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991.
Pedro M. Anastácio Miriam P. Ferreira Filipe Banha César Capinha João E. Rabaça 《Aquatic Ecology》2014,48(1):1-10
Human transport and active dispersal of the red swamp crayfish (Procambarus clarkii) contribute to its rapid spread. However, some small aquatic organisms can be transported by birds. We made two hypotheses related to waterbird-mediated passive dispersal of juvenile crayfish. The first is that, depending on water depth, recently hatched crayfish can attach to ducks, initiating passive external transport (i.e., ectozoochory). The second is that recently hatched crayfish can survive bird flight, being affected by crayfish features, flight distance, and environmental conditions. A first experiment tested the attachment of juvenile crayfish to ducks at different water depths by using a freshly dead duck and tanks with crayfish. Another set of three experiments tested crayfish survival during air transportation. To simulate bird flight, we first used a vehicle moving at bird flight speed, and we then used trained pigeons. Several flight distances, environmental conditions, and crayfish sizes were tested. Our results showed that juvenile crayfish were capable of clinging to duck feathers and were transported when ducks were removed from the water. Furthermore, some juveniles of P. clarkii were able to survive long-distance transport when suspended outside a moving vehicle or when transported by birds. The probability of success was affected by water depth, crayfish size, distance travelled, and relative humidity. Our results support the occurrence of passive transportation of this invader by means of attachment to birds. These findings indicate that waterbird-mediated passive dispersal should be taken into account to explain P. clarkii’s rapid spread and should be considered when managing its invasions. 相似文献
992.
993.
Rafael Luiz Pereira Raphael José Ferreira Felizardo Marcos Ant?nio Cenedeze Meire Ioshie Hiyane ênio José Bassi Mariane Tami Amano Clarice Sylvia Taemi Origassa Reinaldo Correia Silva Cristhiane Fávero Aguiar Sylvia Mendes Carneiro Jo?o Bosco Pesquero Ronaldo Carvalho Araújo Alexandre de Castro Keller Renato C. Monteiro Ivan Cruz Moura Alvaro Pacheco-Silva Niels Olsen Saraiva Camara 《Disease models & mechanisms》2014,7(6):701-710
Focal and segmental glomerulosclerosis (FSGS) is one of the most important renal diseases related to end-stage renal failure. Bradykinin has been implicated in the pathogenesis of renal inflammation, whereas the role of its receptor 2 (B2RBK; also known as BDKRB2) in FSGS has not been studied. FSGS was induced in wild-type and B2RBK-knockout mice by a single intravenous injection of Adriamycin (ADM). In order to further modulate the kinin receptors, the animals were also treated with the B2RBK antagonist HOE-140 and the B1RBK antagonist DALBK. Here, we show that the blockage of B2RBK with HOE-140 protects mice from the development of FSGS, including podocyte foot process effacement and the re-establishment of slit-diaphragm-related proteins. However, B2RBK-knockout mice were not protected from FSGS. These opposite results were due to B1RBK expression. B1RBK was upregulated after the injection of ADM and this upregulation was exacerbated in B2RBK-knockout animals. Furthermore, treatment with HOE-140 downregulated the B1RBK receptor. The blockage of B1RBK in B2RBK-knockout animals promoted FSGS regression, with a less-inflammatory phenotype. These results indicate a deleterious role of both kinin receptors in an FSGS model and suggest a possible cross-talk between them in the progression of disease.KEY WORDS: Focal and segmental glomerulosclerosis, Bradykinin receptors, Inflammation, Podocyte, Fibrosis 相似文献
994.
995.
Li Ping Chung Svetlana Baltic Manuel Ferreira Suzanna Temple Grant Waterer Philip J. Thompson 《PloS one》2014,9(4)
Background
β2 adrenergic receptor (ADRβ2) polymorphisms including ADRβ2+46G>A have been reported to cause adverse outcomes in mild asthmatics. The extent to which ADRβ2 polymorphisms and in particular their haplotypes contribute to severe asthma is unknown.Objective
To determine the association of ADRβ2 polymorphisms and haplotypes with asthma severity.Methods
Caucasians (n = 2979) were genotyped for 11 ADRβ2 polymorphisms. The cohort (mean age 39.6, 60% female) included 2296 non-asthmatics, 386 mild asthmatics, 172 moderate asthmatics and 125 severe asthmatics. Haplotype frequency and haplotype pair for each subject was determined using the PHASE algorithm.Results
The three asthmatic cohorts were comparable in age and gender but were distinguishable from each other in terms of symptoms, spirometry, medication use and health care utilisation (p <0.001). None of the polymorphisms showed a genotypic or allelic association with asthma diagnosis or severity. Nine haplotypes were identified and no association was found with asthma diagnosis or severity per se. Haplotype pair 2/4 was associated with asthma severity (Trend Test, OR 1.42, p = 0.0008) but not with asthma per se. Prevalence of haplotype pair 2/2 appeared to decrease with asthma severity (Trend Test, OR 0.78, p = 0.067). Two new haplotypes were identified, occurring exclusively in asthmatics at a frequency of ≥ 1%. In addition, a positive association between carriage of ADRβ2 +523*C and increased risk of atopy was discovered.Conclusions
ADRβ2 haplotype pair 2/4 is associated with severe asthma and is consistent with findings of poor bronchodilator response in mild asthmatics who are also haplotype 2/4. 相似文献996.
