全文获取类型
收费全文 | 211810篇 |
免费 | 15322篇 |
国内免费 | 753篇 |
专业分类
耳鼻咽喉 | 2293篇 |
儿科学 | 5515篇 |
妇产科学 | 4330篇 |
基础医学 | 27241篇 |
口腔科学 | 4526篇 |
临床医学 | 20161篇 |
内科学 | 45228篇 |
皮肤病学 | 2765篇 |
神经病学 | 20450篇 |
特种医学 | 6981篇 |
外国民族医学 | 13篇 |
外科学 | 33191篇 |
综合类 | 3446篇 |
现状与发展 | 2篇 |
一般理论 | 291篇 |
预防医学 | 19273篇 |
眼科学 | 4417篇 |
药学 | 14482篇 |
1篇 | |
中国医学 | 374篇 |
肿瘤学 | 12905篇 |
出版年
2023年 | 852篇 |
2022年 | 1410篇 |
2021年 | 3463篇 |
2020年 | 2121篇 |
2019年 | 3418篇 |
2018年 | 4003篇 |
2017年 | 3226篇 |
2016年 | 3420篇 |
2015年 | 4093篇 |
2014年 | 6117篇 |
2013年 | 8881篇 |
2012年 | 13180篇 |
2011年 | 14384篇 |
2010年 | 8133篇 |
2009年 | 7336篇 |
2008年 | 13636篇 |
2007年 | 14494篇 |
2006年 | 13971篇 |
2005年 | 14445篇 |
2004年 | 13857篇 |
2003年 | 12955篇 |
2002年 | 12491篇 |
2001年 | 1936篇 |
2000年 | 1511篇 |
1999年 | 2102篇 |
1998年 | 2846篇 |
1997年 | 2456篇 |
1996年 | 2217篇 |
1995年 | 1964篇 |
1994年 | 1768篇 |
1993年 | 1667篇 |
1992年 | 1258篇 |
1991年 | 1187篇 |
1990年 | 1105篇 |
1989年 | 990篇 |
1988年 | 1058篇 |
1987年 | 1051篇 |
1986年 | 1034篇 |
1985年 | 1112篇 |
1984年 | 1494篇 |
1983年 | 1480篇 |
1982年 | 1824篇 |
1981年 | 1649篇 |
1980年 | 1566篇 |
1979年 | 845篇 |
1978年 | 973篇 |
1977年 | 960篇 |
1976年 | 845篇 |
1975年 | 695篇 |
1974年 | 678篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
991.
992.
Lillington DM Kingston JE Coen PG Price E Hungerford J Domizio P Young BD Onadim Z 《Genes, chromosomes & cancer》2003,36(2):121-128
Forty-nine primary retinoblastoma (Rb) tumors were analyzed by the use of comparative genomic hybridization (CGH), and clinical/histological correlations were performed. Adverse histological factors were present in 13 patients. Chromosomal imbalance was a frequent phenomenon, seen in 96% of the tumors. Gain of 6p represented the most frequent event (69% of the tumors), whereas +1q was observed in 57%, confirming that these abnormalities are key secondary events in retinoblastoma tumor progression. Loss of 13q and 16 was significantly associated with tumors displaying adverse histo-prognostic factors, whereas -16q was significantly associated with tumors without adverse features. In three patients who developed an extra-ocular relapse, the tumors showed -13q and 2/3 had -5q, suggesting that these abnormalities may be associated with metastasis. Children >or= 36 months of age at enucleation tended to have more CGH abnormalities per tumor than children < 12 months (median numbers 11 vs. 3). In addition, +1q, +13q, -16, and -16q were more frequent in children with an older age at enucleation. Identical CGH changes were found in both tumors from one patient with bilateral tumors, suggesting a common origin. It is possible that tumors displaying loss of 13q and 5q indicate those patients who may suffer an adverse outcome and who would require alternative or more intensive therapy. CGH analysis on larger cohorts and in prospective clinical trials will be invaluable in determining whether a genetic classification of retinoblastoma represents a reliable measure of prognosis. 相似文献
993.
994.
