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101.
Gross structural changes and neuropil formation in the brain during development were described in Idiosepius paradoxus, a sepioid that we chose as a model cephalopod. The brain originates in 4 pairs of ectodermal placodes, which occur separately in the embryonic surface undergoing epiboly. In the final period of epiboly, neuroblasts internalize from the placodes and gather into 4 pairs of ganglionic masses. The ganglionic masses assemble into a ring-like cluster encircling the inner yolk and the foregut anlage, gradually integrated into the 4 domains of a massive brain, a subesophageal mass (SBM), a supraesophageal mass (SPM), and a pair of optic lobes. In the early brain, neuropil forms a framework composed of a longitudinal ladder lying in the SBM, and a transverse arch standing on the lateral sides of the SBM and crossing the SPM. Differentiation of brain lobes proceeds from ventral to dorsal along this framework; first the magnocellular lobes and the posterior pedal lobe appear first in the SBM, the other lobes in the SBM and the basal lobes follow in the proximal region of the SPM, and the accessory lobes develop last in the most dorsal zone of the SPM. In the hatchlings, the brain lobes show almost the same arrangement as in the adults, but the accessory lobes, particularly the vertical lobe, are much smaller than those in the adults. Comparison of the present results with those in the teuthoid and the octopod indicates that developmental sequences of the brain are highly conserved in the coleoid cephalopods. 相似文献
102.
Isolation and characterization of a sulfur-oxidizing chemolithotroph growing on crude oil under anaerobic conditions 总被引:1,自引:0,他引:1
Molecular approaches have shown that a group of bacteria (called cluster 1 bacteria) affiliated with the epsilon subclass of the class Proteobacteria constituted major populations in underground crude-oil storage cavities. In order to unveil their physiology and ecological niche, this study isolated bacterial strains (exemplified by strain YK-1) affiliated with the cluster 1 bacteria from an oil storage cavity at Kuji in Iwate, Japan. 16S rRNA gene sequence analysis indicated that its closest relative was Thiomicrospira denitrificans (90% identity). Growth experiments under anaerobic conditions showed that strain YK-1 was a sulfur-oxidizing obligate chemolithotroph utilizing sulfide, elemental sulfur, thiosulfate, and hydrogen as electron donors and nitrate as an electron acceptor. Oxygen also supported its growth only under microaerobic conditions. Strain YK-1 could not grow on nitrite, and nitrite was the final product of nitrate reduction. Neither sugars, organic acids (including acetate), nor hydrocarbons could serve as carbon and energy sources. A typical stoichiometry of its energy metabolism followed an equation: S(2-) + 4NO(3)(-) --> SO(4)(2-) + 4NO(2)(-) (Delta G(0) = -534 kJ mol(-1)). In a difference from other anaerobic sulfur-oxidizing bacteria, this bacterium was sensitive to NaCl; growth in medium containing more than 1% NaCl was negligible. When YK-1 was grown anaerobically in a sulfur-depleted inorganic medium overlaid with crude oil, sulfate was produced, corresponding to its growth. On the contrary, YK-1 could not utilize crude oil as a carbon source. These results suggest that the cluster 1 bacteria yielded energy for growth in oil storage cavities by oxidizing petroleum sulfur compounds. Based on its physiology, ecological interactions with other members of the groundwater community are discussed. 相似文献
103.
Sagi K Fujita K Sugiki M Takahashi M Takehana S Tashiro K Kayahara T Yamanashi M Fukuda Y Oono S Okajima A Iwata S Shoji M Sakurai K 《Bioorganic & medicinal chemistry》2005,13(5):1487-1496
An inhibitor of the complex of factor VIIa and tissue factor (fVIIa/TF), 2-substituted-4-amidinophenylpyruvic acid 1a, was structurally modified with the aim of increasing its potency and selectivity. The lead compound 1a was originally found in our factor Xa (fXa) inhibitor library on the basis of structural similarity of the primary binding sites of fVIIa and fXa. The design was based on computational docking studies using the extracted active site of fVIIa. Compound 1j was found to inhibit factor VIIa/TF at nanomolar concentration with improved selectivity versus fXa and thrombin and it preferentially prolonged the clotting time in the TF-dependent extrinsic pathway. 相似文献
104.
