全文获取类型
收费全文 | 1064篇 |
免费 | 62篇 |
出版年
2021年 | 13篇 |
2020年 | 7篇 |
2019年 | 12篇 |
2018年 | 14篇 |
2017年 | 13篇 |
2016年 | 30篇 |
2015年 | 30篇 |
2014年 | 38篇 |
2013年 | 59篇 |
2012年 | 61篇 |
2011年 | 41篇 |
2010年 | 23篇 |
2009年 | 28篇 |
2008年 | 62篇 |
2007年 | 68篇 |
2006年 | 55篇 |
2005年 | 60篇 |
2004年 | 45篇 |
2003年 | 49篇 |
2002年 | 54篇 |
2001年 | 29篇 |
2000年 | 31篇 |
1999年 | 26篇 |
1998年 | 9篇 |
1997年 | 16篇 |
1996年 | 10篇 |
1995年 | 9篇 |
1994年 | 5篇 |
1993年 | 7篇 |
1992年 | 19篇 |
1991年 | 22篇 |
1990年 | 18篇 |
1989年 | 19篇 |
1988年 | 16篇 |
1987年 | 7篇 |
1986年 | 11篇 |
1985年 | 10篇 |
1984年 | 11篇 |
1983年 | 7篇 |
1982年 | 7篇 |
1980年 | 10篇 |
1979年 | 12篇 |
1978年 | 5篇 |
1977年 | 6篇 |
1975年 | 5篇 |
1973年 | 4篇 |
1972年 | 3篇 |
1971年 | 3篇 |
1967年 | 4篇 |
1966年 | 3篇 |
排序方式: 共有1126条查询结果,搜索用时 31 毫秒
61.
62.
Yusuke Sakai Makiko Koike Hideko Hasegawa Kosho Yamanouchi Akihiko Soyama Mitsuhisa Takatsuki Tamotsu Kuroki Kazuo Ohashi Teruo Okano Susumu Eguchi 《PloS one》2013,8(7)
Cell sheet engineering is attracting attention from investigators in various fields, from basic research scientists to clinicians focused on regenerative medicine. However, hepatocytes have a limited proliferation potential in vitro, and it generally takes a several days to form a sheet morphology and multi-layered sheets. We herein report our rapid and efficient technique for generating multi-layered human hepatic cell (HepaRG® cell) sheets using pre-cultured fibroblast monolayers derived from human skin (TIG-118 cells) as a feeder layer on a temperature-responsive culture dish. Multi-layered TIG-118/HepaRG cell sheets with a thick morphology were harvested on day 4 of culturing HepaRG cells by forceful contraction of the TIG-118 cells, and the resulting sheet could be easily handled. In addition, the human albumin and alpha 1-antitrypsin synthesis activities of TIG-118/HepaRG cells were approximately 1.2 and 1.3 times higher than those of HepaRG cells, respectively. Therefore, this technique is considered to be a promising modality for rapidly fabricating multi-layered human hepatocyte sheets from cells with limited proliferation potential, and the engineered cell sheet could be used for cell transplantation with highly specific functions. 相似文献
63.
Tomohiro Iguchi Sho Nambara Takaaki Masuda Hisateru Komatsu Masami Ueda Shinya Kidogami Yushi Ogawa Qingjiang Hu Kuniaki Sato Tomoko Saito Hidenari Hirata Shotaro Sakimura Ryutaro Uchi Naoki Hayashi Shuhei Ito Hidetoshi Eguchi Keishi Sugimachi Yoshihiko Maehara Koshi Mimori 《PloS one》2016,11(11)
miR-146a plays important roles in cancer as it directly targets NUMB, an inhibitor of Notch signaling. miR-146a is reportedly regulated by a G>C polymorphism (SNP; rs2910164). This polymorphism affects various cancers, including colorectal cancer (CRC). However, the clinical significance of miR-146a polymorphism in CRC remains unclear. A total of 59 patients with CRC were divided into 2 groups: a CC/CG genotype (n = 32) and a GG genotype (n = 27), based on the miR-146a polymorphism. cDNA microarray analysis was performed using 59 clinical samples. Significantly enriched gene sets in each genotype were extracted using GSEA. We also investigated the association between miR-146a polymorphism and miR-146a, NUMB expression or migratory response in CRC cell lines. The CC/CG genotype was associated with significantly more synchronous liver metastasis (p = 0.007). A heat map of the two genotypes showed that the expression profiles were clearly stratified. GSEA indicated that Notch signaling and JAK/STAT3 signaling were significantly associated with the CC/CG genotype (p = 0.004 and p = 0.023, respectively). CRC cell lines with the pre-miR-146a/C revealed significantly higher miR-146a expression (p = 0.034) and higher NUMB expression and chemotactic activity. In CRC, miR-146a polymorphism is involved in liver metastasis. Identification of this polymorphism could be useful to identify patients with a high risk of liver metastasis in CRC. 相似文献
64.
