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排序方式: 共有396条查询结果,搜索用时 15 毫秒
51.
52.
Analysis of the Actinobacillus actinomycetemcomitans leukotoxin gene. Delineation of unique features and comparison to homologous toxins 总被引:19,自引:0,他引:19
E T Lally E E Golub I R Kieba N S Taichman J Rosenbloom J C Rosenbloom C W Gibson D R Demuth 《The Journal of biological chemistry》1989,264(26):15451-15456
Actinobacillus actinomycetemcomitans leukotoxin has been implicated as a virulence factor in human infections. To initiate delineation of leukotoxin structure/function relationships, molecular cloning of the leukotoxin gene was carried out. When an A. actinomycetemcomitans genomic DNA library in lambda EMBL3 was screened using a 1.3-kilobase pair restriction fragment containing a portion of the leukotoxin gene, 13 positive recombinants were identified. One recombinant, designated lambda OP8, containing a 16-kilobase pair insert was selected for detailed study. Lysates from lambda OP8, but not control lysates, exhibited leukotoxic activity with target cell specificity identical to the native toxin. Western blots identified the recombinant-produced toxin as a 125-kDa protein doublet identical in mobility to the native toxin. Restriction enzyme and extensive DNA analyses demonstrated that the leukotoxin gene showed strong homology to two other toxins produced by Escherichia coli and Pasteurella haemolytica. As in the other two species, the A. actinomycetemcomitans toxin is contained in a cluster of four genes in which the A gene encodes the toxin and the products of the B, C, and D genes are involved in posttranslational modification of the toxin and its membrane insertion and secretion. The target cell specificity of the A. actinomycetemcomitans toxin differs from the other two toxins and is restricted to human and some non-human primate cells of the monomyelocytic lineage. The A. actinomycetemcomitans leukotoxin is not secreted but remains associated with the bacterial membrane, possibly through a hydrophobic domain at the carboxyl terminus which distinguishes it from the E. coli and P. haemolytica toxins. 相似文献
53.
A novel nucleic acid-binding protein that interacts with human rad51 recombinase. 总被引:2,自引:1,他引:1 下载免费PDF全文
O V Kovalenko E I Golub P Bray-Ward D C Ward C M Radding 《Nucleic acids research》1997,25(24):4946-4953
Using the yeast two-hybrid system, we isolated a cDNA encoding a novel human protein, named Pir51, that strongly interacts with human Rad51 recombinase. Analysis in vitro confirmed the interaction between Rad51 and Pir51. Pir51 mRNA is expressed in a number of human organs, most notably in testis, thymus, colon and small intestine. The Pir51 gene locus was mapped to chromosome 12p13.1-13. 2 by fluorescence in situ hybridization. The Pir51 protein was expressed in Escherichia coli and purified to near homogeneity. Biochemical analysis shows that the Pir51 protein binds both single- and double-stranded DNA, and is capable of aggregating DNA. The protein also binds RNA. The Pir51 protein may represent a new member of the multiprotein complexes postulated to carry out homologous recombination and DNA repair in mammalian cells. 相似文献
54.
55.
Hubbard Jerry S. Hardy James P. Voecks Gerald E. Golub Ellis E. 《Journal of molecular evolution》1973,2(2-3):149-166
Summary
14C-Formic acid and other14C-organic compounds are formed on surface materials when mixtures of14CO,12CO2 or N2 and water vapor are irradiated with ultraviolet light (UV) of > 250 nm. The rate of organic formation is roughly proportional to the quantity of substratum irradiated. The available evidence suggests that14CO adsorbed to or in contact with the substratum is excited by the long wavelength UV and reacts with adsorbed H2O or surface hydroxyl groups yielding the organic products. Photodestruction of the14C-organics yields14CO2 and14CO. A steady state is attained when organic products reach a concentration such that the rate of photodestruction is equal to the rate of synthesis. The product accumulation is greater and the photodestruction is slower when N2 is used as diluent gas.Differences in the rates of synthesis, rates of photodestruction and amounts of product accumulation are observed with different silica and alumina substrata. The substrata with large surface areas are most effective for synthesis while maximum photoprotection of organics is afforded by substrata containing high concentrations of surface hydroxyl groups.The observation of the synthesis on a variety of substrata using realistic simulations of atmospheres and solar energies strengthens previous proposals that this process may occur on Mars and may have been important on the primitive Earth. 相似文献
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Maksym?Golub Mahdi?Hejazi Adrian?K?lsch Heiko?LoksteinView authors OrcID profile D.?C.?Florian?Wieland Athina?Zouni J?rg?PieperEmail author 《Photosynthesis research》2017,133(1-3):163-173
The structure of monomeric and trimeric photosystem I (PS I) of Thermosynechococcus elongatus BP1 (T. elongatus) was investigated by small-angle X-ray scattering (SAXS). The scattering data reveal that the protein–detergent complexes possess radii of gyration of 58 and 78 Å in the cases of monomeric and trimeric PS I, respectively. The results also show that the samples are monodisperse, virtually free of aggregation, and contain empty detergent micelles. The shape of the protein–detergent complexes can be well approximated by elliptical cylinders with a height of 78 Å. Monomeric PS I in buffer solution exhibits minor and major radii of the elliptical cylinder of about 50 and 85 Å, respectively. In the case of trimeric PS I, both radii are equal to about 110 Å. The latter model can be shown to accommodate three elliptical cylinders equal to those describing monomeric PS I. A structure reconstitution also reveals that the protein–detergent complexes are larger than their respective crystal structures. The reconstituted structures are larger by about 20 Å mainly in the region of the hydrophobic surfaces of the monomeric and trimeric PS I complexes. This seeming contradiction can be resolved by the addition of a detergent belt constituted by a monolayer of dodecyl-β-D-maltoside molecules. Assuming a closest possible packing, a number of roughly 1024 and 1472 detergent molecules can be determined for monomeric and trimeric PS I, respectively. Taking the monolayer of detergent molecules into account, the solution structure can be almost perfectly modeled by the crystal structures of monomeric and trimeric PS I. 相似文献
58.
