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161.
Extracellular polysaccharide of Nostoc commune (Cyanobacteria) inhibits fusion of membrane vesicles during desiccation 总被引:6,自引:0,他引:6
Donna R. Hill Thomas W. Keenan Richard F. Helm Malcolm Potts Lois M. Crowe John H. Crowe 《Journal of applied phycology》1997,9(3):237-248
Cells of the cyanobacterium Nostoc commune secrete a complex, high molecular weight, extracellular polysaccharide (EPS) which
accumulates to more than 60% of the dry weight of colonies. The EPS was purified from the clonal isolate N. commune DRH1.
The midpoint of the membrane phase transition (Tm) of desiccated cells of N. commune CHEN was low (Tm
dry = 8 °C) and was comparable to the Tm of rehydrated cells((Tm)H20 = 6 °C). The EPS was not responsible for the depression of Tm. However, the EPS, at low concentrations, inhibited specifically the fusion of phosphatidylcholine membrane vesicles when
they were dried in vitro at0% relative humidity (−400 MPa). Low concentrations of a trehalose:sucrose mixture, in a molar
ratio which corresponded with that present in cells in vivo, together with small amounts of the EPS, were efficient in preventing
leakage of carboxyfloroscein (CF) from membrane vesicles. Freeze-fracture electron microscopy resolved complex changes in
the structure of the EPS and the outer membrane in response to rehydration of desiccated cells. The capacity of the EPS to
prevent membrane fusion, the maintenance of a low Tm
dry in desiccated cells, and the changes in rheological properties of the EPS in response to water availability, constitute what
are likely important mechanisms for desiccation tolerance in this cyanobacterium.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
162.
163.
Selenoprotein P associates with endothelial cells in rat tissues 总被引:11,自引:0,他引:11
R. F. Burk Kristina E. Hill Martha E. Boeglin Ford F. Ebner Harold S. Chittum 《Histochemistry and cell biology》1997,108(1):11-15
Selenoprotein P is an extracellular heparin-binding protein that has been implicated in protecting the liver against oxidant
injury. Its location in liver, kidney, and brain was determined by conventional immunohistochemistry and confocal microscopy
using a polyclonal antiserum. Selenoprotein P is associated with endothelial cells in the liver and is more abundant in central
regions than in portal regions. It is also present in kidney glomeruli associated with capillary endothelial cells. Staining
of selenoprotein P in the brain is also confined to vascular endothelial cells. The heparin-binding properties of selenoprotein
P could be the basis for its binding to tissue. Its localization to the vicinity of endothelial cells is potentially relevant
to its oxidant defense function.
Accepted: 6 March 1997 相似文献
164.
Characterization and crystallization of human uroporphyrinogen decarboxylase. 总被引:4,自引:0,他引:4 下载免费PDF全文
J. D. Phillips F. G. Whitby J. P. Kushner C. P. Hill 《Protein science : a publication of the Protein Society》1997,6(6):1343-1346
The cytosolic enzyme uroporphyrinogen decarboxylase (URO-D) catalyzes the fifth step in the heme biosynthetic pathway, converting uroporphyrinogen to coproporphyrinogen by decarboxylating the four acetate side chains of the substrate. Recombinant human URO-D has been expressed in Escherichia coli with a histidine tag and has been purified to homogeneity. Purified protein was determined to be a monodisperse dimer by dynamic light scattering. Equilibrium sedimentation analysis confirmed that the protein is dimeric, with a dissociation constant of 0.1 microM. URO-D containing an amino-terminal histidine tag was crystallized in space group P3(1)21 or its enantiomer P3(2)21 with unit cell dimensions a = b = 103.6 A, c = 75.2 A. There is one molecule in the asymmetric unit, consistent with generation of the dimer by the twofold axis of this crystallographic operator. Native data have been collected to 3.0 a resolution. 相似文献
165.