65.
Qu Wei-Min Huang Zhi-Li Mochizuki Takatoshi Eguchi Naomi Chen Jiang-Fan Schwarzschild Michael A. Fink Stephen J. Urade Yoshihiro Hayaishi Osamu 《Sleep and biological rhythms》2016,2(1):S55-S55
Sleep and Biological Rhythms - 相似文献
66.
67.
Mari Kawamura Tadashi Yamamoto Keisuke Yamashiro Shinsuke Kochi Chiaki Yoshihara‐Hirata Hidetaka Ideguchi Hiroaki Aoyagi Kazuhiro Omori Shogo Takashiba 《Journal of cellular and molecular medicine》2019,23(2):1211-1223
The recruitment of tissue‐resident stem cells is important for wound regeneration. Periodontal ligament cells (PDL cells) are heterogeneous cell populations with stemness features that migrate into wound sites to regenerate periodontal fibres and neighbouring hard tissues. Cell migration is regulated by the local microenvironment, coordinated by growth factors and the extracellular matrix (ECM). Integrin‐mediated cell adhesion to the ECM provides essential signals for migration. We hypothesized that PDL cell migration could be enhanced by selective expression of integrins. The migration of primary cultured PDL cells was induced by platelet‐derived growth factor‐BB (PDGF‐BB). The effects of blocking specific integrins on migration and ECM adhesion were investigated based on the integrin expression profiles observed during migration. Up‐regulation of integrins α3, α5, and fibronectin was identified at distinct localizations in migrating PDL cells. Treatment with anti‐integrin α5 antibodies inhibited PDL cell migration. Treatment with anti‐integrin α3, α3‐blocking peptide, and α3 siRNA significantly enhanced cell migration, comparable to treatment with PDGF‐BB. Furthermore, integrin α3 inhibition preferentially enhanced adhesion to fibronectin via integrin α5. These findings indicate that PDL cell migration is reciprocally regulated by integrin α3‐mediated inhibition and α5‐mediated promotion. Thus, targeting integrin expression is a possible therapeutic strategy for periodontal regeneration. 相似文献
68.
69.
70.
Xie M Kobayashi I Kiyoshima T Yamaza H Honda JY Takahashi K Enoki N Akamine A Sakai H 《The Journal of biological chemistry》2007,282(32):23275-23283
We examined the functional implication of nucleolin in the mouse first molar development. Both the nucleolin mRNA and protein expressions were demonstrated in the odontogenic epithelial cells in the early stage and in the inner enamel epithelial layer in the late stage. The expression pattern of nucleolin corresponded to the proliferating cells in the tooth germ, thus showing that nucleolin could possibly be related to cell proliferation. No in situ signal of nucleolin was found in the primary enamel knot (PEK). Furthermore, nucleolin protein was demonstrated in the PEK by immunohistochemistry. The existence of nucleolin protein in the PEK may possibly be related to the apoptosis in the PEK cells. An inhibition assay using the hemagglutinating virus of Japan-liposome containing nucleolin antisense phosphorothioated oligonucleotide (AS S-ODN) in cultured mouse mandibles at embryonic day (E) 11.0 showed a marked growth inhibition of tooth germ. Moreover, no developmental arrest was found in the cultured tooth germ at E15.0 treated with nucleolin AS S-ODN. Real time PCR was performed to examine the mRNA expression of nucleolin-related genes, and a significant reduction in the midkine mRNA expression was thus observed in the mouse mandible after being treated with nucleolin AS S-ODN. This inhibition assay indicated that nucleolin could thus be involved in the early stage of tooth germ initiation and morphogenesis, possibly by regulating the midkine expression. 相似文献