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Items: 1 to 20 of 107

1.
Developmental arrest of Drosophila larvae elicits presynaptic depression and enables prolonged studies of neurodegeneration
Sarah Perry, Pragya Goel, Nancy L. Tran, Cristian Pinales, Christopher Buser, Daniel L. Miller, Barry Ganetzky, Dion Dickman
Development. 2020 May 15; 147(10): dev186312. Published online 2020 May 21. doi: 10.1242/dev.186312
PMCID:
PMC7325439
AbstractArticle
2.
Production of systemically circulating Hedgehog by the intestine couples nutrition to growth and development
Jonathan Rodenfels, Oksana Lavrynenko, Sophie Ayciriex, Julio L. Sampaio, Maria Carvalho, Andrej Shevchenko, Suzanne Eaton
Genes Dev. 2014 Dec 1; 28(23): 2636–2651. doi: 10.1101/gad.249763.114
PMCID:
PMC4248294
AbstractArticlePDF–2.1M
3.
Discrete Pulses of Molting Hormone, 20-Hydroxyecdysone, During Late Larval Development of Drosophila melanogaster: Correlations With Changes in Gene Activity
James T. Warren, Yoram Yerushalmi, Mary Jane Shimell, Michael B. O'Connor, Linda Restifo, Lawrence I. Gilbert
Dev Dyn. Author manuscript; available in PMC 2009 Jan 5.
Published in final edited form as: Dev Dyn. 2006 Feb; 235(2): 315–326. doi: 10.1002/dvdy.20626
PMCID:
PMC2613944
AbstractArticlePDF–977K
4.
Glue protein production can be triggered by steroid hormone signaling independent of the developmental program in Drosophila melanogaster
Yuya Kaieda, Ryota Masuda, Ritsuo Nishida, MaryJane Shimell, Michael B. O’Connor, Hajime Ono
Dev Biol. Author manuscript; available in PMC 2018 Apr 25.
Published in final edited form as: Dev Biol. 2017 Oct 1; 430(1): 166–176. Published online 2017 Aug 4. doi: 10.1016/j.ydbio.2017.08.002
PMCID:
PMC5916818
AbstractArticlePDF–1.4M
5.
Endoreplication in the Drosophila melanogaster prothoracic gland is dispensable for the critical weight checkpoint
MaryJane Shimell, Michael B O'Connor
MicroPubl Biol. 2023; 2023: 10.17912/micropub.biology.000741. Published online 2023 Feb 21. doi: 10.17912/micropub.biology.000741
PMCID:
PMC9996309
AbstractArticlePDF–2.0M
6.
A versatile toolkit for CRISPR-Cas13-based RNA manipulation in Drosophila
Nhan Huynh, Noah Depner, Raegan Larson, Kirst King-Jones
Genome Biol. 2020; 21: 279. Published online 2020 Nov 17. doi: 10.1186/s13059-020-02193-y
PMCID:
PMC7670108
AbstractArticlePDF–2.2M
7.
A New Role for Neuropeptide F Signaling in Controlling Developmental Timing and Body Size in Drosophila melanogaster
Jade R. Kannangara, Michelle A. Henstridge, Linda M. Parsons, Shu Kondo, Christen K. Mirth, Coral G. Warr
Genetics. 2020 Sep; 216(1): 135–144. Published online 2020 Jul 16. doi: 10.1534/genetics.120.303475
PMCID:
PMC7463290
AbstractArticlePDF–1.1M
8.
Torso-Like Is a Component of the Hemolymph and Regulates the Insulin Signaling Pathway in Drosophila
Michelle A. Henstridge, Lucinda Aulsebrook, Takashi Koyama, Travis K. Johnson, James C. Whisstock, Tony Tiganis, Christen K. Mirth, Coral G. Warr
Genetics. 2018 Apr; 208(4): 1523–1533. Published online 2018 Feb 13. doi: 10.1534/genetics.117.300601
PMCID:
PMC5887146
AbstractArticlePDF–1.4M
9.
Drosophila enhancer-Gal4 lines show ectopic expression during development
Sergio Casas-Tintó, Mercedes Arnés, Alberto Ferrús
R Soc Open Sci. 2017 Mar; 4(3): 170039. Published online 2017 Mar 29. doi: 10.1098/rsos.170039
PMCID:
PMC5383858
AbstractArticlePDF–2.2M
10.
Nutritional control of body size through FoxO-Ultraspiracle mediated ecdysone biosynthesis
Takashi Koyama, Marisa A Rodrigues, Alekos Athanasiadis, Alexander W Shingleton, Christen K Mirth
eLife. 2014; 3: e03091. Published online 2014 Nov 25. doi: 10.7554/eLife.03091
PMCID:
PMC4337420
AbstractArticlePDF–2.6M
11.
Phantom, a cytochrome P450 enzyme essential for ecdysone biosynthesis, plays a critical role in the control of border cell migration in Drosophila
Elena Domanitskaya, Lauren Anllo, Trudi Schüpbach
Dev Biol. Author manuscript; available in PMC 2014 Aug 15.
