全文获取类型
收费全文 | 319篇 |
免费 | 11篇 |
出版年
2022年 | 5篇 |
2021年 | 8篇 |
2020年 | 5篇 |
2019年 | 4篇 |
2018年 | 9篇 |
2017年 | 9篇 |
2016年 | 8篇 |
2015年 | 14篇 |
2014年 | 13篇 |
2013年 | 21篇 |
2012年 | 25篇 |
2011年 | 26篇 |
2010年 | 11篇 |
2009年 | 14篇 |
2008年 | 25篇 |
2007年 | 24篇 |
2006年 | 16篇 |
2005年 | 14篇 |
2004年 | 10篇 |
2003年 | 14篇 |
2002年 | 13篇 |
2001年 | 4篇 |
2000年 | 4篇 |
1999年 | 1篇 |
1998年 | 5篇 |
1997年 | 1篇 |
1996年 | 4篇 |
1995年 | 2篇 |
1994年 | 2篇 |
1993年 | 2篇 |
1992年 | 3篇 |
1991年 | 1篇 |
1990年 | 1篇 |
1988年 | 1篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1983年 | 1篇 |
1982年 | 5篇 |
1981年 | 1篇 |
1980年 | 1篇 |
1979年 | 1篇 |
排序方式: 共有330条查询结果,搜索用时 15 毫秒
51.
Tomohiro Torii Yuki Miyamoto Kenji Tago Kazunori Sango Kazuaki Nakamura Atsushi Sanbe Akito Tanoue Junji Yamauchi 《The Journal of biological chemistry》2014,289(49):33887-33903
The mechanism of neurite growth is complicated, involving continuous cytoskeletal rearrangement and vesicular trafficking. Cytohesin-2 is a guanine nucleotide exchange factor for Arf6, an Arf family molecular switch protein, controlling cell morphological changes such as neuritogenesis. Here, we show that cytohesin-2 binds to a protein with a previously unknown function, CCDC120, which contains three coiled-coil domains, and is transported along neurites in differentiating N1E-115 cells. Transfection of the small interfering RNA (siRNA) specific for CCDC120 into cells inhibits neurite growth and Arf6 activation. When neurites start to extend, vesicles containing CCDC120 and cytohesin-2 are transported in an anterograde manner rather than a retrograde one. As neurites continue extension, anterograde vesicle transport decreases. CCDC120 knockdown inhibits cytohesin-2 localization into vesicles containing CCDC120 and diffuses cytohesin-2 in cytoplasmic regions, illustrating that CCDC120 determines cytohesin-2 localization in growing neurites. Reintroduction of the wild type CCDC120 construct into cells transfected with CCDC120 siRNA reverses blunted neurite growth and Arf6 activity, whereas the cytohesin-2-binding CC1 region-deficient CCDC120 construct does not. Thus, cytohesin-2 is transported along neurites by vesicles containing CCDC120, and it mediates neurite growth. These results suggest a mechanism by which guanine nucleotide exchange factor for Arf6 is transported to mediate neurite growth. 相似文献
52.
Nakagami H Nishikawa T Tamura N Maeda A Hibino H Mochizuki M Shimosato T Moriya T Morishita R Tamai K Tomono K Kaneda Y 《Journal of cellular and molecular medicine》2012,16(7):1629-1639
We previously identified a novel angiogenic peptide, AG30, with antibacterial effects that could serve as a foundation molecule for the design of wound-healing drugs. Toward clinical application, in this study we have developed a modified version of the AG30 peptide characterized by improved antibacterial and angiogenic action, thus establishing a lead compound for a feasibility study. Because AG30 has an α-helix structure with a number of hydrophobic and cationic amino acids, we designed a modified AG30 peptide by replacing several of the amino acids. The replacement of cationic amino acids (yielding a new molecule, AG30/5C), but not hydrophobic amino acids, increased both the angiogenic and the antimicrobial properties of the peptide. AG30/5C was also effective against methicillin-resistant Staphylococcus aureus (MRSA) and antibiotic-resistant Pseudomonas aeruginosa. In a diabetic mouse wound-healing model, the topical application of AG30/5C accelerated wound healing with increased angiogenesis and attenuated MRSA infection. To facilitate the eventual clinical investigation/application of these compounds, we developed a large-scale procedure for the synthesis of AG30/5C that employed the conventional solution method and met Good Manufacturing Practice guidelines. In the evaluation of stability of this peptide in saline solution, RP-HPLC analysis revealed that AG30/5C was fairly stable under 5°C for 12 months. Therefore, we propose the use of AG30/5C as a wound-healing drug with antibacterial and angiogenic actions. 相似文献
53.
