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91.
92.
The siderophore iron transporter of Candida albicans (Sit1p/Arn1p) mediates uptake of ferrichrome-type siderophores and is required for epithelial invasion
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Heymann P Gerads M Schaller M Dromer F Winkelmann G Ernst JF 《Infection and immunity》2002,70(9):5246-5255
The human fungal pathogen Candida albicans contains a close homologue of yeast siderophore transporters, designated Sit1p/Arn1p. We have characterized the function of SIT1 in C. albicans by constructing sit1 deletion strains and testing their virulence and ability to utilize a range of siderophores and other iron complexes. sit1 mutant strains are defective in the uptake of ferrichrome-type siderophores including ferricrocin, ferrichrysin, ferrirubin, coprogen, and triacetylfusarinine C. A mutation of FTR1 did not impair the use of these siderophores but did affect the uptake of ferrioxamines E and B, as well as of ferric citrate, indicating that their utilization was independent of Sit1p. Hemin was a source of iron for both sit1 and ftr1 mutants, suggesting a pathway of hemin uptake distinct from that of siderophores and iron salts. Heterologous expression of SIT1 in the yeast Saccharomyces cerevisiae confirmed the function of Sit1p as a transporter for ferrichrome-type siderophores. The sit1 mutant was defective in infection of a reconstituted human epithelium as a model for human oral mucosa, while the SIT1 strain was invasive. In contrast, both sit1 and SIT1 strains were equally virulent in the mouse model of systemic infection. These results suggest that siderophore uptake by Sit1p/Arn1p is required in a specific process of C. albicans infection, namely epithelial invasion and penetration, while in the blood or within organs other sources of iron, including heme, may be used. 相似文献
93.
Helicobacter pylori does not require Lewis X or Lewis Y expression to colonize C3H/HeJ mice
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Takata T El-Omar E Camorlinga M Thompson SA Minohara Y Ernst PB Blaser MJ 《Infection and immunity》2002,70(6):3073-3079
Helicobacter pylori strains frequently express Lewis X (Le(x)) and/or Le(y) on their cell surfaces as constituents of the O antigens of their lipopolysaccharide molecules. To assess the effect of Le(x) and Le(y) expression on the ability of H. pylori to colonize the mouse stomach and to adhere to epithelial cells, isogenic mutants were created in which fucT1 alone or fucT1 and fucT2, which encode the fucosyl transferases necessary for Le(x) and Le(y) expression, were deleted. C3H/HeJ mice were experimentally challenged with either wild-type 26695 H. pylori or its isogenic mutants. All strains, whether passaged in the laboratory or recovered after mouse passage, colonized the mice well and without consistent differences. During colonization by the mutants, there was no reversion to wild type. Similarly, adherence to AGS and KatoIII cells was unaffected by the mutations. Together, these findings indicate that Le expression is not necessary for mouse gastric colonization or for H. pylori adherence to epithelial cells. 相似文献
94.
Granulocyte-macrophage colony-stimulating factor (GM-CSF) but not granulocyte colony-stimulating factor (G-CSF) induces plasma membrane expression of proteinase 3 (PR3) on neutrophils in vitro
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Hellmich B Csernok E Trabandt A Gross WL Ernst M 《Clinical and experimental immunology》2000,120(2):392-398
The theoretical risk of triggering vasculitis resulting from administration of G-CSF and GM-CSF to patients with anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV), such as Wegener's granulomatosis (WG), who develop agranulocytosis due to cytotoxic therapy, is unknown. Since there is strong evidence that activation of polymorphonuclear neutrophils (PMN) induced by binding of ANCA to PR3 or myeloperoxidase (MPO) expressed on their plasma membrane is involved in the pathogenesis of systemic vasculitides (SV), we studied the surface expression of PR3 and MPO on PMN from healthy donors in response to G-CSF and GM-CSF in vitro by flow cytometric analysis. Increasing doses of G-CSF did not alter PR3 expression on either untreated or tumour necrosis factor-alpha (TNF-alpha)-primed donor PMN significantly. In contrast, GM-CSF significantly increased PR3 membrane expression on both intact PMN and neutrophils primed with TNF-alpha. MPO expression was not significantly altered by either G-CSF or GM-CSF. In summary, these data demonstrate that GM-CSF, but not G-CSF, induces plasma membrane expression of PR3 on PMN in vitro. Since in AAV accessibility of the antigen (PR3 or MPO) to the antibody (ANCA) on the plasma membrane of PMN is thought to be essential for neutrophil activation by ANCA, the results of the present study suggest that administration of GM-CSF to patients with WG with neutropenia implies a definite theoretical risk of deterioration of vasculitis via this mechanism. 相似文献
95.
Ernst K R?dland Morten Mattingsdal Ole K Olstad Reidun Ovsteb? Peter Kierulf Fredrik Muller Stig S Fr?land 《Medical mycology》2008,46(4):327-336
The objective of these studies was to investigate genes of importance in the pathogenesis of Aspergillus infections. To do so, we employed microarray methodology to explore gene expression in human monocytes infected with Aspergillus conidia as compared with unstimulated monocytes and those stimulated with lipopolysaccharide (LPS) signaling through TOLL-like receptor 4 (TLR4). We found 997 (P相似文献
96.
