全文获取类型
收费全文 | 2104篇 |
免费 | 284篇 |
国内免费 | 9篇 |
专业分类
耳鼻咽喉 | 31篇 |
儿科学 | 81篇 |
妇产科学 | 30篇 |
基础医学 | 435篇 |
口腔科学 | 47篇 |
临床医学 | 226篇 |
内科学 | 449篇 |
皮肤病学 | 29篇 |
神经病学 | 129篇 |
特种医学 | 132篇 |
外科学 | 206篇 |
综合类 | 53篇 |
一般理论 | 1篇 |
预防医学 | 211篇 |
眼科学 | 34篇 |
药学 | 205篇 |
中国医学 | 5篇 |
肿瘤学 | 93篇 |
出版年
2021年 | 41篇 |
2019年 | 21篇 |
2018年 | 23篇 |
2017年 | 16篇 |
2016年 | 33篇 |
2015年 | 40篇 |
2014年 | 49篇 |
2013年 | 74篇 |
2012年 | 105篇 |
2011年 | 78篇 |
2010年 | 57篇 |
2009年 | 71篇 |
2008年 | 78篇 |
2007年 | 101篇 |
2006年 | 92篇 |
2005年 | 91篇 |
2004年 | 79篇 |
2003年 | 94篇 |
2002年 | 85篇 |
2001年 | 63篇 |
2000年 | 59篇 |
1999年 | 71篇 |
1998年 | 59篇 |
1997年 | 58篇 |
1996年 | 48篇 |
1995年 | 33篇 |
1994年 | 42篇 |
1993年 | 42篇 |
1992年 | 54篇 |
1991年 | 46篇 |
1990年 | 32篇 |
1989年 | 39篇 |
1988年 | 47篇 |
1987年 | 27篇 |
1986年 | 49篇 |
1985年 | 32篇 |
1984年 | 29篇 |
1983年 | 22篇 |
1982年 | 22篇 |
1981年 | 19篇 |
1980年 | 23篇 |
1979年 | 24篇 |
1978年 | 28篇 |
1977年 | 12篇 |
1976年 | 19篇 |
1975年 | 10篇 |
1974年 | 21篇 |
1973年 | 27篇 |
1972年 | 12篇 |
1970年 | 10篇 |
排序方式: 共有2397条查询结果,搜索用时 453 毫秒
91.
Intracellular unesterified arachidonic acid signals apoptosis 总被引:46,自引:0,他引:46
Cao Y Pearman AT Zimmerman GA McIntyre TM Prescott SM 《Proceedings of the National Academy of Sciences of the United States of America》2000,97(21):11280-11285
Cyclooxygenase-2 (COX-2) is up-regulated in many cancers and is a rate-limiting step in colon carcinogenesis. Nonsteroidal antiinflammatory drugs, which inhibit COX-2, prevent colon cancer and cause apoptosis. The mechanism for this response is not clear, but it might result from an accumulation of the substrate, arachidonic acid, an absence of a prostaglandin product, or diversion of the substrate into another pathway. We found that colon adenocarcinomas overexpress another arachidonic acid-utilizing enzyme, fatty acid-CoA ligase (FACL) 4, in addition to COX-2. Exogenous arachidonic acid caused apoptosis in colon cancer and other cell lines, as did triacsin C, a FACL inhibitor. In addition, indomethacin and sulindac significantly enhanced the apoptosis-inducing effect of triacsin C. These findings suggested that unesterified arachidonic acid in cells is a signal for induction of apoptosis. To test this hypothesis, we engineered cells with inducible overexpression of COX-2 and FACL4 as "sinks" for unesterified arachidonic acid. Activation of the enzymatic sinks blocked apoptosis, and the reduction of cell death was inversely correlated with the cellular level of arachidonic acid. Inhibition of the COX-2 component by nonsteroidal antiinflammatory drugs restored the apoptotic response. Cell death caused by exposure to tumor necrosis factor alpha or to calcium ionophore also was prevented by removal of unesterified arachidonic acid. We conclude that the cellular level of unesterified arachidonic acid is a general mechanism by which apoptosis is regulated and that COX-2 and FACL4 promote carcinogenesis by lowering this level. 相似文献
92.
