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171.
172.
Phylogenetic analyses of the rbcL sequences from haptophytes and heterokont algae suggest their chloroplasts are unrelated 总被引:2,自引:0,他引:2
Using the large subunit of RuBisCo (rbcL) sequences from cyanobacteria,
proteobacteria, and diverse groups of algae and green plants, we evaluated
the plastid relationship between haptophytes and heterokont algae. The rbcL
sequences were determined from three taxa of heterokont algae
(Bumilleriopsis filiformis, Pelagomonas calceolata, and Pseudopedinella
elastica) and added to 25 published sequences to obtain a data set
comprising 1,434 unambiguously aligned sites (approximately 98% of the
total rbcL gene). Higher levels of mutational saturation in third codon
positions were observed by plotting the pairwise substitutions with and
without corrections for multiple substitutions at the same site for first
and second codon positions only and for third positions only. In accordance
with this finding phylogeny reconstructions were completed by omitting
third codon positions, thus using 956 bp in weighted-parsimony and
maximum-likelihood analyses. The midpoint-rooted phylogenies showed two
major clusters, one containing cyanobacteria, glaucocystophytes, a
phototrophic euglenoid, chlorophytes, and embryophytes (the green lineage),
the other containing proteobacteria, haptophytes, red algae, a cryptophyte,
and heterokont algae (the non-green lineage). In the nongreen lineage, the
haptophytes formed a sister group to the clade containing heterokont algae,
red algae, and the cryptophyte Guillardia theta. This branching pattern was
well supported in terms of bootstrap values in weighted- parsimony and
maximum-likelihood analyses (100% and 92%, respectively). However, the
phylogenetic relationship among red algae, heterokonts, and a cryptophyte
taxon was not especially well resolved. A four- cluster analysis was
performed to further explore the statistical significance of the
relationship between proteobacteria, red algae (including and excluding
Guillardia theta), haptophytes, and heterokont algae. This test strongly
favored the hypothesis that the heterokonts and red algae are more closely
related to each other than either is to proteobacteria or haptophytes.
Hence, this molecular study based on a plastid-encoded gene provides
additional evidence for a distant relationship between haptophytes and the
heterokont algae. It suggests an evolutionary scenario in which the
ancestor of the haptophyte lineage engulfed a phototrophic eukaryote and,
more recently, the heterokont lineage became phototrophic by engulfing a
red alga.
相似文献
173.
ICA 512, an autoantigen of type I diabetes, is an intrinsic membrane protein of neurosecretory granules. 总被引:14,自引:0,他引:14 下载免费PDF全文
M Solimena R Dirkx Jr J M Hermel S Pleasic-Williams J A Shapiro L Caron D U Rabin 《The EMBO journal》1996,15(9):2102-2114
Islet cell autoantigen (ICA) 512 is a novel autoantigen of insulin-dependent diabetes mellitus (IDDM) which is homologous to receptor-type protein tyrosine phosphatases (++PTPases). We show that ICA 512 is an intrinsic membrane protein of secretory granules expressed in insulin-producing pancreatic beta-cells as well as in virtually all other peptide-secreting endocrine cells and neurons containing neurosecretory granules. ICA 512 is cleaved at its luminal domain and, following exposure at the cell surface, recycles to the Golgi complex region and is sorted into newly formed secretory granules. By immunoprecipitation, anti-ICA 512 autoantibodies were detected in 15/17 (88%) newly diagnosed IDDM patients, but not in 10/10 healthy subjects. These results suggest that tyrosine phosphorylation participates in some aspect of secretory granule function common to all neuroendocrine cells and that a subset of autoantibodies in IDDM is directed against an integral membrane protein of insulin-containing granules. 相似文献
174.
Abstract: The monosialoganglioside GM1 has been shown to possess neurotrophic activity in vitro and in vivo and is now used as an experimental treatment for a variety of neurological disorders and trauma. Little is known about the mechanism of action used by GM1. Because GM1 appears to enhance nerve growth factor (NGF) activity, we have used C6trk+ cells, a derivative of C6-2B glioma cells that express the high-affinity receptor for NGF trkA , to determine whether the neurotrophic effects of GM1 occurs through induction of trkA activity. Exposure of C6trk+ cells to NGF (10–50 ng/ml) resulted in a five- to 10-fold increase in trkA tyrosine phosphorylation within 5 min. Incubation of cells with GM1 resulted in a threefold increase in trkA phosphorylation beginning within 1 h and peaking between 3 and 6 h. Optimal responses to GM1 were obtained using 80–100 µ M concentrations. Moreover, tyrosine phosphorylation of known trkA target proteins, such as extracellular signal-regulated kinases, and suc -associated neurotrophic factor-induced tyrosine-phosphorylated target, were activated upon stimulation of C6trk+ cells with GM1. In addition, GM1 potentiated the NGF-mediated activation of tyrosine phosphorylation of trkA . GM1 failed to induce phosphorylation of trkA and target proteins in mock transfected cells. Thus, our data demonstrate that GM1 mimics some of the effects of NGF and suggest that the neurotrophic properties of GM1 may be attributed to its activation of trkA signal transduction. 相似文献
175.
176.
A significant part of the proteome is composed of intrinsically disordered proteins (IDPs). These proteins do not fold into a well-defined structure and behave like ordinary polymers. In this work, we consider IDPs that have the tendency to aggregate, model them as heteropolymers that contain a small number of associating monomers, and use computer simulations to compare the aggregation of such IDPs that are grafted to a surface or free in solution. We then discuss how such grafting may affect the analysis of in vitro experiments and could also be used to suppress harmful aggregation. 相似文献
177.
Herpesvirus saimiri. 3. Plaque formation under multi agar, methyl cellulose and starch overlays 总被引:5,自引:0,他引:5
178.
Subunit structure of Escherichia coli exonuclease VII 总被引:5,自引:0,他引:5
Exonuclease VII has been purified 7,500-fold to 87% homogeneity from Escherichia coli K12 using a new purification procedure. The enzyme has been shown to be composed of two nonidentical subunits of 10,500 and 54,000 daltons. This has been confirmed by restoration of exonuclease VII activity after renaturation of denatured and purified subunits. The structure of the native enzyme consists of one large subunit and four small subunits. We have previously isolated exonuclease VII mutant strains containing defects which map at two distinct loci. Subunit-mixing experiments utilizing wild type enzyme and temperature-sensitive enzyme produced by an xseB mutant strain have shown that the xseB gene codes for the small subunit of the enzymes. 相似文献
179.
180.
Identification of proteins by mass spectrometry (MS) is an essential step in proteomic studies and is typically accomplished by either peptide mass fingerprinting (PMF) or amino acid sequencing of the peptide. Although sequence information from MS/MS analysis can be used to validate PMF-based protein identification, it may not be practical when analyzing a large number of proteins and when high- throughput MS/MS instrumentation is not readily available. At present, a vast majority of proteomic studies employ PMF. However, there are huge disparities in criteria used to identify proteins using PMF. Therefore, to reduce incorrect protein identification using PMF, and also to increase confidence in PMF-based protein identification without accompanying MS/MS analysis, definitive guiding principles are essential. To this end, we propose a value-based scoring system that provides guidance on evaluating when PMF-based protein identification can be deemed sufficient without accompanying amino acid sequence data from MS/MS analysis. 相似文献