Developmental control of xylem hydraulic resistances and vulnerability to embolism in Fraxinus excelsior L.: impacts on water relations 总被引:3,自引:0,他引:3
Welbaum G.E.; Bian D.; Hill D.R.; Grayson R.L.; Gunatilaka M.K. 《Journal of experimental botany》1997,48(3):655-663
The freezing tolerance of many plants, such as pea (Pisum sativum),is increased by exposure to low temperature or abscisic acidtreatment, although the physiological basis of this phenomenonis poorly understood. The freezing tolerance of pea shoot tips,root tips, and epicotyl tissue was tested after cold acclimationat 2C, dehydration/rehydration, applications of 104M abscisic acid (ABA), and deacclimation at 25C. Tests wereconducted using the cultivar Alaska, an ABA-deficientmutant wil, and its wildtype. Freezinginjury was determined graphically as the temperature that caused50% injury (T50) from electrical conductivity. Endogenous ABAwas measured using an indirect enzyme-linked immunosorbant assay,and novel proteins were detected using 2-dimensional polyacrylamidegel electrophoresis. The maximum decrease in T50 for root tissuewas 1C for all genotypes, regardless of treatment. For Alaskashoot tips and epicotyl tissue, exogenous ABA increased thefreezing tolerance by 1.5 to 4.0C, while coldtreatment increased the freezing tolerance by 7.5 to14.8C. Cold treatment increased the freezing toleranceof shoot tips by 9 and 15C for wiland wild-type, respectively. Cold acclimationincreased endogenous ABA concentrations in Alaskashoot tips and epicotyls 3- to 4-fold. Immunogold labeling increasednoticeably in the nucleus and cytoplasm of the epicotyl after7 d at 2C and was greatest after 30 d at the time of maximumfreezing tolerance and soluble ABA concentration. Cold treatmentinduced the production of seven, three, and two proteins inshoot, epicotyl, and root tissue of Alaska, respectively.In Alaska shoot tissue, five out of seven novelproteins accumulated in response to both ABA and cold treatment.However, only a 24 kDa protein was produced in wiland wild-type shoot and epicotyl tissues aftercold treatment. Abscisic acid and cold treatment additivelyincreased the freezing tolerance of pea epicotyl and shoot tissuesthrough apparently independent mechanisms that both resultedin the production of a 24 kDa protein. Key words: Pisum sativum, cold acclimation, immuno-localization 相似文献
166.
Previous studies in our laboratory have shown that Na absorption across the porcine endometrium is stimulated by PGF2α and cAMP-dependent activation of a barium-sensitive K channel located in the basolateral membrane of surface epithelial cells.
In this study, we identify and characterize this basolateral, barium-sensitive K conductance. Porcine uterine tissues were
mounted in Ussing chambers and bathed with KMeSO4 Ringer solution. Amphotericin B (70 μm) was added to the luminal solution to permeabilize the apical membrane and determine the current-voltage relationship of
the basolateral K conductance after activation by 100 μm CPT-cAMP. An inwardly rectifying current was identified which possessed a reversal potential of −53 mV when standard Ringer
solution was used to bathe the serosal surface. The K:Na selectivity ratio was calculated to be 12:1. Administration of 5
mm barium to the serosal solution completely inhibited the current activated by cAMP under these conditions. In addition to
these experiments, amphotericin-perforated whole cell patch clamp recordings were obtained from primary cultures of porcine
surface endometrial cells. The isolated cells displayed an inwardly rectifying current under basal conditions. This current
was significantly stimulated by CPT-cAMP and blocked by barium. These results together with our previous studies demonstrate
that cAMP increases Na absorption in porcine endometrial epithelial cells by activating an inwardly rectifying K channel present
in the basolateral membrane. Similar patch clamp experiments were conducted using cells from a human endometrial epithelial
cell line, RL95-2. An inwardly rectifying current was also identified in these cells which possessed a reversal potential
of −56 mV when the cells were bathed in standard Ringer solution. This current was blocked by barium as well as cesium. However,
the current from the human cells did not appear to be activated by cAMP, indicating that distinct subtypes of inwardly rectifying
K channels are present in endometrial epithelial cells from different species.
Received: 6 February 1997/Revised: 10 July 1997 相似文献
167.
