全文获取类型
收费全文 | 3672篇 |
免费 | 253篇 |
国内免费 | 5篇 |
专业分类
3930篇 |
出版年
2023年 | 13篇 |
2022年 | 23篇 |
2021年 | 54篇 |
2020年 | 21篇 |
2019年 | 47篇 |
2018年 | 50篇 |
2017年 | 56篇 |
2016年 | 87篇 |
2015年 | 126篇 |
2014年 | 150篇 |
2013年 | 253篇 |
2012年 | 243篇 |
2011年 | 267篇 |
2010年 | 129篇 |
2009年 | 135篇 |
2008年 | 261篇 |
2007年 | 234篇 |
2006年 | 248篇 |
2005年 | 255篇 |
2004年 | 253篇 |
2003年 | 217篇 |
2002年 | 189篇 |
2001年 | 31篇 |
2000年 | 19篇 |
1999年 | 40篇 |
1998年 | 53篇 |
1997年 | 36篇 |
1996年 | 38篇 |
1995年 | 35篇 |
1994年 | 41篇 |
1993年 | 35篇 |
1992年 | 21篇 |
1991年 | 17篇 |
1990年 | 21篇 |
1989年 | 27篇 |
1988年 | 12篇 |
1987年 | 14篇 |
1986年 | 14篇 |
1985年 | 31篇 |
1984年 | 23篇 |
1983年 | 17篇 |
1982年 | 16篇 |
1981年 | 10篇 |
1980年 | 10篇 |
1978年 | 11篇 |
1977年 | 5篇 |
1976年 | 9篇 |
1975年 | 4篇 |
1974年 | 6篇 |
1967年 | 3篇 |
排序方式: 共有3930条查询结果,搜索用时 15 毫秒
91.
Optimum conditions for the isolation and culture of protoplasts from high anthocyanin-producing callus of sweet potato (Ipomoea batatas) were investigated. Growth phase of callus and the ratio of callus-enzyme solution affected the yield of protoplasts. Composition of the medium and protoplast density were examined for protoplast culture.Small colonies were regenerated from the protoplasts. Upon transfer to light a high amount of anthocyanin was accumulated in these colonies.Abbreviations 2,4-D
2,4-dichlorophenoxyacetic acid
- MES
2-(N-morpholino)-ethanesulfonic acid 相似文献
92.
Seizaburo Shiraga Masayuki Kawakami Masaji Ishiguro Mitsuyoshi Ueda 《Applied microbiology》2005,71(8):4335-4338
Immobilization of enzymes on some solid supports has been used to stabilize enzymes in organic solvents. In this study, we evaluated applications of genetically immobilized Rhizopus oryzae lipase displayed on the cell surface of Saccharomyces cerevisiae in organic solvents and measured the catalytic activity of the displayed enzyme as a fusion protein with α-agglutinin. Compared to the activity of a commercial preparation of this lipase, the activity of the new preparation was 4.4 × 104-fold higher in a hydrolysis reaction using p-nitrophenyl palmitate and 3.8 × 104-fold higher in an esterification reaction with palmitic acid and n-pentanol (0.2% H2O). Increased enzyme activity may occur because the lipase displayed on the yeast cell surface is stabilized by the cell wall. We used a combination of error-prone PCR and cell surface display to increase lipase activity. Of 7,000 colonies in a library of mutated lipases, 13 formed a clear halo on plates containing 0.2% methyl palmitate. In organic solvents, the catalytic activity of 5/13 mutants was three- to sixfold higher than that of the original construct. Thus, yeast cells displaying the lipase can be used in organic solvents, and the lipase activity may be increased by a combination of protein engineering and display techniques. Thus, this immobilized lipase, which is more easily prepared and has higher activity than commercially available free and immobilized lipases, may be a practical alternative for the production of esters derived from fatty acids. 相似文献
93.
Nakamichi M 《Primates; journal of primatology》2003,44(3):239-246
The present study investigated the influence of dominance rank in combination with kinship on age-related differences in social
grooming among adult females in a free-ranging group of Japanese monkeys (Macaca fuscata). Eighty-three adult females were divided into six sub-groups according to age-class (younger: 5–9 years old; middle: 10–14 years
old; older: 15–22 years old) and dominance rank (high and low rank). The ratio of the number of unrelated females that each
female groomed to the total number of available unrelated females and grooming bouts which she gave to unrelated females decreased
with increasing age for both high- and low-ranking females, whereas age did not appear to affect corresponding values for
related females. On the other hand, compared with low-ranking females, high-ranking females of all age-classes received grooming
more often from a larger number of unrelated females. Moreover, older females of low rank received grooming less often from
a smaller number of unrelated females than younger females of low rank. These results indicate that with increasing age females
are more likely to concentrate on related females when they have grooming interactions with other females. This tendency seems
to be more apparent for low-ranking females. Moreover, the present findings also indicate that older high-ranking females
could maintain their social attractiveness as high as younger high-ranking females. 相似文献
94.
