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1.
We grew 2.4 m2 wheat canopies in a large growth chamber under high photosynthetic photon flux (1000 μmol m−2 s−1) and using two CO2 concentrations, 360 and 1200 μmol mol−1. Photosynthetically active radiation (400–700 nm) was attenuated slightly faster through canopies grown in 360μmol mol−1 than through canopies grown in 1200μmol mol−1, even though high-CO2 canopies attained larger leaf area indices. Tissue fractions were sampled from each 5-cm layer of the canopies. Leaf tissue sampled from the tops of canopies grown in 1200μmol mol−1 accumulated significantly more total non-structural carbohydrate, starch, fructan, sucrose, and glucose (p≤ 0.05) than for canopies grown in 360μmol mol−1. Non-structural carbohydrate did not significantly increase in the lower canopy layers of the elevated CO2 treatment. Elevated CO2 induced fructan synthesis in all leaf tissue fractions, but fructan formation was greatest in the uppermost leaf area. A moderate temperature reduction of 10 °C over 5d increased starch, fructan and glucose levels in canopies grown in 1200μmol mol−1, but concentrations of sucrose and fructose decreased slightly or remained unchanged. Those results may correspond with the use of fructosyl-residues and release of glucose when sucrose is consumed in fructan synthesis.  相似文献   
2.
特定化合物同位素分析(CSIA)可以实现对复杂基质中特定化合物稳定碳同位素组成(δ13C)的精确测定。应用此方法测定树木非结构性碳水化合物(NSC)中特定成分(如糖类、有机酸和糖醇)的δ13C,不仅能够追踪新同化的光合产物在树木中的运移及与外界的碳交换,还能够更敏感地指示树木生理状况对环境变化的响应。本文首先系统介绍了CSIA从样品采集、处理到δ13C测定的方法,然后综述了树木NSC中各成分之间及各成分在不同器官之间的δ13C差异,阐述了树木NSC的δ13C时间动态变化特征及内在机制,最后分析了NSC作为主要呼吸底物,其δ13C与树木呼吸释放CO2的δ13C(δ13CR)之间的联系,并针对CSIA分析技术在后光合分馏、树木逆境生理和年轮δ13C形成机制等研究的应用前景提出了展望。  相似文献   
3.
土壤盐渍化是阻碍林业发展的重要原因, 杨树(Populus spp.)是中国主要的人工林树种, 探究盐胁迫下植物的碳氮代谢特征与抗盐胁迫能力, 将有助于杨树人工林的可持续发展。该研究利用美洲黑杨(P. deltoides)和青杨(P. cathayana)两个物种, 采用去叶与不去叶处理, 在盐胁迫下研究两种杨树的抗逆性差异。研究发现, 盐胁迫下美洲黑杨的总生物量和光合能力均显著高于青杨。盐胁迫与去叶处理导致美洲黑杨叶绿素浓度和光系统II最大光量子效率显著高于青杨, 表明去叶对美洲黑杨影响较小, 但是加重了盐对青杨的毒害作用。美洲黑杨茎叶Na+浓度显著低于青杨, 表明美洲黑杨能够有效地限制Na+向地上部分运输。在盐胁迫条件下, 美洲黑杨茎和根比青杨能够维持更高浓度的淀粉、可溶性糖以及蔗糖, 前者较高的腺苷二磷酸葡萄糖焦磷酸化酶活性促进了光合产物向淀粉转换, 保证植物有充足的非结构性碳水化合物来参与渗透调节和维持其他生命活动, 而去叶使得青杨非结构性碳水化合物严重不足, 受盐胁迫影响更严重。盐胁迫下, 青杨分布在脂溶性蛋白(膜系统相关蛋白质)的氮浓度显著下降, 而NH4+、谷氨酸脱氢酶活性与脯氨酸浓度显著升高。研究结果证明, 非结构性碳水化合物的积累、转化和分配是植物抗逆性的重要特征。  相似文献   
4.
Apoptosis is an important mechanism to maintain homeostasis in mammals, and disruption of the apoptosis regulation mechanism triggers a range of diseases, such as cancer, autoimmune diseases, and developmental disorders. The severity of influenza A virus (IAV) infection is also closely related to dysfunction of apoptosis regulation. In the virus infected cells, the functions of various host cellular molecules involved in regulation of induction of apoptosis are modulated by IAV proteins to enable effective virus replication. The modulation of the intracellular signaling pathway inducing apoptosis by the IAV infection also affects extracellular mechanisms controlling apoptosis, and triggers abnormal host responses related to the disease severity of IAV infections. This review focuses on apoptosis related molecules involved in IAV replication and pathogenicity, the strategy of the virus propagation through the regulation of apoptosis is also discussed.  相似文献   
5.