Published in final edited form as: Dev Biol. 2014 Feb 15; 386(2): 408–418. Published online 2013 Dec 27. doi: 10.1016/j.ydbio.2013.12.013
PMCID:
PMC4028970
AbstractArticlePDF–2.2M
12.
Stop codon readthrough alters the activity of a POU/Oct transcription factor during Drosophila development
Yunpo Zhao, Bo Gustav Lindberg, Shiva Seyedoleslami Esfahani, Xiongzhuo Tang, Stefano Piazza, Ylva Engström
BMC Biol. 2021; 19: 185. Published online 2021 Sep 3. doi: 10.1186/s12915-021-01106-0
PMCID:
PMC8417969
AbstractArticlePDF–7.9M
13.
Matrix Metalloproteinase 2 Is Required for Ovulation and Corpus Luteum Formation in Drosophila
Lylah D. Deady, Wei Shen, Sarah A. Mosure, Allan C. Spradling, Jianjun Sun
PLoS Genet. 2015 Feb; 11(2): e1004989. Published online 2015 Feb 19. doi: 10.1371/journal.pgen.1004989
PMCID:
PMC4335033
AbstractArticlePDF–16M
14.
Genes of the Ecdysone Biosynthesis Pathway Are Regulated by the dATAC Histone Acetyltransferase Complex in Drosophila
T. Pankotai, C. Popescu, D. Martín, B. Grau, N. Zsindely, L. Bodai, L. Tora, A. Ferrús, I. Boros
Mol Cell Biol. 2010 Sep; 30(17): 4254–4266. Published online 2010 Jun 28. doi: 10.1128/MCB.00142-10
PMCID:
PMC2937542
AbstractArticlePDF–1.6M
15.
Drosophila postembryonic nervous system development: a model for the endocrine control of development
James W Truman, Lynn M Riddiford
Genetics. 2023 Mar; 223(3): iyac184. Published online 2023 Jan 16. doi: 10.1093/genetics/iyac184
PMCID:
PMC9991519
AbstractArticlePDF–2.1M
16.
The steroid-hormone ecdysone coordinates parallel pupariation neuromotor and morphogenetic subprograms via epidermis-to-neuron Dilp8-Lgr3 signal induction
Fabiana Heredia, Yanel Volonté, Joana Pereirinha, Magdalena Fernandez-Acosta, Andreia P. Casimiro, Cláudia G. Belém, Filipe Viegas, Kohtaro Tanaka, Juliane Menezes, Maite Arana, Gisele A. Cardoso, André Macedo, Malwina Kotowicz, Facundo H. Prado Spalm, Marcos J. Dibo, Raquel D. Monfardini, Tatiana T. Torres, César S. Mendes, Andres Garelli, Alisson M. Gontijo
Nat Commun. 2021; 12: 3328. Published online 2021 Jun 7. doi: 10.1038/s41467-021-23218-5
PMCID:
PMC8184853
AbstractArticlePDF–5.1M
17.
Ovarian ecdysteroid biosynthesis and female germline stem cells
Tomotsune Ameku, Yuto Yoshinari, Ruriko Fukuda, Ryusuke Niwa
Fly (Austin) 2017; 11(3): 185–193. Published online 2017 Feb 8. doi: 10.1080/19336934.2017.1291472
PMCID:
PMC5552268
AbstractArticlePDF–832K
18.
Pri peptides temporally coordinate transcriptional programs during epidermal differentiation
Maylis Gallois, Delphine Menoret, Simon Marques-Prieto, Audrey Montigny, Philippe Valenti, Bernard Moussian, Serge Plaza, François Payre, Hélène Chanut-Delalande
Sci Adv. 2024 Feb 9; 10(6): eadg8816. Published online 2024 Feb 9. doi: 10.1126/sciadv.adg8816
PMCID:
PMC10857433
AbstractArticlePDF–1007K
19.
Su(var)2-10- and Su(var)205-dependent upregulation of the heterochromatic gene neverland is required for developmental transition in Drosophila
Yuya Ohhara, Yuki Kato, Takumi Kamiyama, Kimiko Yamakawa-Kobayashi
Genetics. 2022 Nov; 222(3): iyac137. Published online 2022 Sep 23. doi: 10.1093/genetics/iyac137
PMCID:
PMC9630985
AbstractArticlePDF–1.1M
20.
Pri smORF Peptides Are Wide Mediators of Ecdysone Signaling, Contributing to Shape Spatiotemporal Responses
Azza Dib, Jennifer Zanet, Alexandra Mancheno-Ferris, Maylis Gallois, Damien Markus, Philippe Valenti, Simon Marques-Prieto, Serge Plaza, Yuji Kageyama, Hélène Chanut-Delalande, François Payre
Front Genet. 2021; 12: 714152. Published online 2021 Aug 30. doi: 10.3389/fgene.2021.714152
PMCID:
PMC8435736
AbstractArticlePDF–5.5M

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