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101.
It has repeatedly been noted that ready availability of well-grown cycad specimens would substantially reduce collection of
plants from their natural habitats. Although some cycads are extensively produced in several countries, there is uncertainty
as to their optimal growing conditions and fertilizer requirements. UsingZamia floridana (sensu lato) as a model, one-year-old seedlings were grown in 30% and 50% light-exclusion shadehouses for one growing season.
They were fertilized with roughly equivalent nutrient proportions of 20-20-20 (N-P-K) Peters solution at 300 ppm applied biweekly,
nine-month 18-6-12 controlled-release Osmocote granules, and 16-8-12 Controlled Release Sierra Tablets plus minors at two
and three tablets per container, and in combinations. There was interaction between shade and fertilizer types in all parameters
measured. Overall, plants grown in 30% shade had a larger caudex, more leaves, and higher leaf and stem-plus-root fresh and
dry weights. Peters fertilizer at 300 ppm was least effective in all growth parameters, as compared with other fertilizer
treatments. Alone, however, it was more effective in caudex enlargement in 50% shade. No differences were observed between
any treatments involving granules, irrespective of supplemental Peters. There was no significant difference between three
tablets plus Peters and two tablets only, in 30% and 50% shade. Two tablets plus Peters and three tablets only, however, had
a significant effect on caudex enlargement in 30% shade. In 50% shade, three tablets plus Peters or granules alone were more
effective. These results and personal experience show that nearly all cycads grow best in ± 30% shade and benefit from fertilizers
that contain micronutrients and a higher ammoniacal nitrogen source. 相似文献
102.
Müller MJ Langemann D Gehrke I Later W Heller M Glüer CC Heymsfield SB Bosy-Westphal A 《PloS one》2011,6(7):e22732
Resting energy expenditure (REE)-power relationships result from multiple underlying factors including weight and height. In addition, detailed body composition, including fat free mass (FFM) and its components, skeletal muscle mass and internal organs with high metabolic rates (i.e. brain, heart, liver, kidneys), are major determinants of REE. Since the mass of individual organs scales to height as well as to weight (and, thus, to constitution), the variance in these associations may also add to the variance in REE. Here we address body composition (measured by magnetic resonance imaging) and REE (assessed by indirect calorimetry) in a group of 330 healthy volunteers differing with respect to age (17-78 years), sex (61% female) and BMI (15.9-47.8 kg/m(2)). Using three dimensional data interpolation we found that the inter-individual variance related to scaling of organ mass to height and weight and, thus, the constitution-related variances in either FFM (model 1) or kidneys, muscle, brain and liver (model 2) explained up to 43% of the inter-individual variance in REE. These data are the first evidence that constitution adds to the complexity of REE. Since organs scale differently as weight as well as height the "fit" of organ masses within constitution should be considered as a further trait. 相似文献
103.
104.
Schröder R Schmidt J Blättermann S Peters L Janssen N Grundmann M Seemann W Kaufel D Merten N Drewke C Gomeza J Milligan G Mohr K Kostenis E 《Nature protocols》2011,6(11):1748-1760
Label-free dynamic mass redistribution (DMR) is a cutting-edge assay technology that enables real-time detection of integrated cellular responses in living cells. It relies on detection of refractive index alterations on biosensor-coated microplates that originate from stimulus-induced changes in the total biomass proximal to the sensor surface. Here we describe a detailed protocol to apply DMR technology to frame functional behavior of G protein-coupled receptors that are traditionally examined with end point assays on the basis of detection of individual second messengers, such as cAMP, Ca(2+) or inositol phosphates. The method can be readily adapted across diverse cellular backgrounds (adherent or suspension), including primary human cells. Real-time recordings can be performed in 384-well microtiter plates and be completed in 2 h, or they can be extended to several hours depending on the biological question to be addressed. The entire procedure, including cell harvesting and DMR detection, takes 1-2 d. 相似文献
105.
Wiebke Neumann Göran Ericsson Holger Dettki 《European Journal of Wildlife Research》2009,55(3):255-265
Previous studies on moose Alces alces have suggested that interactions with humans may trigger anti-predator behaviors and generate a demographical cost. Therefore,
we hypothesized that disturbances from small and big game hunting may have negative effects on moose movements, diurnal activity,
and activity range. Using location data from 64 moose equipped with GPS collars from three populations (Low Alpine, Inland,
Coastal) with different temporal human presence and spatial accessibility, we evaluated the impact of hunting on moose activity
rhythms. On average, female moose in the low human population density (Low Alpine) area (<0.5/km2) had significantly lower movement rates during moose hunting season, but variation in movement rates among individuals were
higher compared with female moose in regions with denser human populations (6–24/km2). We found no evidence that reproductive status influenced female moose sensitivity to disturbance. As expected, females
used smaller activity ranges and were less active nocturnally than males. The high within-group variation suggests that current
hunting disturbance levels do not alter moose population behavior in general. Our data indicate that alterations in movement
were related to rutting activity, not human disturbance induced by hunting. In line with behavioral theory, our study suggests
that some individuals were more sensitive to hunting disturbance than the general population. Our work suggests that individual
moose may perceive human predation risk to be similar to other predation risks. 相似文献
106.
107.
