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561.
Tsukasa Sato Yasuhiko Midorikawa Takao Yamashita Akemi Araki F. Sendo 《Cancer immunology, immunotherapy : CII》1996,43(2):77-86
Effective treatment of a rat transplanted ascites tumor by i. p. injection of a streptococcal biological response modifier,
OK-432, was abrogated by selective in vivo depletion of neutrophils by a monoclonal antibody, RP-3. The mechanisms by which
neutrophils participate in the therapeutic action of OK-432 were studied with Winn’s assay using peritoneal exudate cells
periodically obtained from rats i. p. injected with this biological response modifier. Intraperitoneal resident macrophages
were first activated with OK-432, and within 3 h, tumor-inhibitory activity had moved to the early exuded neutrophils. However,
6 h after injection, exuded macrophages were the only cells involved in tumor inhibition. Considered together with other findings,
it is likely that, in this system, neutrophils may transmit information from resident macrophages to exuded inflammatory macrophages
in a series of responses induced by i. p. injection of OK-432.
Received: 29 April 1996 / Accepted: 27 July 1996 相似文献
562.
563.
Tsukasa Tominari Miyuki Akita Chiho Matsumoto Michiko Hirata Shosei Yoshinouchi Yuki Tanaka Kento Karouji Yoshifumi Itoh Takayuki Maruyama Chisato Miyaura Yukihiro Numabe Masaki Inada 《The Journal of biological chemistry》2022,298(3)
Toll-like receptors (TLRs) are pattern recognition receptors that play a critical role in innate immune diseases. TLR3, which is localized in the endosomal compartments of hematopoietic immune cells, is able to recognize double-stranded RNA (dsRNA) derived from viruses and bacteria and thereby induce innate immune responses. Inflammatory periodontal bone resorption is caused by bacterial infections, which initially is regulated by innate immunity; however, the roles of TLR3 signaling in bone resorption are still not known. We examined the roles of TLR3 signaling in bone resorption using poly(I:C), a synthetic dsRNA analog. In cocultures of mouse bone marrow cells and stromal osteoblasts, poly(I:C) clearly induced osteoclast differentiation. In osteoblasts, poly(I:C) increased PGE2 production and upregulated the mRNA expression of PGE2-related genes, Ptgs2 and Ptges, as well as that of a gene related to osteoclast differentiation, Tnfsf11. In addition, we found that indomethacin (a COX-2 inhibitor) or an antagonist of the PGE2 receptor EP4 attenuated the poly(I:C)-induced PGE2 production and subsequent Tnfsf11 expression. Poly(I:C) also prolonged the survival of the mature osteoclasts associated with the increased mRNA expression of osteoclast marker genes, Nfatc1 and Ctsk. In ex vivo organ cultures of periodontal alveolar bone, poly(I:C) induced bone-resorbing activity in a dose-dependent manner, which was attenuated by the simultaneous administration of either indomethacin or an EP4 antagonist. These data suggest that TLR3 signaling in osteoblasts controls PGE2 production and induces the subsequent differentiation and survival of mature osteoclasts. Endogenous TLR3 in stromal osteoblasts and osteoclasts synergistically induces inflammatory alveolar bone resorption in periodontitis. 相似文献
564.
A conditioned medium (CM) prepared from strawberry suspension cultures greatly stimulated anthocyanin accumulation. CM separated by dialysis membrane showed a significant increase (p 0.05) in anthocyanin synthesis at a fraction smaller than 10,000 Da. The stimulation by CM was eliminated when the CM was treated with alkali. 相似文献
565.
Tatsuro Ikeuchi Ikuko Kondo Motomichi Sasaki Yasuhiko Kaneko Susumu Kodama Tsukasa Hattori 《Human genetics》1976,33(3):327-330
Summary Reexamination was made on a male infant previously reported as 21-monosomy. Extensive chromosome banding analyses in the patient and parents disclosed an unbalanced de novo translocation between chromosomes 13 and 21. The patient's karyotype was interpreted as 45,XY,-13,-21,+der(13),t(13;21) (q2 or 3;q1 or 2)pat. The patient showed many clinical features characteristic of 13q- syndrome. 相似文献
566.
