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T Yamane T Inoue Y Furukawa Y Yasui K Ota Y Nakao H Ohira K Tanaka T Hasuike M Hirai 《Rinsho byori. The Japanese journal of clinical pathology》1991,39(12):1347-1350
CD56 antigen (detected by NKH-1) is distributed on NK cells, monocytes, and ectodermal neural cells. In this study, the blasts of 29.2% of 27 patients with acute nonlymphocytic leukemia (ANLL) expressed CD56 antigen, but not CD16, CD2, or CD3 antigen. Leukemic cells isolated from 3 patients with CD56-positive ANLL did not have NK activity. There were no significant differences between CD56-positive and CD56-negative ANLL in CD13-positive cases, CD33-positive cases, and HLA-DR-positive cases. These results suggest that CD56-positive ANLL could be so-called mixed-lineage leukemia (lymphoid-associated antigen in ANLL). 相似文献
64.
Mizuki N Ota M Katsuyama Y Yabuki K Ando H Yoshida M Onari K Nikbin B Davatchi F Chams H Ghaderi AA Ohno S Inoko H 《Tissue antigens》2001,57(5):457-462
It is well known that Beh?et's disease (BD) is strongly associated with human leukocyte antigen (HLA) B51 in many ethnic groups. However, there has been no published report as yet with respect to this association among the Iranian people. Furthermore, since it is now known that the B51 antigen can be encoded by 21 alleles, B*5101-B*5121, we performed HLA-B*51 allele typing as well as HLA class I genotyping of 48 Iranian patients with this disease. As a result, the frequency of the B*51 allele was significantly higher (62.1%) in the patient group as compared with the ethnically matched control group (31.8%) (Pc=0.067, R.R.=3.51). In the genotyping of B*51 alleles, 33 out of the 36 B*51-positive patients possessed B*5101 and the remaining 3 carried B*5108. This study revealed that Iranian patients with BD also had a strong association with HLA-B51. In addition, this significantly high incidence of HLA-B*51 was found to be caused by an increase in both the HLA-B*5101 and HLA-B*5108 alleles. However, there was no significant difference in the HLA-B*51 allelic distribution between the patient and control groups. 相似文献
65.
A common Ile796Val polymorphism of the human SREBP cleavage-activating protein (SCAP) gene 总被引:3,自引:0,他引:3
We identified a new common amino acid polymorphism of isoleucine/valine at codon 796 in exon 16 of the gene for human sterol
regulatory element binding protein (SREBP) cleavage-activating protein (SCAP), a central regulator of lipid synthesis and
metabolism in animal cells. It can be detected as an MslI restriction fragment length polymorphism. The allelic frequencies were: isoleucine (A) allele, 0.57 and valine (G) allele,
0.43. This polymorphism may be useful for genetic studies of disorders affecting intracellular lipid metabolism and hyperlipidemia.
Received: August 17, 1999 / Accepted: August 19, 1999 相似文献
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Kera J Mizuki N Ota M Katsuyama Y Pivetti-Pezzi P Ohno S Inoko H 《Tissue antigens》1999,54(6):565-571
Beh?et's disease has been known to be strongly associated with human leukocyte antigen (HLA) B51, one of the split antigens of HLA-B5. An increased incidence of HLA-B51 in the patient group has also been reported in an Italian population. Since the B51 antigen has been recently identified to comprise nine alleles, B*5101-B*5109, we performed HLA-B51 allele genotyping by the polymerase chain reaction-sequencing based typing (PCR-SBT) method as well as serological HLA-A and -B typing among 21 Italian patients with Beh?et's disease in order to investigate whether there is any correlation of one particular B51-associated allele with Behcet's disease. In addition, HLA class II genotyping was performed by the PCR-restriction fragment length polymorphism (RFLP) method. As a result, only the phenotype frequency of the B51 antigen was found to be significantly increased in the patient group as compared to the ethnically matched control group by the corrected P-value analysis (71.4% in patients vs. 17.9% in controls; chi2 = 14.26, Pc = 0.0042, R.R. = 11.5). In the B51 allele genotyping, 11 out of 15 B51-positive patients were B*5101 and the remaining four were B*5108, whereas all of 5 normal controls were B*5101, showing significant association of each allele with Beh?et's disease. No significant difference was observed between the patient and control groups in the HLA class II allelic distribution. This study revealed a strong association of Beh?et's disease in Italian with B*5108 as well as B*5101, providing important insight into the molecular mechanism underlying an HLA association with Beh?et's disease. 相似文献
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Surface films formed on titanium specimens immersed in electrolyte solutions (pH 4.5, 5.2, 7.4) at 37 degrees C for 1 h, 1 d, 30 d, and/or 60 d, were characterized using X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared reflection absorption spectroscopy (FTIR-RAS) to understand the reaction between titanium and inorganic ions. For comparison, the surface of Ti-6AI-4V and Ti-50Ni were also characterized. XPS data revealed that calcium phosphates were naturally formed on these specimens. In particular, compared with the calcium phosphates formed on the titanium alloys, the calcium phosphate formed on titanium immersed for 30 d in the solution with pH 7.4 was more like hydroxyapatite. The compositions of the calcium phosphates formed on the specimens changed with the immersion time and the pH value of the solution. The spectrum obtained using FTIR-RAS from titanium immersed in the solution with pH 7.4 for 60 d was similar to that obtained from carbonate-containing hydroxyapatite. The results indicate that a calcium phosphate similar to apatite is naturally formed on titanium in a neutral electrolyte solution in 30 d. In regard to titanium being a biomaterial, we found this to be an intriguing property. It is possible that this calcium phosphate is responsible for the resulting biocompatibility of titanium. 相似文献
70.
Umemura T Yoshizawa K Ota M Katsuyama Y Inada H Tanaka E Kiyosawa K 《Clinical and experimental immunology》2000,121(1):120-126
Many T cells infiltrate into the liver of patients with chronic hepatitis C (CH-C). They are believed to play a crucial role in the immunopathogenesis of hepatic inflammation, but their clonality and specificity are unknown. The aim of this study was to clarify the characteristics of these T cells. We analysed the complementarity-determining region (CDR)3 size lengths of T cell receptor (TCR) beta-chains by size spectratyping, and determined the sequences of Vbeta CDR3 after subcloning Vbeta-specific polymerase chain reaction products. Spectratyping showed clonal expansions in all liver specimens, most of which showed more than two T cell clones. Moreover, many non-clonal T cells also accumulated in the liver. Clonality of the T cells suspected by spectratyping was confirmed by CDR3 sequencing. Although the sequences revealed no whole CDR3-shared clones among different patients, some common motif sequences were observed. Our data suggest that T cells are stimulated by several hepatitis C virus (HCV) epitopes, then accumulate in the liver of CH-C patients. Shared motifs of expanded T cell clones suggest that they might recognize the same regions of HCV peptides, but have differences due to HCV peptide mutational changes. These clones might also interact with non-clonal T cells and play a crucial role in the immunopathogenesis of CH-C. 相似文献