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151.
Cademartiri F La Grutta L Runza G Palumbo A Maffei E Mollet NR Bartolotta TV Somers P Knaapen M Verheye S Midiri M Hamers R Bruining N 《European radiology》2007,17(7):1842-1849
Attenuation variability (measured in Hounsfield Units, HU) of human coronary plaques using multislice computed tomography
(MSCT) was evaluated in an ex vivo model with increasing convolution kernels. MSCT was performed in seven ex vivo left coronary
arteries sunk into oil followingthe instillation of saline (1/∞) and a 1/50 solution of contrast material (400 mgI/ml iomeprol).
Scan parameters were: slices/collimation, 16/0.75 mm; rotation time, 375 ms. Four convolution kernels were used: b30f-smooth,
b36f-medium smooth, b46f-medium and b60f-sharp. An experienced radiologist scored for the presence of plaques and measured
the attenuation in lumen, calcified and noncalcified plaques and the surrounding oil. The results were compared by the ANOVA
test and correlated with Pearson’s test. The signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR) were calculated.
The mean attenuation values were significantly different between the four filters (p < 0.0001) in each structure with both solutions. After clustering for the filter, all of the noncalcified plaque values (20.8 ± 39.1,
14.2 ± 35.8, 14.0 ± 32.0, 3.2 ± 32.4 HU with saline; 74.7 ± 66.6, 68.2 ± 63.3, 66.3 ± 66.5, 48.5 ± 60.0 HU in contrast solution)
were significantly different, with the exception of the pair b36f–b46f, for which a moderate-high correlation was generally
found. Improved SNRs and CNRs were achieved by b30f and b46f. The use of different convolution filters significantly modifief
the attenuation values, while sharper filtering increased the calcified plaque attenuation and reduced the noncalcified plaque
attenuation. 相似文献
152.
RA Stein 《Clinical genetics》2009,75(2):121-123
Age-related macular degeneration is associated with an unstable ARMS2 ( LOC387715 ) mRNA
Fritsche et al. (2008)
Nature Genetics 40 (7): 892–896 相似文献
Fritsche et al. (2008)
Nature Genetics 40 (7): 892–896 相似文献
153.
RA Kumar 《Clinical genetics》2009,76(6):499-501
154.
RA Coleman 《British journal of pharmacology》2009,158(1):180-182
The mechanism of the long duration of action of salmeterol at β2-adrenoceptors has long been a matter of debate, and is still unresolved. Szczuka and colleagues have both summarized the position to date and suggested a new mechanistic contender, receptor rebinding. Despite this, they still do not come to any clear conclusion. Much of the literature data that they have drawn upon appears contradictory, and mathematical models are inevitably flawed by the questionable validity of key values applied to them. Although the issue will undoubtedly eventually be resolved, it will probably require investigators to apply carefully designed studies on simple experimental systems such as isolated membranes or cultured cells. Only then should studies be extended to more complex systems such as isolated preparations of airways smooth muscle, where tissue bulk inevitably presents a complicating factor, particularly where relatively lipophilic compounds are concerned. 相似文献
155.
KD McCloskey UA Anderson RA Davidson YR Bayguinov KM Sanders SM Ward 《British journal of pharmacology》2009,156(2):273-283
Background and purpose:
W/Wv and wild-type murine bladders were studied to determine whether the W/Wv phenotype, which causes a reduction in, but not abolition of, tyrosine kinase activity, is a useful tool to study the function of bladder interstitial cells of Cajal (ICC).Experimental approach:
Immunohistochemistry, tension recordings and microelectrode recordings of membrane potential were performed on wild-type and mutant bladders.Key results:
Wild-type and W/Wv detrusors contained c-Kit- and vimentin-immunopositive cells in comparable quantities, distribution and morphology. Electrical field stimulation evoked tetrodotoxin-sensitive contractions in wild-type and W/Wv detrusor strips. Atropine reduced wild-type responses by 50% whereas a 25% reduction occurred in W/Wv strips. The atropine-insensitive component was blocked by pyridoxal-5-phosphate-6-azophenyl-2′,4′-disulphonic acid in both tissue types. Wild-type and W/Wv detrusors had similar resting membrane potentials of −48 mV. Spontaneous electrical activity in both tissue types comprised action potentials and unitary potentials. Action potentials were nifedipine-sensitive whereas unitary potentials were not. Excitatory junction potentials were evoked by single pulses in both tissues. These were reduced by atropine in wild-type tissues but not in W/Wv preparations. The atropine-insensitive component was abolished by pyridoxal-5-phosphate-6-azophenyl-2′,4′-disulphonic acid in both preparations.Conclusions and implications:
Bladders from W/Wv mice contain c-Kit- and vimentin-immunopositive ICC. There are similarities in the electrical and contractile properties of W/Wv and wild-type detrusors. However, significant differences were found in the pharmacology of the responses to neurogenic stimulation with an apparent up-regulation of the purinergic component. These findings indicate that the W/Wv strain may not be the best model to study ICC function in the bladder. 相似文献156.
157.
158.
Visual identification of bacterially contaminated red cells 总被引:1,自引:0,他引:1
There have been increasing numbers of reports of transfusion-acquired Yersinia enterocolitica bacteremia (including several fatal cases). Fifteen units of whole blood were inoculated with various concentrations of Y. enterocolitica serotype 0:3 and processed into AS-3 preserved red cells (RBCs). Consistent growth of the organism was found at inoculum concentrations greater than or equal to 10 colony-forming units per mL. In all 13 units of RBCs that supported the growth of Y. enterocolitica, a darkening in color (due to hemolysis and a decrease in pO2) was observed in the bag. The attached sample segments, which were sealed from the main unit, remained sterile and did not darken. This color change was apparent in all the contaminated units by Day 35, which was 1.5 to 2 weeks after the bacteria were first detected in cultures of the blood. Hence, by comparison of the color of the segment tubing with that of the unit itself, units grossly contaminated with Y. enterocolitica can be identified prior to transfusion. Moreover, review of photographs on file at the Centers for Disease Control revealed this dramatic color change in 2 units of blood that caused transfusion-transmitted sepsis (Enterobacter agglomerans and an unidentified gram-negative bacillus, not Yersinia sp.), which demonstrated that the color change was not limited to Y. enterocolitica. This method of visual identification of contaminated units of blood could decrease the incidence of posttransfusion bacterial sepsis. 相似文献
159.
160.
The genes encoding effector molecules of mature T cells, IL-2, perforin and
IL-4, were found to be expressed in vivo in the most primitive subsets of
thymocytes of adult mice. These subsets have previously been identified by
their cell surface markers and by their expression of other T
lineage-associated genes. While IL-2, perforin and IL-4 are expressed in
distinct patterns, all three are expressed before the induction of RAG-1
and pre-TCR alpha mRNA expression, and are confined to subsets of cells
that apparently have not yet undergone commitment to the T lineage. Thus,
expression of T cell response genes appears to be one of the earliest
markers of lymphocyte differentiation. Activation events marked by CD69
induction occur in these early cell types, but the response gene expression
by these cells is separable from CD69 expression. IL-2 and perforin are
induced again much later in thymocyte development, during TCR-dependent
repertoire selection. At those stages, IL-2 protein and RNA levels per cell
are higher, but the fraction of cells expressing IL-2 appears to be much
lower than in the most immature stages. In addition, a striking feature of
the immature populations is the robust IL-2 expression by presumptive
immature NK cells. These findings are discussed in terms of the
developmental origins of lineage specificity in T cell response gene
regulation.
相似文献