Moesin Is Not a Receptor for Measles Virus Entry into Mouse Embryonic Stem Cells 总被引:2,自引:0,他引:2
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Yoshinori Doi Mitsue Kurita Misako Matsumoto Takahisa Kondo Tetsuo Noda Sachiko Tsukita Shoichiro Tsukita Tsukasa Seya 《Journal of virology》1998,72(2):1586-1592
The involvement of moesin in measles virus (MV) entry was investigated with moesin-positive and -negative mouse embryonic stem (ES) cells. MV infection of these cells was very ineffective and was independent of moesin expression. Furthermore, when these cells were transfected to express human CD46, a 100-fold increase in syncytium formation was observed with these cells and was independent of the expression of moesin. The only obvious difference between moesin-positive and -negative ES cells was the shape of the syncytia formed. Moesin-negative ES cells expressing or not expressing human CD46 formed separate pieces of fragmented syncytia which were torn apart during spreading, whereas ES cells expressing moesin exhibited typical syncytia. In addition, moesin was not detected on the surface of any murine cells or cell lines that we have tested by a flow cytometric assay with moesin-specific antibodies. These findings indicate that murine moesin is neither a receptor nor a CD46 coreceptor for MV entry into mouse ES cells. Moesin is involved in actin filament-plasma membrane interactions as a cross-linker, and it affects only the spreading and shape of MV-mediated syncytia. 相似文献
567.
Tsutomu Nakanishi Etsuko Yamagata Kaisuke Yoneda Tsukasa Nagashima Ichiro Kawasaki Toshio Yoshida Hideo Mori Iwao Miura 《Phytochemistry》1984,23(9):2066-2067
Three fragrant sesquiterpenes have been isolated as major constituents from the wood of Aquilaria malaccensis and identified as α-agarofuran, (?)-10-epi-γ-eudesmol and oxo-agarospirol. 相似文献
568.
Shinji Hosoi Hiromasa Miyaji Mitsuo Satoh Tsukasa Kurimoto Akira Mihara Nobuo Fujiyoshi Seiga Itoh Seiji Sato 《Cytotechnology》1991,5(Z2):17-34
We investigated the basic technology of cell culture conditions for production of useful substances such as cytokines, and related proteins produced by Namalwa cells. Namalwa cells (Klein, 1972), human B lymphoblastoid cells, were used for large scale production of alpha-interferon (Klein, 1979). Namalwa KJM-1, a subline of Namalwa cells, adapted to serum- and albumin-free medium, can grow at a high density above 1 × 107 cells/ml in suspension mode by the use of a perfusion culture system, Biofermenter, containing a cone-type cell-sedimentation column as cell separator (Sato, 1983).Several kinds of cytokine cDNA can be introduced and expressed in Namalwa KJM-1 cells (Miyaji, 1990a,b,c). Some of these were produced in large quantities by use of a gene amplification method with dhfr (Miyaji, 1990c), even though the Namalwa KJM-1 cells contained endogenous dhfr genes. For stable production of the target protein, Namalwa KJM-1 cells are very useful host cells, because they have no effective endogenous protease activity in the conditioned medium. 相似文献
569.
Tsukasa Fukushi 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1989,166(1):57-64
Summary A new training and testing paradigm for walking sheep blowflies, Lucilia cuprina, is described. A fly is trained by presenting it with a droplet of sugar solution on a patch of coloured paper. After having consumed the sugar droplet, the fly starts a systematic search. While searching, it is confronted with an array of colour marks consisting of four colours displayed on the test cardboard (Fig. 1). Colours used for training and test include blue, green, yellow, orange, red, white and black.Before training, naive flies are tested for their spontaneous colour preferences on the test array. Yellow is visited most frequently, green least frequently (Table 2). Spontaneous colour preferences do not simply depend on subjective brightness (Table 1).The flies trained to one of the colours prefer this colour significantly (Figs. 5 and 9–11). This behaviour reflects true learning rather than sensitisation (Figs. 6–7). The blue and yellow marks are learned easily and discriminated well (Figs. 5, 9, 11). White is also discriminated well, although the response frequencies are lower than to blue and yellow (Fig. 11). Green is discriminated from blue but weakly from yellow and orange (Figs. 5, 9, 10). Red is a stimulus as weak as black (Figs. 8, 9). These features of colour discrimination reflect the spectral loci of colours in the colour triangle (Fig. 14).The coloured papers seem to be discriminated mainly by the hue of colours (Fig. 12), but brightness may also be used to discriminate colour stimuli (Fig. 13). 相似文献
570.
Masayasu Minami Hideyo Takahashi Hirofumi Inagaki Yuko Yamano Sakura Onoue Shun Matsumoto Tsukasa Sasaki Kazuhiro Sakai 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》2009,877(8-9):814-822
During our studies to establish a method for identifying tryptamine-related substances in human urine, we detected three large peaks of unknown origin in an HPLC chromatogram. Fluorometric HPLC and HPLC-TOF-MS/MS analyses led to the identification of these substances as 6-sulphatoxymelatonin, 5-sulphatoxydiacetyltryptamine, and reduced melatonin. This is the first report of the latter two compounds in human urine. Here, we report the results of two fluorometric HPLC assays of these three substances, as well as melatonin, 6-hydroxymelatonin, and 5-hydroxydiacetyltryptamine, using synthesized standards and discuss the possibility that 5-hydroxydiacetyltryptamine (the parent substance of 5-sulphatoxydiacetyltryptamine) and reduced melatonin have radical scavenging activity. 相似文献