Izak J. Bisschoff Christine Zeschnigk Denise Horn Brigitte Wellek Angelika Rieß Maja Wessels Patrick Willems Peter Jensen Andreas Busche Jens Bekkebraten Maya Chopra Hanne Dahlgaard Hove Christina Evers Ketil Heimdal Ann‐Sophie Kaiser Erdmut Kunstmann Kristina Lagerstedt Robinson Maja Linné Patricia Martin James McGrath Winnie Pradel Katrina E. Prescott Bernd Roesler Gorazd Rudolf Ulrike Siebers‐Renelt Nataliya Tyshchenko Dagmar Wieczorek Gerhard Wolff William B. Dobyns Deborah J. Morris‐Rosendahl 《Human mutation》2013,34(1):237-247
OFD1, now recognized as a ciliopathy, is characterized by malformations of the face, oral cavity and digits, and is transmitted as an X‐linked condition with lethality in males. Mutations in OFD1 also cause X‐linked Joubert syndrome (JBTS10) and Simpson–Golabi–Behmel syndrome type 2 (SGBS2). We have studied 55 sporadic and six familial cases of suspected OFD1. Comprehensive mutation analysis in OFD1 revealed mutations in 37 female patients from 30 families; 22 mutations have not been previously described including two heterozygous deletions spanning OFD1 and neighbouring genes. Analysis of clinical findings in patients with mutations revealed that oral features are the most reliable diagnostic criteria. A first, detailed evaluation of brain MRIs from seven patients with cognitive defects illustrated extensive variability with the complete brain phenotype consisting of complete agenesis of the corpus callosum, large single or multiple interhemispheric cysts, striking cortical infolding of gyri, ventriculomegaly, mild molar tooth malformation and moderate to severe cerebellar vermis hypoplasia. Although the OFD1 gene apparently escapes X‐inactivation, skewed inactivation was observed in seven of 14 patients. The direction of skewing did not correlate with disease severity, reinforcing the hypothesis that additional factors contribute to the extensive intrafamilial variability. 相似文献
93.
目的数值模拟抗血管生成因子Angiostatin和Endostatin对肿瘤血管生成的影响。方法建立肿瘤内外血管生成的二维离散数学模型。模型耦合两种抗血管生成因子Angiostatin和Endostatin的抑制效应,数值模拟在促血管生成因子诱导下肿瘤微血管网生成,讨论血管生成抑制因子的影响。结果抗血管生成因子Angiostatin对肿瘤内外血管网络生成的速度和成熟度有抑制作用。抗血管生成因子Angiostatin和Endostatin耦合作用时,在肿瘤血管生成的早期有明显的抑制效应;在肿瘤血管生成的中后期,它们可以降低肿瘤血管化程度。结论本文模型能够较好的模拟抗血管生成因子Angiostatin和Endostatin对内皮细胞迁移和增殖的抑制作用。 相似文献
94.
95.
Abstract In this paper we describe some mathematical and statistical models based on structural equation modeling (SEM) using computer programs like LISREL. We focus on SEM methodology for the simultaneous examination of the internal validity of psychological constructs and the external validity represented by age relations. To illustrate these ideas we use a latent variable path model to examine the organization of intellectual abilities measured by the WAIS-R in the standardization sample. We also examine different ways in which age can be used to structure this organization. This is primarily a methodological paper, but we try to integrate conceptual principles of modeling with some substantive issues of research on the psychology of aging. 相似文献
96.
SMJ Mortazavi MA Mosleh-Shirazi AR Tavassoli M Taheri AR Mehdizadeh SAS Namazi A Jamali R Ghalandari S Bonyadi M Haghani M Shafie 《Dose-response》2013,11(2):281-292
The aim of this study was to investigate the effect of pre-irradiation with microwaves on the induction of radioadaptive response. In the 1st phase of the study, 110 male mice were divided into 8 groups. The animals in these groups were exposed/sham-exposed to microwave, low dose rate gamma or both for 5 days. On day six, the animals were exposed to a lethal dose (LD). In the 2nd phase, 30 male rats were divided into 2 groups of 15 animals. The 1st group received microwave exposure. The 2nd group (controls) received the same LD but there was no treatment before the LD. On day 5, all animals were whole-body irradiated with the LD. Statistically significant differences between the survival rate of the mice only exposed to lethal dose of gamma radiation before irradiation with a lethal dose of gamma radiation with those of the animals pre-exposed to either microwave (p=0.02), low dose rate gamma (p=0.001) or both of these physical adapting doses (p=0.003) were observed. Likewise, a statistically significant difference between survival rates of the rats in control and test groups was observed. Altogether, these experiments showed that exposure to microwave radiation may induce a significant survival adaptive response. 相似文献
97.
