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91.
Anders Sundan Tove Gullstein-Jahr Marit Otterlei Liv Ryan Vladimir Bazilu Samuel D. Wrightu Terje Espevik 《European journal of immunology》1994,24(8):1779-1784
Here we report that soluble CD14 isolated from the urine of nephrotic patients (uCD14) contains a potent cytokine inducing activity. CD14 derived from urine appeared to consist of two major polypeptides of about 54 and 48 kDa. In uCD14 isolated from three different nephrotic patients the cytokine-inducing activity appeared to co-migrate with the 48-kDa polypeptide which upon sequencing had the same N-terminal sequence as native CD14. Treatment of human monocytes and the human astrocytoma cell line U373 with uCD14 resulted in a strong secretion of tumor necrosis factor (TNF) and interleukin-6, respectively. The cytokine-inducing activity of the uCD14 preparations was unaffected by the absence of serum. This is in contrast to the activation of human monocytes and U373 cells by lipopolysaccharide (LPS) which is highly dependent on the presence of serum. The cytokine-inducing activity was not affected by LPS-binding protein (LBP) or polyclonal rabbit antibodies against LBP The TNF-inducing activity of uCD14 was also heat labile in contrast to the cytokine-inducing activity of LPS, which was relatively heat resistant. The results suggest that CD14 may exist in at least two forms of which one is involved in cytokine induction. 相似文献
92.
Urs Bräger Tove Mühle Loannis Fourmousis Niklaus P. Lang rea Mombelli 《Journal of periodontal research》1997,32(7):575-582
The aim of the present experiment was to assess the effect of the administration of the NSAID flurbiprofen (Froben®) on tissue healing after periodontal surgery. Sites from patients with the same treatment modality (modified Widman flap) but receiving a placebo drug and sites within each patient not exposed to surgery served as controls. Nineteen patients suffering from moderate to severe periodontal disease were recruited and they signed informed consent forms. These patients required periodontal surgery as assessed at the periodontal re-evaluation. The sites chosen for the study were all diagnosed with PPD ≥ 5 mm and were bleeding on probing. During the healing phase 10 patients received 50 mg Froben® 3 times per day for 30 d whereas 9 patients received a placebo drug. Two sites with PPD ≥ 5 mm after initial therapy and bleeding on probing served as surgical sites, whereas 2 similar sites were not exposed to surgery. The study design was set up double-blind. The radiographic examination consisted of 2–4 standardized vertical bitewings obtained at the periodontal re-evaluation (BL) at 1, 3 and 6 months post-surgically for digital subtraction and computer assisted densitometric image analysis (CADIA). The regions of interest analysed were mesial or distal crestal sites. Minimal remodelling activity was observed radiographically after periodontal surgery in both patient groups. There were no statistically significant differences between the four groups of sites regarding the mean changes in density when analysing the pairs of radiographs 0–1, 0–3, 0–6 months. A frequency analysis was performed to list the number of sites with different ranges of density change. No differences in the distributions of the numbers of sites were observed when comparing the 4 site groups (Kolmogorov-Smirnov, p > 0.05). A significant reduction of the probing pocket depth and a significant amount of clinical attachment gain was noted at the surgically treated sites irrespective of whether the patients had used flurbiprofen or placebo. Whereas the pathways leading to bone resorption in periodontally diseased sites have been shown, in other studies, to be influenced by NSAID, the results of the present study could not justify general administration of Froben® for the purpose of reduction of bone resorption after periodontal surgical procedures in patients with adult periodontitis. 相似文献
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94.
Gospic K Gunnarsson T Fransson P Ingvar M Lindefors N Petrovic P 《Psychopharmacology》2008,197(2):295-307
Rationale The cholecystokinin (CCK) and opioid neuromodulatory systems work in an antagonistic fashion and can modulate emotional states
and noxious input in opposite directions. In this behavioral study, we generalize this idea and suggest that CCK and opioids
can modulate the processing of other external signals, e.g., visual stimuli rather than only noxious input.
Objectives The objective of this study was to determine whether CCK and an opioid agonist could modulate the emotional experience of
visual stimuli.
