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71.
Polyphenols from some foodstuffs as inhibitors of ovalbumin permeation through caco-2 cell monolayers 总被引:3,自引:0,他引:3
Kobayashi S Watanabe J Fukushi E Kawabata J Nakajima M Watanabe M 《Bioscience, biotechnology, and biochemistry》2003,67(6):1250-1257
Some spices showed high inhibitory activity against ovalbumin permeation through Caco-2 cell monolayers. Pimentol from allspice, rosmarinic acid and luteolin-7-O-beta-glucuronide from thyme, quercetin-3-O-beta-glucuronide from coriander and rutin from tarragon were identified as the active principles. A structure-activity relationship study among the active isolates and their related compounds indicated that the presence of a catechol structure played an important role in the inhibitory activity of each compound. 相似文献
72.
Contractile vacuoles (CVs) released from cells of Amoeba proteus were used to analyze its function in vitro. When CV was transferred to a hypertonic medium, its volume decreased within 10 sec. When it was subsequently returned to its original medium, it quickly started swelling. However, it ruptured before recovering its initial volume. These results suggested that the CV membrane is semi-permeable and that the fluid is collected by the osmotic gradient in vivo. The water permeability of membrane of isolated CV was calculated from the rate of osmotic volume change to be 0.94 microm/sec . OsM. This high value suggested that CV membrane is equipped with water channel. CV contracted (or burst) quickly upon addition of 1 mM ATP. Contraction was induced by ATP, but not by other nucleotides, GTP, ITP, ADP, or the analogues of ATP, AMP-PNP and ATPgammaS. It was suggested that the contraction of isolated CV was caused by increase in the tension of its membrane by ATP. 相似文献
73.
To clarify the structural role of Phe46 inside the hydrophobic core of bovine pancreatic ribonuclease A (RNase A), thermal and pressure unfolding of wild-type RNase A and three mutant forms (F46V, F46E, and F46K) were analyzed by fourth-derivative UV absorbance spectroscopy. All the mutants, as well as the wild type, exhibited a two-state transition during both thermal and pressure unfolding, and both T(m) and P(m) decreased markedly when Phe46 was replaced with valine, glutamic acid, or lysine. The strongest effect was on the F46K mutant and the weakest on F46V. Both unfolding processes produced identical blue shifts in the fourth-derivative spectra, indicating that the tyrosine residues are similarly exposed in the temperature- and pressure-induced unfolded states. A comparison of Gibbs free energies determined from the pressure and temperature unfoldings, however, gave DeltaG(p)/DeltaG(t) ratios (r) of 1.7 for the wild type and 0.92 +/- 0.03 for the mutants. Furthermore, the DeltaV value for each mutant was larger than that for the wild type. CD spectra and activity measurements showed no obvious major structural differences in the folded state, indicating that the structures of the Phe46 mutants and wild type differ in the unfolded state. We propose a model in which Phe46 stabilizes the hydrophobic core at the boundary between two structural domains. Mutation of Phe46 decreases protein stability by weakening the unfolding cooperativity between these domains. This essential function of Phe46 in RNase A stability indicates that it belongs to a chain-folding initiation site. 相似文献
74.
A lateral bud growth inhibitor was isolated from etiolated pea seedlings and identified as indole-3-aldehyde. The indole-3-aldehyde content was significantly higher in the diffusates from explants with apical bud and indole-3-acetic acid treated decapitated explants, in which apical dominance is maintained, than in those from decapitated ones releasing apical dominance. When the indole-3-aldehyde was applied to the cut surface of etiolated decapitated plants or directly to the lateral buds, it inhibited outgrowth of the latter. These results suggest that indole-3-aldehyde plays an important role as a lateral bud growth inhibitor in apical dominance of pea seedlings. 相似文献
75.
Endah Dwi Hartuti Daniel Ken Inaoka Keisuke Komatsuya Yukiko Miyazaki Russell J. Miller Wang Xinying Mohamad Sadikin Erwahyuni Endang Prabandari Danang Waluyo Marie Kuroda Eri Amalia Yuichi Matsuo Nuki B. Nugroho Hiroyuki Saimoto Amila Pramisandi Yoh-Ichi Watanabe Mihoko Mori Kazuro Shiomi Kiyoshi Kita 《BBA》2018,1859(3):191-200
Plasmodium falciparum is an apicomplexan parasite that causes the most severe malaria in humans. Due to a lack of effective vaccines and emerging of drug resistance parasites, development of drugs with novel mechanisms of action and few side effects are imperative. To this end, ideal drug targets are those essential to parasite viability as well as absent in their mammalian hosts. The mitochondrial electron transport chain (ETC) of P. falciparum is one source of such potential targets because enzymes, such as L-malate:quinone oxidoreductase (PfMQO), in this pathway are absent humans. PfMQO catalyzes the oxidation of L-malate to oxaloacetate and the simultaneous reduction of ubiquinone to ubiquinol. It is a membrane protein, involved in three pathways (ETC, the tricarboxylic acid cycle and the fumarate cycle) and has been shown to be essential for parasite survival, at least, in the intra-erythrocytic asexual stage. These findings indicate that PfMQO would be a valuable drug target for development of antimalarial with novel mechanism of action. Up to this point in time, difficulty in producing active recombinant mitochondrial MQO has hampered biochemical characterization and targeted drug discovery with MQO. Here we report for the first time recombinant PfMQO overexpressed in bacterial membrane and the first biochemical study. Furthermore, about 113 compounds, consisting of ubiquinone binding site inhibitors and antiparasitic agents, were screened resulting in the discovery of ferulenol as a potent PfMQO inhibitor. Finally, ferulenol was shown to inhibit parasite growth and showed strong synergism in combination with atovaquone, a well-described anti-malarial and bc1 complex inhibitor. 相似文献
76.
