全文获取类型
收费全文 | 18177篇 |
免费 | 1196篇 |
国内免费 | 67篇 |
专业分类
耳鼻咽喉 | 172篇 |
儿科学 | 401篇 |
妇产科学 | 446篇 |
基础医学 | 2707篇 |
口腔科学 | 699篇 |
临床医学 | 2111篇 |
内科学 | 3793篇 |
皮肤病学 | 351篇 |
神经病学 | 1761篇 |
特种医学 | 491篇 |
外科学 | 1842篇 |
综合类 | 108篇 |
一般理论 | 9篇 |
预防医学 | 1753篇 |
眼科学 | 259篇 |
药学 | 1387篇 |
中国医学 | 104篇 |
肿瘤学 | 1046篇 |
出版年
2024年 | 19篇 |
2023年 | 184篇 |
2022年 | 248篇 |
2021年 | 491篇 |
2020年 | 304篇 |
2019年 | 518篇 |
2018年 | 690篇 |
2017年 | 494篇 |
2016年 | 540篇 |
2015年 | 699篇 |
2014年 | 760篇 |
2013年 | 1059篇 |
2012年 | 1601篇 |
2011年 | 1636篇 |
2010年 | 769篇 |
2009年 | 636篇 |
2008年 | 1193篇 |
2007年 | 1186篇 |
2006年 | 1124篇 |
2005年 | 1056篇 |
2004年 | 1014篇 |
2003年 | 909篇 |
2002年 | 825篇 |
2001年 | 135篇 |
2000年 | 116篇 |
1999年 | 107篇 |
1998年 | 93篇 |
1997年 | 82篇 |
1996年 | 95篇 |
1995年 | 58篇 |
1994年 | 40篇 |
1993年 | 42篇 |
1992年 | 55篇 |
1991年 | 46篇 |
1990年 | 50篇 |
1989年 | 35篇 |
1988年 | 30篇 |
1987年 | 36篇 |
1986年 | 45篇 |
1985年 | 35篇 |
1984年 | 51篇 |
1983年 | 30篇 |
1982年 | 35篇 |
1981年 | 44篇 |
1980年 | 30篇 |
1979年 | 22篇 |
1978年 | 14篇 |
1975年 | 15篇 |
1974年 | 13篇 |
1970年 | 13篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
61.
Jose Carlos de Fraga João Pippi Salle Mauro Boher Carlos R. Antunes 《Pediatric surgery international》1995,10(5-6):376-378
Laryngotracheoesophageal cleft is an uncommon disease that is difficult to diagnose and treat. Repair of the cleft depends on length and localization of the defect as well as the associated anomalies. A successful repair of a type II cleft is reported in this paper. An anterior split of the larynx and trachea was used and provided excellent exposure and safe repair without injury to the neurovascular structures. This is the best approach and should be used to correct all type II defects. 相似文献
62.
The gastrointestinal prokinetic benzamide derivatives are agonists at the non-classical 5-HT receptor (5-HT4) positively coupled to adenylate cyclase in neurons 总被引:24,自引:0,他引:24
Aline Dumuis Michèle Sebben Joël Bockaert 《Naunyn-Schmiedeberg's archives of pharmacology》1989,340(4):403-410
Summary We have previously shown that a non-classical 5-hydroxytryptamine (5-HT4) receptor mediates the stimulation of adenylate cyclase activity in mouse embryo colliculi neurons in primary culture. The pharmacological characteristics of this receptor exclude the possibility that it belongs to the known 5-HT1, 5-HT2 or 5-HT3 receptor types. Here we report that this 5-HT receptor can be stimulated by 4-amino-5-chloro-2-methoxy substituted benzamide derivatives. All these compounds have been reported to be potent stimulants of gastrointestinal motility and some of them are 5-HT3 receptor antagonists. The rank order of potency of these substituted benzamide derivatives in stimulating cAMP formation was: cisapride > BRL 24924 > 5-HT > zacopride > BRL 20627 > metoclopramide. The non-additivity of benzamide and 5-HT activities suggests that 5-HT and the substituted benzamide derivatives act on the same receptor. Only ICS 205930, a recognized 5-HT3 receptor antagonist, competitively antagonized the stimulatory effect of cisapride, zacopride and BRL 24924. However, its pK
i (6–6.3) for this new receptor was very different from its pK
i for 5-HT3 receptors (pK
i = 8 –10). Other selective 5-HT3 receptor antagonists with an indole group (BRL 43694 and GR 38032F), with a benzoate group (cocaïne, MDL 72222) or with a piperazine group (quipazine) were ineffective in reversing the stimulatory effect of benzamide derivatives. Exposure of neuronal cells to potent agonists at this receptor such as BRL 24924 rapidly reduces its capacity to stimulate cAMP production. For example, a preincubation of 10 min with BRL 24924 (100 mol/l) reduced by 42% the ability of 5-HT to stimulate cAMP production. Cross-desensitization occurs between the effects of 5-HT and benzamides. The unique pharmacology of these nonclassical 5-HT receptors that we propose to call 5-HT4 is very close and even identical to the pharmacology of the high affinity 5-HT receptors involved in the indirect stimulation of smooth muscle in the guinea pig ileum. These receptors are different from the 5-HT3 receptors also present in guinea pig ileum.Send offprint requests to A. Dumuis at the above address 相似文献
63.
