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      • KCI등재

        The expression of plasmid mediated afimbrial adhesin genes in an avian septicemic Escherichia coli strain

        Eliana Guedes Stehling,Tatiana Amabile Campos,Marcelo Brocchi,Vasco Ariston de Carvalho Azevedo,Wanderley Dias da Silveira 대한수의학회 2008 Journal of Veterinary Science Vol.9 No.1

        An Escherichia coli strain (SEPT13) isolated from the liver of a hen presenting clinical signs of septicaemia had a LD50 of 4.0 × 105 CFU/ml in one-day-old chickens, expressed Ia, Ib, E1, E3, K and B colicins and aerobactin. The strain was ampicillin and streptomycin resistant, and found to have fimA, csgA and tsh DNA related sequences; it could adhere to and invade HEp-2 and tracheal epithelial cells, expressed fimbriae (observed by electron microscopy), and had five plasmids of 2.7, 4.7, 43, 56, and 88 MDa. Transposon mutagenesis of strain SEPT13, with transposon TnphoA, resulted in a mutant strain named ST16 that had a LD50 of 1.2 × 1012 CFU/ml. All other biological characteristics of strain ST16 were the same as those detected for strain SEPT13 except for the migration of an 88 MDa plasmid to the 93 MDa position indicating the insertion of the transposon into the 88 MDa plasmid. The 93 MDa plasmid of strain ST16 was transferred, by electroporation assay, to non-pathogenic receptor strains (E. coli strains K12 MS101 and HB101), resulting in transformant strains A and B, respectively. These strains exhibited adhesion properties to in vitro cultivated HEp-2 cells but did not have the capacity for invasion. The adherence occurred despite the absence of fimbriae; this finding suggests that the 88 MDa plasmid has afimbrial adhesin genes. An Escherichia coli strain (SEPT13) isolated from the liver of a hen presenting clinical signs of septicaemia had a LD50 of 4.0 × 105 CFU/ml in one-day-old chickens, expressed Ia, Ib, E1, E3, K and B colicins and aerobactin. The strain was ampicillin and streptomycin resistant, and found to have fimA, csgA and tsh DNA related sequences; it could adhere to and invade HEp-2 and tracheal epithelial cells, expressed fimbriae (observed by electron microscopy), and had five plasmids of 2.7, 4.7, 43, 56, and 88 MDa. Transposon mutagenesis of strain SEPT13, with transposon TnphoA, resulted in a mutant strain named ST16 that had a LD50 of 1.2 × 1012 CFU/ml. All other biological characteristics of strain ST16 were the same as those detected for strain SEPT13 except for the migration of an 88 MDa plasmid to the 93 MDa position indicating the insertion of the transposon into the 88 MDa plasmid. The 93 MDa plasmid of strain ST16 was transferred, by electroporation assay, to non-pathogenic receptor strains (E. coli strains K12 MS101 and HB101), resulting in transformant strains A and B, respectively. These strains exhibited adhesion properties to in vitro cultivated HEp-2 cells but did not have the capacity for invasion. The adherence occurred despite the absence of fimbriae; this finding suggests that the 88 MDa plasmid has afimbrial adhesin genes.

      • SCISCIESCOPUS

        Human primordial germ cell commitment <i>in vitro</i> associates with a unique PRDM14 expression profile

        Sugawa, Fumihiro,Araú,zo-Bravo, Marcos J,Yoon, Juyong,Kim, Kee-Pyo,Aramaki, Shinya,Wu, Guangming,Stehling, Martin,Psathaki, Olympia E,,bner, Karin,Schö,ler, Hans R BlackWell Publishing Ltd 2015 The EMBO journal Vol.34 No.8

        <P>Primordial germ cells (PGCs) develop only into sperm and oocytes <I>in vivo</I>. The molecular mechanisms underlying human PGC specification are poorly understood due to inaccessibility of cell materials and lack of <I>in vitro</I> models for tracking the earliest stages of germ cell development. Here, we describe a defined and stepwise differentiation system for inducing pre-migratory PGC-like cells (PGCLCs) from human pluripotent stem cells (PSCs). In response to cytokines, PSCs differentiate first into a heterogeneous mesoderm-like cell population and then into PGCLCs, which exhibit minimal PRDM14 expression. PGC specification in humans is similar to the murine process, with the sequential activation of mesodermal and PGC genes, and the suppression of neural induction and of <I>de novo</I> DNA methylation, suggesting that human PGC formation is induced via epigenesis, the process of germ cell specification via inductive signals from surrounding somatic cells. This study demonstrates that PGC commitment in humans shares key features with that of the mouse, but also highlights key differences, including transcriptional regulation during the early stage of human PGC development (3–6 weeks). A more comprehensive understanding of human germ cell development may lead to methodology for successfully generating PSC-derived gametes for reproductive medicine.</P>

      • KCI등재

        Developing Smart Grids Based on GPRS and ZigBee Technologies Using Queueing Modeling–Based Optimization Algorithm

        Gustavo Batista de Castro Souza,Flávio Henrique Teles Vieira,Cláudio Ribeiro Lima,Getúlio Antero de Deus Júnior,Marcelo Stehling de Castro,Sérgio Granato de Araujo,Thiago Lara Vasques 한국전자통신연구원 2016 ETRI Journal Vol.38 No.1

        Smart metering systems have become widespread around the world. RF mesh communication systems have contributed to the creation of smarter and more reliable power systems. This paper presents an algorithm for positioning GPRS concentrators to attain delay constraints for a ZigBee-based mesh network. The proposed algorithm determines the number and placement of concentrators using integer linear programming and a queueing model for the given mesh network. The solutions given by the proposed algorithm are validated by verifying the communication network performance through simulations.

      • KCI등재

        Refinement of temperature determination in cutting zones

        Michael Storchak,Valerii Kushner,Hans-Christian Möhring,Thomas Stehle 대한기계학회 2021 JOURNAL OF MECHANICAL SCIENCE AND TECHNOLOGY Vol.35 No.8

        A methodology for temperatures calculating in different cutting zones is proposed, taking the peculiarities of heat distribution for moving sources into account. For this, the correlation was established between the heat flow densities and temperatures in the chip forming area, in the stagnation zone as well as in the zone of plastic contact between the chip and the tool. The method for temperature calculation was based on the joint solution of the heat conduction equation and the constitutive equation of the machined material. A significant simplification of the temperature calculation was achieved without sacrificing accuracy by considering the features of the heat propagation from fast-moving sources. Taking into account material softening, the temperature and heat flow density distributions along the tool rake and clearance faces and in the stagnation zone were numerically calculated. The developed models were confirmed by experiment. The comparison showed good agreement between theoretical and experimental results.

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