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51.
Zaccone D Dabrowski K Lauriano ER de Pasquale A Macrì D Satora L Lanteri G 《Acta histochemica》2012,114(4):370-378
Anatomical and functional studies on the autonomic innervation as well as the location of airway receptors in the air-bladder of lepisosteids are very fragmentary. These water-breathing fishes share in common with the bichirs the presence of a glottis (not a ductus pneumaticus) opening into the esophagus. In contrast to a high concentration of neuroepithelial cells (NECs) contained in the furrowed epithelium in the lung of Polypterus, these cells are scattered as solitary cells in the glottal epithelium, and grouped to form neuroepithelial bodies (NEBs) in the mucociliated epithelium investing the main trabeculae in the air-bladder of Lepisosteus osseus and L. oculatus. The present immunohistochemical studies also demonstrated the presence of nerve fibers in the trabecular striated musculature and a possible relation to NEBs in these species, and identified immunoreactive elements of this innervation. Tyrosine hydroxylase (TH), choline acetyltransferase (ChAT), 5-HT and neuropeptide immunoreactivities were detected in the intramural nerve fibers. 5-HT and VIP immunopositive nerve fibers are apparently associated with NEBs. TH, VIP and SP immunoreactivities are also present in nerve fibers coursing in the radially arranged striated muscle surrounding the glottis and its submucosa. 5-HT positive neurons are also found in submucosal and the muscle layers of the glottis. The physiological function of the adrenergic and inhibitory innervation of the striated muscle as well as the neurochemical coding and morphology of the innervation of the NEBs are not known. Future studies are needed to provide evidence for these receptors with the capacity of chemoreceptors and/or mechanoreceptors. 相似文献
52.
Sakamaki Y Sakatsume M Wang X Inomata S Yamamoto T Gejyo F Narita I 《Nephrology (Carlton, Vic.)》2011,16(2):211-218
Aim: SM22α (transgelin) has been focused upon as a player in the process of phenotypic changes of types of cells. The SM22α expression in the rat anti‐glomerular basement membrane (GBM) nephritis model and differences from an established phenotypic marker for the myofibroblast, α‐smooth muscle actin (αSMA), were investigated. Methods: The rat kidney tissues were processed for histological studies, immunohistochemical and immunoelectronmicroscopy analyses on days 0, 7, 28, 42 and 56 after injection of rabbit anti‐GBM serum for the disease induction. Results: Immunohistochemistry with anti‐SM22α antibodies (Ab) revealed that kidneys of the nephritic rats on day 7 expressed SM22α in podocytes, crescentic cells and epithelial cells of Bowman's capsule. After 28 days, SM22α was also expressed in peritubular interstitial cells. Double immunofluorescence with anti‐SM22α Ab and anti‐αSMA Ab showed that SM22α was preferentially expressed in podocytes, whereas αSMA was positive in mesangial cells on day 7. After day 28, both molecules became positive in peritubular interstitial cells. Conclusion: SM22α was expressed in epithelial cells of inflamed glomeruli in the early phase, and then also in peritubular interstitial cells in the later phase of anti‐GBM nephritis model. SM22α presented unique kinetics of expression distinct from αSMA. 相似文献
53.
