全文获取类型
收费全文 | 1614篇 |
免费 | 136篇 |
国内免费 | 455篇 |
出版年
2023年 | 16篇 |
2022年 | 20篇 |
2021年 | 30篇 |
2020年 | 70篇 |
2019年 | 90篇 |
2018年 | 105篇 |
2017年 | 49篇 |
2016年 | 50篇 |
2015年 | 94篇 |
2014年 | 156篇 |
2013年 | 169篇 |
2012年 | 108篇 |
2011年 | 89篇 |
2010年 | 105篇 |
2009年 | 107篇 |
2008年 | 106篇 |
2007年 | 108篇 |
2006年 | 65篇 |
2005年 | 62篇 |
2004年 | 32篇 |
2003年 | 31篇 |
2002年 | 28篇 |
2001年 | 38篇 |
2000年 | 20篇 |
1999年 | 15篇 |
1998年 | 22篇 |
1997年 | 14篇 |
1996年 | 22篇 |
1995年 | 10篇 |
1994年 | 10篇 |
1993年 | 9篇 |
1992年 | 6篇 |
1991年 | 10篇 |
1990年 | 5篇 |
1989年 | 12篇 |
1988年 | 8篇 |
1986年 | 7篇 |
1985年 | 36篇 |
1984年 | 41篇 |
1983年 | 20篇 |
1982年 | 52篇 |
1981年 | 21篇 |
1980年 | 21篇 |
1979年 | 27篇 |
1978年 | 20篇 |
1977年 | 9篇 |
1976年 | 15篇 |
1975年 | 11篇 |
1974年 | 16篇 |
1973年 | 5篇 |
排序方式: 共有2205条查询结果,搜索用时 31 毫秒
81.
82.
Ziguo Zhang Leifu ChangJing Yang Nora ConinKiran Kulkarni David Barford 《Journal of molecular biology》2013
The anaphase-promoting complex or cyclosome (APC/C) is a large E3 RING-cullin ubiquitin ligase composed of between 14 and 15 individual proteins. A striking feature of the APC/C is that only four proteins are involved in directly recognizing target proteins and catalyzing the assembly of a polyubiquitin chain. All other subunits, which account for > 80% of the mass of the APC/C, provide scaffolding functions. A major proportion of these scaffolding subunits are structurally related. In metazoans, there are four canonical tetratricopeptide repeat (TPR) proteins that form homo-dimers (Apc3/Cdc27, Apc6/Cdc16, Apc7 and Apc8/Cdc23). Here, we describe the crystal structure of the N-terminal homo-dimerization domain of Schizosaccharomyces pombe Cdc23 (Cdc23Nterm). Cdc23Nterm is composed of seven contiguous TPR motifs that self-associate through a related mechanism to those of Cdc16 and Cdc27. Using the Cdc23Nterm structure, we generated a model of full-length Cdc23. The resultant “V”-shaped molecule docks into the Cdc23-assigned density of the human APC/C structure determined using negative stain electron microscopy (EM). Based on sequence conservation, we propose that Apc7 forms a homo-dimeric structure equivalent to those of Cdc16, Cdc23 and Cdc27. The model is consistent with the Apc7-assigned density of the human APC/C EM structure. The four canonical homo-dimeric TPR proteins of human APC/C stack in parallel on one side of the complex. Remarkably, the uniform relative packing of neighboring TPR proteins generates a novel left-handed suprahelical TPR assembly. This finding has implications for understanding the assembly of other TPR-containing multimeric complexes. 相似文献
83.
84.
