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Items: 1 to 20 of 96

1.
LARP4 is an RNA-binding protein that binds nuclear-encoded mitochondrial mRNAs to promote mitochondrial function
Benjamin M. Lewis, Chae Yun Cho, Hsuan-Lin Her, Orel Mizrahi, Tony Hunter, Gene W. Yeo
RNA. 2024 Mar; 30(3): 223–239. doi: 10.1261/rna.079799.123
PMCID:
PMC10870378
AbstractArticlePDF–11M
2.
Single molecule poly(A) tail-seq shows LARP4 opposes deadenylation throughout mRNA lifespan with most impact on short tails
Sandy Mattijssen, James R Iben, Tianwei Li, Steven L Coon, Richard J Maraia
eLife. 2020; 9: e59186. Published online 2020 Aug 3. doi: 10.7554/eLife.59186
PMCID:
PMC7413741
AbstractArticlePDF–3.1M
3.
Circular RNA La‐related RNA‐binding protein 4 correlates with reduced tumor stage, as well as better prognosis, and promotes chemosensitivity to doxorubicin in breast cancer
Xiaoyi Zhang, Xinyu Su, Zhe Guo, Xueqing Jiang, Xun Li
J Clin Lab Anal. 2020 Jul; 34(7): e23272. Published online 2020 Mar 18. doi: 10.1002/jcla.23272
PMCID:
PMC7370746
AbstractArticlePDF–653K
4.
circLARP4 induces cellular senescence through regulating miR‐761/RUNX3/p53/p21 signaling in hepatocellular carcinoma
Zhiqiang Chen, Xueliang Zuo, Liyong Pu, Yao Zhang, Guoyong Han, Long Zhang, Jindao Wu, Xuehao Wang
Cancer Sci. 2019 Feb; 110(2): 568–581. Published online 2019 Jan 4. doi: 10.1111/cas.13901
PMCID:
PMC6361555
AbstractArticlePDF–1.8M
5.
The RNA‐binding protein LARP4 regulates cancer cell migration and invasion
Shailaja Seetharaman, Ella Flemyng, Jiazhen Shen, Maria R. Conte, Anne J. Ridley
Cytoskeleton (Hoboken) 2016 Nov; 73(11): 680–690. Published online 2016 Sep 26. doi: 10.1002/cm.21336
PMCID:
PMC5111583
AbstractArticlePDF–633K
6.
Circular RNA LARP4 correlates with decreased Enneking stage, better histological response, and prolonged survival profiles, and it elevates chemosensitivity to cisplatin and doxorubicin via sponging microRNA‐424 in osteosarcoma
Yuhang Hu, Jiaao Gu, Hongtao Shen, Tuo Shao, Song Li, Wei Wang, Zhange Yu
J Clin Lab Anal. 2020 Feb; 34(2): e23045. Published online 2019 Oct 22. doi: 10.1002/jcla.23045
PMCID:
PMC7031593
AbstractArticlePDF–928K
7.
LARP4A recognizes polyA RNA via a novel binding mechanism mediated by disordered regions and involving the PAM2w motif, revealing interplay between PABP, LARP4A and mRNA
Isabel Cruz-Gallardo, Luigi Martino, Geoff Kelly, R Andrew Atkinson, Roberta Trotta, Stefano De Tito, Pierre Coleman, Zainab Ahdash, Yifei Gu, Tam T T Bui, Maria R Conte
Nucleic Acids Res. 2019 May 7; 47(8): 4272–4291. Published online 2019 Mar 1. doi: 10.1093/nar/gkz144
PMCID:
PMC6486636
AbstractArticlePDF–5.6M
8.
LARP4 mRNA codon-tRNA match contributes to LARP4 activity for ribosomal protein mRNA poly(A) tail length protection
Sandy Mattijssen, Aneeshkumar G Arimbasseri, James R Iben, Sergei Gaidamakov, Joowon Lee, Markus Hafner, Richard J Maraia
eLife. 2017; 6: e28889. Published online 2017 Sep 12. doi: 10.7554/eLife.28889
PMCID:
PMC5626478
AbstractArticlePDF–6.8M
9.
Circular RNA_LARP4 inhibits cell proliferation and invasion of gastric cancer by sponging miR-424-5p and regulating LATS1 expression
Jing Zhang, Hui Liu, Lidan Hou, Ge Wang, Rui Zhang, Yanxia Huang, Xiaoyu Chen, Jinshui Zhu
Mol Cancer. 2017; 16: 151. Published online 2017 Sep 11. doi: 10.1186/s12943-017-0719-3
PMCID:
PMC5594516
AbstractArticlePDF–3.7M
10.
LARP4B is an AU-rich sequence associated factor that promotes mRNA accumulation and translation
Maritta Küspert, Yasuhiro Murakawa, Katrin Schäffler, Jens T. Vanselow, Elmar Wolf, Stefan Juranek, Andreas Schlosser, Markus Landthaler, Utz Fischer
RNA. 2015 Jul; 21(7): 1294–1305. doi: 10.1261/rna.051441.115
PMCID:
PMC4478348
AbstractArticlePDF–426K
11.
Conservation of RNA chaperone activity of the human La-related proteins 4, 6 and 7
Rawaa H. Hussain, Mariam Zawawi, Mark A. Bayfield
Nucleic Acids Res. 2013 Oct; 41(18): 8715–8725. Published online 2013 Jul 25. doi: 10.1093/nar/gkt649
PMCID:
PMC3794603
AbstractArticlePDF–2.0M
12.
