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31.
The volume regulation process at work in rabbit kidney cortex slices submitted to hypo-osmotic media show both a swelling limitation and a volume readjustment phase. Swelling limitation is Na+ dependent and is blocked by ouabain 10(-3) M. There is, however, no need to implicate the activity of a ouabain sensitive Na+ /K+ pump in this process. 相似文献
32.
Ellinghaus E Ellinghaus D Stuart PE Nair RP Debrus S Raelson JV Belouchi M Fournier H Reinhard C Ding J Li Y Tejasvi T Gudjonsson J Stoll SW Voorhees JJ Lambert S Weidinger S Eberlein B Kunz M Rahman P Gladman DD Gieger C Wichmann HE Karlsen TH Mayr G Albrecht M Kabelitz D Mrowietz U Abecasis GR Elder JT Schreiber S Weichenthal M Franke A 《Nature genetics》2010,42(11):991-995
33.
34.
Inhibition of HIV-1 protease in infected T-lymphocytes by synthetic peptide analogues. 总被引:22,自引:0,他引:22
T D Meek D M Lambert G B Dreyer T J Carr T A Tomaszek M L Moore J E Strickler C Debouck L J Hyland T J Matthews 《Nature》1990,343(6253):90-92
35.
Agarose-acrylamide composite gels for microfractionation of RNA 总被引:1,自引:0,他引:1
36.
Structure of porphobilinogen deaminase reveals a flexible multidomain polymerase with a single catalytic site. 总被引:11,自引:0,他引:11
G V Louie P D Brownlie R Lambert J B Cooper T L Blundell S P Wood M J Warren S C Woodcock P M Jordan 《Nature》1992,359(6390):33-39
The three-domain structure of porphobilinogen deaminase, a key enzyme in the biosynthetic pathway of tetrapyrroles, has been defined by X-ray analysis at 1.9 A resolution. Two of the domains structurally resemble the transferrins and periplasmic binding proteins. The dipyrromethane cofactor is covalently linked to domain 3 but is bound by extensive salt-bridges and hydrogen-bonds within the cleft between domains 1 and 2, at a position corresponding to the binding sites for small-molecule ligands in the analogous proteins. The X-ray structure and results from site-directed mutagenesis provide evidence for a single catalytic site. Interdomain flexibility may aid elongation of the polypyrrole product in the active-site cleft of the enzyme. 相似文献
37.
Lambert F Delmonte B Petit JR Bigler M Kaufmann PR Hutterli MA Stocker TF Ruth U Steffensen JP Maggi V 《Nature》2008,452(7187):616-619
Dust can affect the radiative balance of the atmosphere by absorbing or reflecting incoming solar radiation; it can also be a source of micronutrients, such as iron, to the ocean. It has been suggested that production, transport and deposition of dust is influenced by climatic changes on glacial-interglacial timescales. Here we present a high-resolution record of aeolian dust from the EPICA Dome C ice core in East Antarctica, which provides an undisturbed climate sequence over the past eight climatic cycles. We find that there is a significant correlation between dust flux and temperature records during glacial periods that is absent during interglacial periods. Our data suggest that dust flux is increasingly correlated with Antarctic temperature as the climate becomes colder. We interpret this as progressive coupling of the climates of Antarctic and lower latitudes. Limited changes in glacial-interglacial atmospheric transport time suggest that the sources and lifetime of dust are the main factors controlling the high glacial dust input. We propose that the observed approximately 25-fold increase in glacial dust flux over all eight glacial periods can be attributed to a strengthening of South American dust sources, together with a longer lifetime for atmospheric dust particles in the upper troposphere resulting from a reduced hydrological cycle during the ice ages. 相似文献
38.
Julie Lecomte Krystel Louis Benoit Detry Silvia Blacher Vincent Lambert Sandrine Bekaert Carine Munaut Jenny Paupert Pierre Blaise Jean-Michel Foidart Jean-Marie Rakic Stephen M. Krane Agn��s Noel 《Cellular and molecular life sciences : CMLS》2011,68(4):677-686
In this study, we evaluate the potential involvement of collagenase-3 (MMP13), a matrix metalloproteinase (MMP) family member, in the exudative form of age-related macular degeneration characterized by a neovascularisation into the choroid. RT-PCR analysis revealed that human neovascular membranes issued from patients with AMD expressed high levels of Mmp13. The contribution of MMP13 in choroidal neovascularization (CNV) formation was explored by using a murine model of laser-induced CNV and applying it to wild-type mice (WT) and Mmp13-deficient mice (Mmp13 ?/? mice). Angiogenic and inflammatory reactions were explored by immunohistochemistry. The implication of bone marrow (BM)-derived cells was determined by BM engraftment into irradiated mice and by injecting mesenchymal stem cells (MSC) isolated from WT BM. The deficiency of Mmp13 impaired CNV formation which was fully restored by WT BM engraftment and partially rescued by several injections of WT MSC. The present study sheds light on a novel function of MMP13 during BM-dependent choroidal vascularization and provides evidence for a role for MSC in the pathogenesis of CNV. 相似文献
39.
以十六烷基三甲基溴化胺和四丙基氢氧化铵为膨化剂,利用超声波的空化作用将合成的层状硅酸盐Magadiite进行层板剥离,从而制备了一种新型介孔材料.采用了XRD、氮气吸附、NMR,IR,SEM和TEM等表征工具对这种材料的结构和形貌进行了详细的表征.研究结果表明:这种材料在长程上是无序的而在短程上是有序的.此外,这种新型介孔材料不仅具有高的比表面,而且约有一半的部分是外表面.形貌观察进一步表明这种介孔材料的孔壁是由不规则的单个晶体片层组成.由于这些结构特点,这种新型介孔材料同时满足了孔壁晶体化,良好的大分子可接近性的要求. 相似文献
40.
AP Gregory CA Dendrou KE Attfield A Haghikia DK Xifara F Butter G Poschmann G Kaur L Lambert OA Leach S Prömel D Punwani JH Felce SJ Davis R Gold FC Nielsen RM Siegel M Mann JI Bell G McVean L Fugger 《Nature》2012,488(7412):508-511
Although there has been much success in identifying genetic variants associated with common diseases using genome-wide association studies (GWAS), it has been difficult to demonstrate which variants are causal and what role they have in disease. Moreover, the modest contribution that these variants make to disease risk has raised questions regarding their medical relevance. Here we have investigated a single nucleotide polymorphism (SNP) in the TNFRSF1A gene, that encodes tumour necrosis factor receptor 1 (TNFR1), which was discovered through GWAS to be associated with multiple sclerosis (MS), but not with other autoimmune conditions such as rheumatoid arthritis, psoriasis and Crohn’s disease. By analysing MS GWAS data in conjunction with the 1000 Genomes Project data we provide genetic evidence that strongly implicates this SNP, rs1800693, as the causal variant in the TNFRSF1A region. We further substantiate this through functional studies showing that the MS risk allele directs expression of a novel, soluble form of TNFR1 that can block TNF. Importantly, TNF-blocking drugs can promote onset or exacerbation of MS, but they have proven highly efficacious in the treatment of autoimmune diseases for which there is no association with rs1800693. This indicates that the clinical experience with these drugs parallels the disease association of rs1800693, and that the MS-associated TNFR1 variant mimics the effect of TNF-blocking drugs. Hence, our study demonstrates that clinical practice can be informed by comparing GWAS across common autoimmune diseases and by investigating the functional consequences of the disease-associated genetic variation. 相似文献