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101.
基于颅脑CT图像的边缘提取 总被引:7,自引:0,他引:7
边缘提取是CT图像三维重建前期工作中的关键步骤.本文一方面利用CT图像分割的等距法求取图像的灰度阈值;另一方面求取图像的梯度阈值,利用这两个阈值将颅脑CT图像中各器官的边缘提取出来,作为三维重建的轮廓输入.实验结果表明:这种方法实时性好,适应性强,提取的边缘清晰完整,准确性较高. 相似文献
102.
Blind source separation assumes that the acquired signal is composed of a weighted sum of a number of basic components corresponding
to a number of limited sources. This work poses the problem of ECG signal diagnosis in the form of a blind source separation
problem. In particular, a large number of ECG signals undergo two of the most commonly used blind source separation techniques,
namely, principal component analysis (PCA) and independent component analysis (ICA), so that the basic components underlying
this complex signal can be identified. Given that such techniques are sensitive to signal shift, a simple transformation is
used that computes the magnitude of the Fourier transformation of ECG signals. This allows the phase components corresponding
to such shifts to be removed. Using the magnitude of the projection of a given ECG signal onto these basic components as features,
it was shown that accurate arrhythmia detection and classification were possible. The proposed strategies were applied to
a large number of independent 3s intervals of ECG signals consisting of 320 training samples and 160 test samples from the
MIT-BIH database. The samples equally represent five different ECG signal types, including normal, ventricular couplet, ventricular
tachycardia, ventricular bigeminy and ventricular fibrillation. The intervals analysed were windowed using either a rectangular
or a Hamming window. The methods demonstrated a detection rate of sensitivity 98% at specificity of 100% using nearest neighbour
classification of features from ICA and a rectangular window. Lower classification rates were obtained using the same classifier
with features from either PCA or ICA and a rectangular window. The results demonstrate the potential of the new method for
clinical use. 相似文献
103.
Ferraris A Rappaport E Santacroce R Pollak E Krantz I Toth S Lysholm F Margaglione M Restagno G Dallapiccola B Surrey S Fortina P 《Human mutation》2002,20(4):312-320
Hereditary hearing loss (HHL) is one of the most common congenital disorders and is highly heterogeneous. Mutations in the connexin 26 (CX26) gene (GJB2) account for about 20% of all cases of childhood deafness, and approach 50% in documented recessive cases of non-syndromic hearing loss. In addition, a single mitochondrial DNA mutation, mt1555A>G, in the 12S rRNA gene (MTRNR1), is associated with familial cases of progressive deafness. Effective screening of populations for HHL necessitates rapid assessment of several of these potential mutation sites. Pyrosequencing links a DNA synthesis protocol for determining sequence to an enzyme cascade that generates light whenever pyrophosphate is released during primer strand elongation. We assessed the ability of Pyrosequencing to detect common mutations causing HHL. Detection of the most common CX26 mutations in individuals of Caucasian (35delG), Ashkenazi (167delT), and Asian (235delC, V37I) descent was confirmed by Pyrosequencing. A total of 41 different mutations in the CX26 gene and the mitochondrial mt1555A>G mutation were confirmed. Genotyping of up to six different adjacent mutations was achieved, including simultaneous detection of 35delG and 167delT. Accurate and reproducible results were achieved taking advantage of assay flexibility and experimental conditions easily optimized for a high degree of standardization and cost-effectiveness. The standardized sample preparation steps, including target amplification by PCR and preparation of single-stranded template combined with automated sequence reaction and automated genotype scoring, positions this approach as a potentially high throughput platform for SNP/mutation genotyping in a clinical laboratory setting. . 相似文献
104.
Natural killer cells and malaria 总被引:3,自引:1,他引:3
Sophie Roetynck Myriam Baratin Sofia Johansson Céline Lemmers Eric Vivier Sophie Ugolini 《Immunological reviews》2006,214(1):251-263
Summary: Malaria, caused by the infection with parasites of the germs Plasmodium , is one of the three most important infectious diseases worldwide, along with tuberculosis and infection with human immunodeficiency virus. Natural killer (NK) cells are lymphocytes classically involved in the early defense against viral infections and intracytoplasmic bacterial infections and are also implicated during the course of tumor development and allogeneic transplantation. These cells display important cytotoxic activity and produce high levels of proinflammatory cytokines. In both mouse and human models of malaria, NK cells appear to be a major source of interferon-γ during the early phase of infection. In humans, indirect signaling through monocytes/macrophages required to optimally stimulate NK cell activity. However, the in vivo functions of NK cells during malaria are still enigmatic, and many issues remain to be dissected, such as the molecular basis of the direct recognition of iRBCs by NK cells. 相似文献
105.
Detection of DNA from infectious laryngotracheitis virus by colourimetric analyses of polymerase chain reactions 总被引:3,自引:0,他引:3
A combination of the polymerase chain reaction and a novel ELISA-type DNA colourimetric assay (developed from studies with a retrovirus from man) was used in a preliminary study to detect DNA from avian infectious laryngotracheitis virus. The method is sensitive, specific and easy to perform. Since it can be readily adapted for the detection of DNA from other sources it could be useful for the identification of a variety of pathogens from other species of veterinary importance. 相似文献
106.