The LARPs, La and related RNA-binding proteins: Structures, functions and evolving perspectives
Richard J. Maraia, Sandy Mattijssen, Isabel Cruz-Gallardo, Maria R. Conte
Wiley Interdiscip Rev RNA. Author manuscript; available in PMC 2018 Nov 1.
Published in final edited form as: Wiley Interdiscip Rev RNA. 2017 Nov; 8(6): 10.1002/wrna.1430. Published online 2017 Aug 7. doi: 10.1002/wrna.1430
PMCID:
PMC5647580
AbstractArticlePDF–5.1M
13.
La-Related Protein 4 Binds Poly(A), Interacts with the Poly(A)-Binding Protein MLLE Domain via a Variant PAM2w Motif, and Can Promote mRNA Stability
Ruiqing Yang, Sergei A. Gaidamakov, Jingwei Xie, Joowon Lee, Luigi Martino, Guennadi Kozlov, Amanda K. Crawford, Amy N. Russo, Maria R. Conte, Kalle Gehring, Richard J. Maraia
Mol Cell Biol. 2011 Feb; 31(3): 542–556. Published online 2010 Nov 22. doi: 10.1128/MCB.01162-10
PMCID:
PMC3028612
AbstractArticlePDF–3.4M
14.
LARP4 Is Regulated by Tumor Necrosis Factor Alpha in a Tristetraprolin-Dependent Manner
Sandy Mattijssen, Richard J. Maraia
Mol Cell Biol. 2016 Feb 15; 36(4): 574–584. Prepublished online 2015 Dec 7. Published online 2016 Feb 1. doi: 10.1128/MCB.00804-15
PMCID:
PMC4751689
AbstractArticlePDF–3.0M
15.
The von Hippel–Lindau Cullin-RING E3 ubiquitin ligase regulates APOBEC3 cytidine deaminases
Gaël K. Scholtès, Aubrey M. Sawyer, Cristina C. Vaca, Isabelle Clerc, Meejeon Roh, Chisu Song, Richard T. D’Aquila
Transl Res. Author manuscript; available in PMC 2022 Nov 1.
Published in final edited form as: Transl Res. 2021 Nov; 237: 1–15. Published online 2021 May 15. doi: 10.1016/j.trsl.2021.05.002
PMCID:
PMC8440357
AbstractArticlePDF–628K
16.
Systematic identification of NF90 target RNAs by iCLIP analysis
Valeria Lodde, Matteo Floris, Rachel Munk, Jennifer L. Martindale, Davide Piredda, Catello Mario Panu Napodano, Francesco Cucca, Sergio Uzzau, Kotb Abdelmohsen, Myriam Gorospe, Ji Heon Noh, M. Laura Idda
Sci Rep. 2022; 12: 364. Published online 2022 Jan 10. doi: 10.1038/s41598-021-04101-1
PMCID:
PMC8748789
AbstractArticlePDF–4.2M
17.
Identification and characterization of a set of conserved and new regulators of cytoskeletal organization, cell morphology and migration
Siau Wei Bai, Maria Teresa Herrera-Abreu, Jennifer L Rohn, Victor Racine, Virginia Tajadura, Narendra Suryavanshi, Stephanie Bechtel, Stefan Wiemann, Buzz Baum, Anne J Ridley
BMC Biol. 2011; 9: 54. Published online 2011 Aug 11. doi: 10.1186/1741-7007-9-54
PMCID:
PMC3201212
AbstractArticlePDF–1.6M
18.
Fyn Regulates Binding Partners of Cyclic-AMP Dependent Protein Kinase A
Anna M. Schmoker, Samuel A. Barritt, Marion E. Weir, Jacqueline E. Mann, Tyler C. Hogan, Bryan A. Ballif, Paula B. Deming
Proteomes. 2018 Dec; 6(4): 37. Published online 2018 Sep 29. doi: 10.3390/proteomes6040037
PMCID:
PMC6313912
AbstractArticlePDF–4.8M
19.
Large-scale cDNA transfection screening for genes related to cancer development and progression
Dafang Wan, Yi Gong, Wenxin Qin, Pingping Zhang, Jinjun Li, Lin Wei, Xiaomei Zhou, Hongnian Li, Xiaokun Qiu, Fei Zhong, Liping He, Jian Yu, Genfu Yao, Huiqiu Jiang, Lianfang Qian, Ye Yu, Huiqun Shu, Xianlian Chen, Huili Xu, Minglei Guo, Zhimei Pan, Yan Chen, Chao Ge, Shengli Yang, Jianren Gu
Proc Natl Acad Sci U S A. 2004 Nov 2; 101(44): 15724–15729. Published online 2004 Oct 21. doi: 10.1073/pnas.0404089101
Correction in:
Proc Natl Acad Sci U S A. 2004 Dec 14; 101(50): 17565.
PMCID:
PMC524842
AbstractArticlePDF–245K
20.
RNF43 G659fs is an oncogenic colorectal cancer mutation and sensitizes tumor cells to PI3K/mTOR inhibition
Lishan Fang, Dane Ford-Roshon, Max Russo, Casey O’Brien, Xiaozhe Xiong, Carino Gurjao, Maximilien Grandclaudon, Srivatsan Raghavan, Steven M. Corsello, Steven A. Carr, Namrata D. Udeshi, James Berstler, Ewa Sicinska, Kimmie Ng, Marios Giannakis
Nat Commun. 2022; 13: 3181. Published online 2022 Jun 8. doi: 10.1038/s41467-022-30794-7
PMCID:
PMC9177965
AbstractArticlePDF–2.2M

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