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Items: 1 to 20 of 32

1.
Ectopic assembly of heterochromatin in Drosophila melanogaster triggered by transposable elements
Monica F. Sentmanat, Sarah C. R. Elgin
Proc Natl Acad Sci U S A. 2012 Aug 28; 109(35): 14104–14109. Published online 2012 Aug 13. doi: 10.1073/pnas.1207036109
PMCID:
PMC3435190
AbstractArticlePDF–735K
2.
Nessun Dorma, a novel centralspindlin partner, is required for cytokinesis in Drosophila spermatocytes
Emilie Montembault, Wei Zhang, Marcin R. Przewloka, Vincent Archambault, Emeric W. Sevin, Ernest D. Laue, David M. Glover, Pier Paolo D'Avino
J Cell Biol. 2010 Dec 27; 191(7): 1351–1365. doi: 10.1083/jcb.201007060
PMCID:
PMC3010078
AbstractArticlePDF–3.6M
3.
What Drosophila spermatocytes tell us about the mechanisms underlying cytokinesis
Maria Grazia Giansanti, Margaret T. Fuller
Cytoskeleton (Hoboken) Author manuscript; available in PMC 2014 Sep 16.
Published in final edited form as: Cytoskeleton (Hoboken). 2012 Nov; 69(11): 869–881. Published online 2012 Sep 21. doi: 10.1002/cm.21063
PMCID:
PMC4165571
AbstractArticlePDF–789K
4.
DAPPER: a data-mining resource for protein-protein interactions
Syed Haider, Zoltan Lipinszki, Marcin R. Przewloka, Yaseen Ladak, Pier Paolo D’Avino, Yuu Kimata, Pietro Lio’, David M. Glover
BioData Min. 2015; 8: 30. Published online 2015 Sep 24. doi: 10.1186/s13040-015-0063-3
PMCID:
PMC4581157
AbstractArticlePDF–594K
5.
Normal dynactin complex function during synapse growth in Drosophila requires membrane binding by Arfaptin
Leo Chang, Tabita Kreko, Holly Davison, Tim Cusmano, Yimin Wu, Adrian Rothenfluh, Benjamin A. Eaton
Mol Biol Cell. 2013 Jun 1; 24(11): 1749–1764. doi: 10.1091/mbc.E12-09-0697
PMCID:
PMC3667727
AbstractArticlePDF–5.9M
6.
Cytokinesis in Drosophila male meiosis
Maria Grazia Giansanti, Stefano Sechi, Anna Frappaolo, Giorgio Belloni, Roberto Piergentili
Spermatogenesis. 2012 Jul 1; 2(3): 185–196. doi: 10.4161/spmg.21711
PMCID:
PMC3469441
AbstractArticlePDF–3.1M
7.
Unbiased Boolean analysis of public gene expression data for cell cycle gene identification
Sarah A. Dabydeen, Arshad Desai, Debashis Sahoo
Mol Biol Cell. 2019 Jul 1; 30(14): 1770–1779. doi: 10.1091/mbc.E19-01-0013
PMCID:
PMC6727750
AbstractArticlePDF–5.4M
8.
Map position and expression of the genes in the 38 region of Drosophila.
H Butler, S Levine, X Wang, S Bonyadi, G Fu, P Lasko, B Suter, R Doerig
Genetics. 2001 Aug; 158(4): 1597–1614. doi: 10.1093/genetics/158.4.1597
PMCID:
PMC1461758
SummaryPDF–776K
9.
Single-cell sequencing of tumor-associated macrophages in a Drosophila model
Dilan Khalili, Mubasher Mohammed, Martin Kunc, Martina Sindlerova, Johan Ankarklev, Ulrich Theopold
Front Immunol. 2023; 14: 1243797. Published online 2023 Sep 19. doi: 10.3389/fimmu.2023.1243797
PMCID:
PMC10546068
AbstractArticlePDF–7.2M
10.
Analysis of Ras-induced overproliferation in Drosophila hemocytes.
H Asha, Istvan Nagy, Gabor Kovacs, Daniel Stetson, Istvan Ando, Charles R Dearolf
Genetics. 2003 Jan; 163(1): 203–215. doi: 10.1093/genetics/163.1.203
PMCID:
PMC1462399
SummaryPDF–236K
11.
Proteomic and Functional Genomic Landscape of Receptor Tyrosine Kinase and Ras to Extracellular Signal–Regulated Kinase Signaling
Adam A. Friedman, George Tucker, Rohit Singh, Dong Yan, Arunachalam Vinayagam, Yanhui Hu, Richard Binari, Pengyu Hong, Xiaoyun Sun, Maura Porto, Svetlana Pacifico, Thilakam Murali, Russell L. Finley, Jr., John M. Asara, Bonnie Berger, Norbert Perrimon
Sci Signal. Author manuscript; available in PMC 2012 Sep 11.
Published in final edited form as: Sci Signal. 2011 Oct 25; 4(196): rs10. Published online 2011 Oct 25. doi: 10.1126/scisignal.2002029
PMCID:
PMC3439136
AbstractArticlePDF–2.4M
12.
