kg body weight while greater doses inhibited the enzyme activity. 相似文献
115.
We reported evidence that horseradish peroxidase (HRP) and chloroperoxidase (CPO) catalyze oxygen transfer from H2O2 to thioanisoles [Kobayashi, S., Nakano, M., Goto, T., Kimura, T., & Schaap, A. P. (1986) Biochem. Biophys. Res. Commun. 135, 166-171]. In the present paper, the reaction mechanism of this oxygen transfer is discussed. The oxidation of para-substituted thioanisoles by HRP compound II showed a large negative rho value of -1.46 vs. the sigma + parameter in a Hammett plot. These results are in accord with the formation of a cation radical intermediate in the rate-determining step. Hammett treatments for HRP- and CPO-dependent S-oxygenations did not provide unequivocal proofs to judge the reaction mechanism, because of the poor correlations for sigma + and sigma p parameters. Different behavior was found in kinetics and stereoselectivity between the two enzymes. Results in the present study and recent studies strongly suggested the formation of a cation radical intermediate. The oxygen atom would transfer by reaction of compound II and the cation radical intermediate. Although involvement of the cation radical was not confirmed in the CPO system, a similar mechanism was proposed for CPO. 相似文献
116.
Spatially resolved cytosolic calcium response to angiotensin II and potassium in rat glomerulosa cells measured by digital imaging techniques 总被引:7,自引:0,他引:7
The response of cytosolic calcium [Ca2+]i to angiotensin II (AII) and potassium (K+) in individual rat glomerulosa cells was determined using the calcium-sensitive fluorescent dye, fura-2 and digital imaging. Control (4 mM K+) cytosolic calcium levels were generally in the 80-120 nM range and increased monotonically as [K+] was increased from 4 to 12 mM. There was no delay in the onset of the response. In most cells the [Ca2+]i decreased from its peak after 3-4 min, even in the presence of superfusate containing elevated K+. The time course of the change in [Ca2+]i in response to AII stimulation, on the other hand, was more variable. It was most often characterized by an early decrease followed by a large delayed increase. The response also was observed to decline during sustained AII stimulation. The majority of the cells showed some response to one or the other secretagogue with a sizeable minority (25%) having an increase in [Ca2+]i in excess of 200%. While the majority showed a response, the cell to cell variation was substantial. Finally, the pattern of cytosolic calcium increase sometimes showed a marked dependence on the secretagogue used, with different regions of the same cell being more strongly affected by one agent or the other. A few cells (10%) responded to AII only at one pole, establishing a large concentration gradient of calcium across the cell. Because of differences in time course, pattern, and degree of responsiveness, it is likely that the mechanisms underlying the Ca2+ elevation with K+ and AII are different. 相似文献
117.
118.
E Imbasciati R Gusmano A Edefonti P Zucchelli C Pozzi C Grassi M Della Volpe F Perfumo P Petrone M Picca et al. 《BMJ (Clinical research ed.)》1985,291(6505):1305-1308
In a multicentre, randomised, prospective trial 89 patients (67 children and 22 adults) with the minimal change nephrotic syndrome were treated with three intravenous pulses of methylprednisolone followed by low dose oral prednisone for six months (group given methylprednisolone) or with high dose oral prednisone for four weeks followed by low dose oral prednisone for five months (control group). Five patients in the group given methylprednisolone and one in the control group did not respond initially. The time to response was shorter in children treated with methylprednisolone. No significant differences between the two groups were observed in the number of patients who relapsed or number of relapses per patient per year. Patients given methylprednisolone tended to relapse earlier than patients in the control group. Side effects related to treatment were significantly fewer in the group given methylprednisolone than in the control group. These data suggest that a short course of methylprednisolone pulses followed by low dose oral prednisone is only marginally less effective than a regimen of high dose oral steroids but can improve the ratio of risk to benefit associated with treatment of the minimal change nephrotic syndrome. 相似文献
119.
Monosomy 21: a new case confirmed by in situ hybridization 总被引:4,自引:0,他引:4
M. C. Pellissier N. Philip M. A. Voelckel-Baeteman M. G. Mattei J. F. Mattei 《Human genetics》1987,75(1):95-96
Summary A new case of total monosomy 21 in a newborn is described. The diagnosis was first made using the cytogenetic data; it was then confirmed by the dosage of copper-superoxide dismutase (SOD-1) which showed a 50% decrease. In situ hybridization with a probe previously assigned to chromosome 21 was used to rule out the possibility of a partial monosomy with an unbalanced reciprocal translocation. 相似文献
120.
W.J. Malaisse F. Malaisse-Lagae A. Sener 《Biochimica et Biophysica Acta (BBA)/General Subjects》1984,797(2):194-202
1. Because L-asparagine augments insulin release evoked by L-leucine, the metabolism of these two amino acids was investigated in rat pancreatic islets. 2. L-Leucine inhibited the uptake and deamidation of L-asparagine, but failed to exert any obvious primary effect upon the further catabolism of aspartate derived from exogenous asparagine. 3. L-Asparagine augmented the oxidation of L-leucine, and effect possibly attributable to activaion of 2-ketoisocaproate dehydrogenase. 4. The association of L-asparagine and L-leucine exerted a sparing action on the utilization of endogenous amino acids, so that the integrated rate of nutrients oxidation was virtually identical in the sole presence of L-leucine and simultaneous presence of L-asparagine and L-leucine, respectively. 5. It is proposed that the enhancing action of L-asparagine upon insulin release evoked by L-leucine is attributable to an increased generation rate of cytosolic NADPH rather than any increase in nutrients oxidation. 相似文献