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1.
G Sansone M Cotugno A Biondi 《Bollettino della Società italiana di biologia sperimentale》1983,59(4):509-513
The Authors have investigated the structural property of organic shell matrix from Mytilus galloprovincialis by scanning microscopy. The microscopic investigation shows differences between matrix from nacreous layer or argonite and matrix from outer layer or calcite. The first shows a "cavernous" surface; the other instead shows a "smooth" surface. The Authors conclude that probably these differences may influence the different crystallographic arrangement of biocrystals. 相似文献
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E. B. Sansone A. M. Losikoff W. B. Lebherz III J. A. Poiley 《In vitro cellular & developmental biology. Plant》1981,17(9):811-815
Summary To estimate worker exposures to, and environmental contamination from, test chemicals and organic solvents used in an in vitro
assay to assess the carcinogenic potential of chemicals, sodium fluorescein, a noncarcinogenic fluorescent material, was dissolved
in tissue culture medium used to maintain early passage hamster embryo cells. Personal and environmental samples were taken
over a 14-d period. The assay was performed according to standard procedures in a ventilated glove box or laminar flow safety
cabinet. Considerably more than 99% of the chemical contamination found was recovered from the interiors of the glove box
and hood and from disposable equipment. Contamination outside the containment units (less than 1 μg) resulted from intralaboratory
transport of chemicals, treated cultures, and contaminated equipment. We conclude that the standard operating practices and
procedures provided adequate safeguards for personnel and the environment.
Research sponsored by the National Cancer Institute under Contract N01-CO-75380, with Litton Bionetics, Inc. 相似文献
5.
Aqueous solutions of a number of biological stains were completely decontaminated to the limit of detection using Amberlite resins. Amberlite XAD-16 was the most generally applicable resin but Amberlite XAD-2, Amberlite XAD-4, and Amberlite XAD-7 could be used to decontaminate some solutions. Solutions of acridine orange, alcian blue 8GX, alizarin red S, azure A, azure B, Congo red, cresyl violet acetate, crystal violet, eosin B, erythrosin B, ethidium bromide, Janus green B, methylene blue, neutral red, nigrosin, orcein, propidium iodide, rose Bengal, safranine O, toluidine blue O, and trypan blue could be completely decontaminated to the limit of detection and solutions of eosin Y and Giemsa stain were decontaminated to very low levels (less than 0.02 ppm) using Amberlite XAD-16. Reaction times varied from 10 min to 18 hr. Up to 500 ml of a 100 micrograms/ml solution could be decontaminated per gram of Amberlite XAD-16. Fourteen of the 23 stains tested were found to be mutagenic to Salmonella typhimurium. None of the completely decontaminated solutions were found to be mutagenic. 相似文献
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Susanna-Assunta Sansone Daniel Schober Helen J. Atherton Oliver Fiehn Helen Jenkins Philippe Rocca-Serra Denis V. Rubtsov Irena Spasic Larisa Soldatova Chris Taylor Andy Tseng Mark R. Viant 《Metabolomics : Official journal of the Metabolomic Society》2007,3(3):249-256
In this article we present the activities of the Ontology Working Group (OWG) under the Metabolomics Standards Initiative
(MSI) umbrella. Our endeavour aims to synergise the work of several communities, where independent activities are underway
to develop terminologies and databases for metabolomics investigations. We have joined forces to rise to the challenges associated
with interpreting and integrating experimental process and data across disparate sources (software and databases, private
and public). Our focus is to support the activities of the other MSI working groups by developing a common semantic framework
to enable metabolomics-user communities to consistently annotate the experimental process and to enable meaningful exchange
of datasets. Our work is accessible via a public webpage and a draft ontology has been posted under the Open Biological Ontology
umbrella. At the very outset, we have agreed to minimize duplications across omics domains through extensive liaisons with
other communities under the OBO Foundry. This is work in progress and we welcome new participants willing to volunteer their
time and expertise to this open effort.
See the MSI Ontology Working Group website for a complete list of members and contributors. Web URL: 相似文献
8.
