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71.
72.
Dominant-Negative Rho, Rac, and Cdc42 Facilitate the Invasion Process of Vibrio parahaemolyticus into Caco-2 Cells
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Yukihiro Akeda Toshio Kodama Takashige Kashimoto Vlademir Cantarelli Yasuhiko Horiguchi Kenichi Nagayama Tetsuya Iida Takeshi Honda 《Infection and immunity》2002,70(2):970-973
To clarify the invasive process of Vibrio parahaemolyticus, an invasion assay was performed using cells expressing dominant negative small GTPases of the Rho family. This assay showed that the dominant negative host phenotype facilitates bacterial invasion, suggesting that the mechanism of V. parahaemolyticus invasion differs from that reported for other invasive bacteria. 相似文献
73.
Toshio Takeuchi Hiroshi Iwasaki Yuko Ohjimi Yasuhiko Kaneko Masako Ishiguro Chikako Fujita Yasusi Mlura Yoshiharu Hiratsuka Kimitaka Sakamoto Masahiro Kikuchi 《Pathology international》1996,46(4):292-297
The cytogenetic and morphologic characteristics of a case with a primitive neuroectodermal tumor (PNET) arising from the left kidney in a 22 year old man are presented. The patient was detected as having a left renal mass with a tumor embolus In the inferior vena cava and multiple pulmonary metastases. A radical nephrectomy with tumor embolectomy of the Inferior vena cava, along with a resection of the pulmonary nodules were performed. Histologic examination revealed a dense proliferation of small round cells with many Homer-Wright type rosettes and perlvascular pseudo-rosettes. Immunohlstochemically, the tumor cells stained strongly positive for HBA71(p30/32M IC2 ), a surface glycopro-teln specific to PNET and Ewlng's sarcoma. In addition, the tumor cells expressed several neural markers (neuron specific enolase, neurofilament, synaptophysin, and Leu-7) and vimentin, while the epithelial, muscular, and lymphocytlc markers were negative in the tumor cells. Cytogenetic analysis of cultured tumor cells showed a reciprocal translocation t(11; 22)(q24; q12) that is considered to be specific to PNET and Ewing's sarcoma. In conclusion, this case suggested that a karyotyping analysis is a useful diagnostic tool for renal PNET, and it may therefore be utilized to help distinguish between difficult cases of small round cell tumors and Wilms' tumor of the kidney. 相似文献
74.
Toshio Nishimura Keizo Tsuruhara Keiko Naito Junko Hirohara Sotokichi Morii 《Pathology international》1989,39(5):281-288
To examine the effect of colchicine on ethionine induced fatty liver, adult female rats were starved overnight and then injected i.p. with 1 g kg ethionine at 11th hour of fasting; then a half of the rats were also injected i.p. with 2.5 mg kg colchicine twice at 3 and 6 h after the single administration of ethionine. Similarly, fasted control rats were injected i.p. with vehicle alone at the above times. All of the rats were sacrificed after a 20 h fast, and the hepatocytes in periportal areas were observed ultra-structurally. In addition, total lipids in the liver tissue were extracted and determined biochemically. Although similar significant increases of triglyceride were observed in the liver tissue of all ethionine-injected rats, the hapatocytes in the group treated with both chemicals had fewer cytoplasmic fat globules (CFG) than those in the group treated with ethionine only. On the other hand, the diameters of markedly increased membrane-bound lipid particles (MLP) in the double treated group were distributed mainly in the range 0.2–0.4 μm, compared with those (0.1-0.2 μm) in the other groups. These findings indicate that colchicine inhibits the development of CFG in ethionine injured hapatocytes. Acta Pathol Jpn 39: 281∼288, 1989. 相似文献
75.
Kazunori Akiyoshi Toshio Masuda Toshinobu Higashimura 《Macromolecular chemistry and physics.》1992,193(3):755-763
Block copolymerizations of 1-chloro-1-octyne (1-ClO) with several substituted acetylenes were examined by means of living polymerization. o-(Trifluoromethyl)phenylacetylene (o-CF3PA), o-(trimethylsilyl)phenylacetylene (o-Me3SiPA), 1-chloro-2-phenylacetylene (1-ClPA), p-butyl-o,o,m,m-tetrafluorophenylacetylene (p-BuF4PA), and tert-butylacetylene (t-BuA) were used as comonomers, and the MoOCl4-n-Bu4Sn-EtOH (mole ratio 1:1:1) catalyst, which is known to effect living polymerization of substituted acetylenes, was employed. When o-CF3PA and 1-CIPA were the comonomers in combination with 1-CIO, block copolymers were exclusively obtained in both orders of monomer addition. In the cases of o-Me3SiPA and p-BuF4PA as comonomers, the copolymerizations initiated from 1-CIO produced block copolymers selectively, whereas the homopolymers of o-Me3SiPA and p-BuF4PA also formed if the order of monomer addition was reversed. The pair of 1-CIO and t-BuA did not selectively yield block copolymers irrespective of the order of monomer addition. Thus, block copolymerization occurred between 1-CIO and monomers that show high “livingness” and close reactivities. 相似文献
76.
