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991.
AbstractSurfactin, a natural lipopeptide produced by Bacillus, is gaining attention for potentially biomedical and pharmaceutical applications. Here, surfactin was assayed for oral delivery of insulin (INS) by its ability to bind to and promote protein to penetrate through the cell membrane. Analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, surfactin was found to form co-precipitates with INS to protect it from acidic and enzymatic attack in the gastrointestinal tract. Further analysis by non-reductive electrophoresis showed surfactin could bind to INS forming heteropolymers. Analysis with circular dichroism, we found this binding significantly influenced the INS structure with decreased rigid α-helix and β-turn, but with increased flexible β-sheet and random coil. The change with more flexible structure was favorable for INS to penetrate through the cell membrane. Fluorescence spectra analysis also showed surfactin could lead Phe and Tyr in the inner of INS exposed outside, further promoting INS permeabilization by improving the hydrophobic-lipophilic interactions between INS and cell membrane. As a result, the effective permeability (Peff) of INS plus surfactin was 4.3 times of that of INS alone. In vivo assay showed oral INS with surfactin displayed excellent hypoglycemic effects with a relative bioavailability of 12.48% and 5.97% in diabetic mice and non-diabetic dogs, respectively. Summary, surfactin is potential for oral delivery of INS by its role as an effective protease inhibitor and permeability enhancer. 相似文献
992.
Chinese scientists have capitalized on the rich flora and the ethnomedical experience in China, in their pursuit of fertility regulating agents from natural products. Discoveries range from anti-implantation agents to abortifacient and pregnancy-terminating compounds, as well as a male contraceptive. Chemistry and bioactivity of these compounds and materials are reviewed in this paper, with the hope that further research and collaboration will take place to help solve the problem of population explosion. 相似文献
993.
目的:探讨四瓣技术在改良结膜囊泪囊鼻腔吻合术中应用的安全性及有效性。方法:回顾性临床研究。选取2017-09/2020-06在我院就诊的泪道疾病患者28例28眼作为研究对象,均行结膜囊泪囊鼻腔吻合术。术后随访6~12mo,观察患者手术效果、满意度及术后并发症情况。结果:本组患者术后荧光素钠染料排泄试验阳性率为96%(27/28),手术成功率为96%(27/28),其中治愈率为68%(19/28),好转率为28%(8/28),无效率为4%(1/28),患者总体满意度为93%(26/28)。术后并发症包括眼部异物感(28眼)、球结膜充血(11眼)、鼻腔结膜囊渗血(8眼)及泪道引流管脱出(1眼)。结论:四瓣技术用于改良结膜囊泪囊鼻腔吻合术手术成功率高,并发症少,安全有效。 相似文献
994.
Li Yingxian Chen Wei Zhao Linchun Zhang Ji-Quan Zhao Yonglong Li Chun Guo Bing Tang Lei Yang Yuan-Yong 《RSC advances》2022,12(32):20550
Amide is a fundamental group that is present in molecular structures of all domains of organic chemistry and the construction of this motif with high atom economy is the focus of the current research. Specifically, N-methyl amides are valuable building blocks in natural products and pharmaceutical science. Due to the volatile nature of methyl amine, the generation of N-methyl amides using simple acids with high atom economy is rare. Herein, we disclose an atom economic protocol to prepare this valuable motif under DABCO/Fe3O4 cooperative catalysis. This protocol is operationally simple and compatible with a range of aliphatic and (hetero)aromatic acids with very good yields (60–99%). Moreover, the Fe3O4 can be easily recovered and high efficiency is maintained for up to ten cycles.The generation of N-methyl amides using simple acids with high atom economy is rare owning to the volatile nature of methyl amine. Herein, an atom economic protocol was disclosed to prepare this valuable motif under DABCO/Fe3O4 cooperative catalysis.Amide is a fundamental group that is present in molecular structures of all domains of organic chemistry.1 It is widely distributed in natural products, synthetic drugs and functional polymers, and is also the key chemical connection in proteins.2 It has been shown that amide bond formation alone accounts for 65% of all preliminary screening reactions in the pharmaceutical industry.3 This means the generation of amide bonds with high atom efficiency is of high practical importance. And not surprisingly, ‘amide formation avoiding poor atom economy reagents’ was voted as the top challenge for organic chemistry by the ACS Green Chemistry Institute in 2007.3From synthetic point of view, the ideal way to produce amide bonds would be the direct coupling of readily available carboxylic acids and amines, but this process is thermodynamically unfavourable due to the formation of the corresponding carboxylate-ammonium salt,4 therefore, stoichiometric amount of coupling reagents, such as DCC, DIC, EDCI, HATU, HBTU, HCTU, SOCl2, BOP, acid chloride etc, are generally required to sidestep thermal conditions for amide bond formation.5 These reagents are highly successful, but the process generally suffers from poor atom economy and side products removal issue especially in the large-scale applications.5 To overcome these drawbacks, “nonclassical” amide bonds formation routes were investigated.6 In these processes, the catalyst takes the role of a coupling reagent in generating an active ester suitable for amidation in a waste-free manner. However, these processes have not been applied in the preparation of N-methyl amides, probably because the methyl amine was delivered in its hydrochloride salt, alcoholic or aqueous form due to its volatile nature.On a different note, N-methyl amides are extensively presented in numerous natural products and pharmaceutical molecules, as shown in Fig. 1,7 and the methylation of amides is a promising way to improve the pharmacological property of molecules.8 However, the synthesis of N-methyl amides compounds relies heavily on non-catalytic approaches.5,9 Catalytic approaches were also investigated by Hisaeda,10 Kundu,11 Li,12 Guo,13 Yu,14 Maruoka,15 Wang,16 Chen,17 Lamaty18 and their co-workers starting from nitriles, primiary amides, aldoximes, aldehydes, lignin, carbamoylsilane and alcohols. Until recently, Thakur,19 Marce,20 Sadeghzadeh21 and their co-workers developed elegant N-methyl amidation approach starting from carboxylic acids under nano-MgO, diatomite Earth@IL/ZrCl4 and Mg(NO3)2·6H2O catalysis respectively, while limitations like poor substrate scope or sophisticated tailored catalyst still persist. Mindful of all the above issues, developing an N-methyl amidation process of simple carboxylic acids, which is still of great challenge in synthesis, and establishing a broad (hetero)aryl scope with high atom economy from commercial available reagents and catalysts were critical considerations in this study. Moreover, the significance of N-methyl amides combined with our interests in the development of green synthetic approaches motivated us to explore the direct coupling of the carboxylic acids and isothiocyanates. To the best of our knowledge, this is the first successful work using isothiocyanatomethane to prepare N-methyl amides.Open in a separate windowFig. 1Marketed drugs bearing N-methyl amide group.Our initial investigation begins with phenylacetic acid and isothiocyanatomethane as model substrate for condition optimization. Using acetonitrile as solvent, only trace amount of product was detected under catalyst free or p-toluenesulfonic acid (PTSA) catalysis conditions ( Entry Additive Time (h) Catalyst Yield (%) 1 — 24 — 5 2 — 24 PTSA — 3 — 48 TEA 17 4 — 48 DBU 45 5 — 48 DMAP 43 6 — 48 DBN 51 7 — 48 DABCO 65 8 LiBr 48 DABCO 71 9 Mn(OAc)2 48 DABCO 75 10 MnO 48 DABCO 79 11 MgO 48 DABCO 88 12 Al2O3 48 DABCO 85 13 Fe3O4 48 DABCO 98 14 Fe3O4 24 DABCO 75 15b Fe3O4 48 DABCO 80