全文获取类型
收费全文 | 3052篇 |
免费 | 214篇 |
专业分类
3266篇 |
出版年
2022年 | 18篇 |
2021年 | 21篇 |
2020年 | 14篇 |
2019年 | 25篇 |
2018年 | 28篇 |
2017年 | 29篇 |
2016年 | 40篇 |
2015年 | 66篇 |
2014年 | 91篇 |
2013年 | 153篇 |
2012年 | 136篇 |
2011年 | 136篇 |
2010年 | 72篇 |
2009年 | 92篇 |
2008年 | 155篇 |
2007年 | 130篇 |
2006年 | 157篇 |
2005年 | 154篇 |
2004年 | 160篇 |
2003年 | 144篇 |
2002年 | 113篇 |
2001年 | 114篇 |
2000年 | 126篇 |
1999年 | 111篇 |
1998年 | 38篇 |
1997年 | 41篇 |
1996年 | 46篇 |
1995年 | 34篇 |
1994年 | 37篇 |
1993年 | 34篇 |
1992年 | 72篇 |
1991年 | 53篇 |
1990年 | 51篇 |
1989年 | 42篇 |
1988年 | 62篇 |
1987年 | 54篇 |
1986年 | 36篇 |
1985年 | 37篇 |
1984年 | 43篇 |
1983年 | 41篇 |
1982年 | 21篇 |
1981年 | 19篇 |
1980年 | 20篇 |
1979年 | 25篇 |
1978年 | 19篇 |
1977年 | 16篇 |
1975年 | 18篇 |
1974年 | 15篇 |
1969年 | 15篇 |
1968年 | 18篇 |
排序方式: 共有3266条查询结果,搜索用时 15 毫秒
61.
In plant cells, the pyruvate dehydrogenase (PDH) complex that requires lipoic acid as an essential coenzyme is located in plastids and mitochondria. The enzyme complex has to be lipoylated in both organelles. However, the lipoyltransferase located in plastids has not been reported. In this study, an Arabidopsis thaliana LIP2p cDNA for a lipoyltransferase located in plastids has been identified. We have shown that this cDNA encodes a lipoyltransferase by demonstrating its ability to complement an Escherichia coli mutant lacking lipoyltransferase activity, and that LIP2p is targeted into chloroplasts. These findings suggest that LIP2p is located in plastids and responsible for lipoylation of the plastidial PDH complex. 相似文献
62.
63.
Hiroshi Tamura Noriko Wada Hong Zhang Hironari Unrin Takafumi Watanabe Tetsuya Suga 《Cell biochemistry and biophysics》2000,32(1-3):325-327
Peroxisome proliferators (PPs) are nongenotoxic compounds causing the emergence of hepatocellular carcinoma in rodents, but
the mechanisms of the hepatocarcinogenesis have been unclear. The authors examined the changes in phosphorylation of nuclear
proteins after treatment with (4-chloro-6-[2,3-xylidino]-2-pyrimidinylthio) acetic acid (Wy-14,643). Wy-14,643 (0.1% w/w in
diet) was given orally to male F-344 rats for up to 80 wk. In the hepatocarcinomas induced by Wy-14,643, phosphorylation of
13 kDa nuclear protein (NP 13), which was resistant to alkaline treatment, was significantly increased. NP 13 phosphorylation
gradually increased, dependent on treatment period. Furthermore, in the hepatocarcinomas induced by other PP, di(2-ethylhexyl)phthalate,
increase in NP13-phospholyration was also observed. Therefore, NP 13-phospholyration may relate to development of preneoplastic
or neoplastic lesions induced by PPs. 相似文献
64.
Cloning of a rat glia maturation factor-gamma (rGMFG) cDNA and expression of its mRNA and protein in rat organs 总被引:4,自引:0,他引:4
Tsuiki H Asai K Yamamoto M Fujita K Inoue Y Kawai Y Tada T Moriyama A Wada Y Kato T 《Journal of biochemistry》2000,127(3):517-523
We isolated a rat glia maturation factor-gamma(rGMFG) cDNA and examined the tissue distribution of GMFG in rat by Northern and Western blot analyses. Sequence analysis of the entire cDNA revealed an open reading frame of 426 nucleotides with a deduced protein of 142 amino acid residues. The deduced amino acid sequence of the putative product is highly homologous (78.9%) to rat glia maturation factor-beta (rGMFB). Northern blot analysis indicated that a 0.9-kb mRNA is predominantly expressed in rat thymus, testis, and spleen. GMFG showed a different tissue distribution from GMFB, being present predominantly in proliferative and differentiative organs. 相似文献
65.
