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841.
842.
- Freshwater fishes are now facing unprecedented environmental changes across their northern ranges, especially due to rapid warming occurring at higher latitudes. However, empirical research that examines co-occurring environmental effects on northern fish communities remains limited.
- We used fish community data from 1587 Alaskan stream sites to examine the potential combined and interacting effects of climate change, current weather, habitat, land use, and fire on two community-level metrics (species richness, relative abundance), and on the distributions of three Alaskan fish species.
- Our models were 71–76% accurate in predicting the distribution of Alaskan stream fishes using a combination of climate and habitat variables. In contrast to other freshwater ecosystems that are most threatened by land use pressures, we did not detect any evidence for the potential stress of anthropogenic land use or fire on stream fishes.
- Warming temperatures increased overall community richness and abundance but produced differing responses at the species level. Juvenile salmon presence was positively associated with several climate variables including warmer spring and autumn temperatures and wetter summers. In comparison, warmer seasonal temperatures contributed to declines for northern-adapted species such as Arctic grayling and Dolly Varden.
- This study highlights the overarching role of current and changing climate in regulating northern stream fish biodiversity. Although many fish species may benefit from climate change across their northern ranges, localised declines are likely to occur and may prove detrimental for communities with limited fishing portfolios. Climate change adaptation and mitigation strategies customised for rapidly changing northern ecosystems will play an essential role in preserving ecologically unique northern species.
843.
Gerwyn Morris Basant K. Puri Ken Walder Michael Berk Michael Maes André F. Carvalho 《Molecular neurobiology》2018,55(12):8765-8787
The endoplasmic reticulum (ER) is the main cellular organelle involved in protein synthesis, assembly and secretion. Accumulating evidence shows that across several neurodegenerative and neuroprogressive diseases, ER stress ensues, which is accompanied by over-activation of the unfolded protein response (UPR). Although the UPR could initially serve adaptive purposes in conditions associated with higher cellular demands and after exposure to a range of pathophysiological insults, over time the UPR may become detrimental, thus contributing to neuroprogression. Herein, we propose that immune-inflammatory, neuro-oxidative, neuro-nitrosative, as well as mitochondrial pathways may reciprocally interact with aberrations in UPR pathways. Furthermore, ER stress may contribute to a deregulation in calcium homoeostasis. The common denominator of these pathways is a decrease in neuronal resilience, synaptic dysfunction and even cell death. This review also discusses how mechanisms related to ER stress could be explored as a source for novel therapeutic targets for neurodegenerative and neuroprogressive diseases. The design of randomised controlled trials testing compounds that target aberrant UPR-related pathways within the emerging framework of precision psychiatry is warranted. 相似文献
844.
Most bacteria are able to generate sufficient amounts of ATP from substrate level phosphorylation, thus rendering the respiratory oxidative phosphorylation non-critical. In mycobacteria, including Mycobacterium tuberculosis, ATP generation by oxidative phosphorylation is an essential process. Of the two types of NADH dehydrogenases (type I and type II), the type II NADH dehydrogenase (Ndh) which is inhibited by phenothiazines has been thought to be essential. In M. tuberculosis there are two Ndh isozymes (Ndh and NdhA) coded by ndh and ndhA genes respectively. Ndh and NdhA share a high degree of amino acid similarity. Both the enzymes have been shown to be enzymatically active and are inhibited by phenothiazines, suggesting a functional similarity between the two. We attempted gene knockout of ndh and ndhA genes in wild type and merodiploid backgrounds. It was found that ndh gene cannot be inactivated in a wild type background, though it was possible to do so when an additional copy of ndh was provided. This showed that in spite of its apparent functional equivalence, NdhA cannot complement the loss of Ndh in M. tuberculosis. We also showed that NdhA is not essential in M. tuberculosis as the ndhA gene could be deleted in a wild type strain of M. tuberculosis without causing any adverse effects in vitro. RT-PCR analysis of in vitro grown M. tuberculosis showed that ndhA gene is actively transcribed. This study suggests that despite being biochemically similar, Ndh and NdhA play different roles in the physiology of M. tuberculosis. 相似文献
845.
Tetraphenyl-p-xylene-glycol, tetraphenyl-phthalein and Dipheno(3-10′)thiazinyl are shown to form dipositive carbonium ions, but triphenyl acetic acid, 2-3-5-6 tetramethyl benzoic acid, 2-3-4-5-6 pentamethyl benzoic acid, tert-butyl alcohol, triphenyl carbinol, tri-p-tolyl carbinol, tri-o-tolyl carbinol, tri-p-chlorophenyl carbinol and tri-p-nitrophenyl carbinol form monopositive carbonium ions in chlorosulphuric acid, as revealed by conductometric and u.v. spectral studies. Oxalyl chloride decomposes while ethylene glycol is sulphonated in chlorosulphuric acid. Dichloroethane behaves as a non-electrolyte but dibromomethane disproportionates in this medium. 相似文献
846.
The thermodynamics of the binding of D-galactopyranoside (Gal), 2-acetamido-2-deoxygalactopyranoside (GalNAc), methyl-alpha-D-galactopyranoside, and methyl-beta-D-galactopyranoside to the basic agglutinin from winged bean (WBAI) in 0.02 M sodium phosphate and 0.15 M sodium chloride buffer have been investigated from 298.15 to 333.15 K by titration calorimetry and at the denaturation temperature by differential scanning calorimetry (DSC). WBAI is a dimer with two binding sites. The titration calorimetry yielded single-site binding constants ranging from 0.56 +/- 0.14 x 10(3) M-1 for Gal at 323.15 K to 7.2 +/- 0.5 x 10(3) M-1 for GalNAc at 298.15 K and binding enthalpies ranging from -28.0 +/- 2.0 kJ mol-1 for GalNAc at 298.15 K to -14.3 +/- 0.1 kJ mol-1 for methyl-beta-D-galactopyranoside at 322.65 K. The denaturation transition consisted of two overlapping peaks over the pH range 5.6-7.4. Fits of the differential scanning calorimetry data to a two-state transition model showed that the low temperature transition (341.6 +/- 0.4 K at pH 7.4) consisted of two domains unfolding as a single entity while the higher temperature transition (347.8 +/- 0.6 K at pH 7.4) is of the remaining WBAI dimer unfolding into two monomers. Both transitions shift to higher temperatures and higher calorimetric enthalpies with increase in added ligand concentration at pH 7.4. Analysis of the temperature increase as a function of added ligand concentration suggests that one ligand binds to the two domains unfolding at 341.6 +/- 0.6 K and one ligand binds to the domain unfolding at 347.8 +/- 0.6 K. 相似文献
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848.