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81.
82.
Jae-Kyung Yang Hee-Dong Yeo Seung-Chul Baik Ji-Young Jung Bo-Min Kim Mi-Jin Jeong Cheul-Ho Lee Chandrakant S. Karigar Han-Min Park Myung-Suk Choi 《Biotechnology and Bioprocess Engineering》2010,15(6):1077-1083
Chemical therapeutics targeted against H. pylori may lead to host toxicity and pathogen eradication failures. In this study, ethanolic extracts from five Lespedeza sp. plants were shown to inhibit the gastric-pathogen H. pylori and to modulate cytokine production. Disc agar diffusion assays showed that Lespedeza sp. ethanol extracts possess potent anti-H. pylori activity. Among the five plant extracts, the extracts from L. cyrtobotrya demonstrated the highest anti-H. pylori effect. The growth inhibitory effect against H. pylori was initiated after six h of treatment with plant extracts and the effect remained for a continuous period of 48 h. Incubation
of the gastric cells infected with H. pylori with 1.25 to 50 mg/mL of sp. plant extracts resulted in a reduction of the production of cytokine IL-8. The plant ethanol
extracts generally had little influence on AGS cell viability, indicating their safety for the treatment of bacterial infections.
Three active fractions of L. cyrtobotrya also demonstrated similar anti-H. pylori and immuno-modulatory effects. Taken together, these results provide evidence that Lespedeza sp. plant extracts might be potential sources of new host friendly anti-H. pylori agents. 相似文献
83.
Evidence of Increased Oxidative Damage in Both Sporadic and Familial Amyotrophic Lateral Sclerosis 总被引:9,自引:13,他引:9
Robert J. Ferrante Susan E. Browne Leslie A. Shinobu Allen C. Bowling M. Jay Baik Usha MacGarvey Neil W. Kowall †Robert H. Brown Jr. M. Flint Beal 《Journal of neurochemistry》1997,69(5):2064-2074
Abstract: Some cases of autosomal dominant familial amyotrophic lateral sclerosis (FALS) are associated with mutations in the gene encoding Cu/Zn superoxide dismutase (SOD1), suggesting that oxidative damage may play a role in ALS pathogenesis. To further investigate the biochemical features of FALS and sporadic ALS (SALS), we examined markers of oxidative damage to protein, lipids, and DNA in motor cortex (Brodmann area 4), parietal cortex (Brodmann area 40), and cerebellum from control subjects, FALS patients with and without known SOD mutations, SALS patients, and disease controls (Pick's disease, progressive supranuclear palsy, diffuse Lewy body disease). Protein carbonyl and nuclear DNA 8-hydroxy-2'-deoxyguanosine (OH8 dG) levels were increased in SALS motor cortex but not in FALS patients. Malondialdehyde levels showed no significant changes. Immunohistochemical studies showed increased neuronal staining for hemeoxygenase-1, malondialdehyde-modified protein, and OH8 dG in both SALS and FALS spinal cord. These studies therefore provide further evidence that oxidative damage may play a role in the pathogenesis of neuronal degeneration in both SALS and FALS. 相似文献
84.
85.
Kisun Ryu Nam Doo Kim Seong Il Choi Cheol Kyu Han Jeong Hyeok Yoon Kyoung Tai No Kyun-Hwan Kim Baik L. Seong 《Bioorganic & medicinal chemistry》2009,17(8):2975-2982
Hepatitis C virus (HCV) is the major etiological agent of non-A, non-B hepatitis where no effective treatment is available. The HCV NS5B with RNA-dependent RNA polymerase (RdRp) activity is a key target for the treatment of HCV infection. Here we report novel NS5B polymerase inhibitors identified by virtual screening and in vitro evaluation of their inhibitory activities. On the basis of a newly identified binding pocket of NS5B, distinct from the nucleotide binding site but highly conserved among various HCV isolates, we performed virtual screening of compounds that fit this binding pocket from the available chemical database of 3.5 million compounds. The inhibitory activities of the in silico selected 119 compounds were estimated with in vitro RdRp assay. Three compounds with IC50 values of about 20 μM were identified, and their kinetic analyses suggest that these compounds are noncompetitive inhibitors with respect to the ribonucleotide substrate. Furthermore, the single-point mutations of the conserved residues in the binding pocket of NS5B resulted in the significant decrease of the RdRp activity, indicating that the binding pocket presented here might be important for the therapeutic intervention of HCV. These novel inhibitors would be useful for the development of effective anti-HCV agents. 相似文献
86.
