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Items: 1 to 20 of 67

1.
Sense and antisense RNA are not toxic in Drosophila models of C9orf72-associated ALS/FTD
Thomas G. Moens, Sarah Mizielinska, Teresa Niccoli, Jamie S. Mitchell, Annora Thoeng, Charlotte E. Ridler, Sebastian Grönke, Jacqueline Esser, Amanda Heslegrave, Henrik Zetterberg, Linda Partridge, Adrian M. Isaacs
Acta Neuropathol. 2018; 135(3): 445–457. Published online 2018 Jan 29. doi: 10.1007/s00401-017-1798-3
PMCID:
PMC6385858
AbstractArticlePDF–1.4M
2.
The translational repressor Glorund uses interchangeable RNA recognition domains to recognize Drosophila nanos
Meghan S Warden, Eugene F DeRose, Joel V Tamayo, Geoffrey A Mueller, Elizabeth R Gavis, Traci M Tanaka Hall
Nucleic Acids Res. 2023 Sep 8; 51(16): 8836–8849. Published online 2023 Jul 10. doi: 10.1093/nar/gkad586
PMCID:
PMC10484662
AbstractArticlePDF–1.4M
3.
Multiple mechanisms collaborate to repress nanos translation in the Drosophila ovary and embryo
Shane Andrews, Danielle R. Snowflack, Ira E. Clark, Elizabeth R. Gavis
RNA. 2011 May; 17(5): 967–977. doi: 10.1261/rna.2478611
PMCID:
PMC3078745
AbstractArticlePDF–586K
4.
Spatial regulation of nanos is required for its function in dendrite morphogenesis
Jillian L. Brechbiel, Elizabeth R. Gavis
Curr Biol. Author manuscript; available in PMC 2009 May 20.
Published in final edited form as: Curr Biol. 2008 May 20; 18(10): 745–750. Published online 2008 May 8. doi: 10.1016/j.cub.2008.04.033
PMCID:
PMC2474551
AbstractArticlePDF–1.9M
5.
The heterogeneous nuclear ribonucleoprotein (hnRNP) glorund functions in the Drosophila fat body to regulate lipid storage and transport
Annabella M. Kolasa, Jasleen K. Bhogal, Justin R. DiAngelo
Biochem Biophys Rep. 2021 Mar; 25: 100919. Published online 2021 Jan 23. doi: 10.1016/j.bbrep.2021.100919
PMCID:
PMC7838711
AbstractArticlePDF–550K
6.
The Drosophila hnRNP F/H Homolog Glorund Uses Two Distinct RNA-binding Modes to Diversify Target Recognition
Joel V. Tamayo, Takamasa Teramoto, Seema Chatterjee, Traci M. Tanaka Hall, Elizabeth R. Gavis
Cell Rep. Author manuscript; available in PMC 2017 Apr 17.
Published in final edited form as: Cell Rep. 2017 Apr 4; 19(1): 150–161. doi: 10.1016/j.celrep.2017.03.022
PMCID:
PMC5392723
AbstractArticlePDF–914K
7.
The Drosophila hnRNP F/H homolog Glorund recruits dFMRP to inhibit nanos translation elongation
Yingshi Peng, Elizabeth R Gavis
Nucleic Acids Res. 2022 Jul 8; 50(12): 7067–7083. Published online 2022 Jun 14. doi: 10.1093/nar/gkac500
PMCID:
PMC9262583
AbstractArticlePDF–4.0M
8.
Glorund interactions in the regulation of gurken and oskar mRNAs
Yossi Kalifa, Stephen T. Armenti, Elizabeth R. Gavis
Dev Biol. Author manuscript; available in PMC 2010 Mar 16.
Published in final edited form as: Dev Biol. 2009 Feb 1; 326(1): 68–74. Published online 2008 Nov 5. doi: 10.1016/j.ydbio.2008.10.032
PMCID:
PMC2839899
AbstractArticlePDF–2.2M
9.
SRSF protein kinase 1 modulates RAN translation and suppresses CGG repeat toxicity
Indranil Malik, Yi‐Ju Tseng, Shannon E Wright, Kristina Zheng, Prithika Ramaiyer, Katelyn M Green, Peter K Todd
EMBO Mol Med. 2021 Nov 8; 13(11): e14163. Published online 2021 Sep 20. doi: 10.15252/emmm.202114163
PMCID:
PMC8573603
AbstractArticlePDF–5.9M
10.
Major hnRNP proteins act as general TDP-43 functional modifiers both in Drosophila and human neuronal cells
Chiara Appocher, Fatemeh Mohagheghi, Sara Cappelli, Cristiana Stuani, Maurizio Romano, Fabian Feiguin, Emanuele Buratti
Nucleic Acids Res. 2017 Jul 27; 45(13): 8026–8045. Published online 2017 May 31. doi: 10.1093/nar/gkx477
PMCID:
PMC5570092
AbstractArticlePDF–6.0M
11.
Pantothenate kinase 2 interacts with PINK1 to regulate mitochondrial quality control via acetyl-CoA metabolism
Yunpeng Huang, Zhihui Wan, Yinglu Tang, Junxuan Xu, Bretton Laboret, Sree Nallamothu, Chenyu Yang, Boxiang Liu, Rongze Olivia Lu, Bingwei Lu, Juan Feng, Jing Cao, Susan Hayflick, Zhihao Wu, Bing Zhou
Nat Commun. 2022; 13: 2412. Published online 2022 May 3. doi: 10.1038/s41467-022-30178-x
PMCID:
PMC9065001
AbstractArticlePDF–5.6M
12.