997.
998.
Cintia Ferreira Marinho Elzinandes Leal Azeredo Amanda Torrentes-Carvalho Alessandro Marins-Dos-Santos Claire Fernandes Kubelka Luiz José de Souza Rivaldo Venancio Cunha Luzia Maria de-Oliveira-Pinto 《PloS one》2014,9(7)
In dengue virus (DENV) infection, complement system (CS) activation appears to have protective and pathogenic effects. In severe dengue fever (DF), the levels of DENV non-structural-1 protein and of the products of complement activation, including C3a, C5a and SC5b-9, are higher before vascular leakage occurs, supporting the hypothesis that complement activation contributes to unfavourable outcomes. The clinical manifestations of DF range from asymptomatic to severe and even fatal. Here, we aimed to characterise CS by their receptors or activation product, in vivo in DF patients and in vitro by DENV-2 stimulation on monocytes. In comparison with healthy controls, DF patients showed lower expression of CR3 (CD11b), CR4 (CD11c) and, CD59 on monocytes. The DF patients who were high producers of SC5b-9 were also those that showed more pronounced bleeding or vascular leakage. Those findings encouraged us to investigate the role of CS in vitro, using monocytes isolated from healthy subjects. Prior blocking with CR3 alone (CD11b) or CR3 (CD11b/CD18) reduced viral infection, as quantified by the levels of intracellular viral antigen expression and soluble DENV non-structural viral protein. However, we found that CR3 alone (CD11b) or CR3 (CD11b/CD18) blocking did not influence major histocompatibility complex presentation neither active caspase-1 on monocytes, thus probably ruling out inflammasome-related mechanisms. Although it did impair the secretion of tumour necrosis factor alpha and interferon alpha. Our data provide strategies of blocking CR3 (CD11b) pathways could have implications for the treatment of viral infection by antiviral-related mechanisms. 相似文献
999.
Renata A. O. Castro Neila M. Silva-Barcellos Carolina S. A. Licio Janine B. Souza Míriam C. Souza-Testasicca Flávia M. Ferreira Mauricio A. Batista Denise Silveira-Lemos Sandra L. Moura Frédéric Frézard Simone A. Rezende 《PloS one》2014,9(8)
Background:
Visceral leishmaniasis (VL) is a chronic debilitating disease endemic in tropical and subtropical areas, caused by protozoan parasites of the genus Leishmania. Annually, it is estimated the occurrence of 0.2 to 0.4 million new cases of the disease worldwide. Considering the lack of an effective vaccine the afflicted population must rely on both, an accurate diagnosis and successful treatment to combat the disease. Here we propose to evaluate the efficacy of trivalent antimonial encapsulated in conventional liposomes, in association with ascorbic acid, by monitoring its toxicity and efficacy in BALB/c mice infected with Leishmania infantum.Methodology/Principal Findings:
Infected mice were subjected to single-dose treatments consisting in the administration of either free or liposome-encapsulated trivalent antimony (SbIII), in association or not with ascorbic acid. Parasite burden was assessed in the liver, spleen and bone marrow using the serial limiting dilution technique. After treatment, tissue alterations were examined by histopathology of liver, heart and kidney and confirmed by serum levels of classic biomarkers. The phenotypic profile of splenocytes was also investigated by flow cytometry. Treatment with liposome-encapsulated SbIII significantly reduced the parasite burden in the liver, spleen and bone marrow. Co-administration of ascorbic acid, with either free SbIII or its liposomal form, did not interfere with its leishmanicidal activity and promoted reduced toxicity particularly to the kidney and liver tissues.Conclusions/Significance:
Among the evaluated posological regimens treatment of L. infantum-infected mice with liposomal SbIII, in association with ascorbic acid, represented the best alternative as judged by its high leishmanicidal activity and absence of detectable toxic effects. Of particular importance, reduction of parasite burden in the bone marrow attested to the ability of SbIII-carrying liposomes to efficiently reach this body compartment. 相似文献1000.
Kennio Ferreira-Paim Thatiana Bragine Ferreira Leonardo Andrade-Silva Delio Jose Mora Deborah J. Springer Joseph Heitman Fernanda Machado Fonseca Dulcilena Matos Márcia Souza Carvalho Melhem Mario León Silva-Vergara 《PloS one》2014,9(9)