Literatura científica selecionada sobre o tema "Homeobox protein engrailed2"
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Artigos de revistas sobre o assunto "Homeobox protein engrailed2"
Hanks, M. C., C. A. Loomis, E. Harris, C. X. Tong, L. Anson-Cartwright, A. Auerbach e A. Joyner. "Drosophila engrailed can substitute for mouse Engrailed1 function in mid-hindbrain, but not limb development". Development 125, n.º 22 (15 de novembro de 1998): 4521–30. http://dx.doi.org/10.1242/dev.125.22.4521.
Texto completo da fontevan den Heuvel, Marcel, John Klingensmith, Norbert Perrimon e Roel Nusse. "Cell patterning in the Drosophila segment: engrailed and wingless antigen distributions in segment polarity mutant embryos". Development 119, Supplement (1 de dezembro de 1993): 105–14. http://dx.doi.org/10.1242/dev.119.supplement.105.
Texto completo da fonteHemmati-Brivanlou, A., J. R. de la Torre, C. Holt e R. M. Harland. "Cephalic expression and molecular characterization of Xenopus En-2". Development 111, n.º 3 (1 de março de 1991): 715–24. http://dx.doi.org/10.1242/dev.111.3.715.
Texto completo da fontePeel, Andrew D., Maximilian J. Telford e Michael Akam. "The evolution of hexapod engrailed-family genes: evidence for conservation and concerted evolution". Proceedings of the Royal Society B: Biological Sciences 273, n.º 1595 (5 de abril de 2006): 1733–42. http://dx.doi.org/10.1098/rspb.2006.3497.
Texto completo da fonteMatsuzaki, M., e K. Saigo. "hedgehog signaling independent of engrailed and wingless required for post-S1 neuroblast formation in Drosophila CNS". Development 122, n.º 11 (1 de novembro de 1996): 3567–75. http://dx.doi.org/10.1242/dev.122.11.3567.
Texto completo da fonteDesjobert, Cecile, Peter Noy, Tracey Swingler, Hannah Williams, Kevin Gaston e Padma-Sheela Jayaraman. "The PRH/Hex repressor protein causes nuclear retention of Groucho/TLE co-repressors". Biochemical Journal 417, n.º 1 (12 de dezembro de 2008): 121–32. http://dx.doi.org/10.1042/bj20080872.
Texto completo da fonteRoyet, J., e R. Finkelstein. "Pattern formation in Drosophila head development: the role of the orthodenticle homeobox gene". Development 121, n.º 11 (1 de novembro de 1995): 3561–72. http://dx.doi.org/10.1242/dev.121.11.3561.
Texto completo da fonteVillanueva, Sandra, Carlos Cespedes, Alexis Gonzalez e Carlos P. Vio. "bFGF induces an earlier expression of nephrogenic proteins after ischemic acute renal failure". American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 291, n.º 6 (dezembro de 2006): R1677—R1687. http://dx.doi.org/10.1152/ajpregu.00023.2006.
Texto completo da fonteMontross, W. T., H. Ji e P. D. McCrea. "A beta-catenin/engrailed chimera selectively suppresses Wnt signaling". Journal of Cell Science 113, n.º 10 (15 de maio de 2000): 1759–70. http://dx.doi.org/10.1242/jcs.113.10.1759.
Texto completo da fonteDibner, Charna, Sarah Elias e Dale Frank. "XMeis3 protein activity is required for proper hindbrain patterning in Xenopus laevis embryos". Development 128, n.º 18 (15 de setembro de 2001): 3415–26. http://dx.doi.org/10.1242/dev.128.18.3415.
Texto completo da fonteTeses / dissertações sobre o assunto "Homeobox protein engrailed2"
Amblard, Irène. "Régulation du transfert intercellulaire des homéoprotéines". Electronic Thesis or Diss., Sorbonne université, 2020. http://www.theses.fr/2020SORUS085.
Texto completo da fonteHomeoproteins (HP) constitute a large family of transcription factors endowed with both autocrine and paracrine activities. Homeoprotein paracrine action controls patterning processes, including axonal guidance and boundary formation. Internalization and secretion, the steps of intercellular transfer, rely on unconventional mechanisms, which still need to be fully characterized. We have deciphered the mechanism of HP transfer, responsible for their paracrine activity, using Engrailed (EN2) as a paradigm. First, I have developed tools to quantify EN2 uptake and secretion. This original strategy allowed us to demonstrate EN2 bidirectional transfer through direct plasma membrane translocation. Then, I identified the molecular requirements for EN2 transfer, highlighting the pivotal role of PIP2, cholesterol, and proteoglycans. This work illustrates how soluble protein are able to cross the plasma membrane, giving new clues to the study of cell-penetrating peptides derived from HP but also to other unconventionnally secreted proteins. Next, I have addressed the contribution of redox signaling in EN2 transfer, and demonstrated that EN2 and H2O2 act in synergy to shape the optic tectum in the zebrafish. Finally, I have extended this study to conventional morphogens and showed that H2O2 regulates the traffic of Sonic Hedgehog. If this regulation of protein trafficking can be generalized to other HPs and morphogens remains unknown, but if so, it would provide an understanding for how tissue morphogenesis and cell metabolism influence each other during development