全文获取类型
收费全文 | 15344篇 |
免费 | 1512篇 |
国内免费 | 1185篇 |
专业分类
耳鼻咽喉 | 81篇 |
儿科学 | 207篇 |
妇产科学 | 179篇 |
基础医学 | 1855篇 |
口腔科学 | 285篇 |
临床医学 | 2172篇 |
内科学 | 2415篇 |
皮肤病学 | 154篇 |
神经病学 | 873篇 |
特种医学 | 661篇 |
外国民族医学 | 13篇 |
外科学 | 1297篇 |
综合类 | 2613篇 |
现状与发展 | 4篇 |
一般理论 | 3篇 |
预防医学 | 915篇 |
眼科学 | 376篇 |
药学 | 1579篇 |
20篇 | |
中国医学 | 971篇 |
肿瘤学 | 1368篇 |
出版年
2024年 | 44篇 |
2023年 | 250篇 |
2022年 | 640篇 |
2021年 | 829篇 |
2020年 | 602篇 |
2019年 | 564篇 |
2018年 | 592篇 |
2017年 | 520篇 |
2016年 | 462篇 |
2015年 | 704篇 |
2014年 | 897篇 |
2013年 | 751篇 |
2012年 | 1085篇 |
2011年 | 1222篇 |
2010年 | 791篇 |
2009年 | 621篇 |
2008年 | 837篇 |
2007年 | 753篇 |
2006年 | 758篇 |
2005年 | 749篇 |
2004年 | 524篇 |
2003年 | 497篇 |
2002年 | 427篇 |
2001年 | 354篇 |
2000年 | 377篇 |
1999年 | 351篇 |
1998年 | 228篇 |
1997年 | 238篇 |
1996年 | 214篇 |
1995年 | 181篇 |
1994年 | 157篇 |
1993年 | 120篇 |
1992年 | 111篇 |
1991年 | 71篇 |
1990年 | 93篇 |
1989年 | 71篇 |
1988年 | 51篇 |
1987年 | 59篇 |
1986年 | 41篇 |
1985年 | 47篇 |
1984年 | 33篇 |
1983年 | 29篇 |
1982年 | 14篇 |
1981年 | 11篇 |
1980年 | 5篇 |
1978年 | 8篇 |
1976年 | 5篇 |
1975年 | 10篇 |
1973年 | 8篇 |
1968年 | 6篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
91.
左心室局部心肌梗塞时的组分式模型及计算机仿真 总被引:1,自引:0,他引:1
为研究左心室局部心肌梗塞时心肌各部分的能量供需状况及心脏辅助装置对改善心肌能量供给的影响,我们建立了一个由左心室正常区域心肌和梗塞区域心肌两部分组成的组分式模型,我们的模型以Sunagawa的模型为基础,并在此基础上加以扩展,与Sunagawa的模型相比,我们的模型允许梗塞区域心肌的收缩性在一定范围内变化,从而可以模拟各种不同范围和不同程度的梗塞情况。用建立好的左心室组分式模型取代我们原有的狗的心 相似文献
92.
基于人膝关节的解剖特征,在文献[3]的基础上,引入了股骨髌骨关节,从而建立了一个完整的人膝关节在矢状面内运动的咬合数学模型。该模型包含了运动膝关节股骨与胫骨间及股骨与髌骨间的咬合滚动和咬合滑动。此模型可用来建立人腿的生物动力模型 相似文献
93.
蝎蜂毒肽对大鼠纤溶系统作用初探 总被引:14,自引:0,他引:14
本研究采用大鼠肢体血管灌流和整体给药两种模型,观察蝎蜂毒(SBP)对血管理灌流液内纤溶酶原激活物(PA)活性、血浆优球蛋白纤溶性(EFA)和纤溶酶(PL)活性的影响。结果说明,SBP有明显激活纤溶系统作用;其机制可能涉及血管内皮细胞释放PA活性增加,进一步促使纤溶酶原活化为PL增多的途径。 相似文献
94.
