全文获取类型
收费全文 | 22786篇 |
免费 | 1766篇 |
国内免费 | 1677篇 |
出版年
2024年 | 30篇 |
2023年 | 221篇 |
2022年 | 518篇 |
2021年 | 1068篇 |
2020年 | 706篇 |
2019年 | 886篇 |
2018年 | 801篇 |
2017年 | 626篇 |
2016年 | 942篇 |
2015年 | 1393篇 |
2014年 | 1606篇 |
2013年 | 1812篇 |
2012年 | 2105篇 |
2011年 | 1907篇 |
2010年 | 1153篇 |
2009年 | 1031篇 |
2008年 | 1276篇 |
2007年 | 1094篇 |
2006年 | 1019篇 |
2005年 | 813篇 |
2004年 | 653篇 |
2003年 | 625篇 |
2002年 | 490篇 |
2001年 | 432篇 |
2000年 | 367篇 |
1999年 | 365篇 |
1998年 | 242篇 |
1997年 | 199篇 |
1996年 | 225篇 |
1995年 | 194篇 |
1994年 | 159篇 |
1993年 | 126篇 |
1992年 | 188篇 |
1991年 | 157篇 |
1990年 | 107篇 |
1989年 | 135篇 |
1988年 | 73篇 |
1987年 | 67篇 |
1986年 | 71篇 |
1985年 | 78篇 |
1984年 | 27篇 |
1983年 | 35篇 |
1982年 | 31篇 |
1981年 | 13篇 |
1980年 | 26篇 |
1979年 | 20篇 |
1978年 | 16篇 |
1977年 | 19篇 |
1974年 | 9篇 |
1972年 | 13篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
131.
Role of protein kinase A and the serine-rich region of herpes simplex virus type 1 ICP4 in viral replication. 总被引:8,自引:6,他引:2
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)
Efficient expression of herpes simplex virus genes requires the synthesis of functional ICP4, a nuclear phosphoprotein that contains a prominent serine-rich region between amino acids 142 and 210. Residues in this region not only are potential sites for phosphorylation but also are involved in the functions of ICP4. By comparing the growth of a virus in which this region is deleted (d8-10) with wild-type virus (KOS) in PC12 cells or PC12 cells that are deficient in cyclic AMP-dependent protein kinase (PKA), two observations were made: (i) the growth of wild-type virus was impaired by 1 to 2 orders of magnitude in the PKA-deficient cells, indicating the involvement of PKA in the growth cycle of herpes simplex virus type 1, and (ii) while the growth of d8-10 was impaired by almost 2 orders of magnitude in wild-type cells, it was not further impaired (as was that of wild-type virus) in PKA-deficient cells, implicating the region deleted in d8-10 as a possible target for cellular PKA. In trigeminal'ganglia of mice, the d8-10 mutant virus grew poorly; however, it established latency in nearly 90% of ganglia tested. Studies of the phosphorylation of wild-type and d8-10 ICP4 proteins revealed that the serine-rich region is a major determinant for phosphorylation of ICP4 in vivo and that the phosphorylation state could change as a function of the PKA activity. Consistent with this observation, the serine-rich region of ICP4 was shown to be a target for PKA in vitro. While intact ICP4 was readily phosphorylated by ICP4 in vitro, the d8-10 mutant ICP4 was not. Moreover, a synthethic peptide representing a sequence in the serine tract that is predicted to be a substrate for PKA was phosphorylated by PKA in vitro, having a Km within the physiological range. These data suggest that PKA plays a role in viral growth through phosphorylation of one or more sites on the ICP4 molecule. 相似文献
132.
133.
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
134.
中国野豌豆属的分类研究 总被引:8,自引:0,他引:8
本文报道了国产野豌豆属43种,4变种及6变型,其中包括4个新种(多叶野豌豆,三尖野豌豆,武山野豌豆,长齿野豌豆);一个新变种(三叶歪头菜)及一个新等级(千山野豌豆)。 相似文献
135.
荧光假单胞菌抗噬菌体菌株的选育 总被引:6,自引:2,他引:4
本实验从荧光假单胞菌(Pseudomonasfluorescens)AS—3菌株的不正常发酵液中分离到一种噬菌体,将其命名为PFAS。AS—3菌株能利用葡萄糖发酵产生D-异维生素C的前体物质2-酮基-D-葡萄糖酸。电镜观察表明PFAS噬菌体呈蝌蚪形,具有直径为66nm的六角形头部及长117nm的尾部。通过紫外线诱变及自然选育两种途径,配合简便有效的初筛方法,经多次分离、纯化、复筛最终在摇并发酵试验中获得6株产量稳定地高于对照敏感菌的抗噬菌体菌株,可望用于生产。 相似文献
136.
Summary All cell-free filtrates of 26 fungal strains containning cellulase activities degraded native cellulose to both reducing sugar and insoluble short fibres. Low-molecular components from the crude filtrates could also degrade native cellulose into short fibres, not accompanied with the production of reducing sugar. Short fibre formation played an important role in cellulose degradation to make the substrate more accessible to attack of cellulases. 相似文献
137.