Van QN Klose JR Lucas DA Prieto DA Luke B Collins J Burt SK Chmurny GN Issaq HJ Conrads TP Veenstra TD Keay SK 《Disease markers》2003,19(4-5):169-183
The advent of systems biology approaches that have stemmed from the sequencing of the human genome has led to the search for new methods to diagnose diseases. While much effort has been focused on the identification of disease-specific biomarkers, recent efforts are underway toward the use of proteomic and metabonomic patterns to indicate disease. We have developed and contrasted the use of both proteomic and metabonomic patterns in urine for the detection of interstitial cystitis (IC). The methodology relies on advanced bioinformatics to scrutinize information contained within mass spectrometry (MS) and high-resolution proton nuclear magnetic resonance (1H-NMR) spectral patterns to distinguish IC-affected from non-affected individuals as well as those suffering from bacterial cystitis (BC). We have applied a novel pattern recognition tool that employs an unsupervised system (self-organizing-type cluster mapping) as a fitness test for a supervised system (a genetic algorithm). With this approach, a training set comprised of mass spectra and 1H-NMR spectra from urine derived from either unaffected individuals or patients with IC is employed so that the most fit combination of relative, normalized intensity features defined at precise m/z or chemical shift values plotted in n-space can reliably distinguish the cohorts used in training. Using this bioinformatic approach, we were able to discriminate spectral patterns associated with IC-affected, BC-affected, and unaffected patients with a success rate of approximately 84%. 相似文献
995.
Dutta Roy T Simon JL Ricci JL Rekow ED Thompson VP Parsons JR 《Journal of biomedical materials research. Part A》2003,67(4):1228-1237
The current study analyzes the in vivo performance of porous sintered hydroxyapatite (HA) bone repair scaffolds fabricated using the TheriForm solid freeform fabrication process. Porous HA scaffolds with engineered macroscopic channels had a significantly higher percentage of new bone area compared with porous HA scaffolds without channels in a rabbit calvarial defect model at an 8-week time point. An unexpected finding was the unusually large amount of new bone within the base material structure, which contained pores less than 20 microm in size. Compared with composite scaffolds of 80% polylactic-co-glycolic acid and 20% beta-tricalcium phosphate with the same macroscopic architecture as evaluated in a previous study, the porous HA scaffolds with channels had a significantly higher percentage of new bone area. Therefore, the current study indicates that scaffold geometry, as determined by the fabrication process, can enhance the ability of a ceramic material to accelerate healing of calvarial defects. 相似文献
996.
Perforin- and Fas-dependent mechanisms of natural killer cell-mediated rejection of incompatible bone marrow cell grafts 总被引:5,自引:0,他引:5
Natural killer (NK) cells eliminate target cells infected with intracellular pathogens and tumor cells by employing the granule exocytosis and death receptor pathways. They also mediate the acute rejection of incompatible bone marrow cell (BMC) grafts. However, the cytotoxic mechanisms employed during acute BMC graft rejection are obscure. Throughout these studies, BMC graft rejection was compared between two inbred strains of mice: 129 mice, which apparently use perforin- and Fas-dependent cytotoxicity, and C57BL/6 (B6) mice, which are able to exploit perforin- and/or Fas-independent mechanisms. Using perforin-knockout (PKO) mice, we have determined that the granule exocytosis pathway can play a major role in NK cell-mediated rejection of allogeneic and MHC class I-deficient BMC, depending upon the genetic background of the recipient and the environmental housing conditions. Although the granule exocytosis pathway seems to be the most potent cytolytic mechanism of NK cell-mediated rejection, alternative perforin-independent mechanisms, such as death receptor-induced apoptosis, also exist. By preventing both perforin- and Fas-mediated interactions concurrently, we observed that 129 mice were impaired in mediating MHC class I-deficient BMC rejection, while B6 mice maintained strong rejection capacities. The administration of neutralizing TNF antibodies to B6PKO mice before challenging with Fas and MHC class I double-deficient BMC still did not reverse rejection. Thus, our studies reveal the relative importance of perforin-, Fas-, and TNF-based cytotoxicity in NK cell-mediated rejection of incompatible BMC. 相似文献
997.