Numanami H Koyama S Sato E Haniuda M Nelson DK Hoyt JC Freels JL Habib MP Robbins RA 《American journal of physiology. Lung cellular and molecular physiology》2003,284(5):L882-L890
Chemotactic chemokines can be released from lung fibroblasts in response to interleukin (IL)-1beta and tumor necrosis factor (TNF)-alpha. An imbalance between proteases and antiproteases has been observed at inflammatory sites, and, therefore, protease inhibitors might modulate fibroblast release of chemotactic cytokines. To test this hypothesis, serine protease inhibitors (FK-706, alpha(1)-antitrypsin, or N(alpha)-p-tosyl-L-lysine chloromethyl ketone) were evaluated for their capacity to attenuate the release of neutrophil chemotactic activity (NCA) or monocyte chemotactic activity (MCA) from human fetal lung fibroblasts (HFL-1). Similarly, the release of the chemoattractants IL-8, granulocyte colony-stimulating factor, monocyte chemoattractant protein-1, macrophage colony-stimulating factor, and granulocyte/macrophage colony-stimulating factor, from HFL-1, were evaluated in response to IL-1beta and TNF-alpha. NCA, MCA, and chemotactic cytokines were attenuated by FK-706. However, matrix metalloproteinase inhibitors were without effect, and cysteine protease inhibitors only slightly attenuated chemotactic or cytokine release. These data suggest that IL-1beta and TNF-alpha may stimulate lung fibroblasts to release NCA and MCA by a protease-dependent mechanism and that serine protease inhibitors may attenuate the release. 相似文献
95.
Yamazaki S Iwamoto R Saeki K Asakura M Takashima S Yamazaki A Kimura R Mizushima H Moribe H Higashiyama S Endoh M Kaneda Y Takagi S Itami S Takeda N Yamada G Mekada E 《The Journal of cell biology》2003,163(3):469-475
Heparin-binding EGF-like growth factor (HB-EGF) is first synthesized as a membrane-anchored form (proHB-EGF), and its soluble form (sHB-EGF) is released by ectodomain shedding from proHB-EGF. To examine the significance of proHB-EGF processing in vivo, we generated mutant mice by targeted gene replacement, expressing either an uncleavable form (HBuc) or a transmembrane domain-truncated form (HBdeltatm) of the molecule. HB(uc/uc) mice developed severe heart failure and enlarged heart valves, phenotypes similar to those in proHB-EGF null mice. On the other hand, mice carrying HBdeltatm exhibited severe hyperplasia in both skin and heart. These results indicate that ectodomain shedding of proHB-EGF is essential for HB-EGF function in vivo, and that this process requires strict control. 相似文献
96.
Ikuzawa M Yasumasu S Inokuchi T Kobayashi K Nomura K Iuchi I 《Journal of biochemistry》2003,134(3):385-394
Cathepsin E (CE) was purified from the foregut of Xenopus laevis tadpoles as a mature dimeric form. The purified enzyme was a typical CE among aspartic proteinases with respect to pH dependence of proteolytic activity, susceptibility to pepstatin, and having N-linked high-mannose type oligosaccharide chains. We isolated two cDNAs for the CE (CE1 and CE2) from adult stomach. The amino acid sequence of the N-terminal region of the purified CE coincided with the corresponding sequence predicted from CE1. Northern blot analysis and in situ hybridization were performed. The CE1 mRNA was highly expressed in surface mucous cells and gland cells constituting the larval epithelium of the foregut of pro-metamorphic tadpoles. As metamorphosis began and progressed, CE1 mRNA drastically decreased in amount, and subsequently both CE1 and CE2 mRNAs gradually increased. The increase in CE2 mRNA was detected shortly after the increase in CE1 mRNA. The decrease in CE1 expression correlated with degeneration of the larval type epithelium, while the increases in both CE1 and CE2 expression correlated with formation of the adult type epithelium. Thus, cathepsin E gene expression was differentially regulated during metamorphosis-associated remodeling of the larval to adult type epithelium in stomach. 相似文献
97.
