Literatura científica selecionada sobre o tema "Plasmide eucaryote"
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Artigos de revistas sobre o assunto "Plasmide eucaryote"
Vasudevachari, M. B., V. Natarajan e N. P. Salzman. "Cotransfection with adenovirus DNA enhances transcription from linear DNA containing eucaryotic promoters". Molecular and Cellular Biology 7, n.º 3 (março de 1987): 1063–69. http://dx.doi.org/10.1128/mcb.7.3.1063-1069.1987.
Texto completo da fonteVasudevachari, M. B., V. Natarajan e N. P. Salzman. "Cotransfection with adenovirus DNA enhances transcription from linear DNA containing eucaryotic promoters." Molecular and Cellular Biology 7, n.º 3 (março de 1987): 1063–69. http://dx.doi.org/10.1128/mcb.7.3.1063.
Texto completo da fonteKaufman, R. J., M. V. Davies, V. K. Pathak e J. W. Hershey. "The phosphorylation state of eucaryotic initiation factor 2 alters translational efficiency of specific mRNAs". Molecular and Cellular Biology 9, n.º 3 (março de 1989): 946–58. http://dx.doi.org/10.1128/mcb.9.3.946-958.1989.
Texto completo da fonteKaufman, R. J., M. V. Davies, V. K. Pathak e J. W. Hershey. "The phosphorylation state of eucaryotic initiation factor 2 alters translational efficiency of specific mRNAs." Molecular and Cellular Biology 9, n.º 3 (março de 1989): 946–58. http://dx.doi.org/10.1128/mcb.9.3.946.
Texto completo da fonteAlwine, J. C. "Transient gene expression control: effects of transfected DNA stability and trans-activation by viral early proteins". Molecular and Cellular Biology 5, n.º 5 (maio de 1985): 1034–42. http://dx.doi.org/10.1128/mcb.5.5.1034-1042.1985.
Texto completo da fonteAlwine, J. C. "Transient gene expression control: effects of transfected DNA stability and trans-activation by viral early proteins." Molecular and Cellular Biology 5, n.º 5 (maio de 1985): 1034–42. http://dx.doi.org/10.1128/mcb.5.5.1034.
Texto completo da fonteChen, XM, SH Zhou, J. Fan, MJ Hu, SQ Wang e YS Yu. "Construction and Identification of an Antisense Glucose Transporter-1 Plasmid". Journal of International Medical Research 36, n.º 5 (outubro de 2008): 1001–7. http://dx.doi.org/10.1177/147323000803600517.
Texto completo da fonteLosos, Jan K., David H. Evans e Ann M. Verrinder Gibbins. "Targeted modification of the complete chicken lysozyme gene by poxvirus-mediated recombination". Biochemistry and Cell Biology 83, n.º 2 (1 de abril de 2005): 230–38. http://dx.doi.org/10.1139/o05-025.
Texto completo da fontePrice, Brian M., Adriane L. Liner, Sukjoon Park, Stephen H. Leppla, Alfred Mateczun e Darrell R. Galloway. "Protection against Anthrax Lethal Toxin Challenge by Genetic Immunization with a Plasmid Encoding the Lethal Factor Protein". Infection and Immunity 69, n.º 7 (1 de julho de 2001): 4509–15. http://dx.doi.org/10.1128/iai.69.7.4509-4515.2001.
Texto completo da fonteChakrabarti, S., e M. M. Seidman. "Intramolecular recombination between transfected repeated sequences in mammalian cells is nonconservative". Molecular and Cellular Biology 6, n.º 7 (julho de 1986): 2520–26. http://dx.doi.org/10.1128/mcb.6.7.2520-2526.1986.
Texto completo da fonteTeses / dissertações sobre o assunto "Plasmide eucaryote"
Quintart, Anne. "Mise au point d'un test de réparation des cassures double-brin de l'ADN, application au déficit immunitaire T(-) B(-) caractérisé par un défaut de recombinaison V(D)J avec radiosensibilité accrue". Paris 5, 2001. http://www.theses.fr/2001PA05P019.