Tong Chen Hao Bai Ying Shao Melanie Arzigian Viktor Janzen Eyal Attar Yi Xie David T Scadden Zack Z Wang 《Stem cells (Dayton, Ohio)》2007,25(2):392-401
The molecular mechanisms that regulate human blood vessel formation during early development are largely unknown. Here we used human ESCs (hESCs) as an in vitro model to explore early human vasculogenesis. We demonstrated that stromal cell-derived factor-1 (SDF-1) and CXCR4 were expressed concurrently with hESC-derived embryonic endothelial differentiation. Human ESC-derived embryonic endothelial cells underwent dose-dependent chemotaxis to SDF-1, which enhanced vascular network formation in Matrigel. Blocking of CXCR4 signaling abolished capillary-like structures induced by SDF-1. Inhibition of the SDF-1/CXCR4 signaling pathway by AMD3100, a CXCR4 antagonist, disrupted the endothelial sprouting outgrowth from human embryoid bodies, suggesting that the SDF-1/CXCR4 axis plays a critical role in regulating initial vessel formation, and may function as a morphogen during human embryonic vascular development. 相似文献
95.
下胫腓联合分离内固定术式的生物力学研究 总被引:2,自引:0,他引:2
目的 探讨下胫腓联合分离采用新型内固定术式———下胫腓钩板固定器 (Hook -platefixation ,HPF)的生物力学特性 ,与螺钉、钢板和带钩固定器三种内固定方式比较 ,为临床提供科学依据。方法 采用新鲜成人尸体足标本 6具 ,运用生物力学实验应力分析方法和压敏片技术 ,测量不同内固定术式的远端胫腓骨强度、应变、负重面积、接触应力和足弓承载能力及踝关节稳定性的变化。结果 新型下胫腓钩板固定器内固定术式无论在胫腓骨强度和刚度、负重面积、接触压力、足弓的变形、移位强度和刚度、承载能力以及踝关节的稳定性方面均优于其它三种内固定术式 ,具有显著性差异 (P <0 .0 1)。结论 实验结果表明 ,采用下胫腓钩板固定器 (HPF) ,既有利于提高生物力学性能 ,又有利于改善踝关节的稳定性 ,与传统手术方式相比可减少一次手术 ,避免了断钉等并发症 ,且能有效地提高足部承载能力 ,是下胫腓联合分离内固定的一种优良术式 相似文献
96.
不同转移特性瘤细胞系的筛选及其生物学特性 总被引:1,自引:0,他引:1
目的:探讨与肿瘤转移相关的某些生物学特性。方法:将小鼠乳腺癌Ca761-FP8/L和Ca761-FL10/L经体内筛选得到细胞系Ca761-P5B和Ca761=L6B,并观察其瘤细胞与凝集反应、靶器官组织条件培养基对瘤细胞真挚化作用等,结果:Ca761-P5B具有高肺转移、低淋巴结转移特性,Ca761-L5B具有低肺、低淋巴结转移特性。两个瘤细胞系的细胞表面的糖基表达,对条件培养的趋化反应不同。结 相似文献
97.
Thioredoxin suppresses 1-methyl-4-phenylpyridinium-induced neurotoxicity in rat PC12 cells 总被引:7,自引:0,他引:7
Thioredoxin (TRX) is a redox-active protein which plays a cytoprotective role against oxidative stress. Geranylgeranylacetone (GGA), used widely as an anti-ulcer drug, has been reported to induce TRX as well as heat shock protein 70 (HSP70) in hepatocytes and other cells. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), causes dopaminergic denervation and Parkinsonism in humans. The 1-methyl-4-phenylpyridinium ion (MPP(+)), an active metabolite of MPTP, induces cell death in a rat pheochromocytoma cell line (PC12 cells). We found that MPP(+) suppresses TRX expression in PC12 cells. Overexpression or administration of TRX attenuates MPP(+)-induced neurotoxicity on PC12 cells. Moreover, GGA induces expression of TRX and HSP70 and attenuates MPP(+)-induced toxicity in PC12 cells. These results indicate that TRX and GGA have a possible potential as new therapeutic agents for Parkinson disease. 相似文献
98.
