全文获取类型
收费全文 | 50345篇 |
免费 | 17523篇 |
国内免费 | 1534篇 |
出版年
2023年 | 292篇 |
2022年 | 689篇 |
2021年 | 1347篇 |
2020年 | 2771篇 |
2019年 | 4408篇 |
2018年 | 4522篇 |
2017年 | 4575篇 |
2016年 | 4843篇 |
2015年 | 5299篇 |
2014年 | 5076篇 |
2013年 | 5708篇 |
2012年 | 3717篇 |
2011年 | 3346篇 |
2010年 | 4141篇 |
2009年 | 2696篇 |
2008年 | 1962篇 |
2007年 | 1427篇 |
2006年 | 1345篇 |
2005年 | 1262篇 |
2004年 | 1175篇 |
2003年 | 1103篇 |
2002年 | 1013篇 |
2001年 | 889篇 |
2000年 | 744篇 |
1999年 | 660篇 |
1998年 | 267篇 |
1997年 | 246篇 |
1996年 | 217篇 |
1995年 | 193篇 |
1994年 | 177篇 |
1993年 | 145篇 |
1992年 | 276篇 |
1991年 | 266篇 |
1990年 | 213篇 |
1989年 | 233篇 |
1988年 | 201篇 |
1987年 | 162篇 |
1986年 | 154篇 |
1985年 | 173篇 |
1984年 | 127篇 |
1983年 | 105篇 |
1982年 | 92篇 |
1981年 | 99篇 |
1979年 | 112篇 |
1978年 | 93篇 |
1977年 | 72篇 |
1976年 | 70篇 |
1975年 | 89篇 |
1974年 | 91篇 |
1973年 | 84篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
991.
992.
993.
994.
995.
996.
Jisub Hwang Chang-Sook Jeong Chang Woo Lee Seung Chul Shin Han-Woo Kim Sung Gu Lee Ui Joung Youn Chang Sup Lee Tae-Jin Oh Hak Jun Kim Hyun Park Hyun Ho Park Jun Hyuck Lee 《Journal of microbiology (Seoul, Korea)》2020,58(7):606-613
Crystal structures of enoyl-coenzyme A (CoA) isomerase from Bosea sp. PAMC 26642 (BoECI) and enoyl-CoA hydratase from Hymenobacter sp. PAMC 26628 (HyECH) were determined at 2.35 and 2.70 Å resolution, respectively. BoECI and HyECH are members of the crotonase superfamily and are enzymes known to be involved in fatty acid degradation. Structurally, these enzymes are highly similar except for the orientation of their C-terminal helix domain. Analytical ultracentrifugation was performed to determine the oligomerization states of BoECI and HyECH revealing they exist as trimers in solution. However, their putative ligand-binding sites and active site residue compositions are dissimilar. Comparative sequence and structural analysis revealed that the active site of BoECI had one glutamate residue (Glu135), this site is occupied by an aspartate in some ECIs, and the active sites of HyECH had two highly conserved glutamate residues (Glu118 and Glu138). Moreover, HyECH possesses a salt bridge interaction between Glu98 and Arg152 near the active site. This interaction may allow the catalytic Glu118 residue to have a specific conformation for the ECH enzyme reaction. This salt bridge interaction is highly conserved in known bacterial ECH structures and ECI enzymes do not have this type of interaction. Collectively, our comparative sequential and structural studies have provided useful information to distinguish and classify two similar bacterial crotonase superfamily enzymes. 相似文献
997.
I. Lamas‐Toranzo A. Martínez‐Moro E. OCallaghan G. Milln‐Blanca J.M. Snchez P. Lonergan P. Bermejo‐lvarez 《Molecular reproduction and development》2020,87(5):542-549
Targeted knock‐in (KI) can be achieved in embryos by clustered regularly interspaced short palindromic repeats (CRISPR)‐assisted homology directed repair (HDR). However, HDR efficiency is constrained by the competition of nonhomologous end joining. The objective of this study was to explore whether CRISPR‐assisted targeted KI rates can be improved in bovine embryos by exposure to the HDR enhancer RS‐1. In vitro produced zygotes were injected with CRISPR components (300 ng/µl Cas9 messenger RNA and 100 ng/µl single guide RNA against a noncoding region) and a single‐stranded DNA (ssDNA) repair template (100 ng/µl). ssDNA template contained a 6 bp XbaI site insert, allowing targeted KI detection by restriction analysis, flanked by 50 bp homology arms. Following microinjection, zygotes were exposed to 0, 3.75, or 7.5 µM RS‐1 for 24 hr. No differences were noted between groups in terms of development or genome edition rates. However, targeted KI rates were doubled in the group exposed to 7.5 µM RS‐1 compared to the others (52.8% vs. 25% and 23.1%, for 7.5, 0, and 3.75 µM, respectively). In conclusion, transient exposure to 7.5 µM RS‐1 enhances targeted KI rates resulting in approximately half of the embryos containing the intended mutation, hence allowing direct KI generation in embryos. 相似文献
998.
