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排序方式: 共有128条查询结果,搜索用时 15 毫秒
91.
Andrew J Pask Anthony T Papenfuss Eleanor I Ager Kaighin A McColl Terence P Speed Marilyn B Renfree 《Genome biology》2009,10(1):R1-8
Background
Genomic imprinting is an epigenetic phenomenon that results in monoallelic gene expression. Many hypotheses have been advanced to explain why genomic imprinting evolved in mammals, but few have examined how it arose. The host defence hypothesis suggests that imprinting evolved from existing mechanisms within the cell that act to silence foreign DNA elements that insert into the genome. However, the changes to the mammalian genome that accompanied the evolution of imprinting have been hard to define due to the absence of large scale genomic resources between all extant classes. The recent release of the platypus genome has provided the first opportunity to perform comparisons between prototherian (monotreme; which appear to lack imprinting) and therian (marsupial and eutherian; which have imprinting) mammals. 相似文献92.
93.
A two-step purification scheme based on affinity chromatography has been developed for bovine and porcine carboxypeptidases A and B. Enzyme preparations of high purity are achieved from extracts of pancreatic acetone powder in less than 1 day by this procedure. The application of trypsin-treated extracts of pancreatic acetone powder to immobilized carboxypeptidase inhibitor from potatoes results in the specific retention of the target exopeptidases. After clution of the bound carboxypeptidases A and B at high pH, the resultant mixture of the two enzymes is resolved by chromatography on a column of ?-amino-n-caproyl-d-arginine-Sepharose 4B. Overall yields of 70–80% of the purified enzymes have been obtained with no cross-contamination of detectable tryptic or chymotryptic activities of the preparations. 相似文献
94.
Chordia Mudit Nordelöf Anders Ellingsen Linda Ager‐Wick 《The International Journal of Life Cycle Assessment》2022,27(8):1123-1125
The International Journal of Life Cycle Assessment - 相似文献
95.
96.
Jimenez JM Davis C Boyall D Fraysse D Knegtel R Settimo L Young S Bolton C Chiu P Curnock A Rasmussen R Tanner A Ager I 《Bioorganic & medicinal chemistry letters》2012,22(14):4645-4649
The identification of a novel series of PKCθ inhibitors and subsequent optimization using docking based on a crystal structure of PKCθ is described. SAR was rapidly generated around an amino pyridine-ketone hit; (6-aminopyridin-2-yl)(2-aminopyridin-3-yl)methanone 2 leading to compound 21 which significantly inhibits production of IL-2 in a mouse SEB-IL2 model. 相似文献
97.
Marcel GA van der Heijden Susanne de Bruin Ludo Luckerhoff Richard SP van Logtestijn Klaus Schlaeppi 《The ISME journal》2016,10(2):389-399
Highly diverse microbial assemblages colonize plant roots. It is still poorly understood whether different members of this root microbiome act synergistically by supplying different services (for example, different limiting nutrients) to plants and plant communities. In order to test this, we manipulated the presence of two widespread plant root symbionts, arbuscular mycorrhizal fungi and nitrogen-fixing rhizobia bacteria in model grassland communities established in axenic microcosms. Here, we demonstrate that both symbionts complement each other resulting in increased plant diversity, enhanced seedling recruitment and improved nutrient acquisition compared with a single symbiont situation. Legume seedlings obtained up to 15-fold higher productivity if they formed an association with both symbionts, opposed to productivity they reached with only one symbiont. Our results reveal the importance of functional diversity of symbionts and demonstrate that different members of the root microbiome can complement each other in acquiring different limiting nutrients and in driving important ecosystem functions. 相似文献
98.
99.
DOMINIK LERMEN BRUNHILDE BLÖMEKE ROBERT BROWNE ANN CLARKE PAUL W. DYCE THOMAS FIXEMER GÜNTER R. FUHR WILLIAM V. HOLT KATARINA JEWGENOW RHIANNON E. LLOYD STEFAN LÖTTERS MARTIN PAULUS GORDON MCGREGOR REID DANIEL H. RAPOPORT DAVID RAWSON JENNIFER RINGLEB OLIVER A. RYDER GABRIELE SPÖRL THOMAS SCHMITT MICHAEL VEITH PAUL MÜLLER 《Molecular ecology》2009,18(6):1030-1033
Cryobanking, the freezing of biological specimens to maintain their integrity for a variety of anticipated and unanticipated uses, offers unique opportunities to advance the basic knowledge of biological systems and their evolution. Notably, cryobanking provides a crucial opportunity to support conservation efforts for endangered species. Historically, cryobanking has been developed mostly in response to human economic and medical needs — these needs must now be extended to biodiversity conservation. Reproduction technologies utilizing cryobanked gametes, embryos and somatic cells are already vital components of endangered species recovery efforts. Advances in modern biological research (e.g. stem cell research, genomics and proteomics) are already drawing heavily on cryobanked specimens, and future needs are anticipated to be immense. The challenges of developing and applying cryobanking for a broader diversity of species were addressed at an international conference held at Trier University (Germany) in June 2008. However, the magnitude of the potential benefits of cryobanking stood in stark contrast to the lack of substantial resources available for this area of strategic interest for biological science — and society at large. The meeting at Trier established a foundation for a strong global incentive to cryobank threatened species. The establishment of an Amphibian Ark cryobanking programme offers the first opportunity for global cooperation to achieve the cryobanking of the threatened species from an entire vertebrate class. 相似文献
100.
Sodium balance determines the extracellular fluid volume and sets arterial blood pressure (BP). Chronically raised BP (hypertension)
represents a major health risk in Western societies. The relationship between BP and renal sodium excretion (the pressure/natriuresis
relationship) represents the key element in defining the BP homeostatic set point. The renin–angiotensin–aldosterone system
(RAAS) makes major adjustments to the rates of renal sodium secretion, but this system works slowly over a period of hours
to days. More rapid adjustments can be made by the sympathetic nervous system, although the kidney can function well without
sympathetic nerves. Attention has now focussed on regulatory mechanisms within the kidney, including extracellular nucleotides
and the P2 receptor system. Here, we discuss how extracellular ATP can control renal sodium excretion by altering the activity
of epithelial sodium channels (ENaC) present in the apical membrane of principal cells. There remains considerable controversy
over the molecular targets for released ATP, although the P2Y2 receptor has received much attention. We review the available data and reflect on our own findings in which ATP-activated
P2Y and P2X receptors make adjustments to ENaC activity and therefore sodium excretion. 相似文献