全文获取类型
收费全文 | 994篇 |
免费 | 56篇 |
国内免费 | 3篇 |
出版年
2023年 | 6篇 |
2022年 | 30篇 |
2021年 | 44篇 |
2020年 | 32篇 |
2019年 | 31篇 |
2018年 | 35篇 |
2017年 | 30篇 |
2016年 | 41篇 |
2015年 | 65篇 |
2014年 | 60篇 |
2013年 | 61篇 |
2012年 | 93篇 |
2011年 | 79篇 |
2010年 | 45篇 |
2009年 | 29篇 |
2008年 | 46篇 |
2007年 | 31篇 |
2006年 | 44篇 |
2005年 | 21篇 |
2004年 | 32篇 |
2003年 | 23篇 |
2002年 | 30篇 |
2001年 | 25篇 |
2000年 | 8篇 |
1999年 | 12篇 |
1998年 | 8篇 |
1997年 | 4篇 |
1996年 | 6篇 |
1995年 | 3篇 |
1994年 | 8篇 |
1993年 | 6篇 |
1992年 | 7篇 |
1991年 | 5篇 |
1990年 | 4篇 |
1989年 | 5篇 |
1988年 | 3篇 |
1987年 | 4篇 |
1986年 | 4篇 |
1985年 | 4篇 |
1984年 | 7篇 |
1983年 | 2篇 |
1982年 | 3篇 |
1979年 | 3篇 |
1975年 | 1篇 |
1974年 | 2篇 |
1970年 | 2篇 |
1967年 | 1篇 |
1963年 | 2篇 |
1962年 | 1篇 |
1960年 | 1篇 |
排序方式: 共有1053条查询结果,搜索用时 15 毫秒
71.
Georgios Tzelepis Akira Hosomi Tanim Jabid Hossain Hiroto Hirayama Mukesh Dubey Dan Funck Jensen Tadashi Suzuki Magnus Karlsson 《Biochemical and biophysical research communications》2014
N-Glycosylation is an important post-translational modification of proteins, which mainly occurs in the endoplasmic reticulum (ER). Glycoproteins that are unable to fold properly are exported to the cytosol for degradation by a cellular system called ER-associated degradation (ERAD). Once misfolded glycoproteins are exported to the cytosol, they are subjected to deglycosylation by peptide:N-glycanase (PNGase) to facilitate the efficient degradation of misfolded proteins by the proteasome. Interestingly, the ortholog of PNGase in some filamentous fungi was found to be an inactive deglycosylating enzyme. On the other hand, it has been shown that in filamentous fungi genomes, usually two different fungi-specific endo-β-N-acetylglucosamidases (ENGases) can be found; one is predicted to be localized in the cytosol and the other to have a signal sequence, while the functional importance of these enzymes remains to be clarified. In this study the ENGases of the filamentous fungus Trichoderma atroviride was characterized. By heterologous expression of the ENGases Eng18A and Eng18B in Saccharomyces cerevisiae, it was found that both ENGases are active deglycosylating enzymes. Interestingly, only Eng18B was able to enhance the efficient degradation of the RTL protein, a PNGase-dependent ERAD substrate, implying the involvement of this enzyme in the ERAD process. These results indicate that T. atroviride Eng18B may deglycosylate misfolded glycoproteins, substituting the function of the cytoplasmic PNGase in the ERAD process. 相似文献
72.
M. Y. Hossain Z. F. Ahmed A. B. M S. Islam S. Jasmine J. Ohtomi 《Zeitschrift fur angewandte Ichthyologie》2010,26(4):550-553
The present study aims to estimate the size at first sexual maturity and fecundity for female Gudusia chapra from the lower Ganges River, northwestern Bangladesh. A total of 250 female specimens, 3.60–13.70 cm in standard length (SL) and 1.00–43.60 g in body weight (BW), were collected during March–August 2006. The gonadosomatic index (GSI) for females was calculated by the equation, GSI (%) = (GW/BW) × 100. The size at first sexual maturity of females was estimated by the relationship between their gonadosomatic index and standard length. The specimen larger (≥8.00 cm in SL) than first size at sexual maturity was used for the estimation of fecundity. The size at first sexual maturity for female G. chapra was considered to be 8.00 cm SL in the Ganges River. The mean total fecundity was 20200 ± 6500 and ranged from 10800 to 36200. This study should be useful for fisheries biologists/managers to impose adequate regulations for sustainable‐fishery management in the Ganges River and elsewhere in Bangladesh. 相似文献
73.
