全文获取类型
收费全文 | 3085篇 |
免费 | 158篇 |
国内免费 | 3篇 |
专业分类
3246篇 |
出版年
2022年 | 12篇 |
2021年 | 20篇 |
2020年 | 14篇 |
2019年 | 18篇 |
2018年 | 36篇 |
2017年 | 28篇 |
2016年 | 45篇 |
2015年 | 66篇 |
2014年 | 87篇 |
2013年 | 240篇 |
2012年 | 143篇 |
2011年 | 174篇 |
2010年 | 100篇 |
2009年 | 109篇 |
2008年 | 176篇 |
2007年 | 190篇 |
2006年 | 214篇 |
2005年 | 205篇 |
2004年 | 198篇 |
2003年 | 195篇 |
2002年 | 192篇 |
2001年 | 29篇 |
2000年 | 28篇 |
1999年 | 32篇 |
1998年 | 33篇 |
1997年 | 44篇 |
1996年 | 39篇 |
1995年 | 50篇 |
1994年 | 33篇 |
1993年 | 44篇 |
1992年 | 40篇 |
1991年 | 23篇 |
1990年 | 24篇 |
1989年 | 19篇 |
1988年 | 25篇 |
1987年 | 19篇 |
1986年 | 12篇 |
1985年 | 28篇 |
1984年 | 22篇 |
1983年 | 29篇 |
1982年 | 32篇 |
1981年 | 29篇 |
1980年 | 26篇 |
1979年 | 10篇 |
1978年 | 20篇 |
1977年 | 15篇 |
1976年 | 12篇 |
1975年 | 9篇 |
1974年 | 11篇 |
1973年 | 13篇 |
排序方式: 共有3246条查询结果,搜索用时 0 毫秒
81.
Hiroshi Sagami Kyozo Ogura Shuichi Seto Tadashi Kurokawa 《Biochemical and biophysical research communications》1978,85(2):572-578
A new prenyltransferase which catalyzes the synthesis of geranyl pyrophosphate as the only product from dimethylallyl pyrophosphate and isopentenyl pyrophosphate has been separated from other known prenyltransferases from . This enzyme fraction is also capable of synthesizing all- geranylgeranyl pyrophosphate from farnesyl pyrophosphate and isopentenyl pyrophosphate though it lacks ability to synthesize farnesyl pyrophosphate. 相似文献
82.
Five triterpenoid saponins isolated from the flowers, the mature fruits and the leaves of Fatsia japonica were identified as 3-O-[β-d-glucopyranosyl(1→4)-β-d-glucopyranosyl]-hederagenin (1), 3-O-[β-d-glucopyranosyl-(1→4)-α-l-arabinopyranosyl]-oleanolic acid (2), 3-O-[α-l-arabinopyranosyl]-hederagenin (3), 3-O-[β-d-glucopyranosyl]-hederagenin (4) and 3-O-[β-d-glucopyranosyl(1→4)-α-l-arabinopyranosyl]-hederagenin (5). The saponins 1 and 2 are new, naturally occurring, triterpenoid saponins. The distribution of the five saponins in three parts of the plant was investigated. Saponins 2, 3 and 5 were present in the flowers, saponins 1, 3, 4 and 5 were in the mature fruits and saponins 2, 3, 4 and 5 were in the leaves. 相似文献
83.
Exposure of Avena coleoptile sections to 8% O2 brought aboutrespiration decrease, resulting in a decrease of ATP production.The pH at the cell wall surface slightly rose in sections exposedto 8% O2, while their growth was greatly accelerated. Moreover,this growth acceleration was observed even in sections treatedwith CCCP known to make membranes permeable for protons. Weconcluded that the growth acceleration with reduction of O2concentration is probably not the result of secretion of H+ions into cell wall compartments. Results of this study provided evidence to support the hypothesisthat there is an inverse relationship between hydroxyproline-proteinlevel and the ability of a cell to undergo rapid cell elongation.Total labeling of the cell wall fraction with 14C-proline wasunaffected by 8% O2 treatment, although the radioactivitiesof hydroxyproline incorporated into this fraction during thetreatments fell to about 45% of the control. Moreover, the radioactivitiesof hydroxyproline incorporated into the SLS-insoluble cell wallfraction of sections exposed to 8% O2 decreased to about 30%of the control. This decrease of hydroxyproline was also observedin sections treated with cycloheximide, which inhibits the secretionof H+ ions into the cell wall compartment. Reduction of O2 concentrationin the surrounding atmosphere affects not only the hydroxylationof peptidyl proline, but also the binding of hydroxyproline-protein(s)to cell wall polysaccharides, and the resulting decrease ofthe protein rigidly bound to them may induce cell elongation. (Received December 5, 1975; ) 相似文献
84.
