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Items: 1 to 20 of 35

1.
A multigene family of intron lacking and containing genes, encoding for mouse ribosomal protein L7.
A Klein, O Meyuhas
Nucleic Acids Res. 1984 May 11; 12(9): 3763–3776. doi: 10.1093/nar/12.9.3763
PMCID:
PMC318788
SummaryPage BrowsePDF–1.8M
2.
Isolation and characterization of BEN, a member of the TFII-I family of DNA-binding proteins containing distinct helix–loop–helix domains
Dashzeveg Bayarsaihan, Frank H. Ruddle
Proc Natl Acad Sci U S A. 2000 Jun 20; 97(13): 7342–7347. doi: 10.1073/pnas.97.13.7342
PMCID:
PMC16547
AbstractArticlePDF–186K
3.
The mouse surfeit locus contains a very tight cluster of four "housekeeping" genes that is conserved through evolution.
T Williams, J Yon, C Huxley, M Fried
Proc Natl Acad Sci U S A. 1988 May; 85(10): 3527–3530. doi: 10.1073/pnas.85.10.3527
PMCID:
PMC280245
SummaryPage BrowsePDF–1.0M
4.
Structural and functional properties of ribosomal protein L7 from humans and rodents.
P Hemmerich, A von Mikecz, F Neumann, O Sözeri, G Wolff-Vorbeck, R Zoebelein, U Krawinkel
Nucleic Acids Res. 1993 Jan 25; 21(2): 223–231. doi: 10.1093/nar/21.2.223
PMCID:
PMC309096
SummaryPage BrowsePDF–1.8M
5.
Primary structure and characterization of an androgen-stimulated autoantigen purified from mouse seminal-vesicle secretion.
L C Yu, J L Chen, W B Tsai, Y H Chen
Biochem J. 1993 Dec 15; 296(Pt 3): 571–576. doi: 10.1042/bj2960571
PMCID:
PMC1137736
SummaryPage BrowsePDF–1.1M
6.
Ribosomal protein L7a is encoded by a gene (Surf-3) within the tightly clustered mouse surfeit locus.
A Giallongo, J Yon, M Fried
Mol Cell Biol. 1989 Jan; 9(1): 224–231. doi: 10.1128/mcb.9.1.224
PMCID:
PMC362164
SummaryPage BrowsePDF–2.1M
7.
Thalamic WNT3 Secretion Spatiotemporally Regulates the Neocortical Ribosome Signature and mRNA Translation to Specify Neocortical Cell Subtypes
Matthew L. Kraushar, Barbara Viljetic, H. R. Sagara Wijeratne, Kevin Thompson, Xinfu Jiao, Jack W. Pike, Vera Medvedeva, Matthias Groszer, Megerditch Kiledjian, Ronald P. Hart, Mladen-Roko Rasin
J Neurosci. 2015 Aug 5; 35(31): 10911–10926. doi: 10.1523/JNEUROSCI.0601-15.2015
PMCID:
PMC4524969
AbstractArticlePDF–6.3M
8.
Cochaperone immunophilin FKBP52 is critical to uterine receptivity for embryo implantation
Susanne Tranguch, Joyce Cheung-Flynn, Takiko Daikoku, Viravan Prapapanich, Marc B. Cox, Huirong Xie, Haibin Wang, Sanjoy K. Das, David F. Smith, Sudhansu K. Dey
Proc Natl Acad Sci U S A. 2005 Oct 4; 102(40): 14326–14331. Published online 2005 Sep 21. doi: 10.1073/pnas.0505775102
PMCID:
PMC1242310
AbstractArticlePDF–800K
9.
Fragile X Related Protein 1 Clusters with Ribosomes and Messenger RNAs at a Subset of Dendritic Spines in the Mouse Hippocampus
Denise Cook, Maria del Rayo Sanchez-Carbente, Claude Lachance, Danuta Radzioch, Sandra Tremblay, Edouard W. Khandjian, Luc DesGroseillers, Keith K. Murai
PLoS One. 2011; 6(10): e26120. Published online 2011 Oct 11. doi: 10.1371/journal.pone.0026120
PMCID:
PMC3191184
AbstractArticlePDF–2.9M
10.
Temporally defined neocortical translation and polysome assembly are determined by the RNA-binding protein Hu antigen R
Matthew L. Kraushar, Kevin Thompson, H. R. Sagara Wijeratne, Barbara Viljetic, Kristina Sakers, Justin W. Marson, Dimitris L. Kontoyiannis, Steven Buyske, Ronald P. Hart, Mladen-Roko Rasin
Proc Natl Acad Sci U S A. 2014 Sep 9; 111(36): E3815–E3824. Published online 2014 Aug 25. doi: 10.1073/pnas.1408305111
PMCID:
PMC4246959
AbstractArticlePDF–2.2M
11.
Protein translation rate determines neocortical neuron fate
Ekaterina Borisova, Andrew G. Newman, Marta Couce Iglesias, Rike Dannenberg, Theres Schaub, Bo Qin, Alexandra Rusanova, Marisa Brockmann, Janina Koch, Marieatou Daniels, Paul Turko, Olaf Jahn, David R. Kaplan, Marta Rosário, Takao Iwawaki, Christian M. T. Spahn, Christian Rosenmund, David Meierhofer, Matthew L. Kraushar, Victor Tarabykin, Mateusz C. Ambrozkiewicz
Nat Commun. 2024; 15: 4879. Published online 2024 Jun 7. doi: 10.1038/s41467-024-49198-w
PMCID:
PMC11161512
AbstractArticlePDF–17M
12.