K. K. Hossain R. D. Itoh G. Yoshimura G. Tokuda H. Oku M. F. Cohen H. Yamasaki 《Russian Journal of Plant Physiology》2010,57(2):222-232
Plant seeds sometimes do not germinate at elevated temperature. The thermoinhibition mechanisms of seed germination have yet
not revealed. Here we describe a chemical approach to improve seed germination at high temperature. We compared the temperature
response of germination between wild-type Arabidopsis thaliana and its T-DNA insertion mutant ΔAtGLB3 that lacks a functional gene encoding GLB3, a homologue of bacterial truncated Hb
(trHb). Under optimal temperature conditions (e.g. 22°C), the seeds of ΔAtGLB3 and the wild type germinated at a frequency
near 100%. In contrast, at 32°C the seeds of ΔAtGLB3 did not germinate while wild-type seeds retained the same high germination
frequency. The germination of ΔAtGLB3 at 32°C was partially restored by supplementation with the nitric oxide-specific scavenger
2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide (carboxy-PTIO; cPTIO), 3-(3,4-dihydroxycinnamoyl)quinic
acid, bovine serum Hb, or isoprene. The results presented in this study suggest that chemical scavengers for reactive nitrogen
species potentially improve seed germination at high temperature. 相似文献
74.
Xiang-Yang Ye Stephanie Chen Hao Zhang Kenneth T. Locke Kevin O’Malley Litao Zhang Raijit Srivastava Bowman Miao Daniel Meyers Hossain Monshizadegan Debra Search Denise Grimm Rongan Zhang Jonathan Lippy Celeste Twamley Jodi K. Muckelbauer Chiehying Chang Yongmi An Vinayak Hosagrahara Lisa Zhang Joseph A. Tino 《Bioorganic & medicinal chemistry letters》2010,20(9):2933-2937
The synthesis and follow-up SAR studies of our development candidate 1 by incorporating 2-aryl-4-oxazolylmethoxy and 2-aryl-4-thiazolylmethoxy moieties into the oxybenzylglycine framework of the PPARα/γ dual agonist muraglitazar is described. SAR studies indicate that different substituents on the aryloxazole/thiazole moieties as well as the choice of carbamate substituent on the glycine moiety can significantly modulate the selectivity of PPARα versus PPARγ. Potent, highly selective PPARα activators 2a and 2l, as well as PPARα activators with significant PPARγ activity, such as 2s, were identified. The in vivo pharmacology of these compounds in preclinical animal models as well as their ADME profiles are discussed. 相似文献
75.
Seon-Yeong Kwak Briony E. Forbes Yoon-Sik Lee Alessia Belgi John D. Wade Mohammed Akhter Hossain 《International journal of peptide research and therapeutics》2010,16(3):153-158
Numerous analogues of insulin have been prepared over the past three decades for use in diabetic therapy. However, only two long-acting insulins have been approved for clinical use. One is Levemir (Novo Nordisk) and the other is Lantus (Sanofi-Aventis). Glargine (commercial name: Lantus) is characterized by a substitution of Gly in place of Asn at the C terminus of the A-chain and addition of two Arg residues to the C terminus of the B-chain. Despite the clinical advantages of glargine, it is not without concern that its increased affinity for the IGF-1 receptor may correlate with increased mitogenic activity. Recently, a systematic study of modified analogues of glargine showed that placement of an extra Arg residue at the N terminus of the A-chain conferred improved insulin:IGF-1 receptor selectivity without significant loss of pharmacological profile. However, as it is difficult to prepare such an analogue in high yield by recombinant DNA methods, we undertook its chemical assembly by our refined solid phase synthesis method. We describe herein its chemical preparation and biological activity in both insulin receptor binding assays and DNA synthesis assays. The synthetic analogue, A0:R glargine, showed slightly reduced affinity for IR-B (twofold) compared to native insulin. In stimulating DNA synthesis, A0:R glargine was slightly less potent compared to insulin or glargine. This result ultimately confirms the previous report that A0:R glargine has a lower potency in mitogenic assays compared to glargine. This glargine analogue thus could be a potential lead compound for drug design and development for the treatment of diabetes. 相似文献
76.