Corson Gary E. Nagashima Kenji V. P. Matsuura Katsumi Sakuragi Yumiko Wettasinghe Ruwanthi Qin Hong Allen Randy Knaff David B. 《Photosynthesis research》1999,59(1):39-52
Sequencing of a 3.4 kb DNA fragment isolated from the photosynthetic purple sulfur bacterium Chromatium vinosum and of PCR products has resulted in identification of the Chr. vinosum pufL, pufM, and pufC genes, reading from the 5 to the 3 direction, and coding, respectively, for the L, M and cytochrome c subunits of the reaction center of this bacterium. Other PCR products have been used to obtain complete sequences for the pufB and pufA genes, located immediately upstream from pufL and encoding the apoproteins of two Chr. vinosum light- harvesting proteins. The 3-portion of the bchZ gene, a gene that codes for a protein involved in the biosynthesis of bacteriochlorophyll, has been located immediately upstream from pufB. A second pufB gene, pufB2, has been located downstream from pufC, as has the 5-portion of a second pufA gene, pufA2. The location of a second set of pufB and pufA genes, encoding light- harvesting proteins, downstream from pufC has not previously been reported for any photosynthetic bacterium. Translation of the gene sequences encoding these Chr. vinosum light-harvesting proteins reveals both similarities to and differences from the amino acid sequences, obtained from direct sequencing of the apoproteins, previously reported for Chr. vinosum light-harvesting proteins. Translation of these gene sequences, and of those for pufL, pufM and pufC, revealed significant homology, at the amino acid level, to the corresponding peptides of photosynthetic purple non-sulfur bacteria. 相似文献
105.
Tsubouchi K Igarashi Y Takasu Y Yamada H 《Bioscience, biotechnology, and biochemistry》2005,69(2):403-405
Human skin fibroblasts were cultured on sericin prepared from cocoon shells. The living cell number after 72 h was enhanced to 250% of the no-sericin control. The increase was due to the acceleration of the initial attachment of the cells. It was found that sericin M, the main component of about 400 kDa, and its serine-rich repetitive domain were the active principles. 相似文献
106.
Komoriya S Haginoya N Kobayashi S Nagata T Mochizuki A Suzuki M Yoshino T Horino H Nagahara T Suzuki M Isobe Y Furugoori T 《Bioorganic & medicinal chemistry》2005,13(12):3927-3954
Compound 7 was identified as the active metabolite of 6 by HPLC and mass spectral analysis. Modification of lead compound 7 by transformation of its N-oxide 6-6 biaryl ring system and fused aromatics produced a series of non-basic fXa inhibitors with excellent potency in anti-fXa and anticoagulant assays. The optimized compounds 73b and 75b showed sub to one digit micromolar anticoagulant activity (PTCT2). Particularly, anti-fXa activity was detected in plasma of rats orally administered with 1mg/kg of compound 75b. 相似文献
107.
Although the study of adaptation is central to biology, two types of adaptation are recognized in the biological field: physiological
adaptation (accommodation or acclimation; an individual organism’s phenotype is adjusted to its environment) and evolutionary–biological
adaptation (adaptation is shaped by natural selection acting on genetic variation). The history of the former concept dates
to the late nineteenth and early twentieth centuries, and has more recently been systemized in the twenty-first century. Approaches
to the understanding of phenotypic plasticity and learning behavior have only recently been developed, based on cellular–histological
and behavioral–neurobiological techniques as well as traditional molecular biology. New developments of the former concepts
in phenotypic plasticity are discussed in bacterial persistence, wing di-/polymorphism with transgenerational effects, polyphenism
in social insects, and defense traits for predator avoidance, including molecular biology analyses. We also discuss new studies
on the concept of genetic accommodation resulting in evolution of phenotypic plasticity through a transgenerational change
in the reaction norm based on a threshold model. Learning behavior can also be understood as physiological phenotypic plasticity,
associating with the brain–nervous system, and it drives the accelerated evolutionary change in behavioral response (the Baldwin
effect) with memory stock. Furthermore, choice behaviors are widely seen in decision-making of animal foragers. Incorporating
flexible phenotypic plasticity and learning behavior into modeling can drastically change dynamical behavior of the system.