Stanislav D. Zakharov Xia Li Taya P. Red'ko Richard A. Dilley 《Journal of bioenergetics and biomembranes》1996,28(6):483-494
The 8-kDa subunit c of theE. coli F0 ATP-synthase proton channel was tested for Ca++ binding activity using a45Ca++ ligand blot assay after transferring the protein from SDS-PAGE gels onto polyvinyl difluoride membranes. The purified subunit c binds45Ca++ strongly with Ca++ binding properties very similar to those of the 8-kDa CF0 subunit III of choloroplast thylakoid membranes. The N-terminal f-Met carbonyl group seems necessary for Ca++ binding capacity, shown by loss of Ca++ binding following removal of the formyl group by mild acid treatment. The dicyclohexylcarbodiimide-reactive Asp-61 is not involved in the Ca++ binding, shown by Ca++ binding being retained in twoE. coli mutants, Asp61Asn and Asp61Gly. The Ca++ binding is pH dependent in both theE. coli and thylakoid 8-kDa proteins, being absent at pH 5.0 and rising to a maximum near pH 9.0. A treatment predicted to increase the Ca++ binding affinity to its F0 binding site (chlorpromazine photoaffinity attachment) caused an inhibition of ATP formation driven by a base-to-acid pH jump in whole cells. Inhibition was not observed when the Ca++ chelator EGTA was present with the cells during the chlorpromazine photoaffinity treatment. An apparent Ca++ binding constant on the site responsible for the UV plus chlorpromazine effect of near 80–100 nM was obtained using an EGTA-Ca++ buffer system to control free Ca++ concentration during the UV plus chlorpromazine treatment. The data are consistent with the notion that Ca++ bound to the periplasimic side of theE. coli F0 proton channel can block H+ entry into the channel. A similar effect occurs in thylakoid membranes, but the Ca++ binding site is on the lumen side of the thylakoid, where Ca++ binding can modulate acid-base jump ATP formation. The Ca++ binding to the F0 and CF0 complexes is consistent with a pH-dependent gating mechanism for control of H+ ion flux across the opening of the H+ channel.This work was supported in part by grants from the Department of Energy and the U.S. Department of Agriculture.On leave from the Institute of Soil Science and Photosynthesis, Russian Academy of Science, Pushchino, Russia. 相似文献
138.
Photoinactivation of Photosystem (PS) II in vivo was investigated by cumulative exposure of pea, rice and spinach leaves to light pulses of variable duration from 2 to 100 s, separated by dark intervals of 30 min. During each light pulse, photosynthetic induction occurred to an extent depending on the time of illumination, but steady-state photosynthesis had not been achieved. During photosynthetic induction, it is clearly demonstrated that reciprocity of irradiance and duration of illumination did not hold: hence the same cumulative photon exposure (mol m–2) does not necessarily give the same extent of photoinactivation of PS II. This contrasts with the situation of steady-state photosynthesis where the photoinactivation of PS II exhibited reciprocity of irradiance and duration of illumination (Park et al. (1995) Planta 196: 401–411). We suggest that, for reciprocity to hold between irradiance and duration of illumination, there must be a balance between photochemical (qP) and non-photochemical (NPQ) quenching at all irradiances. The index of susceptibility to light stress, which represents an intrinsic ability of PS II to balance photochemical and non-photochemical quenching, is defined by the quotient (1-qP)/NPQ. Although constant in steady-state photosynthesis under a wide range of irradiance (Park et al. (1995). Plant Cell Physiol 36: 1163–1169), this index of susceptibility for spinach leaves declined extremely rapidly during photosynthetic induction at a given irradiance, and, at a given cumulative photon exposure, was dependent on irradiance. During photosynthetic induction, only limited photoprotective strategies are developed: while the transthylakoid pH gradient conferred some degree of photoprotection, neither D1 protein turnover nor the xanthophyll cycle was operative. Thus, PS II is more easily photoinactivated during photosynthetic induction, a phenomenon that may have relevance for understorey leaves experiencing infrequent, short sunflecks.Abbreviations D1 protein
psbA gene product
- DTT
dithiothreitol
- Fv, Fm, Fo
variable, maximum, and initial (corresponding to open traps) chlorophyll fluorescence yield, respectively
- NPQ
non-photochemical quenching
- PS
Photosystem
- QA
primary quinone acceptor of PS II
- qP
photochemical quenching coefficient 相似文献
139.
48例原发性闭经患者的细胞遗传学分析 总被引:9,自引:1,他引:8
郑克勤 李永全 潘超仁 周汝滨 廖霞 陈小萍ZHENG Ke-Qin LI Yong-Quan PAN Chao-Ren ZHOU Ru-Bin LIAO Xia CHEN Xiao-Ping 《遗传》1996,18(1):33-35
本文报告对48例原发闭经患者的临床和细胞遣传学分析,共发现染色体异常17例,占35.4%,其中包括45,X,7例;45,X/46,XX,2例;X染色体结构异常5例;核型中有Y染色体3例。讨论了原发闭经的细胞遗传学病因及异常核型与表型的关系。 相似文献
140.