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941.
Inoue Mizuki Michimasa Yamasaki Takehiko Kakutani Yuji Isagi 《Journal of Insect Conservation》2010,14(2):191-198
The genetic diversity of bumblebees can be adversely affected by habitat degradation. An overabundance of deer has altered
the composition and diversity of herbaceous plants in many places of the world, resulting in decreases of herbaceous flowers.
Populations of Bombus diversus may be strongly affected by this degradation of habitat in the Ashiu primary beech forest in Kyoto, Japan. To estimate the
effects of deer browsing on B. diversus populations, we analyzed and compared the genetic diversity of the extant population in Ashiu to museum specimens collected
prior to heavy deer browsing in Ashiu (1980s) and the extant population in Hyonosen primary beech forest in Tottori, Japan,
which has not been as severely degraded by deer. We successfully amplified DNA from ~20-year-old museum specimens and determined
the genetic diversity of B. diversus in Ashiu populations from the 1980s. Results were analyzed for indications of a bottleneck as well as estimates of N
e, allelic richness, rare allelic richness, expected heterozygosity, and the effective number of alleles. Our findings did
not reveal clear evidence of degradation in genetic diversity of the extant Ashiu population compared to the museum specimens
or to the Hyonosen population. Thus, the Ashiu population of B. diversus appears to have maintained a level of genetic diversity during 20 years irrespective of habitat degradation and the levels
have been similar to that of the Hyonosen population. 相似文献
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945.
To investigate the effective depth from the surface sediment, and phosphorus fractions related to phosphorus release under short-term anoxic conditions, varying lengths of sediment cores taken from Lake Kasumigaura, a large shallow polymictic lake in Japan, were incubated for a few weeks and then analyzed. Results showed few differences in total phosphorus (TP) amount per unit area in overlying waters irrespective of the core thickness, and sums of TP in both overlying water and 0- to 2-cm sediment layers were nearly equal before and after the experiment, indicating that phosphorus was released mainly from the 0- to 2-cm layer by dissolution. In contrast, phosphorus was decreased in pore water below a 2-cm depth, probably through sorption to sediment solids. The citrate-dithionite-bicarbonate total phosphorus (CBD-TP) and non-reactive phosphorus extracted by NaOH (NaOH-NRP) in sediment solids in the 0- to 2-cm layer decreased during the experiment. The decreases of CBD-TP were 10 times higher than those of NaOH-NRP, suggesting that the released phosphorus came mainly from the fraction bound to iron in Lake Kasumigaura. 相似文献
946.
Kikuyoshi Yoshida Nobuaki Tamahashi Noboru Matsuura Tohru Takahashi Takehiko Tachibana 《Cell and tissue research》1991,266(2):223-229
Summary Monoclonal antibodies against cellular components of reticular meshworks were produced by immunizing rats with heterogeneous stromal-cell population of mouse spleen. Immunohistochemical screening selected two antibodies, WP-1 and RPSC-2. WP-1 proved to immunostain the meshwork of the B area densely, leaving the marginal zone unstained; it also reacted sparsely with the meshwork of the T-cell region. In contrast, RPSC-2 selectively immunostained the meshwork of the T region. Immuno-electron microscopy clearly visualized, for both antibodies, reaction products being deposited along the cytomembrane of the fibroblastic reticulum cells, along their abundant cytoplasmic processes that were densely intertwined with lymphocytes. Double immunostaining with RPSC-2 followed by WP-1 clearly divided the white pulp into the T and the B domains. The meshwork in the T-cell region proved to be immunostainable with both WP-1 and RPSC-2. Thus, the fibroblastic reticulum cells of the T-and the B-cell areas, while indistinguishable by routine microscopy, are at least partially heterogeneous.Presented at the First International Symposium on Dendritic Cells in Lymphoid Tissues, held in Yamagata, Japan, 7–9 June, 1990 相似文献
947.
Byong Hoon Yoo Xue Wu Yongling Li Mehnaaz Haniff Takehiko Sasazuki Senji Shirasawa Eeva-Liisa Eskelinen Kirill V. Rosen 《The Journal of biological chemistry》2010,285(8):5438-5449
Detachment of non-malignant epithelial cells from the extracellular matrix causes their growth arrest and, ultimately, death. By contrast, cells composing carcinomas, cancers of epithelial origin, can survive and proliferate without being attached to the extracellular matrix. These properties of tumor cells represent hallmarks of malignant transformation and are critical for cancer progression. Previously we identified several mechanisms by which ras, a major oncogene, blocks detachment-induced apoptosis of intestinal epithelial cells, but mechanisms by which Ras promotes proliferation of those cells that remain viable following detachment are unknown. We show here that detachment of non-malignant intestinal epithelial cells promotes formation of autophagosomes, vacuole-like structures that mediate autophagy (a process of cellular self-cannibalization), and that oncogenic ras prevents this autophagosome formation. We also found that ras activates a GTPase RhoA, that RhoA promotes activation of a protease calpain, and that calpain triggers degradation of Beclin-1, a critical mediator of autophagy, in these cells. The reversal of the effect of ras on Beclin-1 (achieved by expression of exogenous Beclin-1) promoted autophagosome formation following cell detachment, significantly reduced the fraction of detached cells in the S phase of the cell cycle and their rate of proliferation without affecting their viability. Furthermore, RNA interference-induced Beclin-1 down-regulation in non-malignant intestinal epithelial cells prevented detachment-dependent reduction of the fraction of these cells in the S phase of the cell cycle. Thus, ras oncogene promotes proliferation of those malignant intestinal epithelial cells that remain viable following detachment via a distinct novel mechanism that involves Ras-induced down-regulation of Beclin-1. 相似文献
948.
