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81.
82.
F. G. Toback M.D. Ph.D. S. Kartha M. M. Walsh-Reitz 《Journal of molecular medicine (Berlin, Germany)》1993,71(10):861-866
Conclusion The mechanisms that regulate regeneration of kidney epithelial cells after acute tubular necrosis are poorly understood. Repair of the nephron can take place in the adverse systemic metabolic setting caused by failure of renal function. This clinical observation suggests that factors released at the site of the tubular insult can mediate repair. Studies carried out in this and other laboratories show that kidney epithelial cells can release and respond to polypeptide growth factors which may thereby contribute to renal regeneration by autocrine and paracrine mechanisms. Specific growth factors secreted by cells and deposited in the tubular basement membrane prior to injury may subsequently participate in nephron repair. In addition, adenine nucleotides released from injured or dying cells at the injury site or provided exogenously could stimulate surviving renal epithelial cells at the edges of the wound to migrate along the basement membrane to rapidly reepithelialize the nephron and subsequently initiate mitogenesis to replace cells lost by necrosis.The nephrotoxic effect of many agents used in cancer chemotherapy and the older age of patients undergoing complicated surgical procedures has increased the incidence of ARF, whereas the mortality rate has not changed since the early 1950s [22]. Thus there is considerable need for innovative therapeutic strategies. An important goal of future research efforts is to identify new growth factors that facilitate migration, differentiation, and proliferation of renal epithelial cells at sites of tubular necrosis. Isolation and use of these agents in combination with dialysis and nutritional support could speed renal regeneration and thereby improve the outcome in patients with this condition.Abbreviations ARF
acute renal failure
- ECM
extracellular matrix
- EGF
epidermal growth factor
- FGF
fibroblast growth factor
- IGF
insulin-like growth factor
- MGSA
melanocyte growth-stimulating activity
- PDGF
platelet-derived growth factor
- IGF
transforming growth factor 相似文献
83.
84.
用体外培养的人的伪表皮作为模型,进行药物毒理学作用的研究,观察了二甲亚砜(DMSO)在不同浓度和不同接触时间条件下,对人的伪表皮细胞脱氧核糖核酸(DNA)、核糖核酸(RNA)和蛋白质合成的影响:随着接触时间的延长,DNA、RNA和蛋白质合成均受抑制。低浓度条件下(1%),DNA、RNA和蛋白质合成增加;在15~50%浓度下,DNA和蛋白质合成抑制,而RNA合成仍增加;在高浓度条件下(70%~100%),DNA、RNA和蛋白质合成均明显抑制。 相似文献
85.
本研究采用先进的三维超声成像技术及多普勒技术对正常育龄妇女月经周期中心血管功能进行研究。结果:月经周期中HR、BP无变化;血清E2是周期性变化,排卵前达高峰。SV、CO、EF在排卵前期升高达峰值,显著高于月经期和黄体期;SVR排卵前期最低,而Ved、Ves无变化。Vmax、A、E在内源性E2高峰时明显加快,而E/A比值无明显变化。结果提示:月经周期中随内源性E2的周期性变化,心脏功能也发生周期性变化。E2高峰时,心输出量、心搏量和射血分数达最高。外周阻力最低,心脏内血流速度加快。 相似文献
86.
Kyung Bok Lee Jong Sig Kim Sang Tae Kwak Wonbo Sim Jong Hwan Kwak Yeong Shik Kim 《Archives of pharmacal research》1998,21(5):555-558
Chondroitin sulfates were isolated from the mud snail. For the quantitative analysis of enzymatic digestion products of isolated
chondroitin sulfates, strong anion exchange-high performance liquid chromatography (SAX-HPLC) was performed. By the action
of chondroitinase ABC, three unsaturated disaccharides 2-acetamide-2-deoxy-3-O-(β-D-gluco-4-enepyranosyluronic acid)-D-galactose (ΔDi-OS), 2-acetamide-2-deoxy-3-O-(β-D-gluco-4-enepyranosyluronic acid)-6-O-sulfo-D-galactose (ΔDi-6S) and 2-acetamide-2-deoxy-3-O-(β-D-gluco-4-enepyranosyluronic acid)-4-O-sulfo-D-galactose (ΔDi-4S) were produced from the mud snail chondroitin sulfates. The analysis showed that relative proportion
of ΔDi-OS/ΔDi-6S/ΔDi-4S was 58.7/3.1/38.2. The immunomodulating activity of chondroitin sulfate was examined by cell proliferation
assay and these results suggest that it might be a immunosuppressant. 相似文献
87.