The interaction of (−)-reboxetine, a non-tricyclic norepinephrine selective reuptake inhibitor, with muscle-type nicotinic acetylcholine receptors (AChRs) in different conformational states was studied by functional and structural approaches. The results established that (−)-reboxetine: (a) inhibits (±)-epibatidine-induced Ca2+ influx in human (h) muscle embryonic (hα1β1γδ) and adult (hα1β1εδ) AChRs in a non-competitive manner and with potencies IC50 = 3.86 ± 0.49 and 1.92 ± 0.48 μM, respectively, (b) binds to the [3H]TCP site with ∼13-fold higher affinity when the Torpedo AChR is in the desensitized state compared to the resting state, (c) enhances [3H]cytisine binding to the resting but activatableTorpedo AChR but not to the desensitized AChR, suggesting desensitizing properties, (d) overlaps the PCP luminal site located between rings 6′ and 13′ in the Torpedo but not human muscle AChRs. In silico mutation results indicate that ring 9′ is the minimum structural component for (−)-reboxetine binding, and (e) interacts to non-luminal sites located within the transmembrane segments from the Torpedo AChR γ subunit, and at the α1/ε transmembrane interface from the adult muscle AChR. In conclusion, (−)-reboxetine non-competitively inhibits muscle AChRs by binding to the TCP luminal site and by inducing receptor desensitization (maybe by interacting with non-luminal sites), a mechanism that is shared by tricyclic antidepressants. 相似文献
85.
Background
Continuing efforts in development of non-invasive prenatal genetic tests have focused on the isolation of fetal nucleated red blood cells (NRBCs) from maternal blood for decades. Because no fetal cell-specific antibody has been described so far, the present study focused on the development of monoclonal antibodies (mAbs) to antigens that are expressed exclusively on fetal NRBCs.Methods: Mice were immunized with fetal erythroid cell membranes and hybridomas screened for Abs using a multi-parameter fluorescence-activated cell sorting (FACS). Selected mAbs were evaluated by comparative FACS analysis involving Abs known to bind erythroid cell surface markers (CD71, CD36, CD34), antigen-i, galactose, or glycophorin-A (GPA). Specificity was further confirmed by extensive immunohistological and immunocytological analyses of NRBCs from umbilical cord blood and fetal and adult cells from liver, bone marrow, peripheral blood, and lymphoid tissues.Results: Screening of 690 hybridomas yielded three clones of which Abs from 4B8 and 4B9 clones demonstrated the desired specificity for a novel antigenic structure expressed on fetal erythroblast cell membranes. The antigenic structure identified is different from known surface markers (CD36, CD71, GPA, antigen-i, and galactose), and is not present on circulating adult erythroid cells, except for occasional detectability in adult bone marrow cells.Conclusions:The new mAbs specifically bind the same or highly overlapping epitopes of a surface antigen that is almost exclusively expressed on fetal erythroid cells. The high specificity of the mAbs should facilitate development of simple methods for reliable isolation of fetal NRBCs and their use in non-invasive prenatal diagnosis of fetal genetic status. 相似文献86.
Filomena Sica Andrea Pica Antonello Merlino Irene Russo Krauss Carmine Ercole Delia Picone 《FEBS letters》2013
Bovine seminal ribonuclease (BS-RNase) acquires an interesting anti-tumor activity associated with the swapping on the N-terminal. The first direct experimental evidence on the formation of a C-terminal swapped dimer (C-dimer) obtained from the monomeric derivative of BS-RNase, although under non-native conditions, is here reported. The X-ray model of this dimer reveals a quaternary structure different from that of the C-dimer of RNase A, due to the presence of three mutations in the hinge peptide 111–116. The mutations increase the hinge peptide flexibility and decrease the stability of the C-dimer against dissociation. The biological implications of the structural data are also discussed. 相似文献
87.
Vasopressin activates Akt/mTOR pathway in smooth muscle cells cultured in high glucose concentration
Daniela K. Montes Marianne Brenet Vanessa C. Muñoz Patricia V. Burgos Carolina I. Villanueva Carlos D. Figueroa Carlos B. González 《Biochemical and biophysical research communications》2013
Mammalian target of rapamycin (mTOR) complex is a key regulator of autophagy, cell growth and proliferation. Here, we studied the effects of arginine vasopressin (AVP) on mTOR activation in vascular smooth muscle cells cultured in high glucose concentration. 相似文献
88.
