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The polypeptide relaxin (RLX) has been suggested to play a role in cardiorenal integration and to be related to the natriuretic peptide system. We hence examined the effects of variations in thoracic blood volume and intravenous volume loading on plasma and urinary RLX levels and associated changes in natriuretic peptide levels in healthy men. Two groups of eight subjects were randomly tilted into a 15 degrees feet-down or a 15 degrees head-down position. Ten volunteers were crossover subjected to an infusion of 15 ml/kg of 0.9% NaCl (over 60 min) or control during an observation period of 10 h. Blood and urine were sampled at timed intervals. RLX, NH(2)-terminal prohormones of atrial natriuretic peptide (NT-pro-ANP), and NH(2)-terminal prohormones of brain natriuretic peptide (NT-pro-BNP) were determined by enzyme, radio-, and electrochemoluminescence immunoassays, respectively. NT-pro-ANP levels (in percentage of baseline levels) were higher (P < 0.05) during the head-down (124 +/- 13%) than during the feet-down position (82 +/- 6%). NT-pro-BNP and RLX were not affected by tilting. Volume loading induced a short-lasting increase in plasma NT-pro-ANP, a delayed increase in plasma NT-pro-BNP, had no effect on plasma RLX, and induced a parallel increase in urine flow, renal excretion of sodium, RLX, and NT-pro-BNP. It is concluded that variations in thoracic blood volume in healthy men are not associated with variations in plasma RLX. Increased urinary RLX and NT-pro-BNP excretion during volume loading suggest renal production and a possible role of kidney-derived RLX and brain natriuretic peptide in sodium homeostasis in men.  相似文献   
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We consider a terminal operator who provides container handling services at multiple terminals within the same port. In this setting, the well-known berth allocation problem can no longer be considered for each terminal in isolation since vessel calls should be spread over the various terminals to avoid peaks and troughs in quay crane utilization, and an allocation of two connecting vessels to different terminals will generate inter-terminal container transport. In this paper, we address the problem of spreading a set of cyclically calling vessels over the various terminals and allocating a berthing and departure time to each of them. The objectives are (1) to balance the quay crane workload over the terminals and over time and (2) to minimize the amount of inter-terminal container transport. We develop a solution approach based on mixed-integer programming that allows to solve real-life instances of the problem within satisfactory time. Additionally, a practical case study is presented based on data from the terminal operator PSA Antwerp who operates multiple terminals in the port of Antwerp, Belgium. The computational results show the cost of the currently agreed schedules, and that relatively small modifications can significantly reduce the required crane capacities and inter-terminal transport.  相似文献   
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Premise of the study: The European Alps harbor a spatially heterogeneous environment. Plants can be adapted genetically to this heterogeneity but may also respond to it by phenotypic plasticity. We expected the important fodder grass Poa alpina to be adapted to elevation either genetically or plastically. • Methods: We investigated in three elevational common gardens whether growth and reproductive allocation of plants reproducing either by seeds or bulbils suggest adaptation to their elevation of origin and to what extent they can respond plastically to different elevations. Additionally, we analyzed genetic diversity using microsatellites and tested whether seeds are of sexual origin. • Key results: In the field, bulbil-producing plants occurred more often at higher elevations, whereas seed-producing plants occurred more often at lower elevations, but bulbil-producing plants were generally less vigorous in the common gardens. The response of plants to elevational transplantation was highly plastic, and vigor was always best at the highest location. The small genetic differences were not clinally related to elevation of origin, underlining the importance of phenotypic plasticity. Reproductive allocation was, however, independent of elevational treatments. Seed-producing plants had higher genetic diversity than the bulbil-producing plants even though we found that seed-producing plants were facultative apomicts mostly reproducing asexually. • Conclusions: Bulbil-producing P. alpina, showing a fitness cost at lower elevations compared with seed-producing plants, seem better adapted to higher elevations. By means of its two reproductive modes and the capacity to adjust plastically, P. alpina is able to occupy a broad ecological niche across a large elevational range.  相似文献   
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A high-throughput genetic screening platform in a single-celled photosynthetic eukaryote would be a transformative addition to the plant biology toolbox. Here, we present ChlaMmeSeq (Chlamydomonas MmeI-based insertion site Sequencing), a tool for simultaneous mapping of tens of thousands of mutagenic insertion sites in the eukaryotic unicellular green alga Chlamydomonas reinhardtii. We first validated ChlaMmeSeq by in-depth characterization of individual insertion sites. We then applied ChlaMmeSeq to a mutant pool and mapped 11,478 insertions, covering 39% of annotated protein coding genes. We observe that insertions are distributed in a manner largely indistinguishable from random, indicating that mutants in nearly all genes can be obtained efficiently. The data reveal that sequence-specific endonucleolytic activities cleave the transforming DNA and allow us to propose a simple model to explain the origin of the poorly understood exogenous sequences that sometimes surround insertion sites. ChlaMmeSeq is quantitatively reproducible, enabling its use for pooled enrichment screens and for the generation of indexed mutant libraries. Additionally, ChlaMmeSeq allows genotyping of hits from Chlamydomonas screens on an unprecedented scale, opening the door to comprehensive identification of genes with roles in photosynthesis, algal lipid metabolism, the algal carbon-concentrating mechanism, phototaxis, the biogenesis and function of cilia, and other processes for which C. reinhardtii is a leading model system.  相似文献   
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During photosynthesis, electrons travel from light-excited chlorophyll molecules along the electron transport chain to the final electron acceptor nicotinamide adenine dinucleotide phosphate (NADP) to form NADPH, which fuels the Calvin–Benson–Bassham cycle (CBBC). To allow photosynthetic reactions to occur flawlessly, a constant resupply of the acceptor NADP is mandatory. Several known stromal mechanisms aid in balancing the redox poise, but none of them utilizes the structurally highly similar coenzyme NAD(H). Using Arabidopsis (Arabidopsis thaliana) as a C3-model, we describe a pathway that employs the stromal enzyme PHOSPHOGLYCERATE DEHYDROGENASE 3 (PGDH3). We showed that PGDH3 exerts high NAD(H)-specificity and is active in photosynthesizing chloroplasts. PGDH3 withdrew its substrate 3-PGA directly from the CBBC. As a result, electrons become diverted from NADPH via the CBBC into the separate NADH redox pool. pgdh3 loss-of-function mutants revealed an overreduced NADP(H) redox pool but a more oxidized plastid NAD(H) pool compared to wild-type plants. As a result, photosystem I acceptor side limitation increased in pgdh3. Furthermore, pgdh3 plants displayed delayed CBBC activation, changes in nonphotochemical quenching, and altered proton motive force partitioning. Our fluctuating light-stress phenotyping data showed progressing photosystem II damage in pgdh3 mutants, emphasizing the significance of PGDH3 for plant performance under natural light environments. In summary, this study reveals an NAD(H)-specific mechanism in the stroma that aids in balancing the chloroplast redox poise. Consequently, the stromal NAD(H) pool may provide a promising target to manipulate plant photosynthesis.

PHOSPHOGLYCERATE DEHYDROGENASE 3, an oxidoreductase in leaf chloroplasts with strong preference to reduce the stromal NAD(H) instead of the NADP(H) pool, is required for full photosynthetic capacity.  相似文献   
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