目的探讨参麦注射液在百草枯中毒所致肺损伤中的作用。方法120只SD大鼠随机分为百草枯中毒组(APP),参麦注射液治疗组(SM1,SM2,SM3)。HE染色观察参麦注射液治疗组组织结构变化,采用免疫组织化学法测定各组肺组织中TGF—β1、IL-1β的表达水平。结果百草枯中毒组肺组织充血水肿明显,肺泡破坏严重,治疗组有所减轻;各治疗组与百草枯中毒组之间转化生长因子β-1(TGF—β1),白细胞介素-1β(IL—1β)水平均较治疗组明显降低,各治疗组随剂量的增加,TGF-β1,IL-1β水平有明显下降,差异有显著性(P〈0.05)。结论参麦注射液在百草枯所致中毒大鼠肺损伤中能使TGF—β1,IL-1β表达水平下调,减轻肺泡炎症和充血程度,减轻百草枯中毒所致肺损伤,延缓和抑制肺纤维化的发生、发展。 相似文献
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Antibodies against hydrophobic antigens are common in several autoimmune diseases. However, detection of such antibodies by standard immune-assays, such as ELISA, is problematic, in part because of the problems with coating hydrophobic molecules onto polystyrene multi-well plates. We describe a novel method of stably associating hydrophobic antigens to ELISA plates. By mixing the antigen with a hydrophobic molecule containing a hydrophilic anchor, we generate mixed lipid aggregates that can attach to ELISA plates, and are resistant to detergent wash. Using the ganglioside GM-1 and phosphatidylethanolamine conjugated to the hapten DNP (dinitrophenyl) as model antigens, we show that hydrophobic antigens incorporated into mixed lipid aggregates expose their antigenic determinants in a correct configuration. The detection limit of both GM-1 and DNP-PE was considerably improved compared to when these antigens were coated on ELISA plates using organic solvents. Furthermore GM-1 incorporated into mixed lipid aggregates can be detected by specific antibodies in patient serum. The method of incorporating hydrophobic antigens into mixed lipid aggregates for stable association to ELISA plates can presumably be applied to a vast array of hydrophobic antigens, and may well be developed into a large scale screening system for serum reactivity towards different hydrophobic antigens. 相似文献
56.
目的 建立盐酸青藤碱(sinomenine hydrochloride,SM-HCl)脂质体包封率的测定方法,并阐明药物在脂质体中的滞留特性。方法 采用薄膜分散法制备SM-HCl脂质体。以HPLC法测定脂质体药物的量,色谱柱为Kromasil ODS C18柱(250 mm×4.6 mm,5 μm),流动相为甲醇-水-乙二胺(55∶45∶0.225),体积流量1.0 mL/min,检测波长265 nm。以离心沉淀-离心超滤法测定SM-HCl脂质体的包封率,并与以枸橼酸缓冲液(pH 7.0)水化的脂质体样品稀释前后的包封率进行对比。结果 辅料与溶剂对青藤碱的定量测定无干扰,青藤碱在9.82~78.56 μg/mL线性关系良好(r=0.999 7),平均回收率在99.29%~100.8%,日内与日间精密度良好(RSD≤2.1%)。50 μL药液可使超滤膜对药物的吸附达到饱和。以枸橼酸缓冲液(pH 7.0)水化的脂质体样品的包封率为33.16%,稀释1倍后该样品的包封率降至14.75%。结论 HPLC法与离心沉淀-离心超滤法结合可用于测定SM-HCl脂质体的包封率,该方法快速、准确;离心超滤中应弃去50 μL初滤液以确保滤液与脂质体外水相药物浓度一致;青藤碱与脂质双分子层有一定的亲和力,但在脂质体中的滞留性较差。 相似文献
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58.
Brian John Angus 《Expert opinion on pharmacotherapy》2020,21(6):645-651
ABSTRACT
Introduction
Severe falciparum malaria stills accounts for around half a million childhood deaths per year in sub-Saharan Africa. Prompt treatment of sick children close to home starting with artesunate given rectally by appropriately trained people can be lifesaving. 相似文献59.
Monoclonal antibodies to human casein 总被引:1,自引:0,他引:1
Two monoclonal antibodies, LICR-LON-32.2 (32.2) and LICR-LON-14.1 (14.1), are described which react with human casein. 32.2 reacts with human beta-casein and 14.1 with human kappa-casein. 32.2 also reacts with rat band 2 casein and bovine beta-casein, but 14.1 appears to be specific for human kappa-casein. These monoclonal antibodies do not cross-react with other milk proteins. 相似文献
60.