A single monkey was trained to perform a grasp, lift, and hold task in which a stationary hand- held object was sometimes subjected to brief, predictable force-pulse perturbations. The displacement, grip, and lifting forces were measured as well the three-dimensional forces and torques to quantify specific motor deficits after reversible inactivation of the cerebellar nuclei. A prior single-cell recording study in the same monkey provided the stereotaxic coordinates used to guide intranuclear injections of muscimol. In total, 34 penetrations were performed at 28 different loci throughout the cerebellar nuclei. On each penetration, two 1.0-microl injections of 5 microg/microl muscimol, were made 1.0 mm apart either within the nuclei or in the white matter just lateral or posterior to the dentate nucleus. Injections in the region corresponding to the anterior interpositus nucleus produced pronounced dynamic tremor and dysmetric movements of the ipsilateral arm when the animal performed unrestrained reaching and grasping movements. In contrast, no relatively short-latency (15-20 min.) deficits were observed after injection in the dentate nucleus, although some effects were observed after several hours. When tested in a primate chair with the forearm supported and restrained at the wrist and elbow, the monkey performed the lift and hold task without tremor or dysmetria. However, with the restraint removed, the forces and torques applied to the manipulandum were poorly controlled and erratic. The monkey's arm was ataxic and a 5-Hz intention tremor was clearly visible. In addition, the animal was generally unable to compensate for the predictable perturbations and the anticipatory grip force increases were absent. However, overall the results suggest that reversible cerebellar nuclear inactivation with muscimol has little effect on isolated distal movements of the wrist and fingers. 相似文献
64.
Breast cancer micrometastases: Different interactions of carcinoma cells with normal and cancer patients' bone marrow stromata 总被引:6,自引:1,他引:6
Nicola MH Bizon R Machado JJ Sollero T Rodarte RS Nobre JS Magalhães MM Takiya CM Borojevic R 《Clinical & experimental metastasis》2003,20(5):471-479
The apparently dormant breast cancer micrometastases in haemopoietic marrow are correlated with distant metastatic carcinoma
dissemination. We studied in vitro interactions of carcinoma cells with adjacent stromata, using connective tissue cell cultures from breast and bone marrow
samples of normal donors, comparing them to the pericancerous breast tissue and bone marrows of 12 selected patients with
invasive breast carcinomas. Cancer cells were detected by immunocytochemistry and RT-PCR in all the bone marrows and in most
blood samples of the studied patients. We monitored the growth and interaction of carcinoma MCF-7 cells with the stromata.
The normal breast stroma sustained typical massive cancer growth. The pericancerous breast stroma induced the invasive mesenchymal
pattern of growth. Normal bone marrow stroma induced the same conversion and was highly adhesive, retaining the cells in the
stroma, but carcinoma patients' bone marrow stromata underwent low adhesive interactions with cancer cells, releasing them
potentially into the circulation. The semi-quantitative RT-PCR indicated an enhanced expression of the hepatocyte growth factor
and its receptor c-met in breast and bone marrow stromata of cancer patients. The input of cancer cells into the normal bone marrow may induce modifications
of the local microenvironment, favourable for growth and release of carcinoma cells into the systemic circulation, which correlate
with the poor prognosis of patients with bone marrow micrometastases.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
65.
The liver regulates T-cell homeostasis, induces T-cell tolerance, and supports intrahepatic T-cell responses against hepatotropic pathogens. Many data from clinical and preclinical systems provide supportive evidence for these diverse roles of the liver in modulating peripheral (systemic, mucosal, and intrahepatic) T-cell immunity. Little information is available on the cellular and molecular mechanisms that mediate the dual role of the liver in tolerizing T-cell responses and in supporting intrahepatic priming of T-cell responses. Understanding these immunoregulatory effects in the liver may offer insight into clinically relevant immunopathologies of this organ. 相似文献
66.
Dina Ruano António Macedo Ana Dourado Maria Jo?o Soares José Valente Isabel Coelho Vítor Santos Maria Helena Azevedo Ann Goodman Mara Helena Hutz Clarissa Gama Maria Inês Lobato Paulo Belmonte-de-Abreu Joana Almeida Palha 《American journal of medical genetics. Part B, Neuropsychiatric genetics》2004,(1):41-45
67.
