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91.
C4d Deposition and Clearance in Cardiac Transplants Correlates With Alloantibody Levels and Rejection in Rats 总被引:4,自引:3,他引:1
K. Minami K. Murata C.-Y. Lee K. Fox-Talbot B. A. Wasowska M. D. Pescovitz W. M. Baldwin III 《American journal of transplantation》2006,6(5P1):923-932
Antibody-mediated rejection of human cardiac transplants is correlated with C4d deposits and macrophage infiltrates in capillaries of endomyocardial biopsies. We produced an antibody to rat C4d to study C4d deposition and clearance in Lewis rats that were sensitized with a blood transfusion from DA rats 7, 14 or 21 days before cardiac transplantation. Cyclosporin A (CsA) immunosuppression was initiated after transplantation at a dose that inhibited graft rejection, antibody production and C4d deposition in unsensitized recipients. Blood transfusion elicited high levels of circulating IgG alloantibodies, predominantly of the complement-activating IgG2b subclass, that peaked 14 days after transplantation. At this time, macrophages accumulated in capillaries, and C4d deposits were diffuse and intense on arteries, capillaries and veins. Grafts that survived 90 days in sensitized recipients still had deposits of C4d that were associated with increased interstitial fibrosis and vasculopathy in arteries. Clearance of C4d was determined by retransplanting DA cardiac allografts from Lewis recipients back to DA recipients. C4d deposits were decreased to minimal levels within 5 days after retransplantation. Thus, C4d deposition is not limited to the capillaries, but extends throughout the arterial tree, and despite formation of a covalent bond, C4d is cleared within days. 相似文献
92.
目的构建并筛选大鼠胶质原纤维酸性蛋白(GFAP)表达抑制短发夹样RNA(shRNA)真核表达载体。方法针对GFAP基因全编码序列设计并合成三对9bp茎环结构、19bp干扰序列特异性shRNA模板,体外定向克隆构建特异性重组质粒真核表达载体;通过体外大鼠脊髓源星形胶质细胞GFAP表达抑制模型,脂质体介导RNA干扰分子转染,实时荧光定量RT—PCR及Wesem blot技术观察RNA干扰后原代星形胶质细胞GFAP表达抑制效果.筛选最佳GFAP表达干扰抑制真核表达载体。结果序列测定证实GFAP—shRNA重组质粒真核表达载体构建成功,三对shRNA模板在mRNA及蛋白表达水平抑制靶基因表达效率分别为81%、63%、56%。结论高效率的GFAP—shRNA真核表达载体在大鼠原代星形胶质细胞GFAP表达抑制模型中能高效抑制GFAP基因表达,为后续多靶点RNA干扰技术在脊髓损伤胶质瘢痕抑制基因治疗中的应用奠定了前期基础。 相似文献
93.
Gsta Holmgren Sven Bergström Ulf Drugge Erik Lundgren Carin Nording-Sikström Ola Sandgren Lars Steen 《Clinical genetics》1992,41(1):39-41
Familial amyloidotic polyneuropathy (FAP) with a mutation in position 30 of transthyretin (TTR) (previously called prealbumin) is an autosomal dominant inherited disorder characterized by varying degrees of peripheral neuropathy, nephropathy, gastrointestinal problems, and vitreous amyloid. We have earlier diagnosed homozygosity for the TTR-Met30-gene using Southern analysis in four Swedish individuals. We have found it possible to detect homozygosity for the Met-30 mutation by amplifying discrete regions of the TTR-gene using polymerase chain reaction (PCR), and the amplification products restricted with NsiI analysed by gel electrophoresis. Clinical data on seven homozygous individuals, including three new cases, are presented. 相似文献
94.
95.
本文检测了140例丙型肝炎病毒(HCV)抗体(抗-HCV)阳性的慢性丙型肝炎(CHC)的HCV核酸(HCVRNA)和IgM抗体(抗-HCVIgM)两项指标。结果表明,原始诊断为不同临床型的肝炎(HC)患者,8年随访时,HCVRNA和抗-HCVIgM阳性率分别为80.7%和90.7%(u=2.39P<0.05).在原始诊断不同临床型HC转慢者中,上述两项指标均未发现统计学上的差别(均为P>0.05)。HCVRNA与抗-HCVIgM配对比较,符合率为78.6%。基因分型初步结果表明,河北省固安HCV以基因Ⅱ型为主。本研究提示,随访8年的CHC患者绝大多数仍有传染性;本文方法检测的抗-HCVIgM不能代表早期感染标志,但代表慢性感染活动化或带毒,所以,在不具备检测HCVRNA的地方更具有实用价值. 相似文献
96.