N. H. Rod M. Grønbæk P. Schnohr E. Prescott T. S. Kristensen 《Journal of internal medicine》2009,266(5):467-475
Objective. The aim of this study was to evaluate the long‐term effects of stress on changes in health behaviour and cardiac risk profile in men and women. Design. A prospective cohort study. Setting. The Copenhagen City Heart Study, Denmark. Subjects. The analyses were based on 7066 women and men from the second (1981–1983) and third (1991–1993) wave of the Copenhagen City Heart Study. All participants were asked questions on stress and health behaviour and they had their weight, height, blood pressure and level of blood lipids measured by trained personnel. Main outcome measures. Changes in health behaviour (smoking, physical activity, alcohol consumption, overweight) and cardiac risk profile (cholesterol, HDL cholesterol, blood pressure, diabetes). Results. Individuals with high levels of stress compared to those with low levels of stress were less likely to quit smoking (OR = 0.58; 95% CI: 0.41–0.83), more likely to become physically inactive (1.90; 1.41–2.55), less likely to stop drinking above the sensible drinking limits (0.43; 0.24–0.79), and stressed women were more likely to become overweight (1.55; 1.12–2.15) during follow‐up. Men and women with high stress were more likely to use antihypertensive medication (1.94; 1.63–2.30), and stressed men were more than two times as likely to develop diabetes during follow‐up (2.36; 1.22–4.59). Conclusion. This longitudinal study supports a causal relation between stress and cardiovascular diseases mediated through unfavourable changes in health behaviour and cardiac risk profile. 相似文献
98.
S Garcovich AR Di Giampetruzzi G Antonelli A Garcovich B Didona 《Journal of the European Academy of Dermatology and Venereology》2010,24(8):881-884
Background Pityriasis rubra pilaris (PRP) is a rare inflammatory dermatosis with frequent clinical presentation as erythroderma. Conventional systemic treatment is often unsatisfactory and limited by long‐term toxicity. The use of tumour necrosis factor (TNF) antagonists has been reported previously in single cases, but lacking long‐term follow‐up or comparison between different biological agents. Objectives To assess the long‐term efficacy and safety of TNF‐alpha antagonist, infliximab and etanercept, either in monotherapy or in combination therapy of severe, refractory adult‐onset PRP. Methods Seven patients of adult‐onset PRP, six newly diagnosed type‐I and 1 type‐II, which were resistant or ineligible to conventional systemic treatment, received a single course of infliximab or etanercept therapy, alone or in combination with low‐dose acitretin (>0.25 mg/kg/daily). After complete remission and treatment discontinuation, a follow‐up period of 12 months was evaluated for relapses. Results Six patients obtained complete remission after a single course of anti‐TNF‐alpha therapy: mean therapy duration was 19.3 weeks (range 6–48 weeks). All patients obtained significant clearing (>75% of body surface area) of skin lesions at week 12. Two patients with marked keratoderma developed localized disease recurrence during treatment. During follow‐up, only a single patient, affected by type II PRP, had disease relapse. Conclusions Both TNF‐alpha antagonists proved successful for the treatment of refractory, adult‐onset PRP, yielding complete and persistent clinical responses in type‐I PRP. Infliximab was associated with a more rapid onset of action, while treatment duration was comparable with etanercept. PRP type II warranted long‐term therapy and showed relapse after drug discontinuation. 相似文献
99.
Matthew S. Comeaux Astrid M. Roy-Engel Dale J. Hedges Prescott L. Deininger 《Genome research》2009,19(4):545-555
The human genome contains nearly 1.1 million Alu elements comprising roughly 11% of its total DNA content. Alu elements use a copy and paste retrotransposition mechanism that can result in de novo disease insertion alleles. There are nearly 900,000 old Alu elements from subfamilies S and J that appear to be almost completely inactive, and about 200,000 from subfamily Y or younger, which include a few thousand copies of the Ya5 subfamily which makes up the majority of current activity. Given the much higher copy number of the older Alu subfamilies, it is not known why all of the active Alu elements belong to the younger subfamilies. We present a systematic analysis evaluating the observed sequence variation in the different sections of an Alu element on retrotransposition. The length of the longest number of uninterrupted adenines in the A-tail, the degree of A-tail heterogeneity, the length of the 3′ unique end after the A-tail and before the RNA polymerase III terminator, and random mutations found in the right monomer all modulate the retrotransposition efficiency. These changes occur over different evolutionary time frames. The combined impact of sequence changes in all of these regions explains why young Alus are currently causing disease through retrotransposition, and the old Alus have lost their ability to retrotranspose. We present a predictive model to evaluate the retrotransposition capability of individual Alu elements and successfully applied it to identify the first putative source element for a disease-causing Alu insertion in a patient with cystic fibrosis. 相似文献