Nucleophosmin Serves as a Rate-Limiting Nuclear Export Chaperone for the Mammalian Ribosome
Leonard B. Maggi, Jr., Michael Kuchenruether, David Y. A. Dadey, Rachel M. Schwope, Silvia Grisendi, R. Reid Townsend, Pier Paolo Pandolfi, Jason D. Weber
Mol Cell Biol. 2008 Dec; 28(23): 7050–7065. Published online 2008 Sep 22. doi: 10.1128/MCB.01548-07
PMCID:
PMC2593371
AbstractArticlePDF–2.0M
13.
Ribosome mediated specificity in Hox mRNA translation and vertebrate tissue patterning
Nadya Kondrashov, Aya Pusic, Craig R. Stumpf, Kunihiko Shimizu, Andrew C. Hsieh, Junko Ishijima, Toshihiko Shiroishi, Maria Barna
Cell. Author manuscript; available in PMC 2015 May 27.
Published in final edited form as: Cell. 2011 Apr 29; 145(3): 383–397. doi: 10.1016/j.cell.2011.03.028
PMCID:
PMC4445650
AbstractArticlePDF–1.5M
14.
Elucidation of the 14-3-3ζ interactome reveals critical roles of RNA-splicing factors during adipogenesis
Yves Mugabo, Mina Sadeghi, Nancy N. Fang, Thibault Mayor, Gareth E. Lim
J Biol Chem. 2018 May 4; 293(18): 6736–6750. Published online 2018 Mar 12. doi: 10.1074/jbc.M117.816272
PMCID:
PMC5936800
AbstractArticlePDF–2.4M
15.
Interaction of tau with the RNA-Binding Protein TIA1 Regulates tau Pathophysiology and Toxicity
Tara Vanderweyde, Daniel J. Apicco, Katherine Youmans-Kidder, Peter E.A. Ash, Casey Cook, Edroaldo Lummertz da Rocha, Karen Jansen-West, Alissa A. Frame, Allison Citro, John D. Leszyk, Pavel Ivanov, Jose F. Abisambra, Martin Steffen, Hu Li, Leonard Petrucelli, Benjamin Wolozin
Cell Rep. Author manuscript; available in PMC 2017 Feb 24.
Published in final edited form as: Cell Rep. 2016 May 17; 15(7): 1455–1466. Published online 2016 May 6. doi: 10.1016/j.celrep.2016.04.045
PMCID:
PMC5325702
AbstractArticlePDF–2.1M
16.
Beads-free protein immunoprecipitation for a mass spectrometry-based interactome and posttranslational modifications analysis
Michal Mikula, Tymon Rubel, Jakub Karczmarski, Malgorzata Statkiewicz, Karol Bomsztyk, Jerzy Ostrowski
Proteome Sci. 2015; 13: 23. Published online 2015 Sep 2. doi: 10.1186/s12953-015-0079-0
PMCID:
PMC4557753
AbstractArticlePDF–1.5M
17.
Cdh1-APC Regulates Protein Synthesis and Stress Granules in Neurons through an FMRP-Dependent Mechanism
Arielle N. Valdez-Sinon, Austin Lai, Liang Shi, Carly L. Lancaster, Avanti Gokhale, Victor Faundez, Gary J. Bassell
iScience. 2020 May 22; 23(5): 101132. Published online 2020 May 1. doi: 10.1016/j.isci.2020.101132
PMCID:
PMC7236060
AbstractArticlePDF–6.1M
18.
Interactome Analysis Reveals Regulator of G Protein Signaling 14 (RGS14) is a Novel Calcium/Calmodulin (Ca2+/CaM) and CaM Kinase II (CaMKII) Binding Partner
Paul R. Evans, Kyle J. Gerber, Eric B. Dammer, Duc M. Duong, Devrishi Goswami, Daniel J. Lustberg, Juan Zou, Jenny J. Yang, Serena M. Dudek, Patrick R. Griffin, Nicholas T. Seyfried, John R. Hepler
J Proteome Res. Author manuscript; available in PMC 2019 Jun 7.
Published in final edited form as: J Proteome Res. 2018 Apr 6; 17(4): 1700–1711. Published online 2018 Mar 20. doi: 10.1021/acs.jproteome.8b00027
PMCID:
PMC6554723
AbstractArticlePDF–2.0M
19.
New roles for the de-ubiquitylating enzyme OTUD4 in an RNA–protein network and RNA granules
Richa Das, Lukas Schwintzer, Stanislav Vinopal, Eva Aguado Roca, Marc Sylvester, Ana-Maria Oprisoreanu, Susanne Schoch, Frank Bradke, Meike Broemer
J Cell Sci. 2019 Jun 15; 132(12): jcs229252. Published online 2019 Jun 17. doi: 10.1242/jcs.229252
PMCID:
PMC6602300
AbstractArticle
20.
The Deubiquitinating Enzyme USP48 Interacts with the Retinal Degeneration-Associated Proteins UNC119a and ARL3
Laura Sánchez-Bellver, Andrea Férriz-Gordillo, Marc Carrillo-Pz, Laura Rabanal, Francesc R. Garcia-Gonzalo, Gemma Marfany
Int J Mol Sci. 2022 Oct; 23(20): 12527. Published online 2022 Oct 19. doi: 10.3390/ijms232012527
PMCID:
PMC9603860
AbstractArticlePDF–3.4M

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