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1.
E. Golomer P. Dupui H. Monod 《European journal of applied physiology and occupational physiology》1997,76(2):140-144
We investigated the effects of maturation on the dynamic body sways of healthy girls. Prepubertal and postpubertal girls
practising professional physical activities requiring a good ability to maintain equilibrium (acrobats and dancers) were asked
to stand on a free seesaw platform and the results compared to those for untrained age-matched girls. This platform (stabilometer)
allows self-induced body sways. Stabilograms were obtained by a double integration of the angular acceleration from the recordings
of the platform sways made with an accelerometer. Fast Fourier transform processing of stabilograms allowed spectral frequency
analysis. The total spectrum energy and the energies of three frequency bands (0–0.5 Hz, 0.5–2 Hz, 2–20 Hz) were determined.
ANOVA showed that, for all groups of different equilibrium activity and independent of visual input, prepubertal girls had
higher energy values than postpubertal girls in the 0- to 0.5-Hz band whereas the opposite was true for 0.5- to 2-Hz band.
Ballet dancers were more dependent than acrobats on visual inputs for the regulation of their postural control but were less
dependent than untrained girls at both ages. Maturation seemed to shift body sways towards higher frequencies and the utilization
of the cues of postural control was different according to the type of equilibrium activity practised by the subjects.
Accepted: 7 February 1997 相似文献
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3.
《Bioorganic & medicinal chemistry letters》2020,30(13):127208
Proinsulin C-peptide has previously been proposed to interact with a G-protein coupled receptor (GPCR), specifically the orphan receptor GPR146. To investigate the potential of C-peptide in treating complications of diabetes, such as kidney damage, it is necessary to understand its mode of action. We used CHO-K1 cells expressing human GPR146 to study human and murine C-peptide in dynamic mass redistribution and GPCR β-arrestin assays, as well as with fluorescence confocal microscopy. Neither assay revealed any significant intracellular response to C-peptide at concentrations of up to 33 µM. We observed no internalisation of C-peptide by fluorescence microscopy. Our results do not support GPR146 as the receptor for C-peptide, but suggest that further investigations of the mode of action of C-peptide should be undertaken. 相似文献
4.
Natalya Y. ERMAKOV Jacob S. ISHAY 《动物学报》2005,51(6):1146-1150
将东方大黄蜂(胡蜂)蛹或幼蜂的棕色表皮层连同含有黑色素的皮细胞层、黄色表皮层及相连的产生黄嘌呤的皮细胞层割下,换化后植入原来的黄蜂体上(原来是黄色的部分用棕色替代,棕色的用黄色替代)。然后将蛹放回原来的子脾中,幼蜂放入一特殊的培养皿中,让其复原和发育。共对200个不同时期的蛹和50只幼蜂进行了试验。结果显示,存活的最主要是将羽化的蛹(差1—2天就羽化的蛹),早期的蛹和幼蜂均死亡。总共有约5%的蛹存活,幼蛹无一存活。在存活的蛹中,棕色表皮植入黄色区域中的不但成活了,而且还保留了棕色色彩。相反,黄色表皮在植入到棕色区域的几天后,就丢失了黄色及膜片。经过表皮异源移植的大黄蜂寿命极短,一般仅几星期。羽化后较敏感,攻击性强,但行走、飞行都很正常[动物学报51(6):1146—1150,2005]。 相似文献
5.
Margarita Eisenberg Inbal Shumacher Rivka Cohen-Luria Gonen Ashkenasy 《Bioorganic & medicinal chemistry》2013,21(12):3450-3457
Repeat proteins are found in almost all cellular systems, where they are involved in diverse molecular recognition processes. Recent studies have suggested that de novo designed repeat proteins may serve as universal binders, and might potentially be used as practical alternative to antibodies. We describe here a novel chemical methodology for producing small libraries of repeat proteins, and screening in parallel the ligand binding of library members. The first stage of this research involved the total synthesis of a consensus-based three-repeat tetratricopeptide (TPR) protein (~14 kDa), via sequential attachment of the respective peptides. Despite the effectiveness of the synthesis and ligation steps, this method was found to be too demanding for the production of proteins containing variable number of repeats. Additionally, the analysis of binding of the individual proteins was time consuming. Therefore, we designed and prepared novel dynamic combinatorial libraries (DCLs), and show that their equilibration can facilitate the formation of TPR proteins containing up to eight repeating units. Interestingly, equilibration of the library building blocks in the presence of the biologically relevant ligands, Hsp90 and Hsp70, induced their oligomerization into forming more of the proteins with large recognition surfaces. We suggest that this work presents a novel simple and rapid tool for the simultaneous screening of protein mixtures with variable binding surfaces, and for identifying new binders for ligands of interest. 相似文献
6.
