全文获取类型
收费全文 | 18400篇 |
免费 | 1395篇 |
国内免费 | 1篇 |
专业分类
19796篇 |
出版年
2021年 | 138篇 |
2020年 | 122篇 |
2019年 | 125篇 |
2018年 | 282篇 |
2017年 | 247篇 |
2016年 | 437篇 |
2015年 | 760篇 |
2014年 | 705篇 |
2013年 | 1042篇 |
2012年 | 1248篇 |
2011年 | 1230篇 |
2010年 | 737篇 |
2009年 | 606篇 |
2008年 | 1100篇 |
2007年 | 1087篇 |
2006年 | 1054篇 |
2005年 | 993篇 |
2004年 | 941篇 |
2003年 | 860篇 |
2002年 | 812篇 |
2001年 | 412篇 |
2000年 | 415篇 |
1999年 | 372篇 |
1998年 | 183篇 |
1997年 | 165篇 |
1996年 | 138篇 |
1995年 | 157篇 |
1994年 | 137篇 |
1993年 | 104篇 |
1992年 | 229篇 |
1991年 | 232篇 |
1990年 | 210篇 |
1989年 | 164篇 |
1988年 | 175篇 |
1987年 | 146篇 |
1986年 | 143篇 |
1985年 | 126篇 |
1984年 | 114篇 |
1983年 | 97篇 |
1982年 | 94篇 |
1981年 | 118篇 |
1980年 | 74篇 |
1979年 | 111篇 |
1978年 | 103篇 |
1977年 | 82篇 |
1976年 | 96篇 |
1975年 | 80篇 |
1974年 | 90篇 |
1973年 | 79篇 |
1971年 | 81篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
111.
112.
113.
Dhruv Khatri Thibault Brugire Chaitanya A. Athale Marie Delattre 《Molecular biology of the cell》2022,33(6)
Cellular functions such as cell division are remarkably conserved across phyla. However, the evolutionary principles of cellular organization that drive them are less well explored. Thus, an essential question remains: to what extent do cellular parameters evolve without altering the basic functions they sustain? Here we have observed six different nematode species for which the mitotic spindle is positioned asymmetrically during the first embryonic division. Whereas the C. elegans spindle undergoes oscillations during its displacement, the spindle elongates without oscillations in other species. We asked which evolutionary changes in biophysical parameters could explain differences in spindle motion while maintaining a constant output. Using laser microsurgery of the spindle, we revealed that all species are subjected to cortical pulling forces of varying magnitudes. Using a viscoelastic model to fit the recoil trajectories and with an independent measurement of cytoplasmic viscosity, we extracted the values of cytoplasmic drag, cortical pulling forces, and spindle elasticity for all species. We found large variations in cytoplasmic viscosity, whereas cortical pulling forces and elasticity were often more constrained. In agreement with previous simulations, we found that increased viscosity correlates with decreased oscillation speeds across species. However, the absence of oscillations in some species despite low viscosity can only be explained by smaller pulling forces. Consequently, we find that spindle mobility across the species analyzed here is characterized by a tradeoff between cytoplasmic viscosity and pulling forces normalized by the size of the embryo. Our work provides a framework for understanding mechanical constraints on evolutionary diversification of spindle mobility. 相似文献
114.
J. Poulton M. Hirano A. Spinazzola M. Arenas Hernandez C. Jardel A. Lombès B. Czermin R. Horvath J.W. Taanman A. Rotig M. Zeviani C. Fratter 《生物化学与生物物理学报:疾病的分子基础》2009,1792(12):1109-1112
These tables list both published and a number of unpublished mutations in genes associated with early onset defects in mitochondrial DNA (mtDNA) maintenance including C10orf2, SUCLG1, SUCLA2, TYMP, RRM2B, MPV17, DGUOK and TK2. The list should not be taken as evidence that any particular mutation is pathogenic. We have included genes known to cause mtDNA depletion, excluding POLG1, because of the existing database (http://tools.niehs.nih.gov/polg/). We have also excluded mutations in C10orf2 associated with dominant adult onset disorders. 相似文献
115.
