全文获取类型
收费全文 | 1209篇 |
免费 | 107篇 |
国内免费 | 4篇 |
专业分类
耳鼻咽喉 | 9篇 |
儿科学 | 119篇 |
妇产科学 | 10篇 |
基础医学 | 161篇 |
口腔科学 | 118篇 |
临床医学 | 148篇 |
内科学 | 167篇 |
皮肤病学 | 34篇 |
神经病学 | 136篇 |
特种医学 | 5篇 |
外科学 | 101篇 |
综合类 | 6篇 |
一般理论 | 1篇 |
预防医学 | 139篇 |
眼科学 | 9篇 |
药学 | 87篇 |
肿瘤学 | 70篇 |
出版年
2024年 | 5篇 |
2023年 | 6篇 |
2022年 | 18篇 |
2021年 | 19篇 |
2020年 | 19篇 |
2019年 | 36篇 |
2018年 | 29篇 |
2017年 | 39篇 |
2016年 | 36篇 |
2015年 | 31篇 |
2014年 | 43篇 |
2013年 | 77篇 |
2012年 | 94篇 |
2011年 | 92篇 |
2010年 | 48篇 |
2009年 | 68篇 |
2008年 | 82篇 |
2007年 | 82篇 |
2006年 | 65篇 |
2005年 | 66篇 |
2004年 | 62篇 |
2003年 | 65篇 |
2002年 | 57篇 |
2001年 | 11篇 |
2000年 | 9篇 |
1999年 | 5篇 |
1998年 | 19篇 |
1997年 | 7篇 |
1996年 | 13篇 |
1995年 | 11篇 |
1994年 | 14篇 |
1993年 | 6篇 |
1992年 | 6篇 |
1990年 | 7篇 |
1988年 | 3篇 |
1987年 | 3篇 |
1984年 | 5篇 |
1983年 | 6篇 |
1982年 | 4篇 |
1980年 | 3篇 |
1979年 | 5篇 |
1978年 | 7篇 |
1977年 | 5篇 |
1976年 | 3篇 |
1975年 | 3篇 |
1974年 | 4篇 |
1973年 | 7篇 |
1972年 | 2篇 |
1970年 | 2篇 |
1967年 | 2篇 |
排序方式: 共有1320条查询结果,搜索用时 15 毫秒
1.
Bacteriophage PRD1 is an icosahedral dsDNA virus with a diameter of 740 A and an outer protein shell composed of 720 copies of major coat protein P3. Spike complexes at the vertices are composed of a pentameric base (protein P31) and a spike structure (proteins P5 and P2) where the N-terminal region of the trimeric P5 is associated with the base and the C-terminal region of P5 is associated with receptor-binding protein P2. The functionality of proteins P3 and P5 was investigated using insertions and deletions. It was observed that P3 did not tolerate changes whereas P5 tolerated changes much more freely. These properties support the hypothesis that viruses have core structures and functions, which remain stable over time, as well as other elements, responsible for host interactions, which are evolutionally more fluid. The insertional probe used was the apex of exposed loop 4 of group B meningococcal outer membrane protein PorA, a medically important subunit vaccine candidate. It was demonstrated that the epitope could be displayed on the virus surface as part of spike protein P5. 相似文献
2.