《Bioorganic & medicinal chemistry》2020,28(9):115436
A polymer based dynamic combinatorial library (DCL) was generated through condensation between aldehyde functionalized linear poly(glycidol) (APG) and galactose containing acylhydrazide derivatives. Pentameric E. coli heat labile enterotoxin B subunit (LTB) was subsequently applied to the DCL as external stimulus, resulting in amplification of a specific acylhydrazone side chain that was further used for the synthesis of a multivalent LTB inhibitor. In the in vitro biological evaluation, this inhibitor exhibited strong inhibition properties as well as low cytotoxicity. 相似文献
7.
Sanjoy K. Bhattacharya 《Systems and synthetic biology》2010,4(2):139-144
Protein–protein interaction networks are currently visualized by software generated interaction webs based upon static experimental
data. Current state is limited to static, mostly non-compartmental network and non time resolved protein interactions. A satisfactory
mathematical foundation for particle interactions within a viscous liquid state (situation within the cytoplasm) does not
exist nor do current computer programs enable building dynamic interaction networks for time resolved interactions. Building
mathematical foundation for intracellular protein interactions can be achieved in two increments (a) trigger and capture the
dynamic molecular changes for a select subset of proteins using several model systems and high throughput time resolved proteomics
and, (b) use this information to build the mathematical foundation and computational algorithm for a compartmentalized and
dynamic protein interaction network. Such a foundation is expected to provide benefit in at least two spheres: (a) understanding
physiology enabling explanation of phenomenon such as incomplete penetrance in genetic disorders and (b) enabling several
fold increase in biopharmaceutical production using impure starting materials. 相似文献
8.
Background and aimAβ1−42 is an amyloidogenic peptide found within senile plaques extracted from those who died with a diagnosis of Alzheimer’s disease. The potent neurotoxicity of this peptide is related to its propensity to form aggregated conformations in vivo, a process that is influenced by the species and concentration of metal ions present within the local environment. This study examines the impact of different metals upon the early aggregatory behaviour and size of Aβ1−42 under simulated physiological conditions.MethodsThe size and aggregatory behaviour of Aβ1−42 in the presence and absence of metal ions was monitored during the initial 30 min of fibril formation in real-time using dynamic light scattering.ResultsIntensity scattering measurements showed a clear tendency towards aggregation with regards to Aβ1−42 only solutions (10 μM). Both equimolar Al3+ & Cu2+ lowered and stabilised the dimensions of Aβ1−42 aggregates; however, a diminutive but significant increase in size was still observed over a 30-min period. While excess Al3+ continued to supress the size of Aβ1−42, a 10-fold increase in the concentration of Cu2+ accelerated peptide aggregation relative to that observed for equimolar metal but not compared to Aβ1−42 alone.ConclusionThese results infer that Al3+ ions stabilise and aid in the maintenance of smaller, toxic intermediates while excess Cu2+ facilitates the formation of larger, more inert, amorphous species exceeding 1 μm in size. Furthermore, we propose that metal-induced toxicity of Aβ1−42 is reflective of their ability to preserve smaller oligomeric species in vitro. 相似文献
9.
We model the vague-to-crisp dynamics of forming percepts in the brain by combining two methodologies: dynamic logic (DL) and operant learning process. Forming percepts upon the presentation of visual inputs is likened to model selection based on sampled evidence. Our framework utilizes the DL in selecting the correct “percept” among competing ones, but uses an intrinsic reward mechanism to allow stochastic online update in lieu of performing the optimization step of the DL framework. We discuss the connection of our framework with cognitive processing and the intentional neurodynamic cycle. 相似文献
10.
《Saudi Journal of Biological Sciences》2022,29(1):526-533
The continuous and rapid development of the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) virus remains a health concern especially with the emergence of numerous variants and mutations worldwide. As with other RNA viruses, SARS-CoV-2 has a genetically high mutation rate. These mutations have an impact on the virus characteristics, including transmissibility, antigenicity and development of drug and vaccine resistance. This work was pursued to identify the differences that exist in the papain-like protease (PLPro) from 58 Saudi isolates in comparison to the first reported sequence from Wuhan, China and determine their implications on protein structure and the inhibitor binding. PLpro is a key protease enzyme for the host cells invasion and viral proteolytic cleavage, hence, it emerges as a valuable antiviral therapeutic target. Two mutations were identified including D108G and A249V and shown to increase the molecular flexibility of PLPro protein and alter the protein stability, particularly with D108G mutation. The effect of these mutations on the stability and dynamic behavior of PLPro structures as well as their effect on the binding of a known inhibitor; GRL0617 were further investigated by molecular docking and dynamic simulation. 相似文献