Abstract: The α-bungarotoxin binding component in mouse brain was purified by affinity chromatography with toxin-Sepharose, gel-chromatography on Sepharose 6B, and ion-exchange chromatography with DE52 resin. The iodinated product of the last step produced one major and one minor band on sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE). The molecular weight of the minor peak was twice as large as that of the major one. The iodinated product could bind α-bungarotoxin, and this binding was inhibited by a nicotinic antagonist, d -tubocurarine, which demonstrated that the iodinated product was a true α-bungarotoxin binding component. The molecular structure of the product was analysed by cross-linking followed by SDS-PAGE. The results fitted the model for an α-bungarotoxin binding component in the mouse brain composed of six identical or very similar subunits of 51,000-52,000. One subunit carrying the binding site for toxin bound one molecule of toxin. This subunit structure of an α-bungarotoxin binding component in the brain is discussed in comparison with that of a nicotinic acetylcholine receptor in the electric organ. 相似文献
949.
Takehiko Fujisawa Stephen R. Waldman Robert H. Yonemoto 《Cancer immunology, immunotherapy : CII》1978,4(2):77-86
Summary 26 breast cancer patients with recurrent disease were studied in order to evaluate whether transfer factor (TF) could abrogate serum blocking factors (SBF) and transfer or amplify immune reactivity directed to tumor-associated antigens (TAA) by using the leukocyte adherence inhibition assay (LAI). When 11 leukocyte samples obtained from patients reactive to cancer extract were preincubated with autologous blocking sera in the presence of PBS, nonspecific TF, or specific TF, leukocytes from these patients gained reactivity against breast cancer extract in none out of 11, one out of 11, and nine out of 11 experiments, respectively. Specific TF was obtained from donors with positive LAI breast cancer extract. Mean percentage LAI differences between control extract and breast cancer extract were –4.5±2.6, 0.5±1.7, and 15.5±2.4. The results of specific TF were significantly different from those of nonspecific TF (P<0.005).When nine leukocyte samples obtained from patients unreactive to cancer extract were preincubated with autologous blocking sera in the presence of PBS, nonspecific TF, or specific TF, leukocytes from these patients gained reactivity against breast cancer extract in none out of nine, one out of nine, and seven out of nine experiments, respectively. Mean percentage LAI differences between control extract and breast cancer extract were –4.6±2.0, 0.6±2.3, and 11.8±3.5. The results of specific TF were again significantly different from those of nonspecific TF (P<0.005).When allogeneic blocking sera were utilized, similar results were obtained. When specific TF was administered in two doses, 1 week apart subcutaneously to six breast cancer patients who were unreactive to breast cancer extracts, four patients gained reactivity against breast cancer extracts.Our in vitro experiments support the presence of a specific component in transfer factor extract which can transfer or amplify cell-mediated reactivity with abrogation of SBF directed at TAA.Abbreviations BSS =
Balanced Salt Solution
- LAI =
Leukocyte Adherence Inhibition
- PBS =
Phosphate Buffered Saline
- RPMI =
Roswell Park Memorial Institute
- SBF =
Serum Blocking Factors
- TAA =
Tumor Associated Antigen
- TF =
Transfer Factor 相似文献
950.
Kazuto Kugou Tomoyuki Fukuda Shintaro Yamada Masaru Ito Hiroyuki Sasanuma Saori Mori Yuki Katou Takehiko Itoh Kouji Matsumoto Takehiko Shibata Katsuhiko Shirahige Kunihiro Ohta 《Molecular biology of the cell》2009,20(13):3064-3076
Spo11-mediated DNA double-strand breaks (DSBs) that initiate meiotic recombination are temporally and spatially controlled. The meiotic cohesin Rec8 has been implicated in regulating DSB formation, but little is known about the features of their interplay. To elucidate this point, we investigated the genome-wide localization of Spo11 in budding yeast during early meiosis by chromatin immunoprecipitation using high-density tiling arrays. We found that Spo11 is dynamically localized to meiotic chromosomes. Spo11 initially accumulated around centromeres and thereafter localized to arm regions as premeiotic S phase proceeded. During this stage, a substantial proportion of Spo11 bound to Rec8 binding sites. Eventually, some of Spo11 further bound to both DSB and Rec8 sites. We also showed that such a change in a distribution of Spo11 is affected by hydroxyurea treatment. Interestingly, deletion of REC8 influences the localization of Spo11 to centromeres and in some of the intervals of the chromosomal arms. Thus, we observed a lack of DSB formation in a region-specific manner. These observations suggest that Rec8 would prearrange the distribution of Spo11 along chromosomes and will provide clues to understanding temporal and spatial regulation of DSB formation. 相似文献