Complementary expression patterns of retinoid acid-synthesizing and -metabolizing enzymes in pre-natal mouse inner ear structures 总被引:1,自引:0,他引:1
Romand R Niederreither K Abu-Abed S Petkovich M Fraulob V Hashino E Dollé P 《Gene expression patterns : GEP》2004,4(2):123-133
Retinoic acid (RA) plays a pivotal role in patterning and differentiation of the embryonic inner ear. Despite its documented effects during embryonic development, the cellular sites that synthesize or metabolize RA in the inner ear have yet to be determined. Here we describe the distribution of three synthesizing enzymes, retinaldehyde dehydrogenases 1, 2 and 3 (RALDH1, RALDH2 and RALDH3) and two catabolizing enzymes (CYP26A1 and CYP26B1) in the mouse inner ear at embryonic day 18.5 when active cell differentiation is underway. Two detection methods, radioactive and non-radioactive in situ hybridization, were employed to elucidate the tissue distribution and cellular localization of these enzymes, respectively. All of the five enzymes examined, with the exception of CYP26A1, were expressed in both vestibular and cochlear end organs. While expression of the three RALDHs was observed in various cell types, CYP26B1 expression was found only in supporting cells of the vestibular and cochlear end organs. In the cochlea, expression domains of RALDH1-3 and CYP26B1 were complementary to one another. These results reveal specific tissue- and cellular expression patterns of RA synthesizing and catabolizing enzymes in the pre-natal inner ear, and suggest that a precise control of RA concentrations in various cell types of the inner ear is achieved by the balance between RALDHs and CYP26B1 activities. 相似文献
77.
Koyama Satoshi Fujita Hiroyuki Shimosato Takeshi Kamijo Aki Ishiyama Yasufumi Yamamoto Eri Ishii Yoshimi Hattori Yukako Hagihara Maki Yamazaki Etsuko Tomita Naoto Nakajima Hideaki 《Probiotics and antimicrobial proteins》2019,11(1):295-298
Probiotics and Antimicrobial Proteins - Probiotic-rich foods are consumed without much restriction. We report here, a case of septic shock caused by yogurt derived Lactobacillus species in a... 相似文献
78.
Akiko Shibui Ayako Takamori Mohammed E.M. Tolba Aya Nambu Eri Shimura Sachiko Yamaguchi Chizu Sanjoba Hajime Suto Katsuko Sudo Ko Okumura Sumio Sugano Hideaki Morita Hirohisa Saito Kenji Matsumoto Susumu Nakae 《Biochemistry and Biophysics Reports》2016
IL-25, IL-33 and TSLP, which are produced predominantly by epithelial cells, can induce production of Th2-type cytokines such as IL-4, IL-5 and/or IL-13 by various types of cells, suggesting their involvement in induction of Th2-type cytokine-associated immune responses. It is known that Th2-type cytokines contribute to host defense against malaria parasite infection in mice. However, the roles of IL-25, IL-33 and TSLP in malaria parasite infection remain unclear. Thus, to elucidate this, we infected wild-type, IL-25?/?, IL-33?/? and TSLP receptor (TSLPR)?/? mice with Plasmodium berghei (P. berghei) ANKA, a murine malaria strain. The expression levels of IL-25, IL-33 and TSLP mRNA were changed in the brain, liver, lung and spleen of wild-type mice after infection, suggesting that these cytokines are involved in host defense against P. berghei ANKA. However, the incidence of parasitemia and survival in the mutant mice were comparable to in the wild-type mice. These findings indicate that IL-25, IL-33 and TSLP are not critical for host defense against P. berghei ANKA. 相似文献
79.
80.
Kazuo GOTO Eri KUWAYAMA Ryoko NOZU Masami UENO Nobuhito HAYASHIMOTO 《Experimental Animals》2015,64(2):191-197
In this study, hypochlorous acid solution, a weak acid, provided as drinking water to
rats, was evaluated for its ability to eradicate and prevent Pseudomonas
aeruginosa infection, while monitoring its simultaneous effect on serum
biochemical variables and microbiota in the rat cecum. The results suggest that the
solution could not eliminate the bacteria in the experimentally infected rats; however,
the administration of a 10-parts-per-million (ppm) hypochlorous acid solution as drinking
water was effective in inhibiting horizontal spread of P. aeruginosa
infection among cage mates. Additionally, exposure to hypochlorous solution did not have
any effect on serum biochemical variables of the rat including levels of total
cholesterol, aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline
phosphatase (ALP), albumin, total bilirubin, lipase, amylase, urea nitrogen, total
protein, calcium (Ca), phosphorus (P), sodium (Na), chlorine (Cl), except for potassium
(K) levels. The most frequently isolated bacteria in the rat cecum included species
belonging to Bacteroidales, Lactobacillus,
Clostridiales, Erysipelotrichaceae,
Akkermansia, Coriobacteriales, and
Firmicutes. The ratio of the terminal restriction fragment length
polymorphism (T-RFLP) peaks did not differ across rats administered with 5 and 10 ppm weak
acid solution as compared to the control group for any of the bacteria, except for
Erysipelotrichaceae and Firmicutes, where the ratio of
T-RFLP peaks was higher in the 5 ppm group for Erysipelotrichaceae and in
the 10 ppm group for Firmicutes than that in the control group
(P<0.01). The results suggest that the weak acid hypochlorous
solution could not eradicate P. aeruginosa completely from rats. The
solution was effective in preventing infection without affecting serum biochemical
variables; however, some of bacterial microbiota may have changed due to administration of
the solution. 相似文献