全文获取类型
收费全文 | 13388篇 |
免费 | 627篇 |
国内免费 | 77篇 |
专业分类
耳鼻咽喉 | 114篇 |
儿科学 | 248篇 |
妇产科学 | 135篇 |
基础医学 | 1646篇 |
口腔科学 | 233篇 |
临床医学 | 840篇 |
内科学 | 3038篇 |
皮肤病学 | 225篇 |
神经病学 | 1241篇 |
特种医学 | 548篇 |
外科学 | 2583篇 |
综合类 | 39篇 |
现状与发展 | 1篇 |
预防医学 | 439篇 |
眼科学 | 297篇 |
药学 | 974篇 |
中国医学 | 18篇 |
肿瘤学 | 1473篇 |
出版年
2023年 | 93篇 |
2022年 | 182篇 |
2021年 | 271篇 |
2020年 | 163篇 |
2019年 | 225篇 |
2018年 | 301篇 |
2017年 | 233篇 |
2016年 | 342篇 |
2015年 | 319篇 |
2014年 | 408篇 |
2013年 | 473篇 |
2012年 | 759篇 |
2011年 | 828篇 |
2010年 | 509篇 |
2009年 | 434篇 |
2008年 | 752篇 |
2007年 | 813篇 |
2006年 | 785篇 |
2005年 | 762篇 |
2004年 | 769篇 |
2003年 | 693篇 |
2002年 | 704篇 |
2001年 | 257篇 |
2000年 | 270篇 |
1999年 | 269篇 |
1998年 | 189篇 |
1997年 | 142篇 |
1996年 | 138篇 |
1995年 | 122篇 |
1994年 | 110篇 |
1993年 | 89篇 |
1992年 | 201篇 |
1991年 | 163篇 |
1990年 | 140篇 |
1989年 | 128篇 |
1988年 | 132篇 |
1987年 | 106篇 |
1986年 | 99篇 |
1985年 | 98篇 |
1984年 | 66篇 |
1983年 | 48篇 |
1982年 | 45篇 |
1981年 | 45篇 |
1980年 | 29篇 |
1979年 | 50篇 |
1978年 | 38篇 |
1976年 | 28篇 |
1973年 | 27篇 |
1971年 | 27篇 |
1970年 | 32篇 |
排序方式: 共有10000条查询结果,搜索用时 13 毫秒
81.
Kazuko Sukegawa Shunji Tomatsu Toshiyuki Fukao Hideki Iwata Xiang-Qian Song Yukiji Yamada Seiji Fukuda Kouji Isogai Tadao Orii 《Human mutation》1995,6(2):136-143
Mucopolysaccharidosis type II (Hunter disease) is a lysosomal storage disorder caused by a deficiency of the enzyme iduronate-2-sulfatase. Varied clinical phenotypes of this disease have been described. To identify mutations in individual patients and to examine possible correlations between mutations and clinical phenotypes, we analyzed the iduronate-2-sulfatase gene in Japanese patients with different clinical phenotypes. Five missense mutations, S333L (severe), R468Q (severe), R468L (severe), W337R (intermediate), R48P (mild), and three nonsense mutations, W345X (severe), R443X (intermediate), Q531X (mild), were identified by the RT-PCR method. Transient expression in the enzyme-deficient fibroblasts revealed that all five missense mutant enzymes were synthesized as the normal-size precursor (73 kD), and the nonsense mutant enzymes were synthesized as truncated ones (W345X:54 kD, R443X:59 kD, and Q531X:69 kD), although stable mature enzymes (45–56 kD) were not detected by Western blot analysis. Further more, expression of the eight mutant cDNAs resulted in severe reductions of iduronate-2-sulfatase enzyme activity in comparison with a normal cDNA. © 1995 Wiley-Liss, Inc. 相似文献
82.
Liposomes could bind and fuse efficiently to human erythrocytes in the presence of HVJ when they contained gangliosides isolated from human erythrocytes. Sialosylparagloboside, which has a terminal sequence of NeuAcα2?3Ga1β1?4GlcNac, has a much higher receptor activity to the virus than GD1a, GD1b, GT1b, and GT1a, all of which contain the terminal sequence of NeuAcα2?3Galβ1?3GalNAc or NeuAcα2?8NeuAcα2?3Galβ1?3GalNAc. The activity of sialosylparagloboside is comparable to that of glycophorin, a major sialoglycoprotein of human erythrocytes, when compared on the basis of the required amount (as sialic acid) of compounds. The high affinity of sialosylparagloboside to the viral HANA protein is also suggested by the finding that it showed high inhibitory activity against HVJ-mediated binding of glycophorin liposomes to erythrocytes. Sialosylparagloboside was also highly susceptible to the viral sialidase, the other biological function of HANA protein. 相似文献
83.
