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581.
582.
Postembryonic development of the ovary through the larval stages was studied in a penicillate diplopod, Eudigraphis nigricans. In the first instar larva a single young cell cluster, consisting of about 20 spherical gonial cells and some smaller interstitial cells, exists beneath the alimentary canal in the third body segment. The gonadal epithelium encompasses the upper surface of this young cell cluster by the end of the first instar. The epithelium then extends forward and backward to form a single long sac-like gonad, leaving the young cell cluster on the center of the gonadal floor as a mound-shaped germarium. In an early second-instar larva, very early previtellogenic oocytes accompanied by some interstitial cells appear in the front and rear surfaces of the ovarian germarium. During the period from the third through the seventh (the last) larval instar, some cell clusters containing several previtellogenic oocytes and interstitial cells successively separate forward and backward from the germarium to form a series of paired patch-shaped vitellarial areas on the extending ventral ovarian epithelium. In each vitellarial area, some of the interstitial cells surround the oocytes to form the follicles. In the seventh instar, the ovarian lumen is extremely expanded, and the late previtellogenic oocytes in the vitellarial areas encroach upward into the ovarian lumen. These oocytes floating in the ovarian lumen are still connected with their own vitellarial areas by partial extensions of their follicles. Some phylogenetic implications of the basic characteristics in structure and postembryonic development of the ovary are discussed. © 1995 Wiley-Liss, Inc. 相似文献
583.
Yu Takahashi Yuji Hori Tomohisa Yamamoto Toshiki Urashima Yasunori Ohara Hideo Tanaka 《Bioscience reports》2015,35(3)
3D (three-dimensional) cultures are considered to be an effective method for toxicological studies; however, little evidence has been reported whether 3D cultures have an impact on hepatocellular physiology regarding lipid or glucose metabolism. In the present study, we conducted physiological characterization of hepatoma cell lines HepG2 and HepaRG cells cultured in 3D conditions using a hanging drop method to verify the effect of culture environment on cellular responses. Apo (Apolipoprotein)B as well as albumin secretion was augmented by 3D cultures. Expression of genes related to not only drug, but also glucose and lipid metabolism were significantly enhanced in 3D cultured HepaRG spheroids. Furthermore, mRNA levels of CYP (cytochrome P450) enzymes following exposure to corresponding inducers increased under the 3D condition. These data suggest that this simple 3D culture system without any special biomaterials can improve liver-specific characteristics including lipid metabolism. Considering that the system enables high-throughput assay, it may become a powerful tool for compound screening concerning hepatocellular responses in order to identify potential drugs. 相似文献
584.
Harvey Schwartz Brad Scroggins Abbey Zuehlke Toshiki Kijima Kristin Beebe Alok Mishra Len Neckers Thomas Prince 《Cell stress & chaperones》2015,20(5):729-741
The merging of knowledge from genomics, cellular signal transduction and molecular evolution is producing new paradigms of cancer analysis. Protein kinases have long been understood to initiate and promote malignant cell growth and targeting kinases to fight cancer has been a major strategy within the pharmaceutical industry for over two decades. Despite the initial success of kinase inhibitors (KIs), the ability of cancer to evolve resistance and reprogram oncogenic signaling networks has reduced the efficacy of kinase targeting. The molecular chaperone HSP90 physically supports global kinase function while also acting as an evolutionary capacitor. The Cancer Genome Atlas (TCGA) has compiled a trove of data indicating that a large percentage of tumors overexpress or possess mutant kinases that depend on the HSP90 molecular chaperone complex. Moreover, the overexpression or mutation of parallel activators of kinase activity (PAKA) increases the number of components that promote malignancy and indirectly associate with HSP90. Therefore, targeting HSP90 is predicted to complement kinase inhibitors by inhibiting oncogenic reprogramming and cancer evolution. Based on this hypothesis, consideration should be given by both the research and clinical communities towards combining kinase inhibitors and HSP90 inhibitors (H90Ins) in combating cancer. The purpose of this perspective is to reflect on the current understanding of HSP90 and kinase biology as well as promote the exploration of potential synergistic molecular therapy combinations through the utilization of The Cancer Genome Atlas.
Electronic supplementary material
The online version of this article (doi:10.1007/s12192-015-0604-1) contains supplementary material, which is available to authorized users. 相似文献585.
586.
Yusuke Sato Seiichi Nishizawa Keitaro Yoshimoto Takehiro Seino Toshiki Ichihashi Kotaro Morita Norio Teramae 《Nucleic acids research》2009,37(5):1411-1422
Here, we report on a significant effect of substitutions on the binding affinity of a series of 2-amino-1,8-naphthyridines, i.e., 2-amino-1,8-naphthyridine (AND), 2-amino-7-methyl-1,8-naphthyridine (AMND), 2-amino-5,7-dimethyl-1,8-naphthyridine (ADMND) and 2-amino-5,6,7-trimethyl-1,8-naphthyridine (ATMND), all of which can bind to cytosine opposite an AP site in DNA duplexes. Fluorescence titration experiments show that the binding affinity for cytosine is effectively enhanced by the introduction of methyl groups to the naphthyridine ring, and the 1:1 binding constant (106 M−1) follows in the order of AND (0.30) < AMND (2.7) < ADMND (6.1) < ATMND (19) in solutions containing 110 mM Na+ (pH 7.0, at 20°C). The thermodynamic parameters obtained by isothermal titration calorimetry experiments indicate that the introduction of methyl groups effectively reduces the loss of binding entropy, which is indeed responsible for the increase in the binding affinity. The heat capacity change (ΔCp), as determined from temperature dependence of the binding enthalpy, is found to be significantly different between AND (−161 cal/mol K) and ATMND (−217 cal/mol K). The hydrophobic contribution appears to be a key force to explain the observed effect of substitutions on the binding affinity when the observed binding free energy (ΔGobs) is dissected into its component terms. 相似文献
587.