Teruomi Jojima Nariyoshi Yoshimura Tetsuo Takematsu Saburo Tamura 《Bioscience, biotechnology, and biochemistry》2013,77(1):96-102
3-Phenoxypyridazines and related compounds were evaluated their pre-emergence activities. Of these, 3-phenoxy-, 3-(2-methylphenoxy)-, and 3-(2-ethylphenoxy)-pyridazines (III, IV and VII) showed powerful effects on barnyardgrass and spikerush, whereas they gave no injury on rice plants. Furthermore, susceptibility of various kinds of cultivated plants as well as of weeds to III and IV were examined. Growth regulating activity of III was compared with that of maleic hydrazide. 相似文献
54.
Michael F. Braby Marianne Espeland Chris J. Müller Rod Eastwood David J. Lohman Akito Y. Kawahara Sarah C. Maunsell Naomi E. Pierce 《Systematic Entomology》2020,45(3):703-722
The butterfly tribe Candalidini is geographically restricted to Australia and mainland New Guinea and its adjacent islands. With 60 species and subspecies, it represents a large radiation of Papilionoidea in the Australian region. Although the species-level taxonomy is relatively well understood, the number of genera is uncertain, varying from two to eight. We reconstructed the phylogeny of the Candalidini based on a 13-locus hybrid enrichment probe set (12.8 Kbp: COI, Thiolase, CAD, CAT, DDC, EF1-a, GAPDH, HCL, IDH, MDH, RPS2, RPS5, Wingless), including all previously recognized genera and 76% (28/37) of the species-level diversity of the tribe. Maximum likelihood analysis recovered the Candalidini as a strongly supported monophyletic group. In conjunction with morphological characters, the phylogeny provided a robust framework for a revised classification in which we recognize four genera, 37 species and 23 subspecies. The genus Nesolycaena Waterhouse & R.E. Turner is considered in synonymy with Candalides Hübner, and four other genera are not recognized, namely, Holochila C. Felder, Adaluma Tindale, Zetona Waterhouse and Microscena Tite. Of the four valid genera, the absimilis group (23 species) is placed in the newly described genus Eirmocides Braby, Espeland & Müller gen. nov. (type species Candalides consimilis Waterhouse). The erinus group (six species) is assigned to Erina Swainson, which is reinstated. Chrysophanus cyprotus Olliff is assigned to Cyprotides Tite, which is also reinstated as a monotypic genus. The remaining seven species are placed in Candalides sensu stricto. Overall, we propose 47 new nomenclatural changes at the species and subspecies levels, including the synonymy of Holochila biaka Tite as Eirmocides tringa biaka (Tite) syn. nov. et comb. nov. and recognition of Candalides hyacinthinus gilesi M.R. Williams & Bollam as a distinct species Erina gilesi (M.R. Williams & Bollam stat. rev. et comb. nov. A dated phylogeny using Bayesian inference in BEAST2 and biogeographical and habitat analyses based on the DEC model in BioGeoBEARS indicated that the ancestor of the Candalidini most likely evolved in rainforest habitats of the mesic biome in situ on the Australian plate of Southern Gondwana during the Eocene (c. 43 Ma). A major period of diversification occurred in the Miocene, which coincided with aridification of the Australian continent, followed by a further episode of radiation in montane New Guinea during the Plio-Pleistocene. This published work has been registered on ZooBank by the authors: Michael Braby: http://zoobank.org/urn:lsid:zoobank.org:author:4D3A7605-EBD0-40F6-A5F2-7F67F59E3D60 ; Marianne Espeland: http://zoobank.org/urn:lsid:zoobank.org:author:00D6F9F9-3902-4A8B-846F-720AB32922A6 ; Chris Müller: http://zoobank.org/urn:lsid:zoobank.org:author:15FE5F26-7596-46C2-9697-1FD92A692D0D ; http://zoobank.org/urn:lsid:zoobank.org:pub:47D5CA34-C294-4FBD-84B6-1C2A82B7CADF . 相似文献
55.
