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101.
Tamalampudi S Talukder MM Hama S Tanino T Suzuki Y Kondo A Fukuda H 《Applied microbiology and biotechnology》2007,75(2):387-395
To expand the industrial applications of Candida antarctica lipase B (CALB), we developed Aspergillus oryzae whole-cell biocatalyst expressing the lipase-encoding gene from C. antarctica. A. oryzae niaD300, which was derived from the wild type strain RIB40, was used as the host strain. The CALB gene was isolated from
C. antarctica CBS6678 and expression plasmids were constructed with and without secretion signal peptide. The lipase gene was expressed
under the control of improved glaA and pNo-8142 promoters of plasmids pNGA142 and pNAN8142, respectively. The Southern blot
analysis demonstrated the successful integration of the CALB gene in the genome of A. oryzae. To determine the role of signal peptide, the expression plasmids were constructed with homologous and heterologous secretion
signal sequences of triacylglycerol lipase gene (tglA) from A. oryzae and lipase B (CALB) from C. antarctica, respectively. The C-terminal FLAG tag does not alter the catalytic properties of the lipase enzyme and Western blotting
analysis using anti-FLAG antibodies demonstrated the presence of cell wall and membrane bound lipase responsible for the biocatalytic
activity of the whole-cell biocatalyst. The resultant recombinant A. oryzae was immobilized within biomass support particles (BSPs) made of polyurethane foam (PUF) and the BSPs were successfully used
for the hydrolysis of para-nitrophenol butyrate (p-NPB) and for the optical resolution of (RS)-1-phenyl ethanol by enantioselective transesterification with vinyl acetate as acyl donor. 相似文献
102.
Matsuki Y Ohmura-Hoshino M Goto E Aoki M Mito-Yoshida M Uematsu M Hasegawa T Koseki H Ohara O Nakayama M Toyooka K Matsuoka K Hotta H Yamamoto A Ishido S 《The EMBO journal》2007,26(3):846-854
The presence of post-translational regulation of MHC class II (MHC II) under physiological conditions has been demonstrated recently in dendritic cells (DCs) that potently function as antigen-presenting cells (APCs). Here, we report that MARCH-I, an E3 ubiquitin ligase, plays a pivotal role in the post-translational regulation of MHC II in B cells. MARCH-I expression was particularly high in B cells, and the forced expression of MARCH-I induced the ubiquitination of MHC II. In B cells from MARCH-I-deficient mice (MARCH-I KO), the half-life of surface MHC II was prolonged and the ubiquitinated form of MHC II completely disappeared. In addition, MARCH-I-deficient B cells highly expressed exogenous antigen-loaded MHC II on their surface and showed high ability to present exogenous antigens. These results suggest that the function of MHC II in B cells is regulated through ubiquitination by MARCH-I. 相似文献
103.
104.
Sakaki J Kishida M Konishi K Gunji H Toyao A Matsumoto Y Kanazawa T Uchiyama H Fukaya H Mitani H Arai Y Kimura M 《Bioorganic & medicinal chemistry letters》2007,17(17):4804-4807
A series of diazepinylbenzoic acid derivatives were synthesized and tested in the inhibition assay of the transactivation of RXR. Oral treatment of cyano derivatives (16f) was found to show anti-diabetic and anti-obesity effects in KK-A(y) mice. 相似文献
105.
106.
Tanabe G Yoshikai K Hatanaka T Yamamoto M Shao Y Minematsu T Muraoka O Wang T Matsuda H Yoshikawa M 《Bioorganic & medicinal chemistry》2007,15(11):3926-3937
De-O-sulfonated analogs (10a, Y(-)=CH(3)OSO(3) and 10b, Y(-)=Cl) of salacinol, a naturally occurring glycosidase inhibitor, and its diastereomer (12a, Y(-)=CH(3)OSO(3)) with L-thiosugar moiety (1,4-dideoxy-1,4-epithio-L-arabinitol) were prepared. Their inhibitory activities against intestinal maltase and sucrase were examined and compared with those of the parent alpha-glycosidase inhibitor, salacinol (1a). Compounds 10a and 10b showed a potent inhibitory activity equal to that of 1a against both enzymes, although 12a was a weak inhibitor against sucrase and maltase. These results indicated that the O-sulfonate anion moiety of 1a is not essential for the inhibitory activity. 相似文献
107.
Miyanishi N Nishi N Abe H Kashio Y Shinonaga R Nakakita S Sumiyoshi W Yamauchi A Nakamura T Hirashima M Hirabayashi J 《Glycobiology》2007,17(4):423-432
Galectin-9 (Gal-9) is a tandem-repeat-type member of the galectin family associated with diverse biological processes, such as apoptosis, cell aggregation, and eosinophil chemoattraction. Although the detailed sugar-binding specificity of Gal-9 has been elucidated, molecular mechanisms that underlie these functions remain to be investigated. During the course of our binding study by affinity chromatography and surface plasmon resonance (SPR) analysis, we found that human Gal-9 interacts with immobilized Gal-9 in the protein-protein interaction mode. Interestingly, this intermolecular interaction strongly depended on the activity of the carbohydrate recognition domain (CRD), because the addition of potent saccharide inhibitors abolished the binding. The presence of multimers was also confirmed by Ferguson plot analysis of result of polyacrylamide gel electrophoresis and matrix-assisted laser-desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry (MS). Moreover, this intermolecular interaction was observed between Gal-9 and other galectin members, such as Gal-3 and Gal-8, but not Gal-1. Because such properties have not been reported yet, they may explain an unidentified mechanism underlying the diverse functions of Gal-9. 相似文献
108.
109.
Sakaki J Konishi K Kishida M Gunji H Kanazawa T Uchiyama H Fukaya H Mitani H Kimura M 《Bioorganic & medicinal chemistry letters》2007,17(17):4808-4811
Synthesis and structure-activity relationship of RXR antagonists employing a diazepinylbenzoic acid scaffold are described. Of those antagonists, sulfonamide derivatives (6v and 6w) reveal a high antagonistic activity and good pharmacokinetic properties. 相似文献
110.
Hidaka M Su GN Chen JK Mukaisho K Hattori T Yamamoto G 《In vitro cellular & developmental biology. Animal》2007,43(2):49-58
Bone is a complex, highly structured, mechanically active, three-dimensional (3-D) tissue composed of cellular and matrix
elements. We previously published a report on in situ collagen gelation using a rotary 3-D culture system (CG–RC system) for
the construction of large tissue specimens. The objective of the current study was to evaluate the feasibility of bone tissue
engineering using our CG–RC system. Osteoblasts from the calvaria of newborn Wistar rats were cultured in the CG–RC system
for up to 3 wk. The engineered 3-D tissues were implanted into the backs of nude mice and calvarial round bone defects in
Wistar rats. Cell metabolic activity, mineralization, and bone-related proteins were measured in vitro in the engineered 3-D
tissues. Also, the in vivo histological features of the transplanted, engineered 3-D tissues were evaluated in the animal
models. We found that metabolic activity increased in the engineered 3-D tissues during cultivation, and that sufficient mineralization
occurred during the 3 wk in the CG–RC system in vitro. One mo posttransplantation, the transplants to nude mice remained mineralized
and were well invaded by host vasculature. Of particular interest, 2 mo posttransplantation, the transplants into the calvarial
bone defects of rats were replaced by new mature bone. Thus, this study shows that large 3-D osseous tissue could be produced
in vitro and that the engineered 3-D tissue had in vivo osteoinductive potential when transplanted into ectopic locations
and into bone defects. Therefore, this system should be a useful model for bone tissue engineering. 相似文献