77.
78.
Arabidopsis thaliana grown in soil amended with barley grain inocula of Penicillium simplicissimum GP17-2 or receiving root treatment with its culture filtrate (CF) exhibited clear resistance to Pseudomonas syringae pv. tomato DC3000 (Pst). To assess the contribution of different defense pathways, Arabidopsis genotypes implicated in salicylic acid (SA) signaling expressing the NahG transgene or carrying disruption in NPR1 (npr1), jasmonic acid (JA) signaling (jar1) and ethylene (ET) signaling (ein2) were tested. All genotypes screened were protected by GP17-2 or its CF. However, the level of protection was significantly lower in NahG and npr1 plants than it was in similarly treated wild-type plants, indicating that the SA signaling pathway makes a minor contribution to the GP17-2-mediated resistance and is insufficient for a full response. Examination of local and systemic gene expression revealed that GP17-2 and its CF modulate the expression of genes involved in both the SA and JA/ET signaling pathways. Subsequent challenge of GP17-2-colonized plants with Pst was accompanied by direct activation of SA-inducible PR-2 and PR-5 genes as well as potentiated expression of the JA-inducible Vsp gene. In contrast, CF-treated plants infected with Pst exhibited elevated expression of most defense-related genes (PR-1, PR-2, PR-5, PDF1.2 and Hel) studied. Moreover, an initial elevation of SA responses was followed by late induction of JA responses during Pst infection of induced systemic resistance (ISR)-expressing plants. In conclusion, we hypothesize the involvement of multiple defense mechanisms leading to an ISR of Arabidopsis by GP17-2. 相似文献
79.
Hossain MT Soga K Wakabayashi K Kamisaka S Fujii S Yamamoto R Hoson T 《Journal of plant physiology》2007,164(4):385-393
Effects of silicon on the mechanical and chemical properties of cell walls in the second leaf of oat (Avena sativa L.) seedlings were investigated. The cell wall extensibility in the basal region of the second leaf was considerably higher than that in the middle and subapical regions. Externally applied silicon increased the cell wall extensibility in the basal region, but it did not affect the extensibility in the middle and subapical regions. The amounts of cell wall polysaccharides and phenolic compounds, such as diferulic acid (DFA) and ferulic acid (FA), per unit length were lower in the basal region than in the middle and subapical regions of the leaf, and silicon altered these amounts in the basal region. In this region, silicon decreased the amounts of matrix polymers and cellulose per unit length and of DFA and FA, both per unit length and unit matrix polymer content. Silicon treatment also lowered the activity of phenylalanine ammonia-lyase (PAL, EC 4.3.1.5) in the basal region. In contrast, the amount of silicon in cell walls increased in response to silicon treatment in three regions. These results suggest that in the basal region, silicon reduces the net wall mass and the formation of phenolic acid-mediated cross-linkages between wall polysaccharides. Such modifications of wall architecture may be responsible for the silicon-induced increase in the cell wall extensibility in oat leaves. 相似文献
80.
Zawacka-Pankau J Issaeva N Hossain S Pramanik A Selivanova G Podhajska AJ 《The Journal of biological chemistry》2007,282(4):2466-2472
Photodynamic therapy (PDT) of cancer is an alternative treatment for tumors resistant to chemo- and radiotherapy. It induces cancer cell death mainly through generation of reactive oxygen species by a laser light-activated photosensitizer. It has been suggested that the p53 tumor suppressor protein sensitizes some human cancer cells to PDT. However, there is still no direct evidence for this. We have demonstrated here for the first time that the photosensitizer protoporphyrin IX (PpIX) binds to p53 and disrupts the interaction between p53 tumor suppressor protein and its negative regulator HDM2 in vitro and in cells. Moreover, HCT116 colon cancer cells exhibited a p53-dependent sensitivity to PpIX in a dose-dependent manner, as was demonstrated using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and fluorescence-activated cell sorter (FACS) analysis of cell cycle profiles. We have also observed induction of p53 target pro-apoptotic genes, e.g. puma (p53-up-regulated modulator of apoptosis), and bak in PpIX-treated cells. In addition, p53-independent growth suppression by PpIX was detected in p53-negative cells. PDT treatment (2 J/cm2) of HCT116 cells induced p53-dependent activation of pro-apoptotic gene expression followed by growth suppression and induction of apoptosis. 相似文献