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Items: 1 to 20 of 188

1.
Gender-specific association between the cytoplasmic poly(A) binding protein 4 rs4660293 single nucleotide polymorphism and serum lipid levels
JIAN WU, RUI-XING YIN, TAO GUO, QUAN-ZHEN LIN, SHAO-WEN SHEN, JIA-QI SUN, GUANG-YUAN SHI, JIN-ZHEN WU, DE-ZHAI YANG, WEI-XIONG LIN
Mol Med Rep. 2015 Sep; 12(3): 3476–3486. Published online 2015 May 22. doi: 10.3892/mmr.2015.3823
PMCID:
PMC4526048
AbstractArticlePDF–1.3M
2.
Importin α-Mediated Nuclear Import of Cytoplasmic Poly(A) Binding Protein Occurs as a Direct Consequence of Cytoplasmic mRNA Depletion
G. Renuka Kumar, Leona Shum, Britt A. Glaunsinger
Mol Cell Biol. 2011 Aug; 31(15): 3113–3125. doi: 10.1128/MCB.05402-11
PMCID:
PMC3147611
AbstractArticlePDF–4.0M
3.
iPABP, an inducible poly(A)-binding protein detected in activated human T cells.
H Yang, C S Duckett, T Lindsten
Mol Cell Biol. 1995 Dec; 15(12): 6770–6776. doi: 10.1128/mcb.15.12.6770
PMCID:
PMC230930
SummaryPDF–945K
4.
Gene variants of coagulation related proteins that interact with SARS-CoV-2
David Holcomb, Aikaterini Alexaki, Nancy Hernandez, Ryan Hunt, Kyle Laurie, Jacob Kames, Nobuko Hamasaki-Katagiri, Anton A. Komar, Michael DiCuccio, Chava Kimchi-Sarfaty
PLoS Comput Biol. 2021 Mar; 17(3): e1008805. Published online 2021 Mar 17. doi: 10.1371/journal.pcbi.1008805
PMCID:
PMC8007013
AbstractArticlePDF–2.1M
5.
Depletion of Nuclear Poly(A) Binding Protein PABPN1 Produces a Compensatory Response by Cytoplasmic PABP4 and PABP5 in Cultured Human Cells
Rumpa Biswas Bhattacharjee, Jnanankur Bag
PLoS One. 2012; 7(12): e53036. Published online 2012 Dec 31. doi: 10.1371/journal.pone.0053036
PMCID:
PMC3534090
AbstractArticlePDF–2.8M
6.
PABPC4 Broadly Inhibits Coronavirus Replication by Degrading Nucleocapsid Protein through Selective Autophagy
Yajuan Jiao, Ning Kong, Hua Wang, Dage Sun, Sujie Dong, Xiaoyong Chen, Hao Zheng, Wu Tong, Hai Yu, Lingxue Yu, Yaowei Huang, Huan Wang, Baokun Sui, Ling Zhao, Ying Liao, Wen Zhang, Guangzhi Tong, Tongling Shan
Microbiol Spectr. 2021 Sep-Oct; 9(2): e00908-21. Published online 2021 Oct 6. doi: 10.1128/Spectrum.00908-21
PMCID:
PMC8510267
AbstractArticlePDF–4.8M
7.
MKRN3-mediated ubiquitination of Poly(A)-binding proteins modulates the stability and translation of GNRH1 mRNA in mammalian puberty
Chuanyin Li, Tianting Han, Qingrun Li, Menghuan Zhang, Rong Guo, Yun Yang, Wenli Lu, Zhengwei Li, Chao Peng, Ping Wu, Xiaoxu Tian, Qinqin Wang, Yuexiang Wang, Vincent Zhou, Ziyan Han, Hecheng Li, Feng Wang, Ronggui Hu
Nucleic Acids Res. 2021 Apr 19; 49(7): 3796–3813. Published online 2021 Mar 21. doi: 10.1093/nar/gkab155
PMCID:
PMC8053111
AbstractArticlePDF–3.8M
8.
Nuclear relocalisation of cytoplasmic poly(A)-binding proteins PABP1 and PABP4 in response to UV irradiation reveals mRNA-dependent export of metazoan PABPs
Hannah M. Burgess, William A. Richardson, Ross C. Anderson, Christine Salaun, Sheila V. Graham, Nicola K. Gray
J Cell Sci. 2011 Oct 1; 124(19): 3344–3355. doi: 10.1242/jcs.087692
PMCID:
PMC3178455
AbstractArticle
9.