Srrm234, but not canonical SR and hnRNP proteins, drive inclusion of Dscam exon 9 variable exons
Pinar Ustaoglu, Irmgard U. Haussmann, Hongzhi Liao, Antonio Torres-Mendez, Roland Arnold, Manuel Irimia, Matthias Soller
RNA. 2019 Oct; 25(10): 1353–1365. doi: 10.1261/rna.071316.119
PMCID:
PMC6800468
AbstractArticlePDF–8.9M
13.
RNA-Seq Analysis of Differential Splice Junction Usage and Intron Retentions by DEXSeq
Yafang Li, Xiayu Rao, William W. Mattox, Christopher I. Amos, Bin Liu
PLoS One. 2015; 10(9): e0136653. Published online 2015 Sep 1. doi: 10.1371/journal.pone.0136653
PMCID:
PMC4556662
AbstractArticlePDF–2.1M
14.
An Interaction Network of RNA-Binding Proteins Involved in Drosophila Oogenesis
Prashali Bansal, Johannes Madlung, Kristina Schaaf, Boris Macek, Fulvia Bono
Mol Cell Proteomics. 2020 Sep; 19(9): 1485–1502. Published online 2020 Nov 25. doi: 10.1074/mcp.RA119.001912
PMCID:
PMC8143644
AbstractArticlePDF–4.1M
15.
Modulation of the Hippo pathway and organ growth by RNA processing proteins
Jana Mach, Mardelle Atkins, Kathleen M. Gajewski, Violaine Mottier-Pavie, Leticia Sansores-Garcia, Jun Xie, Robert Andrew Mills, Weronika Kowalczyk, Leen Van Huffel, Gordon B. Mills, Georg Halder
Proc Natl Acad Sci U S A. 2018 Oct 16; 115(42): 10684–10689. Published online 2018 Sep 26. doi: 10.1073/pnas.1807325115
PMCID:
PMC6196505
AbstractArticlePDF–2.5M
16.
PINK1 and Parkin Control Localized Translation of Respiratory Chain Component mRNAs on Mitochondria Outer Membrane
Stephan Gehrke, Zhihao Wu, Michael Klinkenberg, Yaping Sun, Georg Auburger, Su Guo, Bingwei Lu
Cell Metab. Author manuscript; available in PMC 2016 Jan 6.
Published in final edited form as: Cell Metab. 2015 Jan 6; 21(1): 95–108. doi: 10.1016/j.cmet.2014.12.007
PMCID:
PMC4455944
AbstractArticlePDF–2.7M
17.
Zfrp8 forms a complex with Fragile-X Mental Retardation Protein and regulates its localization and function
William Tan, Curtis Schauder, Tatyana Naryshkina, Svetlana Minakhina, Ruth Steward
Dev Biol. Author manuscript; available in PMC 2017 Feb 15.
Published in final edited form as: Dev Biol. 2016 Feb 15; 410(2): 202–212. Published online 2016 Jan 7. doi: 10.1016/j.ydbio.2015.12.008
PMCID:
PMC4768487
AbstractArticlePDF–2.2M
18.
Cytosolic calcium regulates cytoplasmic accumulation of TDP-43 through Calpain-A and Importin α3
Jeong Hyang Park, Chang Geon Chung, Sung Soon Park, Davin Lee, Kyung Min Kim, Yeonjin Jeong, Eun Seon Kim, Jae Ho Cho, Yu-Mi Jeon, C-K James Shen, Hyung-Jun Kim, Daehee Hwang, Sung Bae Lee
eLife. 2020; 9: e60132. Published online 2020 Dec 11. doi: 10.7554/eLife.60132
PMCID:
PMC7748415
AbstractArticlePDF–6.2M
19.
ChIP-mass spectrometry captures protein interactions and modified histones associated with dosage compensation in Drosophila
C. I. Wang, A. A. Alekseyenko, G. LeRoy, A. E. H. Elia, A. A. Gorchakov, L-M. P. Britton, S. J. Elledge, P. V. Kharchenko, B. A. Garcia, M. I. Kuroda
Nat Struct Mol Biol. Author manuscript; available in PMC 2013 Aug 1.
Published in final edited form as: Nat Struct Mol Biol. 2013 Feb; 20(2): 202–209. Published online 2013 Jan 6. doi: 10.1038/nsmb.2477
PMCID:
PMC3674866
AbstractArticlePDF–1.9M
20.
Hecw controls oogenesis and neuronal homeostasis by promoting the liquid state of ribonucleoprotein particles
Valentina Fajner, Fabio Giavazzi, Simona Sala, Amanda Oldani, Emanuele Martini, Francesco Napoletano, Dario Parazzoli, Giuliana Cesare, Roberto Cerbino, Elena Maspero, Thomas Vaccari, Simona Polo
Nat Commun. 2021; 12: 5488. Published online 2021 Sep 16. doi: 10.1038/s41467-021-25809-8
PMCID:
PMC8446043
AbstractArticlePDF–9.4M

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