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4641por Dambroise, E., Monnier, L., Ruisheng, L., Aguilaniu, H., Joly, J.-S., Tricoire, H., Rera, M.“…To identify the very processes driving aging we have developed in the past years an assay to identify physiologically old individuals in a synchronized population of Drosophila melanogaster. Those individuals show an age-dependent increase of intestinal permeability followed by a high risk of death. …”
Publicado 2016
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4642por Caplan, Stacee Lee, Zheng, Bo, Dawson-Scully, Ken, White, Catherine A., West, Lyndon M.“…The present study probes pseudopterosin A (PsA) for its neuromodulatory properties during oxidative stress using the fruit fly, Drosophila melanogaster. We demonstrate that oxidative stress rapidly reduces neuronal activity, resulting in the loss of neurotransmission at a well-characterized invertebrate synapse. …”
Publicado 2016
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4643“…We study Boolean network ensembles of network motifs as well as three models of biochemical regulation: the segment polarity network in Drosophila melanogaster, the cell cycle of budding yeast Saccharomyces cerevisiae, and the floral organ arrangement in Arabidopsis thaliana. …”
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4644“…In the classic model organism Drosophila melanogaster and the nonmodel scuttle fly Megaselia abdita, early activation and placement of gap gene expression domains show significant quantitative differences, yet the final patterning output of the system is essentially identical in both species. …”
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4645por Bellemer, Andrew“…The fruit fly Drosophila melanogaster is a poikilothermic organism that must detect and respond to both fine and coarse changes in environmental temperature in order maintain optimal body temperature, synchronize behavior to daily temperature fluctuations, and to avoid potentially injurious environmental hazards. …”
Publicado 2015
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4646por Corbett-Detig, Russell B., Zhou, Jun, Clark, Andrew G., Hartl, Daniel L., Ayroles, Julien F.“…In applying this method to a large panel of Drosophila melanogaster recombinant inbred lines(8, 9), we conservatively estimate that any two haploid genomes in this study are expected to harbor 1.15 pairs of incompatible alleles. …”
Publicado 2013
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4647“…RNA interference (RNAi) has emerged as a powerful way of reducing gene function in Drosophila melanogaster tissues. By expressing synthetic short hairpin RNAs (shRNAs) using the Gal4/UAS system, knockdown is efficiently achieved in specific tissues or in clones of marked cells. …”
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4648por Men, Tran Thanh, Thanh, Duong Ngoc Van, Yamaguchi, Masamitsu, Suzuki, Takayoshi, Hattori, Gen, Arii, Masayuki, Huy, Nguyen Tien, Kamei, Kaeko“…The brummer (bmm) gene in Drosophila melanogaster is known to be homologous with human adipocyte triglyceride lipase, which is related to the regulation of lipid storage. …”
Publicado 2016
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4649por Spühler, Isabelle A., Conley, Gaurasundar M., Scheffold, Frank, Sprecher, Simon G.“…With direct stochastic optical reconstruction microscopy, dSTORM, we image synaptic proteins in the brain tissue of the fruit fly, Drosophila melanogaster. Super resolution imaging of brain tissue harbors difficulties due to light scattering and the density of signals. …”
Publicado 2016
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4650por Kuzuoğlu‐Öztürk, Duygu, Bhandari, Dipankar, Huntzinger, Eric, Fauser, Maria, Helms, Sigrun, Izaurralde, Elisa“…An alternative model posits that AGOs repress translation by interfering with eIF4A function during 43S ribosomal scanning and that this mechanism is independent of GW182 and the CCR4–NOT complex in Drosophila melanogaster. Here, we show that miRNAs, AGOs, GW182, the CCR4–NOT complex, and DDX6/Me31B repress and degrade polyadenylated mRNA targets that are translated via scanning‐independent mechanisms in both human and Dm cells. …”
Publicado 2016
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4651por Soldano, Alessia, Alpizar, Yeranddy A, Boonen, Brett, Franco, Luis, López-Requena, Alejandro, Liu, Guangda, Mora, Natalia, Yaksi, Emre, Voets, Thomas, Vennekens, Rudi, Hassan, Bassem A, Talavera, Karel“…Here we show that Drosophila melanogaster display strong aversive responses to LPS and that gustatory neurons expressing Gr66a bitter receptors mediate avoidance of LPS in feeding and egg laying assays. …”
Publicado 2016
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4652“…Here, we report that mating stimulates female germline stem cell (GSC) proliferation in Drosophila melanogaster. Mating-induced increase in GSC number is not simply owing to the indirect effect of emission of stored eggs, but rather is stimulated by a male-derived Sex Peptide (SP) and its receptor SPR, the components of a canonical neuronal pathway that induces a post-mating behavioral switch in females. …”
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4653por Shephard, Freya, Greville-Heygate, Oliver, Liddell, Susan, Emes, Richard, Chakrabarti, Lisa“…To confirm a dynamic localisation of haemoglobin we exposed Drosophila melanogaster to cyclical hypoxia with recovery. …”
Publicado 2016
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4654por Kuzu, Guray, Kaye, Emily G., Chery, Jessica, Siggers, Trevor, Yang, Lin, Dobson, Jason R., Boor, Sonia, Bliss, Jacob, Liu, Wei, Jogl, Gerwald, Rohs, Remo, Singh, Nadia D., Bulyk, Martha L., Tolstorukov, Michael Y., Larschan, Erica“…Once each newly evolved X-chromosome is targeted for dosage compensation in XY males, its active genes are upregulated two-fold to equalize gene expression with XX females. In Drosophila melanogaster, the CLAMP zinc finger protein links the dosage compensation complex to the X-chromosome. …”
Publicado 2016
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4655“…Using the proliferating Drosophila melanogaster wing disc epithelium, we demonstrate that disruption of the junctional vs. basal polarity complexes results in increased epithelial proliferation via distinct downstream signaling pathways. …”
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4656“…Several signaling pathways, including the JAK/STAT and Toll pathways, are known to activate blood cells (hemocytes) in Drosophila melanogaster larvae. They are believed to regulate the immune response against infections by parasitoid wasps, such as Leptopilina boulardi, but how these pathways control the hemocytes is not well understood. …”
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4657“…In the current study, we set out to identify genes involved in the functional decline of the brain with age and study its relevance in a tissue dependent manner using Drosophila melanogaster as a model system. Here we report the age-dependent upregulation of genes involved in the metabolic process of fatty acid β-oxidation in the nervous tissue of female wild-type flies. …”
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4658por Lack, Justin B., Yassin, Amir, Sprengelmeyer, Quentin D., Johanning, Evan J., David, Jean R., Pool, John E.“…We examined the evolution of body and wing size in high‐altitude Drosophila melanogaster from Ethiopia, flies with larger size than any previously known population. …”
Publicado 2016
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4659por Klebanow, Lindsey R., Peshel, Emanuela C., Schuster, Andrew T., De, Kuntal, Sarvepalli, Kavitha, Lemieux, Madeleine E., Lenoir, Jessica J., Moore, Adrian W., McDonald, Jocelyn A., Longworth, Michelle S.“…The pattern of the Drosophila melanogaster adult wing is heavily influenced by the expression of proteins that dictate cell fate decisions between intervein and vein during development. dSRF (Blistered) expression in specific regions of the larval wing disc promotes intervein cell fate, whereas EGFR activity promotes vein cell fate. …”
Publicado 2016
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4660“…Here, we used different laboratory strains and a wild-caught population of the fruit fly Drosophila melanogaster to examine the effect of temperature on the body energy reserves of an ectothermic organism. …”
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