Martyn Kelly Cathy Bennett Michel Coste Cristina Delgado François Delmas Luc Denys Luc Ector Claude Fauville Martial Ferréol Malgorzata Golub Amelie Jarlman Maria Kahlert John Lucey Bernadette Ní Chatháin Isabel Pardo Peter Pfister Joanna Picinska-Faltynowicz Juliette Rosebery Christine Schranz Jochen Schaumburg Herman van Dam Sirje Vilbaste 《Hydrobiologia》2009,621(1):169-182
The European Union (EU)’s Water Framework Directive (WFD) requires that all Member States participate in intercalibration
exercises in order to ensure that ecological status concepts and assessment levels are consistent across the EU. This paper
describes one such exercise, performed by the countries in the Central/Baltic Geographical Intercalibration Group stretching
from Ireland in the west to Estonia in the east and from the southern parts of Scandinavia to the northern regions of Spain
and Italy (but excluding alpine regions, which were intercalibrated separately). In this exercise, methods used to measure
ecological status of rivers using benthic diatoms were compared. Ecological status is estimated as the ratio between the observed
value of a biological element and the value expected in the absence of significant human impact. Approaches to defining the
‘reference sites’, from which these ‘expected’ values were derived, varied from country to country. Minimum criteria were
established as part of the exercise but there was still considerable variation between national reference values, reflecting
typological differences that could not be resolved during the exercise. A simple multimetric index was developed to compare
boundary values using two widely used diatom metrics. Boundary values for high/good status and good/moderate status set by
each participant were converted to their equivalent values of this intercalibration metric using linear regression. Variation
of ±0.05 EQR units around the median value was considered to be acceptable and the exercise provided a means for those Member
States who fell significantly above or below this line to review their approaches and, if necessary, adjust their boundaries.
Handling editor: J. Padisak 相似文献
59.
Golub AS Tevald MA Pittman RN 《American journal of physiology. Heart and circulatory physiology》2011,300(1):H135-H143
We have developed an optical method for the evaluation of the oxygen consumption (Vo(2)) in microscopic volumes of spinotrapezius muscle. Using phosphorescence quenching microscopy (PQM) for the measurement of interstitial Po(2), together with rapid pneumatic compression of the organ, we recorded the oxygen disappearance curve (ODC) in the muscle of the anesthetized rats. A 0.6-mm diameter area in the tissue, preloaded with the phosphorescent oxygen probe, was excited once a second by a 532-nm Q-switched laser with pulse duration of 15 ns. Each of the evoked phosphorescence decays was analyzed to obtain a sequence of Po(2) values that constituted the ODC. Following flow arrest and tissue compression, the interstitial Po(2) decreased rapidly and the initial slope of the ODC was used to calculate the Vo(2). Special analysis of instrumental factors affecting the ODC was performed, and the resulting model was used for evaluation of Vo(2). The calculation was based on the observation of only a small amount of residual blood in the tissue after compression. The contribution of oxygen photoconsumption by PQM and oxygen inflow from external sources was evaluated in specially designed tests. The average oxygen consumption of the rat spinotrapezius muscle was Vo(2) = 123.4 ± 13.4 (SE) nl O(2)/cm(3) · s (N = 38, within 6 muscles) at a baseline interstitial Po(2) of 50.8 ± 2.9 mmHg. This technique has opened the opportunity for monitoring respiration rates in microscopic volumes of functioning skeletal muscle. 相似文献
60.
Kramerov AA Golub AG Bdzhola VG Yarmoluk SM Ahmed K Bretner M Ljubimov AV 《Molecular and cellular biochemistry》2011,349(1-2):125-137
Ubiquitous protein kinase CK2 is a key regulator of cell migration, proliferation and tumor growth. CK2 is abundant in retinal astrocytes, and its inhibition suppresses retinal neovascularization in a mouse retinopathy model. In human astrocytes, CK2 co-distributes with GFAP-containing intermediate filaments, which implies its association with cytoskeleton. Contrary to astrocytes, CK2 is co-localized in microvascular endothelial cells (HBMVEC) with microtubules and actin stress fibers, but not with vimentin-containing intermediate filaments. Specific CK2 inhibitors (TBB, TBI, TBCA and DMAT) and nine novel CK2 inhibiting compounds (TID43, TID46, Quinolone-7, Quinolone-39, FNH28, FNH62, FNH64, FNH68 and FNH74) were tested at 10-200 μM for their ability to induce morphological alterations in cultured human astrocytes (HAST-40), and HBMVEC (For explanation of the inhibitor names, see "Methods" section). CK2 inhibitors caused dramatic changes in shape of cultured cells with effective inhibitor concentrations between 50 and 100 μM. Attached cells retracted, acquired shortened processes, and eventually rounded up and detached. CK2 inhibitor-induced morphological alterations were completely reversible and were not blocked by caspase inhibition. However, longer treatment or higher inhibitor concentration did cause apoptosis. The speed and potency of the CK2 inhibitors effects on cell shape and adhesion were inversely correlated with serum concentration. Western analyses showed that TBB and TBCA elicited a significant (about twofold) increase in the activation of p38 and ERK1/2 MAP kinases that may be involved in cytoskeleton regulation. This novel early biological cell response to CK2 inhibition may underlie the anti-angiogenic effect of CK2 suppression in the retina. 相似文献