Therapy of bovine ocular squamous-cell carcinoma with local doses of interleukin-2: 67% complete regressions after 20 months of follow-up 总被引:1,自引:1,他引:0
F. W. Willem Den Otter Graham Hill Wim R. Klein Jan Willem Koten Peter A. Steerenberg Pieter H. M. De Mulder Christopher Rhode Rachel Stewart Joop A. J. Faber E. Joost Ruitenberg Victor P. M. G. Rutten 《Cancer immunology, immunotherapy : CII》1995,41(1):10-14
We have tested the therapeutic potency of peritumorally injected low doses of interleukin-2(IL-2). Seventy tumours of the bovine ocular squamous-cell carcinoma (BOSCC), 1–3 cm in diameter, were treated with 5000, 20 000 or 200 000 U IL-2 from Eurocetus (Chiron) to find the optimal dose for treatment. Injections were given peritumorally on Monday to Friday on 2 consecutive weeks. The size of the tumours was measured before treatment and 1, 3, 4, 9 and 20 months after treatment. After 9 months complete regression was observed in 89% of the tumours treated with 5000 U IL-2, 80% treated with 20 000 U and 67% treated with 200 000 U. After 20 months, there was complete regression of 35%, 31% and 67% of the tumours respectively. The 9-and 20-month results of the 200 000-U treatment are significantly better than those of the 5000-U and 20 000-U treatments taken together. This protocol may be useful to treat advanced inoperable tumours (e.g. of the nasopharynx or skin) of human patients. 相似文献
168.
C. J. Lord S. K. Bohlander E. A. Hopes C. T. Montague N. J. Hill J. -B. Prins R. J. Renjilian L. B. Peterson L. S. Wicker J. A. Todd P. Denny 《Mammalian genome》1995,6(9):563-570
Development of novel congenic mouse strains has allowed us to better define the location of the diabetogenic locus, Idd3, on Chromosome (Chr) 3. Congenic strains were identified by use of published and newly developed microsatellite markers, their genomes fingerprinted by a rapid, fluorescence-based approach, and their susceptibility to type 1 diabetes evaluated. The maximum interval containing Idd3 is now approximately 4 cM. 相似文献
169.
Numbers of viable fungal propagules in corn dusts in southern Georgia were estimated during various farm and grain elevator operations in 1979, 1980, and 1982. A six-stage Andersen sampler for viable microbial particles was used to sample the dusts with various agar media. The most abundant fungi in corn dusts were species of yeasts: Aspergillus, Penicillium, Cladosporium, Alternaria. Helminthosporium, and Fusarium. However, the relative abundance of these fungi differed between years. There was a greater incidence of the Aspergillus flavus group in the hot, dry year of 1980 compared with the cooler, wetter years of 1979 and 1982. Fungi in the corn dusts sampled numbered between 10(4) and 10(9) viable propagules per m3 of air. By contrast, outdoor air often contained fewer than 10(4) viable fungal propagules per m3. Most A. flavus propagules were deposited at stages three and four of the Andersen sampler, with correspond to the trachea, primary bronchi, and secondary bronchi in the human respiratory system. In an assessment of the air spores by exposing sterile petri dishes, more large-spored fungi, like Alternaria tenuis, and fewer small-spored fungi, such as A. flavus, were detected when compared with colony counts from petri dishes exposed to air in the Anderson sampler. 相似文献
170.
J. S. Hill Gaston Lesley E. Wallace Alan B. Rickinson M. Anthony Epstein Donald Pious 《Immunogenetics》1984,19(6):475-486
Mutants of the EB virus-transformed cell line T5-1 (HLA-Al, 2; B8, 27), bearing well-characterized alterations in HLA-A2 antigen expression and unable to bind the HLA-A2-specific monoclonal antibody 13137.2, have been tested for their susceptibility to EB virus-specific cytolysis using effector T-cell preparations functionally restricted through relevant HLA antigens. Initial experiments first confirmed that the parent line T5-1 was susceptible to cytolysis by both common A2-restricted and 1327-restricted effector cells. While those T5-1 mutants with little or no surface A2 expression were not lysed by A2-restricted effectors, those targets with quantitatively normal expression of mutant A2 molecules were as susceptible to A2-restricted lysis as the parent line itself. In contrast, all the T5-1 mutant lines were susceptible to B27-restricted cytolysis. The results demonstrate that experimentally induced mutations of HLA-A2 antigen structure, affecting a serologically defined site on the molecule, can occur without altering that same molecule's expression of the T cell-restricting determinant(s). Such experimentally induced mutations are quite different from the naturally occurring variant A2 antigens which are present within the serologically defined A2 antigen group and which show changes at the T cell-restricting site. 相似文献