HIV- 1 Protease Inhibits Cap- and Poly(A)-Dependent Translation upon eIF4GI and PABP Cleavage
Alfredo Castelló, David Franco, Pablo Moral-López, Juan J. Berlanga, Enrique Álvarez, Eckard Wimmer, Luis Carrasco
PLoS One. 2009; 4(11): e7997. Published online 2009 Nov 24. doi: 10.1371/journal.pone.0007997
PMCID:
PMC2776998
AbstractArticlePDF–745K
10.
Chromosomal localization of three human poly(A)-binding protein genes and four related pseudogenes
Chloé Féral, Marie-Geneviève Mattéi, André Pawlak, Georges Guellaën
Hum Genet. Author manuscript; available in PMC 2007 May 10.
Published in final edited form as: Hum Genet. 1999 Oct; 105(4): 347–353. doi: 10.1007/s004399900148
PMCID:
PMC1865476
AbstractArticle
11.
O‐GlcNAcylated LARP1 positively regulated by circCLNS1A facilitates hepatoblastoma progression through DKK4/β‐catenin signalling
Zhongqi Cui, Jiangtu He, Jiabei Zhu, Wenxuan Ni, Li Liu, Zhixuan Bian, Siwei Mao, Song Gu, Yuhua Shan, Zhexuan Chu, Qi Wu, Jiayi Lu, Ya Liu, Fenyong Sun, Qiuhui Pan, Yue Zhang, Nan Huang, Ji Ma
Clin Transl Med. 2023 Apr; 13(4): e1239. Published online 2023 Apr 17. doi: 10.1002/ctm2.1239
PMCID:
PMC10111636
AbstractArticlePDF–10M
12.
Prion protein is required for tumor necrosis factor α (TNFα)-triggered nuclear factor κB (NF-κB) signaling and cytokine production
Gui-Ru Wu, Tian-Chen Mu, Zhen-Xing Gao, Jun Wang, Man-Sun Sy, Chao-Yang Li
J Biol Chem. 2017 Nov 17; 292(46): 18747–18759. Published online 2017 Sep 12. doi: 10.1074/jbc.M117.787283
PMCID:
PMC5704461
AbstractArticlePDF–2.9M
13.
Epstein-Barr Virus Immediate-Early Protein Zta Co-Opts Mitochondrial Single-Stranded DNA Binding Protein To Promote Viral and Inhibit Mitochondrial DNA Replication
Andreas Wiedmer, Pu Wang, Jing Zhou, Andrew J. Rennekamp, Valeria Tiranti, Massimo Zeviani, Paul M. Lieberman
J Virol. 2008 May; 82(9): 4647–4655. Published online 2008 Feb 27. doi: 10.1128/JVI.02198-07
PMCID:
PMC2293061
AbstractArticlePDF–783K
14.
miRNA repression involves GW182-mediated recruitment of CCR4–NOT through conserved W-containing motifs
Marina Chekulaeva, Hansruedi Mathys, Jakob T Zipprich, Jan Attig, Marija Colic, Roy Parker, Witold Filipowicz
Nat Struct Mol Biol. Author manuscript; available in PMC 2014 Jan 8.
Published in final edited form as: Nat Struct Mol Biol. 2011 Oct 7; 18(11): 10.1038/nsmb.2166. Published online 2011 Oct 7. doi: 10.1038/nsmb.2166
PMCID:
PMC3885283
AbstractArticlePDF–2.3M
15.
RNF168 and USP10 regulate topoisomerase IIα function via opposing effects on its ubiquitylation
Kiran Kumar Naidu Guturi, Miyuki Bohgaki, Toshiyuki Bohgaki, Tharan Srikumar, Deborah Ng, Ramya Kumareswaran, Samah El Ghamrasni, Justin Jeon, Parasvi Patel, Mohamed Saad Eldin, Rob Bristow, Peter Cheung, Grant S. Stewart, Brian Raught, Anne Hakem, Razqallah Hakem
Nat Commun. 2016; 7: 12638. Published online 2016 Aug 25. doi: 10.1038/ncomms12638
PMCID:
PMC5007378
AbstractArticlePDF–1.7M
16.