Holán V Vítová A Krulová M Zajícová A Neuwirth A Filipec M Forrester JV 《Immunology letters》2005,100(2):211-213
The effects of passive transfer of antisera containing cytotoxic antibodies to allo- and xenoantigens on survival of corneal allografts and xenografts were evaluated in experimental models. Corneas from allogeneic B10 or xenogeneic rat Lewis donors were grafted orthotopically into BALB/c mice. Recipient mice were treated with donor-specific antisera administered at the period of grafting or at 2 weeks after transplantation. Rejection was determined by the severity of corneal opacity using a standard scoring system. Treatment of graft recipients with donor-specific antisera accelerated the onset of graft rejection and significantly shortened survival times of both corneal allografts and xenografts. Corneal xenografts, which had been accepted after treatment with anti-CD4 monoclonal antibody, were acutely rejected by the passive transfer of antiserum against xenoantigens. The results suggest that corneal grafts are vulnerable to antibody-dependent immunity and that cytotoxic antibodies against graft donor antigens can mediate rejection of both corneal allografts and xenografts. 相似文献
998.
John E. Burnes David C. Kaelber Bruno Taccardi Robert L. Lux Philip R. Ershler Yoram Rudy 《Annals of biomedical engineering》1998,26(1):37-47
Mapping of bioelectric potentials over a given surface (e.g., the torso surface, the scalp) often requires interpolation of potentials into regions of missing data. Existing interpolation methods introduce significant errors when interpolating into large regions of high potential gradients, due mostly to their incompatibility with the properties of the three-dimensional (3D) potential field. In this paper, an interpolation method, inverse-forward (IF) interpolation, was developed to be consistent with Laplace's equation that governs the 3D field in the volume conductor bounded by the mapped surface. This method is evaluated in an experimental heart–torso preparation in the context of electrocardiographic body surface potential mapping. Results demonstrate that IF interpolation is able to recreate major potential features such as a potential minimum and high potential gradients within a large region of missing data. Other commonly used interpolation methods failed to reconstruct major potential features or preserve high potential gradients. An example of IF interpolation with patient data is provided to illustrate its applicability in the actual clinical setting. Application of IF interpolation in the context of noninvasive reconstruction of epicardial potentials (the inverse problem) is also examined. © 1998 Biomedical Engineering Society.
PAC98: 8710+e, 0260Ed 相似文献
999.
Virginia Attanasio Frank Andrasik Edward B. Blanchard John G. Arena 《Journal of behavioral medicine》1984,7(2):247-257
The Psychosomatic Symptom Checklist (PSC), a questionnaire assessing psychosomatic symptoms, was administered to two separate samples of college students. For Sample 1 (N=698),the questionnaire was readministered to three separate subsets at intervals of either 1 week (N=143),4 weeks (N=74),or 8 weeks (N=48).Each subset of subjects recompleted the PSC on only one of the three retest intervals. Based on the initial administration an analysis of the normative data revealed a mean total score of 23.7, suggesting a relatively low degree of psychosomatic symptoms in this group. Although total scores decreased slightly over time, test-retest correlations remained high (r>0.80, P<0.0001).Individual item correlations varied and also decreased across time; however, the majority of correlations was greater than r=0.50 throughout. Sample 2 (N=249)completed the PSC, Beck Depression Inventory (BDI), State-Trait Anxiety Inventory (STAI-X), and Rathus Assertiveness Scale (RAS), and intercorrelations were computed between these measures. This analysis revealed little overlap between the psychosomatic complaints assessed by the PSC and other commonly used measures of psychological distress. Finally, a factor analysis revealed one major factor on which all but 2 of the 17 questionnaire items loaded significantly. These results suggest that the PSC is sensitive to psychosomatic distress and remains reliable over time.This reaserch was supported in part by Grants NS-15235 and NS-16891 from NINCDS. 相似文献
1000.
Michael S. Watson W. Roy Breg John C. Hobbins Maurice J. Mahoney 《American journal of medical genetics. Part A》1984,19(4):805-813
Cytogenetic studies on fetal blood cells obtained at 18–25 weeks gestation have provided information for decision making in 25 cases identified as being at high risk of having an abnormal fetus. In particular, in the 21 cases studied to consider the possibility of true mosaicism, confirmation in fetal blood was obtained in three, one of which presented as a pseudomosaic on the original amniotic fluid cell study. Fetal blood was also informative in two cases (one positive and the other negative) in which a diagnosis of the fragile X syndrome was being considered. Furthermore, when high risk pregnancies presented late in gestation (21–24 weeks), these methods allowed for a rapid cytogenetic diagnosis. The procedure has proved useful in most of these cases since the couples involved had indicated that they would probably have terminated the pregnancy without the reassurance of normal fetal lymphocyte studies. Since the technique carries a much higher risk of pregnancy loss than does amniocentesis, its use should only be considered when there are compelling indications. 相似文献