87.
Jun Cheul Ahn Won Seog Chong Young Soon Kim Baik Hwang 《Biotechnology and Bioprocess Engineering》2006,11(2):121-126
Saikosaponin productivity was examined in aBupleurum falcatum L. BFHR2 hairy root culture in response to changes in the sucrose content (2≈8%), nitrogen content (0≈250 mM NH4NO3), phosphate content (0≈12 mM NaH2PO4), and the potassium content (0≈87.2 mM KCl) of the culture media. We found that the conditions for maximal saikosaponin production
differed from those for optimal root growth. Highest saikosaponin yield was achieved for 8% sucrose, 62 mM NH4NO3, 1.2 mM NaH2PO4, and 0.5 mM KCl. 相似文献
88.
89.
J Bussenius CM Blazey N Aay NK Anand A Arcalas T Baik OJ Bowles CA Buhr S Costanzo JK Curtis SC Defina L Dubenko TS Heuer P Huang C Jaeger A Joshi AR Kennedy AI Kim K Lara J Lee J Li JC Lougheed S Ma S Malek JC Manalo JF Martini G McGrath M Nicoll JM Nuss M Pack CJ Peto TH Tsang L Wang SW Womble M Yakes W Zhang KD Rice 《Bioorganic & medicinal chemistry letters》2012,22(17):5396-5404
With structural guidance, tropane-derived HTS hits were modified to optimize for HSP90 inhibition and a desirable in vivo profile. Through an iterative SAR development process 12i (XL888) was discovered and shown to reduce HSP90 client protein content in PD studies. Furthermore, efficacy experiments performed in a NCI-N87 mouse xenograft model demonstrated tumor regression in some dosing regimens. 相似文献
90.
Jong-Hyun Jung Dong-Ho Seo Suk-Jin Ha Myoung-Chong Song Jaeho Cha Sang-Ho Yoo Tae-Jip Kim Nam-In Baek Moo-Yeol Baik Cheon-Seok Park 《Carbohydrate research》2009,344(13):1612-1619
Amylosucrase (ASase, EC 2.4.1.4) is a member of family 13 of the glycoside hydrolases that catalyze the synthesis of an α-(1→4)-linked glucan polymer from sucrose instead of an expensive activated sugar, such as ADP- or UDP-glucose. Transglycosylation reactions mediated by the ASases of Deinococcus geothermalis (DGAS) and Neisseria polysaccharea (NPAS) were applied to the synthesis of salicin glycosides with sucrose serving as the glucopyranosyl donor and salicin as the acceptor molecule. Two salicin glycoside transfer products were detected by TLC and HPLC analyses. The synthesis of salicin glycosides was very efficient with NPAS with a yield of over 90%. In contrast, DGAS specifically synthesized only one salicin transglycosylation product. The transglycosylation products were identified as α-d-glucopyranosyl-(1→4)-salicin (glucosyl salicin) and α-d-glucopyranosyl-(1→4)-α-d-glucopyranosyl-(1→4)-salicin (maltosyl salicin) by NMR analysis. The ratio between donor and acceptor had a significant effect on the type of product that resulted from the transglycosylation reaction. With more acceptors present in the reaction, more glucosyl salicin and less maltosyl salicin were synthesized. 相似文献