66.
Masakazu Atobe Natsumi Yamakawa Yasuhiro Wada Tokuhito Goto Masashi Kawanishi Takeshi Ito Makoto Saito Masahiro Takeda Takanori Tabata Hirokazu Arai 《Bioorganic & medicinal chemistry letters》2017,27(21):4828-4831
A series of indazole derivatives were identified as Sirt 1 activators though high-throughput screening. Optimization of each substituent on the indazole ring led to the identification of compound 13. Compound 13 appeared to give the best Sirt 1 activity of the compounds tested and also showed osteogenesis activity in a cell assay. Sirt 1 activators are therefore potential candidates for the treatment of osteoporosis. 相似文献
67.
Enzymatic activities of uridine and thymidine phosphorylase in normal and cancerous uterine cervical tissues 总被引:1,自引:0,他引:1
Kobayashi Y Wada Y Ohara T Okuda Y Suzuki N Hasegawa K Kiguchi K Ishizuka B 《Human cell》2007,20(4):107-110
In this study, the preliminary analyses were conducted of enzymatic activities of uridine phosphorylase (UP) and thymidine phosphorylase (TP) in normal tissues and cancer tissues of the uterine cervix. The study was performed on 27 patients of cervical cancer, treated first in our hospital. Normal cervical tissues obtained from 15 patients undergoing hysterectomy for benign diseases were used as controls. The supernatant of the homogenated cervical tissues and the stroma (5-FU and ribose-1-P or deoxyribose-1-P) were analyzed by high performance liquid chromatography, and then the UP and TP activities calculated. TP activity was significantly greater than UP activity (P < 0.0001). Both UP and TP showed significantly greater activity in cancer tissues than in normal tissues (P < 0.0001). In the TP activity of the cancer tissues, there was no significant difference among the histological types, while the TP activity tended to be significantly higher in the cases with lymph node metastasis. These results showed that the TP-mediated route seemed important as the 5FU metabolic pathway in the uterine cervical tissues, and TP enzymatic activity might be associated with lymph node metastasis. 相似文献
68.
69.
70.
Mizohata E Sakai H Fusatomi E Terada T Murayama K Shirouzu M Yokoyama S 《Journal of molecular biology》2005,354(2):317-329
Peroxiredoxins (Prxs) are thiol-dependent peroxidases that catalyze the detoxification of various peroxide substrates such as H2O2, peroxinitrite, and hydroperoxides, and control some signal transduction in eukaryotic cells. Prxs are found in all cellular organisms and represent an enormous superfamily. Recent genome sequencing projects and biochemical studies have identified a novel subfamily, the archaeal Prxs. Their primary sequences are similar to those of the 1-Cys Prxs, which use only one cysteine residue in catalysis, while their catalytic properties resemble those of the typical 2-Cys Prxs, which utilize two cysteine residues from adjacent monomers within a dimer in catalysis. We present here the X-ray crystal structure of an archaeal Prx from the aerobic hyperthermophilic crenarchaeon, Aeropyrum pernix K1, determined at 2.3 A resolution (Rwork of 17.8% and Rfree of 23.0%). The overall subunit arrangement of the A.pernix archaeal Prx is a toroid-shaped pentamer of homodimers, or an (alpha2)5 decamer, as observed in the previously reported crystal structures of decameric Prxs. The basic folding topology and the peroxidatic active site structure are essentially the same as those of the 1-Cys Prx, hORF6, except that the C-terminal extension of the A.pernix archaeal Prx forms a unique helix with its flanking loops. The thiol group of the peroxidatic cysteine C50 is overoxidized to sulfonic acid. Notably, the resolving cysteine C213 forms the intra-monomer disulfide bond with the third cysteine, C207, which should be a unique structural characteristic in the many archaeal Prxs that retain two conserved cysteine residues in the C-terminal region. The conformational flexibility near the intra-monomer disulfide linkage might be necessary for the dramatic structural rearrangements that occur in the catalytic cycle. 相似文献