Morphologic characterization of osteoblast-like cell cultures isolated from newborn rat calvaria 总被引:4,自引:0,他引:4
Dominique Masquelier Béatrice Herbert Nadine Hauser Pascal Mermillod Edgard Schonne Claude Remacle Ph.D. 《Calcified tissue international》1990,47(2):92-104
Summary Two methods for harvesting osteoblast-like cell populations from newborn (10 days) rat calvaria were compared. The first one
consisted in culturing the periosteum-free bones and then trypsinizing the cells on the bone surface. The second one involved
the migration of the osteoblasts on glass fragments before trypsinization. Since the plating efficiency, the proportion of
alkaline phosphatase-positive cells, the population doubling time, and the calcium deposition were more adequate, the second
method was used to further characterize the behavior of the cultures. During the first week of culture, the cells featured
shapes similar to those observedin vivo on the surface of periosteum-free calvaria. They formed multilayers and, in the presence of ascorbic acid, synthetized an
organic matrix containing exclusively type I collagen. Later, small amounts of type III collagen appeared. The cells were
embedded in the matrix and progressively acquired the morphologic phenotype of osteocyte-like cells. The matrix mineralized
in the presence of β-glycerophosphate. The technique of dropinoculation (high concentration of cells in a small volume of
medium) promoted the multilayer formation and the achievement of large mineralized plates (about 1 cm2) in 3 weeks of culture. 相似文献
88.
采用MTT方法观察癌光啉结合^60Coγ射线放射对四株人鼻咽癌细胞体外放射增敏作用,结果表明在一定的PsD007浓度范围内,随PsD007浓度的升高,放射对细胞的杀灭作用明显增强,当浓度分别为1.25,6.25,12.5,25和50μg/ml时,对四株细胞杀灭增加倍数分别为1.01-1.06,1.15-1.29,1.28-1.59,1.79-3.18,2.86-5.55;放射量效存活曲线按多靶单击 相似文献
89.
细胞内钙信号的变化调节血管平滑肌细胞增殖 总被引:4,自引:0,他引:4
目的探讨细胞内钙信号的变化对大鼠血管平滑肌细胞(VSMC)增殖作用的影响及其对细胞内信号转导机制的变化。方法以培养的大鼠VSMC为模型,用雷尼丁(RY)剌激VSMC内贮Ca2 释放入胞浆,用3H亮氨酸及3H胸腺嘧啶掺入量作为反应VSMC增殖的指标,加入不同的细胞内信号转导阻断剂,观察对RY效应的影响。结果与对照组相比,RY浓度依赖性地促进细胞内游离钙浓度的增高,差异显著(P<0.05或0.01)。RY剌激组蛋白核酸合成速率明显增高,与对照组相比差异显著(P<0.01);尼卡地平(Nicardipine),蛋白激酶C抑制剂(H7),钙调素激酶(CaMPK)抑制剂(W7)和丝裂素活化蛋白激酶(MAPK)抑制剂(PD98059)能明显抑制RY介导的VSMC蛋白核酸合成速率增高,与RY剌激组相比差异显著(P<0.01)。结论细胞内钙信号的变化明显促进VSMC增殖,但其效应可能通过Ca2 、PKC、MAPK来介导。钙离子拮抗剂可抑制血管平滑肌细胞增殖。 相似文献
90.
动态旋转系统构建组织工程化血管模型中血管内皮细胞分泌功能监测 总被引:3,自引:2,他引:1
目的 比较静态和动态旋转系统中构建组织工程化血管模型中血管内皮细胞分泌功能。方法新型可降解材料聚羟基丁酸酯(PHB),用胶原包埋,形成多孔状PHB 胶原管形支架。分离传代、分化人脐静脉内皮细胞,接种于PHB管型支架内腔面,分别在静态、动态旋转系统中培养14 d后,测定血管内皮细胞分泌一氧化氮(NO)、前列环素(PGI2)水平。结果 在动态旋转系统构建组织工程化血管模型中血管内皮细胞分泌NO、PGI2水平显著高于静态系统,在11 d NO分别为(120.52±3.83)μmmol/L、(80.98±5.98)μmmol/L,PGI2分另9为(20.48±1.52)μg/L,(16.59±1.29)μg/L,与静态系统相比,差异有显著性(P<0.05)。结论胶原包埋PHB支架有利于细胞的黏附和生长,可作为组织工程化血管的支架材料。在动态旋转系统构建组织工程化血管模型中血管内皮细胞,具有与正常血管类似的"生理功能"。 相似文献