Fu J Hato M Ohmae H Matsuoka H Kawabata M Tanabe K Miyamoto Y Leafasia JL Chinzei Y Ohta N 《Parasitology research》2000,86(5):345-351
We analyzed the relationships between levels of antibody specific for merozoite surface glycoprotein-1 (MSP1) of Plasmodium falciparum and clinical manifestations in humans. We prepared recombinant MSP1 proteins representing block 3 (M3), block 6 (M6), blocks
1–6 (M1/6), and block 17. When we divided the slide-positive individuals in Guadalcanal into symptomatic and asymptomatic
groups, the former group showed lower IgG levels against M6 and block 17, but not against M3, than did the asymptomatic group
(P < 0.01). The possibility of nonspecific suppression was unlikely, given that the levels of antibody against poliomyelitis
virus observed in the two groups were almost the same. Among the IgG subclasses tested, production of cytophilic IgG3 seemed to be dominant. When we analyzed epitopes recognized by antibodies against block 17, a peptide (SSSNFLGIS) was preferentially
recognized by sera from asymptomatic individuals. These results suggest that clinical symptoms occurring during falciparum
malaria seem to be associated with the development of levels of antibody against particular epitopes on MSP1, which is under
the control of an immunoregulatory mechanism.
Received: 1 October 1999 / Accepted: 21 October 1999 相似文献
84.
Joji Haratake Atsuo Jimi Akio Horie Taizoh Inokuma Masato Ohno 《Pathology international》1984,34(4):925-933
This is a case report of a malignant mesenchymoma of the esophagus in a 50?year-old Japanese man. The tumor was a sessile polypoid mass showing a downward invasion limited to the submucosa of the esophagus. Histologically, the lesion contained rhabdomyosarcomatous and osteosarcomatous areas, in addition to an ill-defined fibrosarcomatous element. In contrast with reports of carcinosarcoma up to the present, this tumor lacked any invasive lesion of an epithelial malignancy. The morphogenesis of these tumor groups was discussed from a hamartoblastomatous standpoint. Acta pathol. jpn. 34: 925~933, 1984. 相似文献
85.
Abeta-degrading endopeptidase,neprilysin, in mouse brain: synaptic and axonal localization inversely correlating with Abeta pathology 总被引:5,自引:0,他引:5
Fukami S Watanabe K Iwata N Haraoka J Lu B Gerard NP Gerard C Fraser P Westaway D St George-Hyslop P Saido TC 《Neuroscience research》2002,43(1):39-56
Metabolism of amyloid-beta peptide (Abeta) is closely associated with the pathology and etiology of Alzheimer's disease (AD). Since neprilysin is the only rate-limiting catabolic peptidase proven by reverse genetics to participate in Abeta metabolism in vivo, we performed detailed immunohistochemical analysis of neprilysin in mouse brain using neprilysin-deficient mice as a negative control. The aim was to assess, at both the cellular and subcellular levels, where Abeta undergoes neprilysin-dependent degradation in the brain and how neprilysin localization relates to Abeta pathology in amyloid precursor protein (APP)-transgenic mice. In hippocampus, neprilysin was present in the stratum pyramidale and stratum lacunosum-moleculare of the CA1-3 fields and the molecular layer of the dentate gyrus. Confocal double immunofluorescence analyses revealed the subcellular localization of neprilysin along axons and at synapses. This observation suggests that after synthesis in the soma, neprilysin, a type II membrane-associated protein, is axonally transported to the terminals, where Abeta degradation is likely to take place. Among various cell types, GABAergic and metabotropic glutamate 2/3 receptor-positive neurons but not catecholaminergic or cholinergic neurons, expressed neprilysin in hippocampus and neocortex, implying the presence of a cell type-specific mechanism that regulates neprilysin gene expression. As expected, Abeta deposition correlated inversely with neprilysin expression in TgCRND8 APP-transgenic mice. These observations not only support the notion that neprilysin functions as a major Abeta-degrading enzyme in the brain but also suggest that down-regulation of neprilysin activity, which may be caused by aging, is likely to elevate local concentrations of Abeta at and around neuronal synapses. 相似文献
86.
Masato Matsuda Mika Sato Hiroki Sakata Takahisa Ogawa Ken-ichiro Yamamoto Taiji Yakushiji Makoto Fukuda Takehiro Miyasaka Kiyotaka Sakai 《Journal of artificial organs》2008,11(3):148-155
When uremic blood flows through dialyzers during hemodialysis, dialysis membrane surfaces are exposed to shear stress and internal filtration, which may affect the surface characteristics of the dialysis membranes. In the present study, we evaluated changes in the characteristics of membrane surfaces caused by shear stress and internal filtration using blood substitutes: water purified by reverse osmosis and 6.7 wt% dextran70 solution. We focused on the levels of a hydrophilic modifier, polyvinylpyrrolidone (PVP), on the membrane surface measured by attenuated total reflectance Fourier transform infrared spectroscopy. Experiments involving 4 h dialysis, 0-144 h shear-stress loading, and 4 h dead-end filtration were performed using polyester-polymer alloy (PEPA) and polysulfone (PS) membranes. After the dialysis experiments with accompanying internal filtration, average PVP retention on the PEPA membrane surface was 93.7% in all areas, whereas that on the PS membrane surface was 98.9% in all areas. After the shear-stress loading experiments, PVP retention on the PEPA membrane surface decreased as shear-stress loading time and the magnitude of shear stress increased. However, with the PS membrane, PVP retention scarcely changed. After the dead-end filtration experiments, PVP retention decreased in all areas for both PEPA and PS membranes, but PVP retention on the PEPA membrane surface was lower than that on the PS membrane surface. PVP on the PEPA membrane surface was eluted by both shear stress and internal filtration, while that on the PS membrane surface was eluted only by internal filtration. 相似文献
87.
