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101.
Efficient RT-PCR on platelet mRNA after long-term storage 总被引:1,自引:0,他引:1
We have developed a procedure permitting RT-PCR from mRNA even after a long-term storage (1 year) of platelet samples in ethanol (EtOH-platelets) at −80°C. To validate our method, we have analysed the human platelet alloantigen system (HPA-1) which is coded by β3 mRNA. We have also demonstrated the efficiency of amplification of part of the coding region for (i) αIIb subunit mRNA, (ii) αv subunit mRNA, and (iii) the seven transmembrane domain thrombin receptor mRNA. 相似文献
102.
应用肿瘤相关糖蛋白72抗原(TAG-72)的单抗72-45及两种凝集素PNA和DBA对不同组织分型的大肠癌及癌旁组织进行了研究。结果表明:大肠癌中TAG-72抗原及PNA受体的表达阳性率分别为85.3%和89.3%,DBA受体呈阴性;在癌旁组织中三者的表达阳性率分别为50%、53.3%和63.3%;在正常大肠粘膜中TAG-72抗原及PNA受体均呈阴性,而DBA受体全部呈阳性。由此认为72-45单抗和PNA可做为大肠癌的有效标记物,有助于大肠癌的诊断和预后。 相似文献
103.
股骨多段闭合骨折病人术前凝血功能的变化 总被引:12,自引:0,他引:12
目的 探讨股骨多段闭合骨折病人术前凝血功能的变化。方法 选择创伤股骨多段闭合骨折后当天入院的病人20例,年龄19-45岁,ASA Ⅰ级,为试验组(Ⅰ组);选择健康成年人15人,年龄21-39岁,作为对照组(Ⅱ组);Ⅱ组于清晨空腹采上肢静脉血标本,Ⅰ组病人入院后于骨折的第2天、第6天(手术当天清晨)空腹采上肢静脉血样本,检测血栓弹力图(TEG)指标[R时间、K时间、α角、血栓最大幅度(MA)、血栓硬度(G)]、D-二聚体浓度(D-Di)、血小板计数(PLC)及血小板聚集率(PAgR)的变化。结果 Ⅱ组TEG指标、D-Di、PLC及PAgR均在正常范围。与Ⅱ组比较,Ⅰ组骨折后第2天,K时间缩短(P<0.05),α角、MA、G及D-Di增高(P<0.01);骨折后第6天,R时间缩短(P<0.05),α角、MA、G、D-Di、PLC及PagR增高(P<0.01)。与骨折后第2天比较,Ⅰ组骨折后第6天MA、G、PLT及PAgR增高(P<0.05或0.01)。结论 病人创伤骨折后凝血功能24 h内增强,随时间的延长至术日呈高凝状态,应加强术中管理,并采取相应措施预防术中静脉血栓的发生。 相似文献
104.
重叠细胞的判别在细胞计数和参数测量中有非常重要的意义.本文根据重叠细胞的形态特征,提出根据形状因子来判断细胞是否重叠.首先研究了形状因子的计算方法,对重叠细胞形状因子的阈值P0进行了探讨和实验,得出P0=0.5:当PE≤P0,认为目标存在细胞重叠;PE>P0,认为目标不存在细胞重叠.实验结果证明本技术能检测出不同形状的重叠细胞,准确率为95%. 相似文献
105.
粉防己碱与牛磺酸合用对血小板聚集与血栓形成的影响 总被引:4,自引:0,他引:4
粉防己碱(Tet)和牛磺酸(Tau)均能抑制ADP、胶原和凝血酶诱导的大鼠血小板聚集及血栓形成。Tet抑制ADP诱导聚集较强,Tau则对胶原作用最明显,二药减半量合并应用时,较各药单用强 相似文献
106.
107.
Joen-Rong sheu Chao-Hsin Lin Jih-Luan chung Che-Ming Teng Tur-Fu Huang 《Thrombosis research》1992,66(6):679-691
Triflavin, an Arg-Gly-Asp (RGD)-containing peptide, purified from snake venom of Trimeresurus flavoviridis, inhibits human platelet aggregation through the blockade of fibrinogen binding to fibrinogen receptors associated with glycoprotein IIb/IIIa complex. In this report, we examined the effect of triflavin on tumor cells (human hepatoma J-5)-induced platelet aggregation (TCIPA) of heparinized platelet-rich plasma (PRP). ADP-scavenger agents, apyrase (10 U/ml) and creatine phosphate (5 mM)/creatine phosphokinase (5 U/ml) did not inhibit TCIPA while hirudin (5u/ml) completely inhibited it. J-5 cells initially induced platelet aggregation, then blood coagulation occurred. J-5 cells concentration-dependently shortened the recalcification time of normal as well as Factor VIII, IX-deficient human plasmas, while it was inactive at shortening the recalcification time of Factor VII-deficient plasma, suggesting J-5 cells induced platelet aggregation through activation of extrinsic pathway, leading to thrombin formation as evidenced by the amidolytic activity on S-2238 by expressing tissue factor-like activity. Triflavin inhibited TCIPA in a dose-dependent manner (IC50, 0.02 μM). When compared on molar ratio, triflavin was approximately 30,000 times more potent than GRGDS (IC50,0.58 mM). On the other hand, GRGES showed no significant effect on TCIPA, even its concentration was raised to 4 mM. Additionally, the monoclonal antibodies, raised against glycoprotein IIb/IIIa complex (i.e., 7E3 and 10 E5) inhibited J-5 TCIPA. In conclusion, we suggest the inhibitory effect of triflavin on J-5 TCIPA may be chiefly mediated by the binding of triflavin to the fibrinogen receptor associated with glycoprotein IIb/IIIa complex on platelet surface membrane. 相似文献
108.
