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1.
Chie Amano Hideki Minematsu Kazuyo Fujita Shinki Iwashita Masaki Adachi Koichi Igarashi Shuji Hinuma 《PloS one》2015,10(9)
To explore a novel method using liposomes to suppress macrophages, we screened food constituents through cell culture assays. Curcumin was one of the strongest compounds exhibiting suppressive effects on macrophages. We subsequently tried various methods to prepare liposomal curcumin, and eventually succeeded in preparing liposomes with sufficient amounts of curcumin to suppress macrophages by incorporating a complex of curcumin and bovine serum albumin. The diameter of the resultant nanoparticles, the liposomes containing curcumin, ranged from 60 to 100 nm. Flow cytometric analyses revealed that after intraperitoneal administration of the liposomes containing curcumin into mice, these were incorporated mainly by macrophages positive for F4/80, CD36, and CD11b antigens. Peritoneal cells prepared from mice injected in vivo with the liposomes containing curcumin apparently decreased interleukin-6-producing activities. Major changes in body weight and survival rates in the mice were not observed after administrating the liposomes containing curcumin. These results indicate that the liposomes containing curcumin are safe and useful for the selective suppression of macrophages in vivo in mice. 相似文献
2.
Distribution of Ankyrin Isoforms and Their Proteolysis After Ischemia and Reperfusion in Rat Brain 总被引:1,自引:0,他引:1
Kazuki Harada Shiro Fukuda †Manabu Kunimoto Ken-ichi Yoshida 《Journal of neurochemistry》1997,69(1):371-376
Abstract: The distribution of brain-type ankyrin (ankyrinB , 212 kDa) and erythrocyte-type ankyrin (ankyrinR , 239 kDa) was investigated in the subcellular fractions of rat forebrain (P1, 1,000 g pellet; P2, 15,000 g pellet; P3, 100,000 g pellet; S, 100,000 g supernatant) by immunoblotting using specific antibodies. The P2 fraction contained ∼40% of the 212- and 163-kDa isoforms of ankyrinB and the 239-kDa isoform of ankyrinR . Further subfractionation of the P2 by Percoll gradient centrifugation followed by separation of myelin showed association of the three ankyrin isoforms with the synaptosome-rich fraction but not with the myelin-rich fraction. The plasma membrane-rich P3 fraction contained a concentration of ankyrin isoforms similar to that in the P2 fraction. In vitro proteolysis of ankyrin in the P2 fraction with calpain showed that the 212-kDa ankyrinB was more susceptible to calpain than was ankyrinR . In the two-vessel occlusion model, ischemia for 30 min generated the 160-kDa fragment of ankyrinR , and reperfusion for 60 min after 30 min of ischemia remarkably increased the 160-kDa fragment. The reperfusion also significantly decreased the 212-kDa isoform of ankyrinB . Both ischemia-reperfusion and in vitro proteolysis with calpain generated the 160-kDa fragment of ankyrinR , suggesting the involvement of calpain. 相似文献
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Lin Cui Kenoki Ohuchida Kazuhiro Mizumoto Taiki Moriyama Manabu Onimaru Kohei Nakata Toshinaga Nabae Takashi Ueki Norihiro Sato Yohei Tominaga Masao Tanaka 《PloS one》2010,5(8)
Although CD133 has been reported to be a promising colon cancer stem cell marker, the biological functions of CD133+ colon cancer cells remain controversial. In the present study, we investigated the biological differences between CD133+ and CD133− colon cancer cells, with a particular focus on their interactions with cancer-associated fibroblasts, especially CD10+ fibroblasts. We used 19 primary colon cancer tissues, 30 primary cultures of fibroblasts derived from colon cancer tissues and 6 colon cancer cell lines. We isolated CD133+ and CD133− subpopulations from the colon cancer tissues and cultured cells. In vitro analyses revealed that the two populations showed similar biological behaviors in their proliferation and chemosensitivity. In vivo analyses revealed that CD133+ cells showed significantly greater tumor growth than CD133− cells (P = 0.007). Moreover, in cocultures with primary fibroblasts derived from colon cancer tissues, CD133+ cells exhibited significantly more invasive behaviors than CD133− cells (P<0.001), especially in cocultures with CD10+ fibroblasts (P<0.0001). Further in vivo analyses revealed that CD10+ fibroblasts enhanced the tumor growth of CD133+ cells significantly more than CD10− fibroblasts (P<0.05). These data demonstrate that the in vitro invasive properties and in vivo tumor growth of CD133+ colon cancer cells are enhanced in the presence of specific cancer-associated fibroblasts, CD10+ fibroblasts, suggesting that the interactions between these specific cell populations have important roles in cancer progression. Therefore, these specific interactions may be promising targets for new colon cancer therapies. 相似文献
8.