Yoko Kamitani Eiji Kajii Toshio Suda Shigenori Ikemoto 《Journal of human genetics》1992,37(4):271-283
Summary In order to examine expression of the Tn antigen on erythroid cells from a patient with Tn syndrome, we applied a selective two phase liquid culture system for human erythroid progenitors in peripheral blood. The cells were analyzed with flow cytometry employing an anti-Tn antibody and a lectin ofVicia villosa which recognizes only the Tn determinant. In the second phase, the Tn antigen was expressed on the cultured cells from the patient on day 3 and Tn-positive cells reached 62.7% on day 9. On the other hand, Tn-positive cells were not detected in the volunteer's cultured cells. When the patient's cells were co-cultured with the cells from a healthy voluteer, the percentage of Tn-positive cells was much lower than the expected value, suggesting that the normal cells suppressed the expression of Tn antigen on the patient's cells. 相似文献
77.
Toshio Shikata 《Pathology international》1967,17(2):191-215
An attempt of pathogenetic analysis of Wilson's disease and Inose's disease, the two most important varieties of hepatocerebral diseases, was made from the facette of the hepatic pathology. The liver changes of a total of 43 human autopsy cases(19 of Wilson's and 24 of Inose's disease) were reevaluated. Concurrently an attempt of experimental production in animals of hepatic lesions compatible with those of Wilson's disease was made. Inose's special type of hepatocerebral disease is divided into two subgroups, a shunt form and a nutritional form. Cerebral damage in the shunt form is attributed to the portal-systemic collaterals, while the clinicopathological survey of the cases with the nutritional form indicates that functional disturbances, related unbalanced diet or endocrine abnormality, seem to cause brain damage. In Wilson's disease, three stages are noted from the analysis of the liver changes; fibrosis or monolobular cirrhosis in the first stage, submassive necrosis or active postnecrotic cirrhosis in the second stage and multilobular cirrhosis or arrested postnecrotic cirrhosis in the third stage. Experimentally, monolobular cirrhosis could be produced in animals by copper administration alone, whereas postnecrotic cirrhosis was first reproduced by a combination of copper administration and low protein diet, anti-kidney serum, or copper nephrosis. It is suggested that for the development of postnecrotic cirrhosis in the second and third stages of Wilson's disease an additional factor other than copper is needed, and that this second factor may be the deficiency of SH- containing aminoacids. 相似文献
78.
The study of the reaction of some methylenebisphenols with chloranil in ethanol and also of a phenol formaldehyde condensate prepared by acid catalysis, reveals that quinone methide is formed in the self-cure of quinoid phenol formaldehyde resin. The quinone methide reacts with ethanol to give an adduct. The structure of the alcohol adduct is identified by NMR and IR data and by means of pyrolysis. 相似文献
79.
Nomura H Nishimori H Yasoshima T Hata F Tanaka H Nakajima F Honma T Araya J Kamiguchi K Isomura H Sato N Denno R Hirata K 《Clinical & experimental metastasis》2002,19(5):391-399
To elucidate the mechanisms of metastasis, we established two sublines HPC-1H5 with a highly liver metastatic cell line and
HPC-1P5a with a highly peritoneal disseminating cell line, which were sequentially selected from the parental pancreatic cancer
cell line HPC-1. Using these three cell lines, we investigated several biological properties and mRNA levels of differentially-expressed
genes involved in cancer metastasis by cDNA macroarray. Microscopic findings for the three cell lines were the same. The tumorigenicity,
in vitro growth ability, motile activity, adhesive activity and the production of IL-8 of metastatic sublines were higher than those
of parental HPC-1 cells. Particularly, HPC-1H5 cells showed clearly higher levels of IL-8 expression and tumors of HPC-1H5
cells grew faster and bigger than those of HPC-1P5a cells. In cDNA macroarray analysis of HPC-1H5 cells, 22 genes were up-regulated
and 44 genes were down-regulated compared with parental HPC-1 cells. In HPC-1P5a cells, 9 genes were up-regulated and 28 genes
were down-regulated compared with parental HPC-1 cells. This study provides a demonstration of global gene expression analysis
of pancreatic cancer cells with liver metastasis and peritoneal dissemination. Furthermore, our results provide a new insight
into the study of liver metastasis and peritoneal dissemination of human pancreatic cancer.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
80.
Jo EK Wang Y Kanegane H Futatani T Song CH Park JK Kim JS Kim DS Ahn KM Lee SI Park HJ Hahn YS Lee JH Miyawaki T 《Journal of human genetics》2003,48(6):322-326
Mutations in the Bruton's tyrosine kinase (BTK) gene are responsible for X-linked agammaglobulinemia (XLA). We identified BTK mutations in six patients with presumed XLA from unrelated Korean families. Four out of six mutations were novel: two missense
mutations (P565T, C154Y), a point mutation in a splicing donor site (IVS11+1G>A), and a large deletion (a 6.1-kb deletion
including BTK exons 11–18). The large deletion, identified by long-distance PCR, revealed Alu-Alu mediated recombination extended from an Alu sequence in intron 10 to another Alu sequence in intron 18, spanning a distance of 6.1 kb. The two known mutations consisted of one missense (G462D) mutation,
and a point mutation in a splicing acceptor site (IVS7−9A>G). This study suggests that large genomic rearrangements involving Alu repeats are few but an important component of the spectrum of BTK mutations. 相似文献