J. A. Doebler W. R. Markesbery A. Anthony S. W. Scheff R. E. Rhoads 《Acta neuropathologica》1988,75(3):272-276
Summary A new double-staining procedure, in which the techniques of immunocytochemistry of glial fibrillary acidic protein (GFAP) and quantitative microdensitometry of azure B-RNA were combined, was used to study nucleic acid alterations in fibrous astrocytes in Alzheimer's disease (AD). RNA contents of GFAP-positive cells of the hippocampal endplate (Rose's H3-H5 fields) and the dentate gyrus molecular layer were determined in ten autopsy-proven AD patients (ages 51–88) and ten age-matched, non-demented control. In addition, RNA contents of pyramidal neurons of the endplate were examined. While there were no differences in RNA contents of astrocytes of either region between AD patients and controls, neuronal RNA was markedly depleted. These data suggest that astrocytes maintain protein synthetic capabilities in AD and that RNA loss is limited to the neuronal compartment.Supported by Grants 1P01-AG05119 and 1P50-AG05144 from the National Institutes of Health and by a Small Research Project Award from the University of Kentucky Medical Center 相似文献
97.
丙型肝炎患者外周血单核细胞中丙型肝炎病毒复制的研究 总被引:2,自引:0,他引:2
9例临床诊断为丙型肝炎患者,研究其外周血单核细胞中HCVRNA的存在及复制。9例患者血清标本抗-HCV及HCVRNA均为阳性,采用高敏感的逆转录一套式PCR法测定其外周血单核细胞中HCV正、负链RNA,结果9例患者外周血单核细胞中7例HCV正链RNA阳性,3例HCV负链RNA阳性,证实部分丙肝患者外周血单核细胞中存在HCV的复制,表明肝细胞并非为HCV感染与复制的唯一场所。 相似文献
98.
Soonmyoung Paik M.D. 《Breast cancer research and treatment》1992,22(1):31-38
Summary Expression of IGF-I and IGF-II was studied in human breast cancer tissues by in situ hybridization. IGF-I mRNA was detected only in stromal cells adjacent to normal breast epithelial cells. Stromal cells associated with the tumor cells did not contain IGF-I, nor did malignant or benign breast epithelial cells. In contrast, IGF-II mRNA was found in both the malignant epithelial cells and their adjacent stromal cells. These data imply that stromal cells associated with breast epithelium may switch expression from IGF-I to IGF-II during breast cancer evolution. This appearance of IGF-II expression may identify cancer-associated stromal cells that have a fetal phenotype. 相似文献
99.
甲硫氨酸脑啡肽对抗体的产生和T细胞免疫功能具有调节作用。为了明确这种作用机制,本实验观察了抗体和白细胞介素-2(IL-2)的产生和基因表达。甲硫氨酸脑啡肽对3F3杂交瘤细胞的抗体产生及其轻链和重链基因表达影响不明显。较高浓度的甲硫氨酸脑啡肽(0.1nmol·L ̄(-1)-1μmol·L(-1))不仅促进IL-2的产生和IL-2mRNA的转录,而且能提高IL-2mRNA的稳定性。 相似文献
100.
本资料对93例不同性质的卵巢肿瘤细胞DNA及RNA含量进行了定量研究,其中50例良性、43例恶性。并对患者进行1~5年的随访。结果是卵巢良性肿瘤的异倍率(假阳性)为44%,恶性肿瘤异倍率为86.0%。以“标准DI”及“标准RI”为指标判断卵巢肿瘤性质的准确率较以“异倍性”为高,且双指标同时应用高于任一单指标:对卵巢良恶性肿瘤的诊断准确率分别为90%和95.3%。提出“标准DI”和“标准RI”是判断卵巢肿瘤性质的理想指标。且DNA及RNA含量与卵巢癌预后有密切关系。 相似文献