Development of hatching blastocysts from immature human oocytes following in-vitro maturation and fertilization using a co-culture system 总被引:8,自引:0,他引:8
Hwu YM; Lee RK; Chen CP; Su JT; Chen YW; Lin SP 《Human reproduction (Oxford, England)》1998,13(7):1916-1921
Recently, in-vitro maturation (IVM) of immature human oocytes recovered
from non-stimulated follicles has been applied in the treatment of
infertility. However, in previous reports, very few embryos cultured in
conventional medium have reached the expanded blastocyst stage following
in-vitro maturation and fertilization (IVM/IVF). The objective of this
study was to investigate whether the developmental competence of human
embryos following IVM/IVF could be enhanced by the use of a human ampullary
cell co-culture system. Immature human oocytes were aspirated from small
follicles at Caesarean section and then cultured in medium containing human
menopausal gonadotrophin for 36 to 48 h, followed by insemination. Zygotes
were randomly cultured either in conventional culture medium alone or in
the co-culture system. Of 48 embryos cultured in conventional medium alone,
all arrested at the 2-16- cell stage on day 3 after insemination. Of 46
embryos cultured in the co-culture system, 26 embryos (56.5%) arrested at
the 2-16-cell stage. Six embryos (13%) developed to the morula stage.
Fourteen embryos (30.4%) developed to expanded blastocysts and two
blastocysts were hatching on day 7 after insemination. We conclude that
co-culture significantly enhances the development of blastocysts in embryos
resulting from IVM/IVF.
相似文献
99.
Functional tyrosine kinase inhibitor profiling: a generally applicable method points to a novel role of platelet-derived growth factor receptor-beta in tuberous sclerosis 总被引:1,自引:0,他引:1
下载免费PDF全文
![点击此处可从《The American journal of pathology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Arbiser JL Govindarajan B Bai X Onda H Kazlauskas A Lim SD Amin MB Claesson-Welsh L 《The American journal of pathology》2002,161(3):781-786
A ubiquitous herpesvirus that establishes life-long infection, the Epstein-Barr virus (EBV) has yielded little insight into how a single agent in general accord with its host can produce diverse pathologies ranging from oral hairy leukoplakia to nasopharyngeal carcinoma, from infectious mononucleosis to Hodgkin's disease (HD) and Burkitt's lymphoma. Its pathogenesis is further confounded by the less than total association of virus with histologically similar tumors. In other viral systems, defective (interfering) viral genomes are known to modulate outcome of infection, with either ameliorating or intensifying effects on disease processes initiated by prototype strains. To ascertain whether defective EBV genomes are present in HD, we examined paraffin-embedded tissue from 56 HD cases whose EBV status was first determined by cytohybridization for nonpolyadenylated EBV RNAs (EBERs). Using both standard polymerase chain reaction (PCR) and PCR in situ hybridization, we successfully amplified sequences that span abnormally juxtaposed BamHI W and Z fragments characteristic of defective heterogeneous (het) EBV DNA from 10 of 32 (31%) EBER-positive tumors. Of 24 EBER-negative HD, 8 yielded PCR products indicating presence of het EBV DNA. Two of these contained defective EBV in the apparent absence of the prototype virus. Of the 42 tumors analyzed for defective EBV by both PCR techniques, there was concordance of results in 38 (90%). Detection of defective EBV genomes with the potential to disrupt viral gene regulation suggests one mechanism for pathogenic diversity that may also account for loss of prototypic EBV from individual tumor cells. 相似文献
100.
Converging collimation increases the geometric efficiency for imaging small organs, such as the heart, but also increases the difficulty of correcting for the physical effects of attenuation, geometric response and scatter in SPECT. In this paper, 3D first-order Compton scatter in non-uniform scattering media is modelled by using an efficient slice by-slice incremental blurring technique in both parallel and converging beam SPECT. The scatter projections are generated by first forming an effective scatter source image (ESSI), then forward-projecting the ESSI. The Compton scatter cross section described by the Klein-Nishina formula is used to obtain spatial scatter response functions (SSRFs) of scattering slices which are parallel to the detector surface. Two SSRFs of neighbouring scattering slices are used to compute two small orthogonal 1D blurring kernels used for the incremental blurring from the slice which is further from the detector surface to the slice which is closer to the detector surface. First-order Compton scatter point response functions (SPRFs) obtained using the proposed model agree well with those of Monte Carlo (MC) simulations for both parallel and fan beam SPECT. Image reconstruction in fan beam SPECT MC simulation studies shows increased left ventricle myocardium-to-chamber contrast (LV contrast) and slightly improved image resolution when performing scatter compensation using the proposed model. Physical torso phantom fan beam SPECT experiments show increased myocardial uniformity and image resolution as well as increased LV contrast. The proposed method efficiently models the 3D first-order Compton scatter effect in parallel and converging beam SPECT. 相似文献