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221por Lopes, Jeyson Césary, Machado, Nayane Moreira, Saturnino, Rosiane Soares, Nepomuceno, Júlio César“…In view of these experimental conditions and results, it was concluded that Pantoprazole is associated with recombinogenic effects in Drosophila melanogaster.…”
Publicado 2015
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222por Morgante, Fabio, Sørensen, Peter, Sorensen, Daniel A., Maltecca, Christian, Mackay, Trudy F. C.“…Here, we quantified genetic variation for micro-environmental plasticity for three quantitative traits in the inbred, sequenced lines of the Drosophila melanogaster Genetic Reference Panel. We found substantial genetic variation for micro-environmental plasticity for all traits, with broad sense heritabilities of the same magnitude or greater than those of trait means. …”
Publicado 2015
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223por Sakata, Kazuki, Kawasaki, Haruhisa, Suzuki, Takahiro, Ito, Kumpei, Negishi, Osamu, Tsuno, Takuo, Tsuno, Hiromi, Yamazaki, Youta, Ishida, Norio“…Accumulating evidence indicates that the molecular circadian clock underlies the mating behavior of Drosophila melanogaster. However, information about which food components affect circadian mating behavior is scant. …”
Publicado 2015
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224“…Dscam2, a cell surface protein that mediates cellular repulsion, plays a crucial role in the development of the Drosophila melanogaster visual system. Dscam2 generates boundaries between neighboring modules in the fly optic lobe; in Dscam2 mutants this visual system modularity is compromised. …”
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225por Schwartz, Yuri B, Boykova, Tatiana, Belyaeva, Elena S, Ashburner, Michael, Zhimulev, Igor F“…In Drosophila the transformation of the larva into the pupa and the subsequent metamorphosis to the adult stage is triggered by changes in the titer of the steroid hormone 20-hydroxyecdysone. singed wings (swi) is the only gene known in Drosophila melanogaster for which mutations specifically interrupt the transmission of the regulatory signal from early to late ecdysone inducible genes. …”
Publicado 2004
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226por Jasper, HeinrichEnlace del recurso
Publicado 2015
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227“…Here we estimated costs and benefits in thermal tolerance limits in relation to winter acclimatization of Drosophila melanogaster. We sampled flies from a natural habitat during winter in Denmark (field flies) and compared heat and cold tolerance of these to that of flies collected from the same natural population, but acclimated to 25 °C or 13 °C in the laboratory (laboratory flies). …”
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228“…Here we present a simple methodology to quantitatively assess bi-allelic TALEN cutting, as well as approaches that permit accurate measures of somatic and germline mutation rates in Drosophila melanogaster. We report that percent lethality from pilot injection of candidate TALEN mRNAs into Lig4 null embryos can be used to effectively gauge bi-allelic TALEN cutting efficiency and occurs in a dose-dependent manner. …”
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229por Webster, Claire L., Waldron, Fergal M., Robertson, Shaun, Crowson, Daisy, Ferrari, Giada, Quintana, Juan F., Brouqui, Jean-Michel, Bayne, Elizabeth H., Longdon, Ben, Buck, Amy H., Lazzaro, Brian P., Akorli, Jewelna, Haddrill, Penelope R., Obbard, Darren J.“…Drosophila melanogaster is a valuable invertebrate model for viral infection and antiviral immunity, and is a focus for studies of insect-virus coevolution. …”
Publicado 2015
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230por Sanchez-Díaz, Iván, Rosales-Bravo, Fernando, Reyes-Taboada, José Luis, Covarrubias, Alejandra A, Narvaez-Padilla, Verónica, Reynaud, EnriqueEnlace del recurso
Publicado 2015
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231por Crosby, Madeline A., Gramates, L. Sian, dos Santos, Gilberto, Matthews, Beverley B., St. Pierre, Susan E., Zhou, Pinglei, Schroeder, Andrew J., Falls, Kathleen, Emmert, David B., Russo, Susan M., Gelbart, William M.“…In the context of the FlyBase annotated gene models in Drosophila melanogaster, we describe the many exceptional cases we have curated from the literature or identified in the course of FlyBase analysis. …”
Publicado 2015
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232por Liu, Chang, Haynes, Paula R., Donelson, Nathan C., Aharon, Shani, Griffith, Leslie C.“…The fruit fly Drosophila melanogaster is a diurnal insect active during the day with consolidated sleep at night. …”
Publicado 2015
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233por Philip, Philge, Boija, Ann, Vaid, Roshan, Churcher, Allison M., Meyers, David J., Cole, Philip A., Mannervik, Mattias, Stenberg, PerEnlace del recurso
Publicado 2015
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234“…Likewise, in the invertebrate model organism Drosophila melanogaster, inductive microenvironments known as larval Hematopoietic Pockets (HPs) have been identified as anatomical sites for the development and regulation of blood cells (hemocytes), in particular of the self-renewing macrophage lineage. …”
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235“…RESULTS: Here, we compare the genomes of lab-reared and wild-caught Drosophila melanogaster to understand the genetic basis of these recently endowed behaviors common to laboratory models. …”
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237por Mukunda, Latha, Miazzi, Fabio, Sargsyan, Vardanush, Hansson, Bill S., Wicher, DieterEnlace del recurso
Publicado 2016
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238por Perry, Jennifer C., Joag, Richa, Hosken, David J., Wedell, Nina, Radwan, Jacek, Wigby, Stuart“…Here, we use a genetic manipulation of mating frequency in Drosophila melanogaster to create a novel, highly promiscuous mating system. …”
Publicado 2016
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239por Schnorrenberg, Sebastian, Grotjohann, Tim, Vorbrüggen, Gerd, Herzig, Alf, Hell, Stefan W, Jakobs, Stefan“…Here, we report on the use of rsEGFP2 for live-cell RESOLFT nanoscopy of sub-cellular structures of intact Drosophila melanogaster larvae and of resected tissues. We generated flies expressing fusion proteins of alpha-tubulin and rsEGFP2 highlighting the microtubule cytoskeleton in all cells. …”
Publicado 2016
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240por Riedel, Falko, Gillingham, Alison K., Rosa-Ferreira, Cláudia, Galindo, Antonio, Munro, Sean“…The use of Drosophila melanogaster as a model organism has been pivotal to understanding the developmental processes of metazoans. …”
Publicado 2016
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