A newly developed noninvasive tissue reflectance oximeter utilizes 5 light emitting diodes operating at the wavelengths of 0.635, 0.665, 0.795, 0.910, and 0.955 μ, and photodiodes to sample the tissue reflectance spectra. Since the tissue reflectance is affected by changes in both hemoglobin content (Hb T) and hemoglobin oxygen saturation (OS T),Hb T is first determined using the reflectance at 0.795 μ. The hemoglobinOS T is then estimated using the reflectances at the 5 wavelengths in conjunction with the diffuse reflectance equation which has previously been verified applicable to tissue reflectance oximetry. A quantitative estimation of bothHb T andOS T in intestinal mucosa of dogs obtained using this instrument showed thatHb T values agreed fairly well with those of others and that the standard errors ofOS T were around 5.0% inOS as compared with theOS values of blood samples for minimized arterial-venousOS differences. The continuous on-line measurement ofHb T andOS T should be possible using the reflectance technique and should be valuable for clinical evaluation of the patients. 相似文献
97.
Epithelial membranes are multicompartment structures of microscopic and submicroscopic dimensions. Therefore, interpretations
of kinetic data on solute fluxes, based on the standard three compartment model are open to criticism. We have obtained an
integrated view of the kinetics of Na+ transport in frog skin epidermis by application of the computer simulation method. Epidermis and whole skin models were designed
which resemble photomicrographs of these tissues. Justification is given for the way in which internal and external chamber
compartments are connected (topology). The epidermis model has eight passive, and two active transfer sites. Our primary aims
were 1) simulation of the transepidermal Na+ influx and the concomitant Na+ backflux saturation kinetics, and 2) localization of the so-called “outer” and “inner” Na+ responsive borders in epidermis. The analysis, based on methodical variations of transfer coefficients, suggests involvement
of the “composite desmosomes” and the transepithelial Na+-pump leak pathway. These are located in the outer and the inner region of the epidermis, respectively. Reasonable functional
agreement between epidermis and model was also seen in 1) Na+ saturation kinetics in ouabain, poisoned system, 2) relative independence of the two borders to the “trans” [Na+] in the external solutions, and 3) equal energy requirement, for the transmembrane Na+ pump, Na+/O2∼-20.
This work was supported by NIH Grant GM 03545-23 相似文献
98.
Modification of collagen matrices for enhancing angiogenesis 总被引:3,自引:0,他引:3
Yao C Prével P Koch S Schenck P Noah EM Pallua N Steffens G 《Cells, tissues, organs》2004,178(4):189-196
The vascularization of engineered tissues in many cases does not keep up with the ingrowth of cells. Nutrient and oxygen supply are not sufficient, which ultimately leads to the death of the invading cells. The enhancement of the angiogenic capabilities of engineered tissues therefore represents a major challenge in the field of tissue engineering. The immobilization of angiogenic growth factors may be useful for enhancing angiogenesis. The most potent angiogenic growth factor specific to endothelial cells, vascular endothelial growth factor (VEGF), occurs in several splice variants. The variant with 165 amino acids both has a high angiogenic activity and a high affinity for heparin. We therefore incorporated heparin molecules into collagen matrices by covalently cross-linking them to amino functions on the collagen. Physical binding of VEGF to the heparin may then prevent a rapid clearance from the implant, while the release rate may become coupled to the degradation of the collagen matrix. The modified matrices were characterized by determination of the extent of the heparin immobilization, the in vitro degradation rate by collagenase. For testing the angiogenic properties, non-modified and heparinized collagen specimens were--either loaded with VEGF or non-loaded--subcutaneously implanted on the back of rats. Specimens were explanted after varying periods of implantation, the dry weights and the hemoglobin contents, as well as immunostained histological sections were evaluated: heparinized collagen matrices loaded with VEGF are vascularized to a substantially higher extent as compared to non-modified matrices. 相似文献
99.
100.
An efficient method to generate chromosomal rearrangements by targeted DNA double-strand breaks in Drosophila melanogaster
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Homologous recombination (HR) is an indispensable tool to modify the genome of yeast and mammals. More recently HR is also being used for gene targeting in Drosophila. Here we show that HR can be used efficiently to engineer chromosomal rearrangements such as pericentric and paracentric inversions and translocations in Drosophila. Two chromosomal double-strand breaks (DSBs), introduced by the rare-cutting I-SceI endonuclease on two different mobile elements sharing homologous sequences, are sufficient to promote rearrangements at a frequency of 1% to 4%. Such rearrangements, once generated by HR, can be reverted by Cre recombinase. However, Cre-mediated recombination efficiency drops with increasing distance between recombination sites, unlike HR. We therefore speculate that physical constraints on chromosomal movement are modulated during DSB repair, to facilitate the homology search throughout the genome. 相似文献