56.
Akito Kawai Keishi Yamasaki Taisuke Enokida Shuichi Miyamoto Masaki Otagiri 《Biochemistry and Biophysics Reports》2018
Sodium 4-phenylbutyrate (PB) is an orphan drug for the treatment of urea cycle disorders. It also inhibits the development of endoplasmic reticulum stress, the action of histone deacetylases and as a regulator of the hepatocanalicular transporter. PB is generally considered to have the potential for use in the treatment of the diseases such as cancer, neurodegenerative diseases and metabolic diseases. In a previous study, we reported that PB is primarily bound to human serum albumin (HSA) in plasma and its binding site is drug site 2. However, details of the binding mode of PB to HSA remain unknown. To address this issue, we examined the crystal structure of HSA with PB bound to it. The structure of the HSA–PB complex indicates that the binding mode of PB to HSA is quite similar to that for octanoate or drugs that bind to drug site 2, as opposed to that for other medium-chain length of fatty acids. These findings provide useful basic information related to drug–HSA interactions. Moreover, the information presented herein is valuable in terms of providing safe and efficient treatment and diagnosis in clinical settings. 相似文献
57.
Shingo Yamamoto Katsuhisa Nakata Kazuyo Yuri Hiromi Katae Akito Terai Hisao Kurazono Yoshifumi Takeda Osamu Yoshida 《Microbiology and immunology》1996,40(9):607-610
Four Escherichia coli strains, isolated from cystitis patients, belonging to serotype O2:H? and possessing different combinations of urovirulence factors were examined in an experimental pyelonephritis mouse model to assess the relative importance of virulence factors in causation of urinary tract infections (UTI). The results suggest not only that the each virulence factor has a role in causation of UTI but also that the presence of P fimbriae and production of hemolysin significantly reduced the LD50 and ID50 of the strains in the mouse model. The results also demonstrate that the presence of additional virulence factors acts in an additive or synergetic fashion enhancing the cumulative impact of the strain. 相似文献
58.
59.
60.
Hiroaki Kawasaki Masatoshi Itoh Tatsuo Nakahara Akito Nohtomi Motofumi Fukahori 《Neurochemical research》1991,16(11):1227-1233
Endogenous substances which inhibited the binding of [3H]flunitrazepam ([3H]FNZ) to bovine synaptosomal membranes have been purified from the hot acetic acid extracts of the bovine brain. Three peaks of inhibitory activity were obtained by Sephadex G-10 gel chromatography. Two of the peaks (Peak 2, and Peak 3) which had lower molecular weights that that of peak 1 were identified as inosine and hypoxanthine by TLC methods. Another peak (Peak 1) was further purified to homogeneity using both cation and anion ion-exchange chromatography and the following two-step reversed-phase HPLC. The purified substance inhibited the [3H]FNZ binding dose-dependently and competitively but did not have an effect on the binding of the peripheral-type BZ ligand [3H]Ro 5-4864. It was also shown that the substance was heat-stable and resistant to proteolytic degradation (trypsin, -chymotrypsin, pronase). However, a significant loss of inhibitory activity to [3H]FNZ binding was observed after acid hydrolysis. Molecular weight estimates based on gel filtration methods were less than 500 dalton, and the maximal ultraviolet absorption peak was at 314 nm. These results suggest that this substance is a new endogenous ligand for the central BZ receptor and may play an important role in regulating the GABAergic tone in the central nervous system. 相似文献