Immunocytochemical localization of zinc transporter 3 in the ependyma of the mouse spinal cord 总被引:2,自引:0,他引:2
We report, for the first time, the light microscopical and ultrastructural appearance of ZnT3-immunoreactivities in the ependymal cells of the central canal of the mouse spinal cord. Light microscopy revealed the presence of ZnT3-immunoreactive (Ir) ependymal cells in 1 microm thick epon sections stained by the ABC method. The ZnT3-Ir cells were observed at all levels of the spinal cord, but were a little more numerous in lumbosacral segments than in cervicothoracic segments. The ZnT3-Ir cells had large, ovoid nuclei with abundant cytoplasm, and protruded into the lumen of the central canal. Our ultrastructural findings suggest that the ZnT3-Ir ependymal cells possess secretory activity directed towards the central canal. We propose that they may play a role in the trans-ependymal mechanism responsible for zinc homeostasis between cerebrospinal fluid and the central area of the gray matter. 相似文献
68.
Kevin P Weinfurt Michaela A Dinan Jennifer S Allsbrook Jo?lle Y Friedman Mark A Hall Kevin A Schulman Jeremy Sugarman 《Academic medicine》2006,81(2):113-118
PURPOSE: To document the current state of institutional review board (IRB) and conflict of interest committee policies regarding disclosures of financial conflicts of interest to potential research participants, and to use this information to identify and share models for effectively achieving disclosure. METHOD: The authors identified the 123 U.S. academic medical centers that have IRBs and sought their IRB and institutional policies regarding financial conflicts of interest. In February and March 2004, using manual and key word searches, each institution's Web site was searched to identify documents containing information regarding the disclosure of financial conflicts of interest. Letters were sent to 24 institutions that had either no information or incomplete information posted on their Web sites. To assess institutions' guidelines for disclosure, the authors extracted and content coded each institution's information on disclosure. RESULTS: Relevant information was obtained from 120 (98%) academic medical centers (AMCs), of which 57 (48%) mentioned disclosing financial conflicts to potential research participants. Of these 57, 33 (58%) included verbatim language that could be used in informed consent documents. AMCs' recommendations and requirements for disclosure included details of the financial arrangement, administrative management of conflicts of interest, and encouragement of dialogue between the investigator and the potential research participant. CONCLUSIONS: Considerable variability exists concerning the specific information that should be disclosed. Most of the AMCs' policies were consistent with the goal of protection from legal liability. Significant questions remain, however, concerning the goals of disclosure and the most effective methods for achieving those goals. 相似文献
69.
Genetic mapping ofPim-1 putative oncogene to mouse chromosome 17 总被引:10,自引:0,他引:10
John Hilkens H. Theo Cuypers Gerard Selten Vera Kroezen Jo Hilgers Anton Berns 《Somatic Cell and Molecular Genetics》1986,12(1):81-88
Pim-1 is a putative oncogene activated in T-cell lymphomas induced by Moloney and AKR mink cell focus forming (MCF) viruses. We have determined the chromosomal localization of the Pim-1gene in mice by Southern blot analysis of DNAs obtained from a panel of mouse-Chinese hamster somatic cell hybrids. The Pim-1gene was localized on chromosome 17, a chromosome frequently aberrant in T-cell lymphomas. Two chromosomal regions, containing sequences homologous to regions within the Pim-1locus, were localized on chromosome 6 and 16. 相似文献
70.
M. Joëls I. J. A. Urban 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》1984,54(3):455-462
Summary Electrical stimulation of fimbria-fornix (fifx) fibers monosynaptically activated many of the neurons tested in the lateral septal complex (LSC) of the rat. The orthodromically activated LSC neurons were classified as strongly orthodromically activated (SOA) or weakly orthodromically activated (WOA) cells according to their threshold for eliciting a response, stability of the response latency, frequency following and the stimulus-response ratio.Microiontophoretically applied glutamate (GLU) could excite both SOA and WOA neurons. However, the expelling currents needed to activate the SOA cells were often considerably lower than those necessary to excite the WOA cells suggesting higher sensitivity to GLU of those cells which receive a strong fi-fx innervation. Iontophoretically administered glutamic acid diethylester (GDEE) in general reversibly attenuated excitatory responses of LSC cells to GLU but not to acetylcholine. GDEE was also effective in blocking the synaptic responses of SOA septal cells to fi-fx stimuli. In addition, GDEE administered topically reversibly suppressed the field potential induced in the LSC by fi-fx stimulation.These electrophysiological and pharmacological results support recent biochemical observations suggesting that the excitatory innervation of LSC neurons by fi-fx fibers is mediated by GLU or a closely related excitatory amino acid.The investigations were supported by the Foundation for Medical Research FUNGO which is subsidized by the Netherlands Organization for Advancement of Pure Research (Z.W.O.), grant 13-31-045 awarded to I.J. A. Urban 相似文献