Masataka Saito Sara N. Stahley Christopher Y. Caughman Xuming Mao Dana K. Tucker Aimee S. Payne Masayuki Amagai Andrew P. Kowalczyk 《PloS one》2012,7(12)
Pemphigus vulgaris (PV) is an autoimmune epidermal blistering disease caused by autoantibodies directed against the desmosomal cadherin desmoglein-3 (Dsg3). Significant advances in our understanding of pemphigus pathomechanisms have been derived from the generation of pathogenic monoclonal Dsg3 antibodies. However, conflicting models for pemphigus pathogenicity have arisen from studies using either polyclonal PV patient IgG or monoclonal Dsg3 antibodies. In the present study, the pathogenic mechanisms of polyclonal PV IgG and monoclonal Dsg3 antibodies were directly compared. Polyclonal PV IgG cause extensive clustering and endocytosis of keratinocyte cell surface Dsg3, whereas pathogenic mouse monoclonal antibodies compromise cell-cell adhesion strength without causing these alterations in Dsg3 trafficking. Furthermore, tyrosine kinase or p38 MAPK inhibition prevents loss of keratinocyte adhesion in response to polyclonal PV IgG. In contrast, disruption of adhesion by pathogenic monoclonal antibodies is not prevented by these inhibitors either in vitro or in human skin explants. Our results reveal that the pathogenic activity of polyclonal PV IgG can be attributed to p38 MAPK-dependent clustering and endocytosis of Dsg3, whereas pathogenic monoclonal Dsg3 antibodies can function independently of this pathway. These findings have important implications for understanding pemphigus pathophysiology, and for the design of pemphigus model systems and therapeutic interventions. 相似文献
98.
Microtubules play multiple roles in a wide range of cellular phenomena, including cell polarity establishment and chromosome segregation. A number of microtubule regulators have been identified, including microtubule-associated proteins and kinases, and knowledge of these factors has contributed to our molecular understanding of microtubule regulation of each relevant cellular process. The known regulators, however, are insufficient to explain how those processes are linked to one another, underscoring the need to identify additional regulators. To find such novel mechanisms and microtubule regulators, we performed a screen that combined genetics and microscopy for fission yeast mutants defective in microtubule organization. We isolated approximately 900 mutants showing defects in either microtubule organization or the nuclear envelope, and these mutants were classified into 12 categories. We particularly focused on one mutant, kis1, which displayed spindle defects in early mitosis. The kis1 mutant frequently failed to assemble a normal bipolar spindle. The responsible gene encoded a kinetochore protein, Mis19 (also known as Eic1), which localized to the interface of kinetochores and spindle poles. We also found that the inner kinetochore proteins Mis6/CENP-I and Cnp1/CENP-A were delocalized from kinetochores in the kis1 cells and that kinetochore-microtubule attachment was defective. Another mutant, mis6, also displayed similar spindle defects. We conclude that Kis1 is required for inner kinetochore organization, through which Kis1 ensures kinetochore-microtubule attachment and spindle integrity. Thus, we propose an unexpected relationship between inner kinetochore organization and spindle integrity. 相似文献
99.
Keizo Nishikawa Shigeto Seno Toshitada Yoshihara Ayako Narazaki Yuki Sugiura Reito Shimizu Junichi Kikuta Reiko Sakaguchi Norio Suzuki Norihiko Takeda Hiroaki Semba Masamichi Yamamoto Daisuke Okuzaki Daisuke Motooka Yasuhiro Kobayashi Makoto Suematsu Haruhiko Koseki Hideo Matsuda Masayuki Yamamoto Seiji Tobita Yasuo Mori Masaru Ishii 《EMBO reports》2021,22(12)
Oxygen plays an important role in diverse biological processes. However, since quantitation of the partial pressure of cellular oxygen in vivo is challenging, the extent of oxygen perturbation in situ and its cellular response remains underexplored. Using two‐photon phosphorescence lifetime imaging microscopy, we determine the physiological range of oxygen tension in osteoclasts of live mice. We find that oxygen tension ranges from 17.4 to 36.4 mmHg, under hypoxic and normoxic conditions, respectively. Physiological normoxia thus corresponds to 5% and hypoxia to 2% oxygen in osteoclasts. Hypoxia in this range severely limits osteoclastogenesis, independent of energy metabolism and hypoxia‐inducible factor activity. We observe that hypoxia decreases ten‐eleven translocation (TET) activity. Tet2/3 cooperatively induces Prdm1 expression via oxygen‐dependent DNA demethylation, which in turn activates NFATc1 required for osteoclastogenesis. Taken together, our results reveal that TET enzymes, acting as functional oxygen sensors, regulate osteoclastogenesis within the physiological range of oxygen tension, thus opening new avenues for research on in vivo response to oxygen perturbation. 相似文献
100.
Ryu Tashiro Masahiro Iwamoto Hironobu Morinaga Tomoko Emura Kumi Hidaka Masayuki Endo Hiroshi Sugiyama 《Nucleic acids research》2015,43(14):6692-6700
DNA has recently emerged as a promising material for the construction of nanosized architectures. Chemically modified DNA has been suggested to be an important component of such architectural building blocks. We have designed and synthesized a novel H-shaped DNA oligonucleotide dimer that is cross-linked with a structurally rigid linker composed of phenylene and ethynylene groups. A rotatable DNA unit was constructed through the self-assembly of this H-shaped DNA component and two complementary DNA oligonucleotides. In addition to the rotatable unit, a locked DNA unit containing two H-shaped DNA components was also constructed. As an example of an extended locked structure, a hexagonal DNA origami dimer and oligomer were constructed by using H-shaped DNA as linkers. 相似文献