Materials and methods Thirteen healthy male volunteers viewed standardized pictures with either neutral or unpleasant content. Simultaneously, one
of three treatments was administered in a randomized, double-blind crossover design: the CCKb receptor agonist pentagastrin (0.1 μg/kg), the mu-opioid receptor agonist remifentanil (0.0625 μg/kg), or saline. Self-ratings
of the emotional experience of pictures and drugs were sampled together with psychological tests and recording of heart rate.
Results Pentagastrin treatment increased the rating of unpleasantness for both neutral and unpleasant pictures, while it decreased
the rating of pleasantness for the neutral pictures. These effects did not correlate with the degree of general unpleasantness
induced by the drug. Remifentanil treatment increased the pleasantness for the neutral pictures. While pentagastrin treatment
induced a heart rate increase, unpleasant pictures induced a heart rate decrease, and the magnitude of change in heart rate
correlated positively for these conditions.
Conclusions This study shows that the CCK and the opioid system modulate how external stimuli are emotionally perceived, suggesting a
possible involvement in affective disorders. 相似文献
95.
Blood metabolism of [methyl-
11C]choline; implications for in vivo imaging with positron emission tomography 总被引:1,自引:1,他引:0
Anne Roivainen Sarita Forsback Tove Grönroos Pertti Lehikoinen Meri Kähkönen Eija Sutinen Heikki Minn 《European journal of nuclear medicine and molecular imaging》2000,27(1):25-32
[methyl-11C]Choline (11C-choline) is a radioligand potentially useful for oncological positron emission tomography (PET). As a first step towards
the development of a kinetic model for quantification of 11C-choline uptake, blood metabolism of 11C-choline during PET imaging was studied in humans. High-performance liquid chromatography (HPLC) and thin-layer chromatography
(TLC) were used for the analysis of 11C-choline and its radioactive metabolites. Prior to human PET imaging we studied ex vivo the biodistribution and metabolism
of intravenously administered 11C-choline in rats. Our results revealed that the radioactivity accumulated particularly in kidney, lung, adrenal gland and
liver. Chromatographic analysis showed that the level of unmetabolized 11C-choline in rat plasma decreased from 42%±20% (mean±SD) at 5 min to 21%±10% at 15 min after injection. In accordance with
these findings, in humans the unmetabolized 11C-choline represents 62%±19% of the total radioactivity in arterial plasma at 5 min after injection and 27%±12% at 15 min.
In human venous plasma the corresponding values were 85%±12% and 48%±12% at 5 and 10 min, respectively. The major metabolite
observed in both human and rat plasma was identified as 11C-betaine. In human arterial plasma this maximally represented 82%±9% of the total radioactivity at 25 min after radiotracer
injection. By 20 min after injection, the 11C-choline and 11C-betaine in human arterial plasma reached a plateau, and their fractional activities remained nearly constant thereafter.
Although most of the circulating 11C-choline in blood is transported to tissues, it does not disappear totally from blood within the first 40 min after tracer injection.
Received 7 July and in revised form 16 September 1999 相似文献
96.
The skin barrier, located in the stratum corneum, is influenced mainly by the lipid and protein composition of this layer. In eczematous diseases impairment of the skin barrier is thought to be of prime importance. Topical anti-inflammatory drugs and emollients are the most widely used eczema treatments. The aim of this study was to examine the effects of topically applied corticosteroid, tacrolimus and emollient on stratum corneum lipids and barrier parameters. Nineteen healthy volunteers participated in the study. Both forearms of the subjects were divided into four areas, which were treated twice daily for one week with betamethasone, tacrolimus, emollient, or left untreated, respectively. After one week each area was challenged with a 24 h sodium lauryl sulphate patch test. The lipids were collected using the cyanoacrylate method and evaluated by high performance thin layer chromatography. For evaluation of the skin barrier, transepidermal water loss, erythema and electrical capacitance were measured. The ceramide/cholesterol ratio was increased in betamethasone- (p?=?0.008) and tacrolimus-treated (p?=?0.025) skin compared with emollient-treated skin. No differences in ceramide subgroups were found between treatment regimes. Pretreatment with betamethasone (p?=?0.01) or with tacrolimus (p?=?0.001) causes a decreased inflammatory response to sodium lauryl sulphate compared with emollient. In conclusion, treatment with betamethasone and tacrolimus has a positive effect on the ceramide/cholesterol ratio and susceptibility to irritant reaction compared with an emollient. 相似文献
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