In Eubacteria, de novo translation of some internal cistrons may be inefficient or impossible unless the 5' neighboring cistron is also translated (translational coupling). Translation reinitiation is an extreme case of translational coupling in which translation of a message depends entirely on the presence of a nearby terminating ribosome. In this work, the characteristics of mRNA cis-elements inducing the reinitiation process in Escherichia coli have been investigated using a combinatorial approach. A number of novel translational reinitiation sequences (TRSs) were thus identified, which show a wide range of reinitiation activities fully dependent on a translational coupling event and unrelated to the presence/absence of secondary structure or mRNA stability. Moreover, some of the isolated TRSs are similar to intercistronic sequences present in the E. coli genome. 相似文献
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Lucia Polletta Enza Vernucci Ilaria Carnevale Tania Arcangeli Dante Rotili Silvia Palmerio Clemens Steegborn Theresa Nowak Mike Schutkowski Laura Pellegrini Luigi Sansone Lidia Villanova Alessandra Runci Bruna Pucci Emanuela Morgante Massimo Fini Antonello Mai Matteo A Russo Marco Tafani 《Autophagy》2015,11(2):253-270
In liver the mitochondrial sirtuin, SIRT5, controls ammonia detoxification by regulating CPS1, the first enzyme of the urea cycle. However, while SIRT5 is ubiquitously expressed, urea cycle and CPS1 are only present in the liver and, to a minor extent, in the kidney. To address the possibility that SIRT5 is involved in ammonia production also in nonliver cells, clones of human breast cancer cell lines MDA-MB-231 and mouse myoblast C2C12, overexpressing or silenced for SIRT5 were produced. Our results show that ammonia production increased in SIRT5-silenced and decreased in SIRT5-overexpressing cells. We also obtained the same ammonia increase when using a new specific inhibitor of SIRT5 called MC3482. SIRT5 regulates ammonia production by controlling glutamine metabolism. In fact, in the mitochondria, glutamine is transformed in glutamate by the enzyme glutaminase, a reaction producing ammonia. We found that SIRT5 and glutaminase coimmunoprecipitated and that SIRT5 inhibition resulted in an increased succinylation of glutaminase. We next determined that autophagy and mitophagy were increased by ammonia by measuring autophagic proteolysis of long-lived proteins, increase of autophagy markers MAP1LC3B, GABARAP, and GABARAPL2, mitophagy markers BNIP3 and the PINK1-PARK2 system as well as mitochondrial morphology and dynamics. We observed that autophagy and mitophagy increased in SIRT5-silenced cells and in WT cells treated with MC3482 and decreased in SIRT5-overexpressing cells. Moreover, glutaminase inhibition or glutamine withdrawal completely prevented autophagy. In conclusion we propose that the role of SIRT5 in nonliver cells is to regulate ammonia production and ammonia-induced autophagy by regulating glutamine metabolism. 相似文献
10.
Jan Bartacek Isabella Manconi Gerardo Sansone Roberta Murgia Piet N.L. Lens 《Nitric oxide》2010,22(2):101-105
Hydrogen sulfide (H2S) inhibits the last step of the denitrification process, i.e. the reduction of nitrous oxide (N2O) to dinitrogen gas (N2), both in natural environments (marine sediments) and industrial processes (activated sludge, methanogenic sludge, BioDeNOx process). In a previously published study, we showed that the inhibitory effect of sulfide to N2O reduction in mixed microbial communities is reversible and can be counteracted by dosing trace amounts of copper. It remained, however, unclear if this was due to copper sulfide precipitation or a retrofitting of the copper containing N2O-reductase (N2OR). The present study aimed to elucidate the mechanism of the restoration of sulfide-inhibited N2O reducing activity by metal addition to a pure Pseudomonas aeruginosa culture. This was done by using other metals (zinc, cobalt and iron) in comparison with copper. Zinc and cobalt clearly alleviated the sulfide inhibition of N2OR to the same extent as copper and the activity restoration was extremely fast (within 15 min, Fig. 3) for zinc, cobalt and copper. This suggests that the alleviation of the inhibitory effect of sulfide is due to metal sulfide precipitation and thus not exclusively limited to Cu. This work also underlines the importance of metal speciation: supply of iron did not restore the N2OR activity because it was precipitated by the phosphates present in the medium and thus could not precipitate the sulfide. 相似文献