Dodier Y Banderali U Klein H Topalak O Dafi O Simoes M Bernatchez G Sauvé R Parent L 《The Journal of biological chemistry》2004,279(8):6853-6862
The substituted cysteine accessibility method (SCAM) was used to map the external vestibule and the pore region of the ECaC-TRPV5 calcium-selective channel. Cysteine residues were introduced at 44 positions from the end of S5 (Glu515) to the beginning of S6 (Ala560). Covalent modification by positively charged MTSET applied from the external medium significantly inhibited whole cell currents at 15/44 positions. Strongest inhibition was observed in the S5-linker to pore region (L520C, G521C, and E522C) with either MTSET or MTSES suggesting that these residues were accessible from the external medium. In contrast, the pattern of covalent modification by MTSET for residues between Pro527 and Ile541 was compatible with the presence of a alpha-helix. The absence of modification by the negatively charged MTSES in that region suggests that the pore region has been optimized to favor the entrance of positively charged ions. Cysteine mutants at positions -1, 0, +1, +2 around Asp542 (high Ca2+ affinity site) were non-functional. Whole cell currents of cysteine mutants at +4 and +5 positions were however covalently inhibited by external MTSET and MTSES. Altogether, the pattern of covalent modification by MTS reagents globally supports a KcsA homology-based three-dimensional model whereby the external vestibule in ECaC-TRPV5 encompasses three structural domains consisting of a coiled structure (Glu515 to Tyr526) connected to a small helical segment of 15 amino acids (527PTALFSTFELFLT539) followed by two distinct coiled structures Ile540-Pro544 (selectivity filter) and Ala545-Ile557 before the beginning of S6. 相似文献
116.
Anion channels and transporters in plant cell membranes 总被引:2,自引:0,他引:2
de Angeli A Thomine S Frachisse JM Ephritikhine G Gambale F Barbier-Brygoo H 《FEBS letters》2007,581(12):2367-2374
117.
118.
Hélène Cheap Sophie Bernad Valérie Derrien László Gerencsér Julia Tandori Pedro de Oliveira Deborah K. Hanson Péter Maróti Pierre Sebban 《BBA》2009,1787(12):1505-1515
Bacterial reaction centers use light energy to couple the uptake of protons to the successive semi-reduction of two quinones, namely QA and QB. These molecules are situated symmetrically in regard to a non-heme iron atom. Four histidines and one glutamic acid, M234Glu, constitute the five ligands of this atom. By flash-induced absorption spectroscopy and delayed fluorescence we have studied in the M234EH and M234EL variants the role played by this acidic residue on the energetic balance between the two quinones as well as in proton uptake. Delayed fluorescence from the P+QA? state (P is the primary electron donor) and temperature dependence of the rate of P+QA? charge recombination that are in good agreement show that in the two RC variants, both QA? and QB? are destabilized by about the same free energy amount: respectively ~ 100 ± 5 meV and 90 ± 5 meV for the M234EH and M234EL variants, as compared to the WT. Importantly, in the M234EH and M234EL variants we observe a collapse of the high pH band (present in the wild-type reaction center) of the proton uptake amplitudes associated with formation of QA? and QB?. This band has recently been shown to be a signature of a collective behaviour of an extended, multi-entry, proton uptake network. M234Glu seems to play a central role in the proton sponge-like system formed by the RC protein. 相似文献
119.
Development of a 16S rRNA gene-based prototype microarray for the detection of selected actinomycetes genera 总被引:1,自引:0,他引:1
Kyselková M Kopecký J Felföldi T Cermák L Omelka M Grundmann GL Moënne-Loccoz Y Ságová-Marecková M 《Antonie van Leeuwenhoek》2008,94(3):439-453
Actinomycetes are known for their secondary metabolites, which have been successfully used as drugs in human and veterinary medicines. However, information on the distribution of this group of Gram-positive bacteria in diverse ecosystems and a comprehension of their activities in ecosystem processes are still scarce. We have developed a 16S rRNA-based taxonomic microarray that targets key actinomycetes at the genus level. In total, 113 actinomycete 16S rRNA probes, corresponding to 55 of the 202 described genera, were designed. The microarray accuracy was evaluated by comparing signal intensities with probe/target-weighted mismatch values and the Gibbs energy of the probe/target duplex formation by hybridizing 17 non-actinomycete and 29 actinomycete strains/clones with the probe set. The validation proved that the probe set was specific, with only 1.3% of false results. The incomplete coverage of actinomycetes by a genus-specific probe was caused by the limited number of 16S rRNA gene sequences in databases or insufficient 16S rRNA gene polymorphism. The microarray enabled discrimination between actinomycete communities from three forest soil samples collected at one site. Cloning and sequencing of 16S rRNA genes from one of the soil samples confirmed the microarray results. We propose that this newly constructed microarray will be a valuable tool for genus-level comparisons of actinomycete communities in various ecological conditions. 相似文献
120.
Functional domains of the human glucocorticoid receptor 总被引:96,自引:0,他引:96