A Targeted LC‐MS Strategy for Low‐Abundant HLA Class‐I‐Presented Peptide Detection Identifies Novel Human Papillomavirus T‐Cell Epitopes 下载免费PDF全文
Renata Blatnik Nitya Mohan Maria Bonsack Lasse G. Falkenby Stephanie Hoppe Kathrin Josef Alina Steinbach Sara Becker Wiebke M. Nadler Marijana Rucevic Martin R. Larsen Mogjiborahman Salek Angelika B. Riemer 《Proteomics》2018,18(11)
For rational design of therapeutic vaccines, detailed knowledge about target epitopes that are endogenously processed and truly presented on infected or transformed cells is essential. Many potential target epitopes (viral or mutation‐derived), are presented at low abundance. Therefore, direct detection of these peptides remains a challenge. This study presents a method for the isolation and LC‐MS3‐based targeted detection of low‐abundant human leukocyte antigen (HLA) class‐I‐presented peptides from transformed cells. Human papillomavirus (HPV) was used as a model system, as the HPV oncoproteins E6 and E7 are attractive therapeutic vaccination targets and expressed in all transformed cells, but present at low abundance due to viral immune evasion mechanisms. The presented approach included preselection of target antigen‐derived peptides by in silico predictions and in vitro binding assays. The peptide purification process was tailored to minimize contaminants after immunoprecipitation of HLA‐peptide complexes, while keeping high isolation yields of low‐abundant target peptides. The subsequent targeted LC‐MS3 detection allowed for increased sensitivity, which resulted in successful detection of the known HLA‐A2‐restricted epitope E711–19 and ten additional E7‐derived peptides on the surface of HPV16‐transformed cells. T‐cell reactivity was shown for all the 11 detected peptides in ELISpot assays, which shows that detection by our approach has high predictive value for immunogenicity. The presented strategy is suitable for validating even low‐abundant candidate epitopes to be true immunotherapy targets. 相似文献
108.
Clostridium difficile causes infections ranging from mild C. difficile-associated diarrhea to severe pseudomembranous colitis. Since 2003 new hypervirulent C. difficile strains (PCR ribotype 027) emerged characterized by a dramatically increased mortality. The secretomes of the three C. difficile strains CDR20291, CD196, and CD630 were analyzed and compared. Proteins were separated and analyzed by means of SDS--PAGE and LC-MS. MS data were analyzed using Mascot and proteins were checked for export signals with SecretomeP and SignalP. LC-MS analysis revealed 158 different proteins in the supernatant of C. difficile. Most of the identified proteins originate from the cytoplasm. Thirty-two proteins in CDR20291, 36 in CD196 and 26 in CD630 were identified to be secreted by C. difficile strains. Those were mainly S-layer proteins, substrate-binding proteins of ABC-transporters, cell wall hydrolases, pilin and unknown hypothetical proteins. Toxin A and toxin B were identified after growth in brain heart infusion medium using immunological techniques. The ADP-ribosyltransferase-binding component protein, which is a part of the binary toxin CDT, was only identified in the hypervirulent ribotype 027 strains. Further proteins that are secreted specifically by hypervirulent strains were identified. 相似文献
109.
Géraud C Evdokimov K Straub BK Peitsch WK Demory A Dörflinger Y Schledzewski K Schmieder A Schemmer P Augustin HG Schirmacher P Goerdt S 《PloS one》2012,7(4):e34206
Liver sinusoidal endothelium is strategically positioned to control access of fluids, macromolecules and cells to the liver parenchyma and to serve clearance functions upstream of the hepatocytes. While clearance of macromolecular debris from the peripheral blood is performed by liver sinusoidal endothelial cells (LSECs) using a delicate endocytic receptor system featuring stabilin-1 and -2, the mannose receptor and CD32b, vascular permeability and cell trafficking are controlled by transcellular pores, i.e. the fenestrae, and by intercellular junctional complexes. In contrast to blood vascular and lymphatic endothelial cells in other organs, the junctional complexes of LSECs have not yet been consistently characterized in molecular terms. In a comprehensive analysis, we here show that LSECs express the typical proteins found in endothelial adherens junctions (AJ), i.e. VE-cadherin as well as α-, β-, p120-catenin and plakoglobin. Tight junction (TJ) transmembrane proteins typical of endothelial cells, i.e. claudin-5 and occludin, were not expressed by rat LSECs while heterogenous immunreactivity for claudin-5 was detected in human LSECs. In contrast, junctional molecules preferentially associating with TJ such as JAM-A, B and C and zonula occludens proteins ZO-1 and ZO-2 were readily detected in LSECs. Remarkably, among the JAMs JAM-C was considerably over-expressed in LSECs as compared to lung microvascular endothelial cells. In conclusion, we show here that LSECs form a special kind of mixed-type intercellular junctions characterized by co-occurrence of endothelial AJ proteins, and of ZO-1 and -2, and JAMs. The distinct molecular architecture of the intercellular junctional complexes of LSECs corroborates previous ultrastructural findings and provides the molecular basis for further analyses of the endothelial barrier function of liver sinusoids under pathologic conditions ranging from hepatic inflammation to formation of liver metastasis. 相似文献
110.
Guido Grossmann Jan Malinsky Wiebke Stahlschmidt Martin Loibl Ina Weig-Meckl Wolf B. Frommer Miroslava Opekarov Widmar Tanner 《The Journal of cell biology》2008,183(6):1075-1088
In this study, we investigate whether the stable segregation of proteins and lipids within the yeast plasma membrane serves a particular biological function. We show that 21 proteins cluster within or associate with the ergosterol-rich membrane compartment of Can1 (MCC). However, proteins of the endocytic machinery are excluded from MCC. In a screen, we identified 28 genes affecting MCC appearance and found that genes involved in lipid biosynthesis and vesicle transport are significantly overrepresented. Deletion of Pil1, a component of eisosomes, or of Nce102, an integral membrane protein of MCC, results in the dissipation of all MCC markers. These deletion mutants also show accelerated endocytosis of MCC-resident permeases Can1 and Fur4. Our data suggest that release from MCC makes these proteins accessible to the endocytic machinery. Addition of arginine to wild-type cells leads to a similar redistribution and increased turnover of Can1. Thus, MCC represents a protective area within the plasma membrane to control turnover of transport proteins. 相似文献