BACKGROUND: It is established that the A3 domain in von Willebrand factor (VWF) contains the major collagen-binding site. However, there are conflicting reports describing the capacity of the A1 domain to interact with collagen types I and III. METHODS: In this study, we have used recombinant VWF-A1 polypeptides, as well as conformation-specific monoclonal antibodies (mAb), to analyze the A1-collagen interaction. RESULTS: The A1 domain bound to collagen with K(d) approximately 8.0 nm and this binding was blocked by the mAb 6G1, which blocks the interaction between ristocetin and VWF. In addition, collagen-bound A1 protein was able to support flow-dependent adhesion of platelets, demonstrating that the binding sites for collagen and glycoprotein (GP)Ib are different. Analysis with two conformation-specific mAb demonstrated that the structure of the A1 domain changed as a result of the binding to collagen. In contrast, the antibodies failed to detect conformational change in the G1324S mutant (type 2M von Willebrand disease). Thus, direct binding to collagen induces a change in the structural conformation within the VWF-A1 domain, and the G1324S substitution prevents this conformational change. CONCLUSION: This study has shown that the isolated A1 domain can simultaneously bind to collagen and platelet GPIb, supporting platelet adhesion under high-flow conditions. In addition, this study has used mAb to demonstrate that the binding of the isolated A1 domain or full-length VWF to collagen is accompanied by a conformational change in A1 domain. 相似文献
109.
目的观测糖尿病肾病患者血液白细胞的变化,分析炎症在糖尿病肾病中的作用。方法对436例糖尿病住院病人,分为糖尿病肾病组(n=102)和糖尿病无肾病组(n=334),检测血液白细胞总数和中性粒细胞数。结果糖尿病肾病组白细胞总数为(7.10±2.21)×109/L,糖尿病无肾病组为(5.61±1.34)×109/L,两组相比,差异有非常显著性意义(t=8.270,P<0.001);中性粒细胞计数值糖尿病肾病组(4.47±2.03)×109/L明显高于糖尿病无肾病组(3.18±1.04)×109/L,差异有非常显著性意义(t=8.481,P<0.001)。相关分析,白细胞数与肌酐(C r)呈正相关(r=0.155,P>0.05)、与尿素(Urea)呈明显正相关(r=0.295,P<0.01)、与血糖(GLU)无明显相关(r=0.055,P>0.05);中性粒细胞与C r、Urea呈明显正相关(r=0.260,0.398,P<0.01)、与GLU呈正相关(r=0.163,P>0.05)。结论糖尿病肾病患者血液白细胞计数升高,与肌酐、尿素水平呈正相关。糖尿病肾病患者存在炎症反应,炎症在糖尿病肾病发生发展中起一定作用。 相似文献
110.
SUMMARY. This study compared plateletpheresis on the Haemonetics PCS Plus (PCS Plus) and the Baxter Autopheresis C (Auto C) using the same 100 selected donors. The number of packs meeting UK BTS/NIBSC specification (>2.2 times 1011 platelets per pack) was achieved by 99% of PCS Plus and 82% of Auto C procedures. The positive correlation found between donor precount and final platelet yield was better for the PCS Plus. Both machines met U.K. specification for white-cell contamination but this was significantly greater for the Auto C. Plasma yields were similar.
As a result of this study we chose to use the PCS Plus for routine plateletpheresis in our unit. This has enabled us not only to comply with UK BTS/NIBSC specifications for apheresis platelets easily and cost effectively but also to meet our own higher specification (2.75 times 1011 platelets per pack) using existing staff and without extending the working day. 相似文献
As a result of this study we chose to use the PCS Plus for routine plateletpheresis in our unit. This has enabled us not only to comply with UK BTS/NIBSC specifications for apheresis platelets easily and cost effectively but also to meet our own higher specification (2.75 times 10