Adult development and production of up to 400 eggs within the pupal case of female silkmoths are both dependent on 20-hydroxyecdysone (20E), the steroid hormone of insects. When adult development was initiated with tebufenozide, the non-steroidal ecdysteroid agonist, instead of 20E, full development of all epidermal tissues like the wing was witnessed, but ovarian growth and egg formation was minimal. Administration of tebufenozide to female pharate adults caused disruption of the follicular epithelium, produced nurse cell damage, and inhibited oogenesis. Reduced ability to synthesize RNA and protein accompanied these tebufenozide induced morphological disturbances of the follicles. In vivo accumulation of vitellogenin (Vg) from the hemolymph was reduced in tebufenozide treated female ovaries as well as their ability to accumulate Vg in vitro. Determination of protein staining intensity and antibody reactivity of Vg pointed out that hemolymph Vg level remained fairly constant all through adult development whether induced by 20E or tebufenozide. Measurement of hemolymph volumes and hemolymph Vg levels of control and experimental animals allowed us to conclude that egg development involves the uptake of all the hemolymph proteins and not Vg alone. The loss of hemolymph that accompanies egg maturation was considerably reduced in tebufenozide initiated female pharate adults. 20E could not overcome ovarian growth inhibitory effects of tebufenozide. Dual mechanisms, one involving ecdysteroid antagonist action at the beginning of development, and the other unrelated to that function during heightened egg formation, are needed explain the biphasic inhibitory actions of tebufenozide on silkmoth ovaries. 相似文献
89.
选取缙云山针阔混交林、常绿阔叶林、楠竹林和灌木林作为研究对象,对4种林分的凋落物储量和营养元素释放量等进行观测,并应用室内模拟酸雨实验对4种林分凋落物进行淋溶模拟。结果表明:缙云山各林分现存凋落物厚度为1.4~4.5 cm,具有明显的分层结构;林分未分解U层、半分解S层和分解D层现存凋落物量分别为1.97~8.59、2.84~10.18和3.58~17.43 t·hm-2,林分年凋落物量为2.17~9.86 t·hm-2·a-1,凋落物总储量为14.21~32.42 t·hm-2,凋落物分解常数为0.15~0.31,林下凋落物分解95%时所需时间针阔混交林和楠竹林均在10年以上,凋落物分解速率比较缓慢;林下凋落物层营养元素含量以Ca、N为主,Fe、K、Mg次之;凋落物总的营养元素释放率表现为常绿阔叶林(0.80)>灌木林(0.72)>针阔混交林(0.50)>楠竹林(-0.17);与叶片相比,凋落物中N、K、Mn 3种营养元素含量明显降低;为探明酸雨影响营养元素循环的作用机理,对模拟酸雨的离子含量与凋落物淋滤液盐基离子含量进行了分析,其相关性大小表现为楠竹林(相关系数0.895)>针阔混交林(0.826)>灌木(0.700)>常绿阔叶林(0.699),楠竹林凋落物营养元素的淋滤受酸雨影响最大,常绿阔叶林受其影响最弱;推测在这一过程中以凋落物的吸附作用为主。 相似文献
90.
为评价水域环境中铬元素对两栖动物幼体的急性毒性,将中国林蛙(Rana chensinensis)28~29期蝌蚪分别暴露于30~35 mg·L-1Cr(Ⅲ)6个不同浓度和10 ~ 45mg·L-1Cr(Ⅵ)6个不同浓度的水体中,分别在24、48、72和96 h统计蝌蚪的死亡率及半致死浓度(LC50).结果表明:暴露24、48、72和96 h,Cr(Ⅲ)对蝌蚪的LC50分别为34.09±1.06、33.47±0.65、32.58±0.11和(32.05±0.20) mg·L-1,安全浓度(SC)为(3.21±0.02)mg·L-1;Cr(Ⅵ)对蝌蚪的LC50分别为91.97±5.32、51.19±4.62、35.79±1.40和(28.81±1.87) mg·L-1,安全浓度(SC)为(2.88±0.19) rng·L-1.观察表明:Cr(Ⅲ)的急性毒性是通过与蝌蚪皮肤表面的分泌物结合后粘附在鳃部,导致呼吸障碍致死;而Cr(Ⅵ)的强氧化性可导致蝌蚪的表皮溃变,鳃部萎缩致死;另外,将28~29期蝌蚪暴露于安全浓度(SC)以下的含铬水体进行慢性实验,通过检测蝌蚪的体长、体重和完全变态时间显示,低浓度的Cr(Ⅲ)和Cr(Ⅵ)对蝌蚪的生长发育仍具有一定的抑制作用,并可导致畸型发生,其作用强度呈现剂量效应,但时间累积效应不规律. 相似文献