目的旨在探讨脑干听觉传入通路中GABA能神经递质及GABAA受体对电刺激位听神经传入冲动的影响.方法使用出生后0~5 d的ddy/ddy小鼠制备脑干切片.脑片经电压敏感染料NK3041染色,电刺激与脑片相连的位听神经残端.使用16×16像素的硅光电二极管阵列测量光学信号.所采集的数据使用ARGUS50/PDA软件分析.结果多部位的光学记录方法显示了从位听神经到耳蜗核和前庭核的兴奋性传导的时间-空间分布.其中每一个光学成分由快峰电位样反应和慢反应组成.抑制性神经递质GABA可降低诱发的光学信号的快反应和慢反应,GABAA受体拮抗剂荷包牡丹碱可增强这些反应.结论16×16像素的硅光电二极管阵列可记录位听神经刺激诱发的多部位光学信号,每一个光学信号含有突触前及突触后电位成分.抑制性神经递质GABA和GJBAA受体拮抗剂可调节光学信号的兴奋性传导. 相似文献
85.
86.
Yoneda T Kumagai T Nagatomo I Furukawa M Yamane H Hoshino S Mori M Takeda Y Horai T Nishida S Watanabe D Kijima T Yoshida M Osaki T Tachibana I Greene MI Kawase I 《DNA and cell biology》2006,25(9):530-540
EGFR is involved in the density-dependent inhibition of cell growth, while coexpression of EGFR with erbB2 can render normal cells transformed. In this study, we have examined the effect of a species of p185 that contains the transmembrane domain and the extracellular domain of p185(c-neu), on growth properties of a human malignant mesothelioma cell line that coexpresses EGFR and erbB2. The ectodomain form of p185(c-neu) enhanced density-dependent inhibition of cell growth and we found that p21 induction appeared to be responsible for this inhibitory effect. Previously, the extracellular domain species was shown to suppress the transforming abilities of EGFR and p185(c-neu/erbB2) in a dominant-negative manner. The ability of this subdomain to affect tumor growth is significant, as it reduced in vivo tumor growth. Unexpectedly, we found that the domain did not abrogate all of EGFR functions. We noted that EGFR-induced density-dependent inhibition of cell growth was retained. Tyrosine kinase inhibitors of EGFR did not cause density-dependent inhibition of cell growth of malignant mesothelioma cells. Therefore, simultaneously inhibiting the malignant phenotype and inducing density-dependent inhibition of cell growth in malignant mesothelioma cells by the extracellular domain of p185(c-neu) may represent an important therapeutic advance. 相似文献
87.
Togi S Ikeda O Kamitani S Nakasuji M Sekine Y Muromoto R Nanbo A Oritani K Kawai T Akira S Matsuda T 《The Journal of biological chemistry》2011,286(21):19170-19177
88.
Suzuki T Hara I Nakano M Zhao G Lennarz WJ Schindelin H Taniguchi N Totani K Matsuo I Ito Y 《The Journal of biological chemistry》2006,281(31):22152-22160
Peptide:N-glycanase (PNGase) is the deglycosylating enzyme, which releases N-linked glycan chains from N-linked glycopeptides and glycoproteins. Recent studies have revealed that the cytoplasmic PNGase is involved in the degradation of misfolded/unassembled glycoproteins. This enzyme has a Cys, His, and Asp catalytic triad, which is required for its enzymatic activity and can be inhibited by "free" N-linked glycans. These observations prompted us to investigate the possible use of haloacetamidyl derivatives of N-glycans as potent inhibitors and labeling reagents of this enzyme. Using a cytoplasmic PNGase from budding yeast (Png1), Man9GlcNAc2-iodoacetoamide was shown to be a strong inhibitor of this enzyme. The inhibition was found to be through covalent binding of the carbohydrate to a single Cys residue on Png1, and the binding was highly selective. The mutant enzyme in which Cys191 of the catalytic triad was changed to Ala did not bind to the carbohydrate probe, suggesting that the catalytic Cys is the binding site for this compound. Precise determination of the carbohydrate attachment site by mass spectrometry clearly identified Cys191 as the site of covalent attachment. Molecular modeling of N,N'-diacetylchitobiose (chitobiose) binding to the protein suggests that the carbohydrate binding site is distinct from but adjacent to that of Z-VAD-fmk, a peptide-based inhibitor of this enzyme. These results suggest that cytoplasmic PNGase has a separate binding site for chitobiose and other carbohydrates, and haloacetamide derivatives can irreversibly inhibit that catalytic Cys in a highly specific manner. 相似文献
89.
Molecular Characterization and Heterologous Expression of the Gene Encoding a Low-Molecular-Mass Endoglucanase from Trichoderma reesei QM9414 总被引:3,自引:0,他引:3 下载免费PDF全文
90.
Abnormal spermatogenesis and male infertility in testicular zinc finger protein Zfp318‐knockout mice 下载免费PDF全文