The Drosophila Helicase Maleless (MLE) is Implicated in Functions Distinct From its Role in Dosage Compensation
Simona Cugusi, Satish Kallappagoudar, Huiping Ling, John C. Lucchesi
Mol Cell Proteomics. 2015 Jun; 14(6): 1478–1488. Published online 2015 Mar 16. doi: 10.1074/mcp.M114.040667
PMCID:
PMC4458714
AbstractArticlePDF–625K
13.
Genes conserved in bilaterians but jointly lost with Myc during nematode evolution are enriched in cell proliferation and cell migration functions
Albert J. Erives
Dev Genes Evol. 2015; 225(5): 259–273. Published online 2015 Jul 15. doi: 10.1007/s00427-015-0508-1
PMCID:
PMC4568025
AbstractArticlePDF–2.8M
14.
Proteome-wide association studies identify biochemical modules associated with a wing-size phenotype in Drosophila melanogaster
Hirokazu Okada, H. Alexander Ebhardt, Sibylle Chantal Vonesch, Ruedi Aebersold, Ernst Hafen
Nat Commun. 2016; 7: 12649. Published online 2016 Sep 1. doi: 10.1038/ncomms12649
PMCID:
PMC5025782
AbstractArticlePDF–2.2M
15.
CRISPR-based modular assembly of a UAS-cDNA/ORF plasmid library for more than 5500 Drosophila genes conserved in humans
Ping Wei, Wen Xue, Yun Zhao, Guang Ning, Jiwu Wang
Genome Res. 2020 Jan; 30(1): 95–106. doi: 10.1101/gr.250811.119
PMCID:
PMC6961578
AbstractArticlePDF–3.6M
16.
Phylostratigraphic Bias Creates Spurious Patterns of Genome Evolution
Bryan A. Moyers, Jianzhi Zhang
Mol Biol Evol. 2015 Jan 1; 32(1): 258–267. Published online 2014 Oct 13. doi: 10.1093/molbev/msu286
Correction in:
Mol Biol Evol. 2016 Nov; 33(11): 3031.
PMCID:
PMC4271527
AbstractArticlePDF–618K
17.
A global in vivo Drosophila RNAi screen identifies NOT3 as a conserved regulator of heart function
G. Gregory Neely, Keiji Kuba, Anthony Cammarato, Kazuya Isobe, Sabine Amann, Liyong Zhang, Mitsushige Murata, Lisa Elmén, Vaijayanti Gupta, Suchir Arora, Rinku Sarangi, Debasis Dan, Susumu Fujisawa, Takako Usami, Cui-ping Xia, Alex C. Keene, Nakissa N. Alayari, Hiroyuki Yamakawa, Ulrich Elling, Christian Berger, Maria Novatchkova, Rubina Koglgruber, Keiichi Fukuda, Hiroshi Nishina, Mitsuaki Isobe, J. Andrew Pospisilik, Yumiko Imai, Arne Pfeufer, Andrew A Hicks, Peter P. Pramstaller, Sai Subramaniam, Akinori Kimura, Karen Ocorr, Rolf Bodmer, Josef M. Penninger
Cell. Author manuscript; available in PMC 2011 Apr 2.
Published in final edited form as: Cell. 2010 Apr 2; 141(1): 142–153. doi: 10.1016/j.cell.2010.02.023
PMCID:
PMC2855221
AbstractArticlePDF–5.3M
18.
A genome-wide Drosophila screen for heat nociception identifies α2δ3 as an evolutionary-conserved pain gene
G. Gregory Neely, Andreas Hess, Michael Costigan, Alex C. Keene, Spyros Goulas, Michiel Langeslag, Robert S Griffin, Inna Belfer, Feng Dai, Shad Smith, Luda Diatchenko, Vaijayanti Gupta, Cui-ping Xia, Sabina Amann, Silke Kreitz, Cornelia Heindl-Erdmann, Susanne Wolz, Cindy V. Ly, Suchir Arora, Rinku Sarangi, Debasis Dan, Maria Novatchkova, Mark Rosenzweig, Dustin Gibson, Darwin Truong, Daniel Schramek, Tamara Zoranovic, Shane J. F. Cronin, Belinda Angjeli, Kay Brune, Georg Dietzl, William Maixner, Arabella Meixner, Winston Thomas, J. Andrew Pospisilik, Mattias Alenius, Michaela Kress, Sai Subramaniam, Paul A. Garrity, Hugo J. Bellen, Clifford J. Woolf, Josef M. Penninger
Cell. Author manuscript; available in PMC 2011 Nov 12.
Published in final edited form as: Cell. 2010 Nov 12; 143(4): 628–638. doi: 10.1016/j.cell.2010.09.047
PMCID:
PMC3040441
AbstractArticlePDF–2.0M
19.
High-fidelity promoter profiling reveals widespread alternative promoter usage and transposon-driven developmental gene expression
Philippe Batut, Alexander Dobin, Charles Plessy, Piero Carninci, Thomas R. Gingeras
Genome Res. 2013 Jan; 23(1): 169–180. doi: 10.1101/gr.139618.112
PMCID:
PMC3530677
AbstractArticlePDF–1.5M
20.
Landscape and evolution of tissue-specific alternative polyadenylation across Drosophila species
Piero Sanfilippo, Jiayu Wen, Eric C. Lai
Genome Biol. 2017; 18: 229. Published online 2017 Nov 30. doi: 10.1186/s13059-017-1358-0
PMCID:
PMC5707805
AbstractArticlePDF–3.2M

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