A second Warburg-like effect in cancer metabolism: The metabolic shift of glutamine-derived nitrogen
Manabu Kodama Keiichi I. Nakayama 《BioEssays : news and reviews in molecular, cellular and developmental biology》2020,42(12):2000169
Carbon and nitrogen are essential elements for life. Glucose as a carbon source and glutamine as a nitrogen source are important nutrients for cell proliferation. About 100 years ago, it was discovered that cancer cells that have acquired unlimited proliferative capacity and undergone malignant evolution in their host manifest a cancer-specific remodeling of glucose metabolism (the Warburg effect). Only recently, however, was it shown that the metabolism of glutamine-derived nitrogen is substantially shifted from glutaminolysis to nucleotide biosynthesis during malignant progression of cancer—which might be referred to as a “second” Warburg effect. In this review, address the mechanism and relevance of this metabolic shift of glutamine-derived nitrogen in human cancer. We also examine the clinical potential of anticancer therapies that modulate the metabolic pathways of glutamine-derived nitrogen. This shift may be as important as the shift in carbon metabolism, which has long been known as the Warburg effect. 相似文献
9.
Masafumi Komiya Shigehiro Asano Nobuyuki Koike Erina Koga Junetsu Igarashi Shogo Nakatani Yoshiaki Isobe 《Bioorganic & medicinal chemistry》2012,20(23):6840-6847
Based on 2-(4-phenoxybenzoyl)-5-hydroxyindole (2), a novel structural class of CaMKII inhibitors were synthesized and further optimized. The strong acidity of the hydroxyl group and the lipophilic group at the 4 and 6-positions were found to be necessary for strong CaMKII inhibition. Compound 25 was identified as a promising compound with 50-fold more potent inhibitory activity for CaMKII than 2. Compound 25 also showed high selectivity for CaMKII over off-target kinases. 相似文献
10.
H. Akita Taeko Miyagi Keiko Hata Manabu Kagayama 《Histochemistry and cell biology》1997,107(6):495-503
Histochemical evidence is required to demonstrate the presence of biochemically defined cytosolic sialidase. To meet this
requirement, we examined the immunohistochemical localization of the enzyme in rat skeletal muscles. Sections of chemically
fixed tissues were incubated with a polyclonal antibody raised against a synthetic peptide which corresponded to a part of
the enzyme protein. After incubation with the primary antibody, cryosections for fluorescence microscopy and resin sections
for electron microscopy were incubated with a fluorochrome- and colloidal gold-labeled secondary antibody, respectively. Immunofluorescence
was diffusely distributed in the muscle fibers and was also found in the perimysium and blood vessels. Many immunogold particles
were scattered over the sarcoplasm, myofibrils, nucleoplasm, and matrix of mitochondria. The immunogold particles were also
found in the equivalent compartments of axons, Schwann cells, and cells of endomysium and blood vessels. The specificity of
the primary antibody was elucidated by immunoblotting and an immunoprecipitation test. These findings clearly indicate that
this type of sialidase is essentially located in the cytosolic compartment. Consequently, the name, cytosolic sialidase, will
be appropriate for this enzyme. Additionally it is indicated that this enzyme is also present in cells other than skeletal
muscle fibers.
Accepted: 29 January 1997 相似文献