Unification of biological sciences will be facilitated and integrated, such as behavioral ecology and behavioral neurobiology
in the area of learning, and evolutionary ecology and molecular developmental biology in the theme of phenotypic plasticity. 相似文献
108.
Xuesong Wang Rashmi Ray Sven Kratochvil Eleonora Melzi YingCing Lin Sophie Giguere Liling Xu John Warner Diane Cheon Alessia Liguori Bettina Groschel Nicole Phelps Yumiko Adachi Ryan Tingle Lin Wu Shane Crotty Kathrin H Kirsch Usha Nair William R Schief Facundo D Batista 《The EMBO journal》2021,40(2)
B‐cell receptor (BCR) knock‐in (KI) mouse models play an important role in vaccine development and fundamental immunological studies. However, the time required to generate them poses a bottleneck. Here we report a one‐step CRISPR/Cas9 KI methodology to combine the insertion of human germline immunoglobulin heavy and light chains at their endogenous loci in mice. We validate this technology with the rapid generation of three BCR KI lines expressing native human precursors, instead of computationally inferred germline sequences, to HIV broadly neutralizing antibodies. We demonstrate that B cells from these mice are fully functional: upon transfer to congenic, wild type mice at controlled frequencies, such B cells can be primed by eOD‐GT8 60mer, a germline‐targeting immunogen currently in clinical trials, recruited to germinal centers, secrete class‐switched antibodies, undergo somatic hypermutation, and differentiate into memory B cells. KI mice expressing functional human BCRs promise to accelerate the development of vaccines for HIV and other infectious diseases. 相似文献
109.
Post-translational regulation of CND41 protease activity in senescent tobacco leaves 总被引:2,自引:0,他引:2
The degradation of chloroplast proteins is an important occurrence in the mobilization of nutrients from senescing leaves
to reproductive organs during senescence. Recently, we proved that tobacco CND41 protease is involved in Rubisco degradation
and the translocation of nitrogen during senescence. In this study, we show the post-translational regulation of CND41 protease.
Using very specific antibodies that were prepared against CND41-specific peptide (anti-Val 186 to Ser 206), immunoblot analysis
clearly indicated a change in the accumulation and processing of CND41 during the maturation of leaves in whole plants. The
developmental modification of CND41 was also observed in transgenic tobacco with constitutive expression of CND41 under cauliflower
mosaic virus 35S promoter. Further studies of seedlings under senescence induced by combined treatment with nitrogen-starvation
and high sucrose confirmed that the processing of CND41 was important for protease activity and senescence. A possible mechanism
for the regulation of CND41 activity is discussed. 相似文献
110.
A clear parallelism was demonstrated between the efficiency as substrate of the substituted oligopeptides corresponding to the carboxy-terminal (C-terminal) sequence of the precursor D1 protein (pD1) in the in vitro enzymatic assay and their competitive inhibitory capacity toward the proteolytic C-terminal processing of the full-length pD1 integrated in the intact photosystem II complex embedded in the thylakoid membrane of Scenedesmus obliquus LF-1 mutant, as shown e.g. by the influence of L343A, A345G and A345V substitutions and the effect of C-terminal fragments. This suggests that the basic mechanism for substrate recognition by the processing protease elucidated in the enzymatic analysis using synthetic oligopeptides is also effective in vivo, although it can sometimes be difficult to detect the consequence of amino acid substitution in the integrated systems. 相似文献