Monfraix S Bayat S Porra L Berruyer G Nemoz C Thomlinson W Suortti P Sovijärvi AR 《Physics in medicine and biology》2005,50(1):1-11
The aim of this study was to assess the feasibility of a novel respiration-gated spiral synchrotron radiation computed tomography (SRCT) technique for direct quantification of absolute regional lung volumes, using stable xenon (Xe) gas as an inhaled indicator. Spiral SRCT with K-edge subtraction using two monochromatic x-ray beams was used to visualize and directly quantify inhaled Xe concentrations and airspace volumes in three-dimensional (3D) reconstructed lung images. Volume measurements were validated using a hollow Xe-filled phantom. Spiral images spanning 49 mm in lung height were acquired following 60 breaths of an 80% Xe-20% O2 gas mixture, in two anaesthetized and mechanically ventilated rabbits at baseline and after histamine aerosol inhalation. Volumetric images of 20 mm lung sections were obtained at functional residual capacity (FRC) and at end-inspiration. 3D images showed large patchy filling defects in peripheral airways and alveoli following histamine provocation. Local specific lung compliance was calculated based on FRC/end-inspiration images in normal lung. This study demonstrates spiral SRCT as a new technique for direct determination of regional lung volume, offering possibilities for non-invasive investigation of regional lung function and mechanics, with a uniquely high spatial resolution. An example of non-uniform volume distribution in rabbit lung following histamine inhalation is presented. 相似文献
3.
Saana Mnkre Liina Kuuluvainen Celia Kun-Rodrigues Susana Carmona Johanna Schleutker Jose Bras Minna Pyhnen Rita Guerreiro Liisa Myllykangas 《European journal of human genetics : EJHG》2021,29(4):663
Cerebral small vessel disease (CSVD) is the most important cause of vascular cognitive impairment (VCI). Most CSVD cases are sporadic but familial monogenic forms of the disorder have also been described. Despite the variants identified, many CSVD cases remain unexplained genetically. We used whole-exome sequencing in an attempt to identify novel gene variants underlying CSVD. A cohort of 35 Finnish patients with suspected CSVD was analyzed. Patients were screened negative for the most common variants affecting function in NOTCH3 in Finland (p.Arg133Cys and p.Arg182Cys). Whole-exome sequencing was performed to search for a genetic cause of CSVD. Our study resulted in the detection of possibly pathogenic variants or variants of unknown significance in genes known to associate with CSVD in six patients, accounting for 17% of cases. Those genes included NOTCH3, HTRA1, COL4A1, and COL4A2. We also identified variants with predicted pathogenic effect in genes associated with other neurological or stroke-related conditions in seven patients, accounting for 20% of cases. This study supports pathogenic roles of variants in COL4A1, COL4A2, and HTRA1 in CSVD and VCI. Our results also suggest that vascular pathogenic mechanisms are linked to neurodegenerative conditions and provide novel insights into the molecular basis of VCI.Subject terms: Stroke, Sequencing, Genetics research, Dementia 相似文献
4.
We show here that T cell cross-reactivity between heterologous viruses influences the immunodominance of virus-specific CD8(+) T cells by two mechanisms. First, T cells specific for cross-reactive epitopes dominate acute responses to viral infections; second, within the memory pool, T cells specific for cross-reactive epitopes are maintained while those specific for non-cross-reactive epitopes are selectively lost. These findings suggest an immunological paradigm in which viral infections shape the available T cell repertoire, causing alterations in the hierarchies of both the primary and memory CD8(+) T cell responses elicited by subsequent viral infections. Thus, immunodominance is a function of the host's previous exposure to unrelated pathogens, and this may have an impact on protective immunity and immunopathology. 相似文献
5.
6.
The present study investigated sex differences and the effect of a high level of estradiol in the female meadow vole on performance in the forced swim test (FST) and the Morris water maze in meadow voles. Female meadow voles were ovariectomized (OVX) and administered either vehicle (sesame oil) or estradiol for 2 days prior to performing the FST. Four days following the FST, all animals were run in the Morris water maze. Results indicated that estradiol-injected female meadow voles showed more 'depressive-like' behaviors in the FST (greater time spent immobile and less time spent swimming) than vehicle-treated female or male meadow voles. In addition, estradiol-treated females had impaired performance (greater latencies and distance swam to reach the hidden platform) than both vehicle-treated female and male meadow voles, consistent with previous data. Despite the fact that estradiol administration increased 'depressive-like' behaviors in the FST and impaired performance in the Morris water maze, there was no correlation between the two behaviors indicating that 'depressive-like' behaviors did not account for the differences seen in spatial performance in the Morris water maze. To our knowledge, this is the first demonstration in rodents indicating that estradiol-mediated changes in behavior in the FST is not indicative of subsequent performance in the Morris water maze. 相似文献
7.