林恬  郑怀舟  朱锦懋 《生态学报》2022,42(18):7641-7651
植物叶片中的非结构性碳水化合物(NSC)和碳(C)、氮(N)、磷(P)含量可反映植物和生态系统对水分亏缺环境的响应及适应程度。以福建省长汀县25a马尾松(Pinus massoniana)为对象,原位观测分析了3年持续100%隔离降雨对成年马尾松针叶NSC与C、N、P的影响。结果表明:(1)持续隔离降雨导致马尾松针叶NSC含量先显著增加后减少,最终导致针叶NSC含量季节变化消失;且针叶可溶性糖含量、可溶性糖/淀粉比值在后期显著增加;(2)持续隔离降雨使马尾松针叶N含量、P含量、N∶P均表现为前期与对照组差异不显著,后期显著高于对照组;(3)马尾松针叶NSC含量、可溶性糖含量、P含量、N∶P与土壤水分含量呈显著或极显著相关,且均与P含量显著或极显著相关,与N素无相关性。以上研究结果表明,随着土壤水分含量的持续减少马尾松可通过调整针叶中NSC含量的积累及分配和提高针叶N、P含量来适应缺水环境,P含量的增加对NSC含量波动及可溶性糖和淀粉的相互转化起促进作用。  相似文献   
6.
Rice ragged stunt disease, caused by rice ragged stuntoryzavirus (RRSV), was first discovered in 1976–1977 inIndonesia and Philippines [1]. Subsequently the diseasewas found in most rice-growing countries in south-easternand far-eastern Asia [2] and may inflict heavy loss on thecrop. RRSV is the type species of the genus Oryzavirus in thefamily Reoviridae. The virus particle is icosahedral witha diameter of about 65–70 nm and the genome consistsof 10 double stranded RNA (dsRNA) segm…  相似文献   
7.
Hepatitis C virus encodes an autoprotease, NS2-3, which is required for processing of the viral polyprotein between the non-structural NS2 and NS3 proteins. This protease activity is vital for the replication and assembly of the virus and therefore represents a target for the development of anti-viral drugs. The mechanism of this auto-processing reaction is not yet clear but the protease activity has been shown to map to the C-terminal region of NS2 and the N-terminal serine protease region of NS3. The NS2-3 precursor can be expressed in Escherichia coli as inclusion bodies, purified as denatured protein and refolded, in the presence of detergents and the divalent metal ion zinc, into an active form capable of auto-cleavage. Here, intrinsic tryptophan fluorescence has been used to assess refolding in the wild-type protein and specific active site mutants. We also investigate the effects on protein folding of alterations to the reaction conditions that have been shown to prevent auto-cleavage. Our data demonstrate that these active site mutations do not solely affect the cleavage activity of the HCV NS2-3 protease but significantly affect the integrity of the global protein fold.  相似文献   
8.
We have identified a membrane-active region in the HCV NS5A protein by performing an exhaustive study of membrane rupture induced by a NS5A-derived peptide library on model membranes having different phospholipid compositions. We report the identification in NS5A of a highly membranotropic region located at the suggested membrane association domain of the protein. We report the binding and interaction with model membranes of two peptides patterned after this segment, peptides 1A and 1B, derived from the strains 1a_H77 and 1b_HC-4J respectively. We show that they insert into phospholipid membranes, interact with them, and are located in a shallow position in the membrane. The NS5A region where this segment resides might have an essential role in the membrane replication and/or assembly of the viral particle through the modulation of the replication complex, and consequently, directly implicated in the HCV life cycle.  相似文献   
9.
Avian influenza viruses belong to the genus influenza A virus of the family Orthomyxoviridae. The influenza virus consists of eight segmented minus stranded RNA that encode 11 known proteins. Among the 11 viral proteins, NS1 (non-structural protein 1, encoded on segment 8) has been implicated in the regulation of several important intra-cellular functions.In this report, we investigated the functional interaction of NS1 with serine threonine kinase Akt, a core intra-cellular survival regulator. In co-immunoprecipitation assays and GST pull-down assays, NS1 directly interacted with Akt. The interaction was mediated primarily through the Akt-PH (Pleckstrin Homology) domain and the RNA-binding domain of NS1. NS1 preferentially interacted with phosphorylated Akt, but not with non-phosphorylated Akt. Functionally, the NS1-Akt interaction enhanced Akt activity both in the intra-cellular context and in in vitro Akt kinase assays. Confocal microscopic analysis revealed that phosphorylated Akt interacted with NS1 during the interphase of the cell cycle predominantly within the nucleus. Finally, mass spectrometric analysis demonstrated the position at Thr215 of NS1 protein is primary phosphorylation target site through Akt activation. The results together supported the functional importance of influenza virus NS1 with Akt, a core intra-cellular survival regulator.  相似文献   
10.
This study investigates the role of magnesium ions in coupling ATP hydrolysis to the nucleic acid unwinding catalyzed by the NS3 protein encoded by the hepatitis C virus (HCV). Analyses of steady-state ATP hydrolysis rates at various RNA and magnesium concentrations were used to determine values for the 15 dissociation constants describing the formation of a productive enzyme-metal-ATP-RNA complex and the four rate constants describing hydrolysis of ATP by the possible enzyme-ATP complexes. These values coupled with direct binding studies, specificity studies and analyses of site-directed mutants reveal only one ATP binding site on HCV helicase centered on the catalytic base Glu291. An adjacent residue, Asp290, binds a magnesium ion that forms a bridge to ATP, reorienting the nucleotide in the active site. RNA stimulates hydrolysis while decreasing the affinity of the enzyme for ATP, magnesium, and MgATP. The binding scheme described here explains the unusual regulation of the enzyme by ATP that has been reported previously. Binding of either free magnesium or free ATP to HCV helicase competes with MgATP, the true fuel for helicase movements, and leads to slower hydrolysis and nucleic acid unwinding.  相似文献   
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