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111.
1临床资料输尿管结石560(男324,女236)例,年龄16~68(平均38)岁.其中左侧输尿管246例,右侧输尿管268例,双侧输尿管46例,合并肾功能减退者28例,合并妊娠12例,孤肾合并输尿管结石5例,上段输尿管139例,中段输尿管154例,下段输尿管267例,合并输尿管狭窄68例,合并输尿管息肉156例,合并输尿管扩张及不同程度肾积水286例,36例有肾或输尿管切开取石史,196例行体外震波碎石效果不佳,其中16例形成石街.本组经X线诊断的阳性结石388例,经B超或静脉肾盂造影诊断的阴性结石148例,未发现结石经输尿管镜诊断的结石24例. 相似文献
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114.
目的;在经典法与药典法基础上,提出了异步六点法。方法:采用异步六点法与经典法进行盐酸普奈洛尔片剂溶出度试验。结果:两者所得溶出度参数Td、T0.75基本一致。结论:试验表明本法可成倍减少工作量,省时实用。 相似文献
115.
2-(Allylthio)pyrazine (2-AP), synthesized for its possible use as a
hepatoprotective agent, has been found to selectively inhibit rat hepatic
cytochrome P450 2E1 (Kim et al., Biochem. Pharmacol., 53, 261- 269, 1997),
while it enhances the activities of phase II detoxification enzymes such as
glutathione S-transferase and epoxide hydrolase. As part of a program in
evaluating the chemopreventive potential of 2-AP, we have determined its
effects on hepatotoxicity, mutagenicity and tumorigenicity of vinyl
carbamate (VC), a prototypic hepatocarcinogen preferentially activated by
P450 2E1 to the ultimate carcinogenic metabolite vinyl carbamate epoxide
(VCO), which undergoes detoxification by glutathione conjugation and
oxirane hydrolysis. Administration of 2-AP (100 mg/kg body wt) to male
Sprague-Dawley rats by gavage, 2 days, 1 day and 4 h prior to VC or VCO,
markedly ameliorated the hepatotoxicity of these compounds as determined by
decreased serum aspartate aminotransferase and alanine aminotransferase
activities. Furthermore, 2-AP pre-treatment significantly suppressed the
VC-induced hepatocarcinogenesis in infant male B6C3F1 mice. In a separate
experiment, the multiplicities of skin tumors formed in female ICR mice
treated with 5.8 micromol of VC or VCO were inhibited 58 and 70%,
respectively, by pre-treatment with 2-AP by oral administration. The
mutational spectrum of ras-oncogene in papillomas was not altered by 2-AP
pre-treatment. 2-AP also inhibited the mutagenicity of VC in the
Salmonella-microsome assay. Taken together, these findings suggest that
2-AP is a potential chemopreventive agent.
相似文献
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辽东楤本化学成分的研究 总被引:11,自引:0,他引:11
从辽东楤本(Aralia elata)的根皮中分得8个化合物,利用理化和光谱方法鉴定分别为胡萝卜甙-6’-棕榈酸酯(6’-O-palmitoyl-β-sitosterol-3-O-β-D-glucoside,A5)、罗盘草甙A(silphioside A,A9)、楤木皂甙A甲酯(araloside A methyl ester,A10)、竹节人参甙Ib(chikusetusaponin Ib,A11)、楤木皂甙A(araloside A,A12)、楤木皂甙C(araloside C,A15、楤木皂甙G(araloside G,A16)、无梗五加甙D(acanthoside D,B1)。化合物A5,A9,A11和B1为首次从该植物中分得,A10为新天然产物,A16为新化合物命名为楤木皂甙G,归属了化合物A9,A15的13C-NMR化学位移。 相似文献
118.
Although approximately two-thirds of breast cancers are estrogen receptor
(ER)-positive, only a small proportion of epithelial cells in the mammary
gland express the ER. The origin of the ER-positive breast cancers is
unknown. Recently, we have developed a culture method to grow two
morphologically and antigenically distinguishable types of normal human
breast epithelial cells (HBEC) derived from reduction mammoplasty. In this
report, we studied the expression of ER in these two types of cells and
their transformed cell lines. The results indicate that Type I HBEC with
luminal and stem cell characteristics expressed a variant ER (approximately
48 kd) by Western blot analysis. This variant ER contains a deletion in the
DNA binding domain (exon 2) as revealed by RT-PCR analysis. The lack of the
DNA-binding domain of the variant ER was also confirmed by the ER-estrogen
responsive element binding assay, as well as by the immunofluorescence
staining of the ER using anti-ER antibodies which recognize either the
C-terminal or N- terminal region. In contrast, Type II HBEC with basal
epithelial phenotype are ER-negative. Simian virus 40 (SV40) transformed
Type I and Type II HBEC lines also expressed the variant ER. Tumors formed
in athymic nude mice by in vitro transformed tumorigenic Type I cell lines,
however, expressed a high level of wild type ER which was undetectable in
these cells grown in vitro before and after tumor formation. Thus, there
appears to be a differential ER mRNA splicing between the in vitro and in
vivo mileu.
相似文献
119.
褪黑激素(N-乙酰基-5-甲氧基色胺)的合成 总被引:5,自引:0,他引:5
This paper reports the synthesis of melatonin(N-acetyl-5-methoxytryptamine).The structure of all the compounds synthesized were characterized by elemental analysis,IR, MS and 1HNMR spectra. 相似文献
120.
马缨丹根的三萜成分研究 总被引:4,自引:0,他引:4
从马缨丹(Lantana camara L.)根中分离到八个三萜成分,通过光谱(UV,IR,1HNMR,13CNMR,MS)分析和理化常数测定,分别鉴定为lantanolic acid(Ⅰ),22β-O-angeloyl-lantanolic acid(Ⅱ),oleanolic acid(Ⅲ),22βO-angeloyt-oleanolic acid(Ⅳ),22β-O-senecioyl-oleanolic acid(Ⅴ),22β-hydroxy-oleanolic acid(Ⅵ),19α-hydroxyursolic acid(Ⅶ),3β-isovaleroyl-19α-hydroxyursolic acid(Ⅷ)。Ⅱ系首次从植物中分离到。Ⅷ是新化合物,命名为lantaiursolic acid。 相似文献