Meta-analysis of genome-wide association studies in >80,000 subjects identifies multiple loci for C-reactive protein levels
Abbas Dehghan, Josée Dupuis, Maja Barbalic, Joshua C Bis, Gudny Eiriksdottir, Chen Lu, Niina Pellikka, Henri Wallaschofski, Johannes Kettunen, Peter Henneman, Jens Baumert, David P Strachan, Christian Fuchsberger, Veronique Vitart, James F Wilson, Guillaume Paré, Silvia Naitza, Megan E Rudock, Ida Surakka, Eco JC de Geus, Behrooz Z Alizadeh, Jack Guralnik, Alan Shuldiner, Toshiko Tanaka, Robert YL Zee, Renate B Schnabel, Vijay Nambi, Maryam Kavousi, Samuli Ripatti, Matthias Nauck, Nicholas L Smith, Albert V Smith, Jouko Sundvall, Paul Scheet, Yongmei Liu, Aimo Ruokonen, Lynda M Rose, Martin G Larson, Ron C Hoogeveen, Nelson B Freimer, Alexander Teumer, Russell P Tracy, Lenore J Launer, Julie E Buring, Jennifer F Yamamoto, Aaron R Folsom, Eric JG Sijbrands, James Pankow, Paul Elliott, John F Keaney, Wei Sun, Antti-Pekka Sarin, João D Fontes, Sunita Badola, Brad C Astor, Albert Hofman, Anneli Pouta, Karl Werdan, Karin H Greiser, Oliver Kuss, Henriette E Meyer zu Schwabedissen, Joachim Thiery, Yalda Jamshidi, Ilja M Nolte, Nicole Soranzo, Timothy D Spector, Henry Völzke, Alexander N Parker, Thor Aspelund, David Bates, Lauren Young, Kim Tsui, David S Siscovick, Xiuqing Guo, Jerome I Rotter, Manuela Uda, David Schlessinger, Igor Rudan, Andrew A Hicks, Brenda W Penninx, Barbara Thorand, Christian Gieger, Joe Coresh, Gonneke Willemsen, Tamara B Harris, Andre G Uitterlinden, Marjo-Riitta Järvelin, Kenneth Rice, Dörte Radke, Veikko Salomaa, Ko Willems van Dijk, Eric Boerwinkle, Ramachandran S Vasan, Luigi Ferrucci, Quince D Gibson, Stefania Bandinelli, Harold Snieder, Dorret I Boomsma, Xiangjun Xiao, Harry Campbell, Caroline Hayward, Peter P Pramstaller, Cornelia M van Duijn, Leena Peltonen, Bruce M Psaty, Vilmundur Gudnason, Paul M Ridker, Georg Homuth, Wolfgang Koenig, Christie M Ballantyne, Jacqueline CM Witteman, Emelia J Benjamin, Markus Perola, Daniel I Chasman
Circulation. Author manuscript; available in PMC 2011 Aug 1.
Published in final edited form as: Circulation. 2011 Feb 22; 123(7): 731–738. Published online 2011 Feb 7. doi: 10.1161/CIRCULATIONAHA.110.948570
PMCID:
PMC3147232
AbstractArticlePDF–336K
17.
A proteomics approach for the identification of cullin-9 (CUL9) related signaling pathways in induced pluripotent stem cell models
Natalya A. Ortolano, Alejandra I. Romero-Morales, Megan L. Rasmussen, Caroline Bodnya, Leigh A. Kline, Piyush Joshi, Jon P. Connelly, Kristie L. Rose, Shondra M. Pruett-Miller, Vivian Gama
PLoS One. 2021; 16(3): e0248000. Published online 2021 Mar 11. doi: 10.1371/journal.pone.0248000
PMCID:
PMC7951927
AbstractArticlePDF–3.8M
18.
Proline-rich Sequence Recognition: II. PROTEOMICS ANALYSIS OF Tsg101 UBIQUITIN-E2-LIKE VARIANT (UEV) INTERACTIONS
Andreas Schlundt, Jana Sticht, Kirill Piotukh, Daniela Kosslick, Nadin Jahnke, Sandro Keller, Michael Schuemann, Eberhard Krause, Christian Freund
Mol Cell Proteomics. 2009 Nov; 8(11): 2474–2486. Published online 2009 Jun 20. doi: 10.1074/mcp.M800337-MCP200
PMCID:
PMC2773715
AbstractArticlePDF–529K
19.
An unexpected role for BAG3 in regulating PARP1 ubiquitination in oxidative stress-related endothelial damage
Naijin Zhang, Ying Zhang, Wei Miao, Chuning Shi, Zihan Chen, Boquan Wu, Yuanming Zou, Qiushi Ma, Shilong You, Saien Lu, Xinyue Huang, Jingwei Liu, Jiaqi Xu, Liu Cao, Yingxian Sun
Redox Biol. 2022 Apr; 50: 102238. Published online 2022 Jan 17. doi: 10.1016/j.redox.2022.102238
PMCID:
PMC8783151
AbstractArticlePDF–9.4M
20.
ZBTB10 binds the telomeric variant repeat TTGGGG and interacts with TRF2
Alina Bluhm, Nikenza Viceconte, Fudong Li, Grishma Rane, Sandra Ritz, Suman Wang, Michal Levin, Yunyu Shi, Dennis Kappei, Falk Butter
Nucleic Acids Res. 2019 Feb 28; 47(4): 1896–1907. Published online 2019 Jan 10. doi: 10.1093/nar/gky1289
PMCID:
PMC6393293
AbstractArticlePDF–4.9M

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