Rb基因在鼻咽癌中存在状态的研究 总被引:1,自引:1,他引:1
首次应用生物素-14-dUTP标记Rb3.8kb探针,结合亲合素-碱性磷酸酶发光及自显影法,对Rb基因在鼻咽癌中存在状态进行了研究。杂交结果表明,3例正常胎儿鼻咽组织出现分子量为12.8、10.2、8.0、6.2、5.6、5.2及4.8kb的7条杂文区带,11例鼻咽癌组织均发现有Rb基因缺失或失活,其中4例为5.6kb片段缺失,4例为4.8kb缺失并有2例伴5.6kb减弱,2例为10.2kb缺失,1例为5.6及5.2kb片段显著减弱,说明在上述11例鼻咽癌中均有Rb基因的改变。这种高频率的异常变化,提示Rb基因的缺失或失活,与鼻咽癌的发生有密切关系。 相似文献
107.
Mimicking cell membrane and the biomolecular recognition associated with membranes represents a great technical challenge, yet it has opened doors to innovative diagnostic and therapeutic methods. Our work has focused on design and synthesis of a class of smart materials exploiting biological principals for use in biosensors: these materials are functional polymeric assemblies that mimic the cell membrane and conveniently report the presence of pathogens with a color change. Biologically active cell membrane components are incorporated into conjugated polymers with desirable optical properties and the binding of the target molecules onto the material triggers conformational and electronic shifts that are reflected in a chromatic change (a so-called biochromic shift) that is conveniently observed and recorded. Langmuir–Blodgett thin films and vesicle bilayers provide ideal configurations for precise delivery of the biological binding entity to the sensing interface, and for control of molecular orientation for effective biomolecular interaction. Polydiacetylenic membrane-mimicking materials containing cell surface receptor gangliosides and sialic acid residues, respectively were formulated into these architectures and used for colorimetric detection of bacterial toxins and influenza virus. One advantage of these biochromic conjugated polymer (BCP) sensors is that their molecular recognition and signal transduction functionalities are resident in a single functional unit, making them amenable to convenient microfabrication and use. 相似文献
108.
马凡综合征微纤维蛋白1基因突变检测及单倍型连锁分析 总被引:1,自引:0,他引:1
目的:检测中国人马凡综合征(Marfan syndrome,MFS)患者微纤维蛋白1(fibillin-1,FBN1)基因的突变及对马凡综合征患者的家系成员进行症状前诊断。方法:应用聚合酶链反应-单链构象多态性技术和测序方法,对汉族9个家系中共17个MFS患者进行基因突变检测;运用FBN1基因内4个内含子中的可变串联重复序列构建染色体单倍型,进行家系单倍型连锁分析和基因诊断。结果:发现MFS(A)家系Ⅱ1患者有单链构象改变,测序证实为位于FBN1基因第25号外显子3243-3256核苷酸之间有I个13bp的小片段缺失,为新位点基因移码突变,其序列为gcctctgcaccca;单倍型连锁分析发现MFS(B)家系Ⅲ1是1个无症状期患者。结论:中国人FBN1基因突变可以引起马凡综合征,应用突变检测与单倍型连锁分析方法能为马凡综合征基因诊断提供依据。 相似文献
109.
A Miettinen H Turunen J Paavonen E Jansson P Leinikki 《Journal of immunological methods》1984,69(2):267-275
A 4-layer modification of enzyme immunoassay (EIA) was developed for the detection of Mycoplasma hominis antigen in clinical specimens. Microtiter plates were sensitized with rabbit anti-mycoplasma immunoglobulin, guinea pig anti-mycoplasma immunoglobulin was used as the secondary antibody, and horseradish peroxidase-conjugated anti-guinea pig immunoglobulin was used as the indicator antibody. The specificity of the assay was confirmed by using guinea pig immunoglobulins from preimmunization sera. The sensitivity of the assay is down to 10 ng/ml of antigen protein. Marked cross-reactivity was demonstrated for different strains within the species M. hominis, whereas the other genital mycoplasma species tested showed no reactivity in the assay. A comparison was made of EIA and conventional culture of vaginal specimens from 24 women. All 6 specimens positive by culture were also positive for M. hominis antigen by EIA. Antigen detection by EIA is a sensitive, rapid and simple method for the detection of M. hominis in clinical specimens. 相似文献
110.
GKT原理的模拟犯罪测试范式实验研究 总被引:2,自引:0,他引:2
目的:本实验旨在以实际犯罪较接近的实验场景验证GKT的测谎机制,并探讨其对罪犯以及其他嫌疑人的判定有效性。方法:以72名健康大学生为被试,让被试在模拟犯罪的背景下采用三种包含不同说谎和认知成分的回答方式进行测谎测试,采用Limestone测谎仪测量被试皮肤电反应。结果:回答方式与角色两因子在判定分数上的主效应均显著,交互作用不显著。结论:在模拟犯罪测试范式下,GKT模式中认知与说谎机制是共存的,其中认知成分不占主要地位,说谎成分占主要地位,GKT模式无法兼顾有效地判定"犯罪"和"知情无辜"角色,需进一步改进。 相似文献