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71.
Tuxworth RI Stephens S Ryan ZC Titus MA 《The Journal of biological chemistry》2005,280(28):26557-26564
Myosin VII (M7) plays a role in adhesion in both Dictyostelium and mammalian cells where it is a component of a complex of proteins that serve to link membrane receptors to the underlying actin cytoskeleton. The nature of this complex is not fully known, prompting a search for M7-binding proteins. Co-immunoprecipitation experiments reveal that Dictyostelium M7 (DdM7) interacts with talinA, an actin-binding protein with a known role in cell-substrate adhesion. No additional proteins are observed in the immunoprecipitate, indicating that the interaction is direct. The N-terminal region of the DdM7 tail that lies between the region of predicted coil and the first MyTH4 domain is found to harbor the talinA binding site. Localization experiments reveal that talinA does not serve as a membrane receptor for DdM7 and vice versa. These findings reveal that talinA is a major DdM7 binding partner and suggest that their interaction induces a conformational change in each that, in combination with membrane receptor binding, promotes the assembly of a high avidity receptor complex essential for adhesion of the cell to substrata. 相似文献
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Zachary A. Bacigalupa Chaitali H. Bhadiadra Mauricio J. Reginato 《Journal of bioenergetics and biomembranes》2018,50(3):189-198
Elevated O-GlcNAcylation is emerging as a general characteristic of most cancers. Although O-GlcNAcylation can regulate many cell biological pathways, recent evidence suggests that it is a key regulator of metabolic pathways including glycolysis in cancer cells. This review summarizes our current understanding of how O-GlcNAcylation regulates glycolytic pathways and contributes to alterations in cancer cell metabolism. 相似文献
73.
Shape disparity of bovid (Mammalia,Artiodactyla) horn sheaths and horn cores allows discrimination by species in 3D geometric morphometric analyses 下载免费PDF全文
The bony cranial structures of even‐toed hoofed mammals are important for understanding ecology and behavior of ruminants. Horns, the cranial appendages of the family Bovidae, are covered in a layer of keratin that is often not preserved in the fossil record; however, this keratin sheath is intimately involved in the processes that influence horn shape evolution. To understand the relationship between these two components of horns, we quantified both core and sheath shape for four extant species using three‐dimensional geometric morphometric analyses in separate, core‐ and sheath‐specific morphospaces as well as a combined morphospace. We assessed correlations between the horn and sheath morphospaces using two‐block partial least squares regression, a Mantel test of pairwise distances between species, and Procrustes ANOVA. We measured disparity in the combined morphospace as Procrustes distances between mean shapes of cores and sheaths within and between species and as Procrustes variance. We also tested whether core and sheath shapes could be discriminated by taxon with a canonical variate analysis. Results show that horn core and sheath morphospaces are strongly correlated. The differences in shape between a species' core and sheath were statistically significant, but not as great as those between the cores and sheaths of different species when close relatives were not considered, and core and sheath Procrustes variances are not significantly different within species. Cores and sheath shapes were highly identifiable and were assigned to the correct clade 93% of the time in the canonical variate analysis. Based on these tests, horn cores are distinguishable in geometric morphometric analyses, extending the possibility of using geometric morphometrics to study the ecology and evolution of bovid horns to the fossil record. 相似文献
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Zachary L. Rinkes Michael N. Weintraub Jared L. DeForest Daryl L. Moorhead 《Fungal Ecology》2011,4(6):396-407
The Guild Decomposition Model (GDM) hypothesized that temporal shifts in microbial “guilds,” each with distinct substrate preferences, drive decomposition dynamics and regulate soil carbon (C) losses and sequestration. To test this hypothesis, we established a laboratory incubation of Acer saccharum litter and monitored respiration, microbial biomass and enzyme activities, inorganic nutrients and shifts in functional groups of decomposers using phospholipid fatty acid (PLFA) analysis. Biomass and respiration peaked within the first 2 d of incubation, and the Gram negative PLFA biomarker 18:1ω7c predominated during the first 5 d. Hydrolytic enzyme activities and two fungal biomarkers (18:2ω6,9c and 18:3ω6c) increased by 25 d and lignolytic enzyme activity was detected at 68 d. Our results suggest that decomposers preferentially use labile substrates and that shifts in decomposer groups occur in response to changes in available substrates, which supports the GDM. 相似文献
75.
Monika Oláhová Wan Hee Yoon Kyle Thompson Sharayu Jangam Liliana Fernandez Jean M. Davidson Jennifer E. Kyle Megan E. Grove Dianna G. Fisk Jennefer N. Kohler Matthew Holmes Annika M. Dries Yong Huang Chunli Zhao Kévin Contrepois Zachary Zappala Laure Frésard Daryl Waggott Matthew T. Wheeler 《American journal of human genetics》2018,102(3):494-504
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Zachary Castonguay Christopher AugerSean C. Thomas M’hamed ChahmaVasu D. Appanna 《Biochemical and biophysical research communications》2014
It is becoming increasingly apparent that the nucleus harbors metabolic enzymes that affect genetic transforming events. Here, we describe a nuclear isoform of lactate dehydrogenase (nLDH) and its ability to orchestrate histone deacetylation by controlling the availability of nicotinamide adenine dinucleotide (NAD+), a key ingredient of the sirtuin-1 (SIRT1) deacetylase system. There was an increase in the expression of nLDH concomitant with the presence of hydrogen peroxide (H2O2) in the culture medium. Under oxidative stress, the NAD+ generated by nLDH resulted in the enhanced deacetylation of histones compared to the control hepatocytes despite no discernable change in the levels of SIRT1. There appeared to be an intimate association between nLDH and SIRT1 as these two enzymes co-immunoprecipitated. The ability of nLDH to regulate epigenetic modifications by manipulating NAD+ reveals an intricate link between metabolism and the processing of genetic information. 相似文献
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Ricardo Cáceda Tori Moskovciak Stefania Prendes-Alvarez Justyna Wojas Anzhelika Engel Samantha H. Wilker Jorge L. Gamboa Zachary N. Stowe 《PloS one》2014,9(9)