Texto completo da fonteGirard, Fabien. "Tethering of molecular parasites on inactive chromatin in eukaryote nucleus". Electronic Thesis or Diss., Sorbonne université, 2023. http://www.theses.fr/2023SORUS661.
Texto completo da fonteNatural plasmids are common in prokaryotes but few have been documented in eukaryotes. The natural 2µ plasmid present in budding yeast Saccharomyces cerevisiae is one of the most well characterized. This highly stable genetic element coexists with its host for millions of years, efficiently segregating at each cell division through a mechanism that remains poorly understood. Using proximity ligation (Hi-C, MicroC) to map the contacts between the 2µ and yeast chromosomes under dozens of different biological conditions, we found that the plasmid tether preferentially on regions with low transcriptional activity, often corresponding to long inactive genes, throughout the cell cycle. Common players in chromosome structure such as members of the structural maintenance of chromosome complexes (SMC) are not involved in these contacts, and depend instead on a nucleosomal signal associated with a depletion of RNA Pol II. These contacts are highly stable, and can be established within minutes. Our data show that the plasmid segregates by binding to transcriptionally silent regions of the host chromosomes. This strategy may concern other types of DNA molecules and species beyond S. cerevisiae, as suggested by the binding pattern of the natural Ddp5 plasmid along Dictyostelium discoideum chromosomes’ silent regions
Gatignol, Anne. "Expression de genes plasmidiques de resistance a la phleomycine chez les eucaryotes". Toulouse 3, 1987. http://www.theses.fr/1987TOU30257.
Texto completo da fonteBaudry, Bernadette. "Séquences plasmidiques responsables de l'entrée de Shigella flexneri dans les cellules eucaryotes". Paris 11, 1988. http://www.theses.fr/1988PA112035.
Texto completo da fonteDebuchy, Robert. "Mise au point d'un systeme de transformation du champignon filamenteux podospora anserina et recherche de sequences susceptibles d'assurer l'autonomie de replication". Paris 6, 1987. http://www.theses.fr/1987PA066103.
Texto completo da fonteDupou, Laurence. "Contribution a l'etude de la dynamique et de la distribution laterale des lipides dans les membranes plasmiques de cellules eucaryotes". Toulouse 3, 1987. http://www.theses.fr/1987TOU30043.
Texto completo da fonteLe, Guyader Laurent. "Utilisation de sondes pyréniques in vivo pour caractériser l'état de phase global de la membrane plasmique de cellules eucaryotes : application à la détection de la liaison d'agonistes au récepteur "delta" opioïde murin". Toulouse 3, 2007. http://thesesups.ups-tlse.fr/53/.
Texto completo da fonteThe development of tools for the screening of new receptors’ agonists is a major issue for pharmaceutical research. Currently, the main targets used are the G-protein coupled receptor of the plasma membrane which the activation trigger the signaling pathways involved in many cell functions. The goal of this thesis is the detection, using a spectrofluorometry approach in vivo, of the signaling pathway ignition by the mouse delta opioid receptor (mDOR). DOR is assumed to generate a relocalisation of some lipids (cholesterol) while agonist binding leading to the formation of a liquid-ordered phase (lo). Thus two fluorescent probes have been synthesized, which the 3beta-hydroxy-pregn-5-ene-21-(1-methylpyrenyl)-20-methylidene. Data from calorimetry and RMN-2H studies show that this probe induces the same lipid membranes disturbance than cholesterol. Absorption data of the probe allowed the assessment of a self-association process of cholesterol in model membranes, which is as a function of the acyl-chains saturation degree of phospholipids. Then the polarity sensitive property of the probe has been used to distinguish between ld and lo phases in model membranes. Finally, we incorporated the probes in CHO cells over-expressing mDOR to monitor, by fluorescence spectroscopy, the mean phase state change of the plasma membrane triggered by a mDOR agonist. This is the first step of a new screening approach
Livros sobre o assunto "Plasmide eucaryote"
Plasmids of Eukaryotes. Springer Verlag, 1986.
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