An exploration of the role of Sertoli cells on fetal testis development using cell ablation strategy
Yu‐Qian Wang Jin‐Mei Cheng Qing Wen Ji‐Xin Tang Jian Li Su‐Ren Chen Yi‐Xun Liu 《Molecular reproduction and development》2020,87(2):223-230
Sertoli cells (SCs) are presumed to be the center of testis differentiation because they provide both structural support and biological regulation for spermatogenesis. Previous studies suggest that SCs control germ cell (GC) count and Leydig cell (LC) development in mouse testes. However, the regulatory role of SCs on peritubular myoid (PTM) cell fate in fetal testis has not been clearly reported. Here, we employed Amh‐Cre; diphtheria toxin fragment A (DTA) mouse model to selectively ablate SCs from embryonic day (E) 14.5. Results found that SC ablation in the fetal stage caused the disruption of testis cords and the massive loss of GCs. Furthermore, the number of α‐smooth muscle actin‐labeled PTM cells was gradually decreased from E14.5 and almost lost at E18.5 in SC ablation testis. Interestingly, some Ki67 and 3β‐HSD double‐positive fetal LCs could be observed in Amh‐Cre; DTA testes at E16.5 and E18.5. Consistent with this phenomenon, the messenger RNA levels of Hsd3b1, Cyp11a1, Lhr, Star and the protein levels of 3β‐HSD and P450Scc were significantly elevated by SC ablation. SC ablation appears to induce ectopic proliferation of fetal LCs although the total LC number appeared reduced. Together, these findings bring us a better understanding of SCs’ central role in fetal testis development. 相似文献
999.
Plants have evolved a battery of mechanisms that potentially act as polyspermy barriers. Supernumerary sperm fusion to one egg cell has consequently long remained a hypothetical concept. The recent discovery that polyspermy in flowering plants is not lethal but generates viable triploid plants is a game changer affecting the field of developmental biology, evolution, and plant breeding. The establishment of protocols to artificially induce polyspermy together with the development of a high‐throughput assay to identify and trace polyspermic events in planta now provide powerful tools to unravel mechanisms of polyspermy regulation. These achievements are likely to open new avenues for animal polyspermy research as well, where forward genetic approaches are hampered by the fatal outcome of supernumerary sperm fusion. 相似文献
1000.
Xue‐Chen Wu Zhe Han Xin Hao Yi‐Tong Zhao Cheng‐Jie Zhou Xin Wen Cheng‐Guang Liang 《Molecular reproduction and development》2020,87(2):262-273
Phosphodiesterase (PDE)‐mediated reduction of cyclic adenosine monophosphate (cAMP) activity can initiate germinal vesicle (GV) breakdown in mammalian oocytes. It is crucial to maintain oocytes at the GV stage for a long period to analyze meiotic resumption in vitro. Meiotic resumption can be reversibly inhibited in isolated oocytes by cAMP modulator forskolin, cAMP analog dibutyryl cAMP (dbcAMP), or PDE inhibitors, milrinone (Mil), Cilostazol (CLZ), and 3‐isobutyl‐1‐methylxanthine (IBMX). However, these chemicals negatively affect oocyte development and maturation when used independently. Here, we used ICR mice to develop a model that could maintain GV‐stage arrest with minimal toxic effects on subsequent oocyte and embryonic development. We identified optimal concentrations of forskolin, dbcAMP, Mil, CLZ, IBMX, and their combinations for inhibiting oocyte meiotic resumption. Adverse effects were assessed according to subsequent development potential, including meiotic resumption after washout, first polar body extrusion, early apoptosis, double‐strand DNA breaks, mitochondrial distribution, adenosine triphosphate levels, and embryonic development. Incubation with a combination of 50.0 μM dbcAMP and 10.0 μM IBMX efficiently inhibited meiotic resumption in GV‐stage oocytes, with low toxicity on subsequent oocyte maturation and embryonic development. This work proposes a novel method with reduced toxicity to effectively arrest and maintain mouse oocytes at the GV stage. 相似文献