Seiko Iwata Yukiko Shibata Jun-ichi Kawada Shinya Hara Yukihiro Nishiyama Tsuneo Morishima Masaru Ihira Tetsushi Yoshikawa Yoshizo Asano Hiroshi Kimura 《Journal of clinical virology》2006,37(2):128-133
BACKGROUND: The loop-mediated isothermal amplification (LAMP) method is a novel technique for the amplification of specific DNA sequences. OBJECTIVES: To establish the LAMP method for amplifying Epstein-Barr virus (EBV) DNA and to examine its reliability for the detection of EBV DNA in clinical specimens. STUDY DESIGN: Sera from 108 patients, who were initially suspected of primary EBV infection, were tested by the EBV LAMP method, and the results were compared with those of the real-time PCR assay. Serological examination was regarded as the standard diagnostic method. RESULTS: To diagnose primary EBV infection, the sensitivity of LAMP was 86.4% and the specificity was 100%. The sensitivity of the real-time PCR assay was 84.1% and the specificity was 98.4%. Longitudinal analysis showed that the detection rate of EBV DNA in serum by the LAMP method decreased with time in accordance with the decrease of the EBV load. EBV DNA could not be detected in serum 40 days after onset of symptoms. CONCLUSIONS: These results indicate that the sensitivity and specificity of the LAMP method are comparable to those of real-time PCR and that detecting EBV DNA in serum by this method is potentially useful for diagnosing primary EBV infection. 相似文献
88.
89.
Komada H Ito M Nishio M Kawano M Ohta H Tsurudome M Kusagawa S O'Brien M Bando H Ito Y 《Medical microbiology and immunology》2000,189(1):1-6
cDNAs encoding human parainfluenza virus type 4B (hPIV-4B) hemagglutinin neuraminidase (HN) protein were cloned and the nucleotide
sequences were determined. A high degree of identity (81.4%) was observed between the nucleotide sequences of hPIV-4A and
-4B HN proteins, and an 87.3% identity was found between the deduced amino acid sequences. This degree of identity is considered
to be greater than immunological similarity between hPIV-4A and -4B HN proteins determined using monoclonal antibodies. To
elucidate the causes of the antigenic difference between HN proteins of hPIV-4A and -4B, we constructed three cDNAs of hPIV-4B
HN whose potential N-glycosylation sites were partially or completely the same as in hPIV-4A HN cDNA. We compared the antigenicity of the expressed
wild-type and mutant proteins, and found that the antigenicities of the mutant hPIV-4B HN proteins were more similar to the
hPIV-4A HN protein than to the non-mutant hPIV-4B HN protein. This study indicated that the antigenic diversity between hPIV-4A
and -4B was partly caused by deletion or creation of glycosylation sites, showing that the point mutations resulting in deletion
or creation of glycosylation sites is one of the initial steps leading to the division of virus into subtypes.
Received: 21 January 2000 相似文献
90.
Mutsuo Furihata Tamotsu Takeuchi Jun Iwata Hiroshi Sonobe Yuji Ohtsuki Akihiko Wakatsuki Nobuyuki Morioka Yusuke Sagara 《Pathology international》1998,48(12):967-973
Primary ovarian angiosarcoma is extremely rare. Only 16 cases have histologicaliy been reported to date In the Ilterature. A case of angiosarcoma arising In the right ovary of a 46-year-old female is presented. Grossly, the resected right ovary was completely replaced by a solid tumor mass, which revealed multiple necrotic and/or hemorrhagic foci. This case revealed the typical histological features of angiosarcoma with sinusoldal and solid patterns of anaplastic tumor cells. Immunohlstochemically, tumor cells were strongly and diffusely positive for CD31 and CD34, in particular, along the cytoplasmic membrane of the tumor cells. Ultrastructurally, tumor cells possessed the intermediate junctions between tumor cells, discontinuous basal laminae attached to the irregularly shaped blood vessels and occasional cytoplasmic pinocytotlc vesicles. These findings confirmed the case as being one of angiosarcoma of the ovary. The patient died 9 months after surgery as a result of developed multlfocal brain metastases. A total of 17 cases reported as primary ovarian anglosarcoma, including this presented case, are clinicopathologically reviewed. 相似文献