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131.
Bernardo Hochman Felipe Contoli Isoldi José Octávio Gonçalves de Freitas Guilherme Abbud Franco Lapin Paulo Rogério Quieregatto Erica Calcagno Raymundo Da Silva Gerson Chadi Lydia Masako Ferreira 《Central European Journal of Biology》2014,9(12):1140-1146
Background. The skin neurogenic inflammation is mainly related to Substance P (SP) and Calcitonin Gene-related Peptide (CGRP). There is no data on their availability in the dynamics of skin nerve endings, concerning their release and replenishment after a nociceptive stimulus, so this was investigated. Materials and methods. 25 rats were randomly distributed in 5 groups. The animals of the control group (CG) determined the baseline levels of neuropeptides in the skin. The groups S0 and S30 did not receive any cutaneous stimulus at 30 and 60 minutes, respectively. In the group S1, an “incision stimulus” was made at 30 minutes. In the group S31, a nociceptive stimulus was performed by subdermal scratching at 30 minutes and, at 60 minutes, the “incision stimulus” was carried out in the same location (“nociceptive hyperstimulation”). The skin samples of the other animals were harvested from the back 1 minute after their death. SP, pro-CGRP and CGRP were quantified by Western Blotting. Results. The “incision stimulus” released SP, S1 compared to S0 (p <0.05) detected in the first minute, and the replenishment time was more than 30 minutes. Also, it cleaved pro-CGRP, S1 compared to S31 (p <0.05) in the first minute, and its replenishment time less than 30 minutes. Release of CGRP was not detected. Conclusion. The incision released SP already detected in the first minute; its replenishment time is more than 30 minutes. The incision decreased pro-CGRP, also detected in the first minute; and its replenishment time is less than 30 minutes. 相似文献
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Richter SH Garner JP Zipser B Lewejohann L Sachser N Touma C Schindler B Chourbaji S Brandwein C Gass P van Stipdonk N van der Harst J Spruijt B Võikar V Wolfer DP Würbel H 《PloS one》2011,6(1):e16461
In animal experiments, animals, husbandry and test procedures are traditionally standardized to maximize test sensitivity and minimize animal use, assuming that this will also guarantee reproducibility. However, by reducing within-experiment variation, standardization may limit inference to the specific experimental conditions. Indeed, we have recently shown in mice that standardization may generate spurious results in behavioral tests, accounting for poor reproducibility, and that this can be avoided by population heterogenization through systematic variation of experimental conditions. Here, we examined whether a simple form of heterogenization effectively improves reproducibility of test results in a multi-laboratory situation. Each of six laboratories independently ordered 64 female mice of two inbred strains (C57BL/6NCrl, DBA/2NCrl) and examined them for strain differences in five commonly used behavioral tests under two different experimental designs. In the standardized design, experimental conditions were standardized as much as possible in each laboratory, while they were systematically varied with respect to the animals' test age and cage enrichment in the heterogenized design. Although heterogenization tended to improve reproducibility by increasing within-experiment variation relative to between-experiment variation, the effect was too weak to account for the large variation between laboratories. However, our findings confirm the potential of systematic heterogenization for improving reproducibility of animal experiments and highlight the need for effective and practicable heterogenization strategies. 相似文献
134.
Sun LQ Zhao J Zhang TT Qu L Wang X Xue B Li XJ Mu YM Lu JM 《Neurochemical research》2012,37(5):996-1010
Diabetic peripheral neuropathy (DPN) is one of the most common and debilitating microvascular complications of diabetes, and
there is no effective therapy for the prevention or treatment of DPN. Oxidative stress triggers several pathways of injury
and may be the unifying factor of hyperglycemia. The aim of this study was to investigate protective effect of Salvianolic
acid B (Sal B) on the high glucose (HG)-induced oxidative stress-induced mitochondrial pathway activation and Schwann cells
(SCs) apoptosis in vitro. We found that Sal B inhibited the HG-induced oxidative stress by reducing ROS and 8-hydroxy-2-deoxy
Guanosine (8-OHdG) production, and mitochondrial depolarization and apoptosis in SCs in a dose-dependent manner. Furthermore,
Sal B down-regulated the HG-mediated Bax expression and AIF nuclear translocation and the release of cytochrome c, but up-regulated
the HG-induced BcL-2 expression in SCs. In addition, Sal B attenuated the HG-induced activation of caspase 3 and 9 and minimized
the cleavage of PARP in SCs. Our results indicated that Sal B antagonized the HG-induced oxidative stress, activation of the
mitochondrial pathway and apoptosis in SCs. 相似文献
135.
Gurfein BT Stamm AW Bacchetti P Dallman MF Nadkarni NA Milush JM Touma C Palme R Di Borgo CP Fromentin G Lown-Hecht R Konsman JP Acree M Premenko-Lanier M Darcel N Hecht FM Nixon DF 《Molecular medicine (Cambridge, Mass.)》2012,18(1):606-617
Chronic stress is associated with negative health outcomes and is linked with neuroendocrine changes, deleterious effects on innate and adaptive immunity, and central nervous system neuropathology. Although stress management is commonly advocated clinically, there is insufficient mechanistic understanding of how decreasing stress affects disease pathogenesis. Therefore, we have developed a "calm mouse model" with caging enhancements designed to reduce murine stress. Male BALB/c mice were divided into four groups: control (Cntl), standard caging; calm (Calm), large caging to reduce animal density, a cardboard nest box for shelter, paper nesting material to promote innate nesting behavior, and a polycarbonate tube to mimic tunneling; control exercise (Cntl Ex), standard caging with a running wheel, known to reduce stress; and calm exercise (Calm Ex), calm caging with a running wheel. Calm, Cntl Ex and Calm Ex animals exhibited significantly less corticosterone production than Cntl animals. We also observed changes in spleen mass, and in vitro splenocyte studies demonstrated that Calm Ex animals had innate and adaptive immune responses that were more sensitive to acute handling stress than those in Cntl. Calm animals gained greater body mass than Cntl, although they had similar food intake, and we also observed changes in body composition, using magnetic resonance imaging. Together, our results suggest that the Calm mouse model represents a promising approach to studying the biological effects of stress reduction in the context of health and in conjunction with existing disease models. 相似文献
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Sunny E. Townsend I Putu Sumantra Pudjiatmoko Gusti Ngurah Bagus Eric Brum Sarah Cleaveland Sally Crafter Ayu P. M. Dewi Dewa Made Ngurah Dharma Jonathan Dushoff Janice Girardi I Ketut Gunata Elly F. Hiby Corlevin Kalalo Darryn L. Knobel I Wayan Mardiana Anak Agung Gde Putra Luuk Schoonman Helen Scott–Orr Mike Shand I Wayan Sukanadi Pebi Purwo Suseno Daniel T. Haydon Katie Hampson 《PLoS neglected tropical diseases》2013,7(8)