Summary To clarify the effects of withdrawal from chronic morphine treatment on cerebral dopamine (DA) turnover, we have measured the -methyl-p-tyrosine (MT)-induced depletion of DA in five brain areas of male Wistar rats given morphine twice daily for 40 or 60 days. After the last morphine dose (50 or 70 mg/kg) the rats were withdrawn for 1, 2 or 4 days. In order to study the development of tolerance some of the rats were challenged with 10 mg/kg of morphine.Withdrawal of morphine retarded the MT-induced DA depletion in the limbic forebrain and after long enough chronic treatment in the striatum, too. The challenge dose of morphine accelerated the cerebral DA depletion slightly less in rats withdrawn for 1 day from 60-day chronic morphine treatment than in rats treated chronically with saline, but it enhanced the DA depletion more in rats withdrawn from morphine for 2 and 4 days than in chronic saline rats. This enhancement was clearest in rats withdrawn for 4 days from 60-day treatment. Thus withdrawal from morphine seems to sensitize the rats to the DA depletion accelerating effect of morphine.Our results show that repeated administration of morphine creates no marked tolerance to the DA depletion accelerating effect of morphine. In contrast, the dopaminergic neurones of the chronically treated rats seem to depend on continuous morphine administration for their normal functioning. Furthermore, the retarded DA turnover after discontinuation of morphine treatment seems to sensitize the dopaminergic neurones to the DA depletion accelerating effect of morphine. The limbic dopaminergic neurones are more easily affected by both acute and chronic morphine treatment than the striatal ones. 相似文献
8.
Summary The minimum inhibitory concentrations (MIC) for 100 strains ofStreptococcus agalactiae varied as follows: ampicillin 0.1 to >1 mg/l, amoxicillin 0.03 to 0.5 mg/l, cephalexin 2 to >16 mg/l, nitrofurantoin 8 to >64 mg/l, suphadiazine all >500 mg/l and trimethoprim <3.9 to >250 mg/l. The MICs of the -lactams were not affected by inoculum density. Amoxicillin was 2.5 times as active as ampicillin. Sulphadiazine and trimethoprim acted synergistically, and the average factor of potentiation exceeded 5.9. The growth curves and drug susceptibilities of 19 strains isolated from urine were similar to those of the 81 strains isolated from other sources.
In-vitro-Aktivität von Ampicillin, Amoxicillin, Cephalexin, Nitrofurantoin, Sulphadiazin und Trimethoprim gegenüber Isolaten von Streptococcus agalactiae aus Urin und anderem infektiösen Material
Zusammenfassung Die minimalen Hemmkonzentrationen (MHK) für 100 Stämme vonStreptococcus agalactiae variierten wie folgt: Ampicillin 0,1 bis >1 mg/l, Amoxicillin 0,03 bis 0,5 mg/l, Cephalexin 2 bis >16 mg/l, Nitrofurantoin 8 bis >64 mg/l; die MHK von Sulphadiazin lag für alle Stämme bei >500 mg/l, die MHK von Trimethoprim bei <3,9 bis >250 mg/l. Die MHKs der -Laktame wurden von der Inokulumdichte nicht beeinflußt. Amoxicillin besaß die 2,5fache Aktivität von Ampicillin. Sulphadiazin und Trimethoprim wirkten synergistisch mit einem durchschnittlichen Potenzierungsfaktor von über 5,9. Die Wachstumskurven und Antibiotikaempfindlichkeit der 19 Urinisolate waren mit denjenigen der 81 aus anderem infektiösen Material isolierten Stämme vergleichbar.相似文献
9.