Soichiro Fukushima Takao Ohki Makoto Koizumi Hiroki Ohta Toshiki TakahasHi Hirotaka James Okano 《Experimental Animals》2021,70(2):257
A reproducible swine thoracic aortic aneurysm (TAA) model is useful for investigating new therapeutic interventions. We report a surgical method for creating a reproducible swine saccular TAA model. We used eight female swine weighing 20–25 kg (LWD; ternary species). All procedures were performed under general anesthesia and involved left thoracotomy. Following aortic cross-clamping, the thoracic aorta was surgically dissected and the media and intima were resected, and the dissection plane was extended by spreading the outer layer for aneurysmal space. Subsequently, only the adventitial layer of the aorta was sutured. At 2 weeks after these procedures, angiography and computed tomography were performed. After follow-up imaging, the model animals were euthanized. Macroscopic, histological, and immunohistological examinations were performed. All model animals survived, and a saccular TAA was confirmed by follow-up imaging in all cases. The mean length of the shorter and the longer aortic diameter after the procedure were 14.01 ± 1.0 mm and 18.35 ± 1.4 mm, respectively (P<0.001). The rate of increase in the aortic diameter was 131.7 ± 13.8%, and the mean length of aneurysmal change at thoracic aorta was 22.4 ± 1.9 mm. Histological examination revealed intimal tears and defects of elastic fibers in the media. Immunostaining revealed MMP-2 and MMP-9 expressions at the aneurysm site. We report our surgical method for creating a swine saccular TAA model. Our model animal may be useful to investigate new therapeutic interventions for aortic disease. 相似文献
588.
Maruyama Takuma Kamihama Haruka Watanabe Mutsuto Matsuo Toshiki Matsuda Kenshiro Tanaka Akane 《Bioscience, biotechnology, and biochemistry》2018,82(7):1101-1106
The chondroprotective effect of olive leaf extract (OLE) on knee osteoarthritis (OA) was studied with STR/ort mice (n = 5). OLE was administrated with a dosage of 100 mg/kg for 8 weeks and the OA severity score of hind limb knee joints was then measured. The Mankin scores of the knee joints of the non-OA control group, OA control group and OLE-treated group were 3.50, 11.13 and 7.20, respectively. This suggests that oral OLE supplements help prevent cartilage degeneration in STR/ort mice. In vitro, the synthesis of high molecular weight hyaluronan in synovial cells (HIG-82) was increased by OLE stimulation. This suggests that OLE modulates hyaluronan metabolism in synovial cells and improves OA symptoms. Our findings indicate that OLE intake inhibits cartilage destruction by increasing high molecular weight hyaluronan and thus preventing OA progress. 相似文献
589.
Divergent synthesis of kinase inhibitor derivatives,leading to discovery of selective Gck inhibitors
Takanori Matsumaru Makoto Inai Kana Ishigami Toshiki Iwamatsu Hiroshi Maita Satoko Otsuguro Takao Nomura Akira Matsuda Satoshi Ichikawa Masahiro Sakaitani Satoshi Shuto Katsumi Maenaka Toshiyuki Kan 《Bioorganic & medicinal chemistry letters》2017,27(10):2144-2147
We accomplished divergent synthesis of potent kinase inhibitor BAY 61-3606 (1) and 27 derivatives via conjugation of imidazo[1,2-c]pyrimidine and indole ring compounds with aromatic (including pyridine) derivatives by means of palladium-catalyzed cross-coupling reaction. Spleen tyrosine kinase (Syk) and germinal center kinase (Gck, MAP4K2) inhibition assays showed that some of the synthesized compounds were selective Gck inhibitors. 相似文献
590.
Detection of the Leghemoglobin Gene on Two Chromosomes of Phaseolus vulgaris by in situ PCR Linked-Fluorescent in situ Hybridization (FISH) 总被引:1,自引:0,他引:1
Uchiumi Toshiki; Kuwashiro Ryoko; Miyamoto Junko; Abe Mikiko; Higashi Shiro 《Plant & cell physiology》1998,39(7):790-794
The leghemoglobin (Lb) gene on the metaphase chromosomes ofPhaseolus vulgaris was amplified by in situ PCR. The amplifiedLb gene could be detected on two chromosomes by fluorescentin situ hybridization (FISH) using the short Lb gene probe. (Received January 9, 1998; Accepted April 30, 1998) 相似文献