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Items: 1 to 20 of 37

1.
Binding of factor VIIa to tissue factor induces alterations in gene expression in human fibroblast cells: Up-regulation of poly(A) polymerase
Usha R. Pendurthi, Deoraj Alok, L. Vijaya Mohan Rao
Proc Natl Acad Sci U S A. 1997 Nov 11; 94(23): 12598–12603. doi: 10.1073/pnas.94.23.12598
PMCID:
PMC25051
AbstractArticlePDF–344K
2.
Poly(A) Polymerase and the Nuclear Poly(A) Binding Protein, PABPN1, Coordinate the Splicing and Degradation of a Subset of Human Pre-mRNAs
Lisa Muniz, Lee Davidson, Steven West
Mol Cell Biol. 2015 Jul; 35(13): 2218–2230. Prepublished online 2015 Apr 20. Published online 2015 Jun 4. doi: 10.1128/MCB.00123-15
PMCID:
PMC4456446
AbstractArticlePDF–1.7M
3.
CstF-64 and 3′-UTR cis-element determine Star-PAP specificity for target mRNA selection by excluding PAPα
Divya T. Kandala, Nimmy Mohan, Vivekanand A, Sudheesh AP, Reshmi G, Rakesh S. Laishram
Nucleic Acids Res. 2016 Jan 29; 44(2): 811–823. Published online 2015 Oct 22. doi: 10.1093/nar/gkv1074
Correction in:
Nucleic Acids Res. 2019 Feb 20; 47(3): 1598.
PMCID:
PMC4737136
AbstractArticlePDF–5.4M
4.
Regulation of poly(A) polymerase by 14-3-3ε
Hana Kim, June Hyung Lee, Younghoon Lee
EMBO J. 2003 Oct 1; 22(19): 5208–5219. doi: 10.1093/emboj/cdg486
PMCID:
PMC204469
AbstractArticlePDF–378K
5.
The nuclear poly(A) binding protein of mammals, but not of fission yeast, participates in mRNA polyadenylation
Uwe Kühn, Juliane Buschmann, Elmar Wahle
RNA. 2017 Apr; 23(4): 473–482. doi: 10.1261/rna.057026.116
PMCID:
PMC5340911
AbstractArticlePDF–862K
6.
Multiple forms of poly(A) polymerases in human cells.
A C Thuresson, J Aström, A Aström, K O Grönvik, A Virtanen
Proc Natl Acad Sci U S A. 1994 Feb 1; 91(3): 979–983. doi: 10.1073/pnas.91.3.979
PMCID:
PMC521437
SummaryPage BrowsePDF–1.2M
7.
Tat-dependent occlusion of the HIV poly(A) site.
C Weichs an der Glon, M Ashe, J Eggermont, N J Proudfoot
EMBO J. 1993 May; 12(5): 2119–2128. doi: 10.1002/j.1460-2075.1993.tb05860.x
PMCID:
PMC413433
SummaryPage BrowsePDF–2.4M
8.
Human Fip1 is a subunit of CPSF that binds to U-rich RNA elements and stimulates poly(A) polymerase
Isabelle Kaufmann, Georges Martin, Arno Friedlein, Hanno Langen, Walter Keller
EMBO J. 2004 Feb 11; 23(3): 616–626. Published online 2004 Jan 29. doi: 10.1038/sj.emboj.7600070
PMCID:
PMC1271804
AbstractArticlePDF–580K
9.
Inositol 1,4,5-Triphosphate Receptor-binding Protein Released with Inositol 1,4,5-Triphosphate (IRBIT) Associates with Components of the mRNA 3′ Processing Machinery in a Phosphorylation-dependent Manner and Inhibits Polyadenylation
Hélène Kiefer, Akihiro Mizutani, Shun-Ichiro Iemura, Tohru Natsume, Hideaki Ando, Yukiko Kuroda, Katsuhiko Mikoshiba
J Biol Chem. 2009 Apr 17; 284(16): 10694–10705. doi: 10.1074/jbc.M807136200
PMCID:
PMC2667756
AbstractArticlePDF–808K
10.
A promiscuous biotin ligase fusion protein identifies proximal and interacting proteins in mammalian cells
Kyle J. Roux, Dae In Kim, Manfred Raida, Brian Burke
J Cell Biol. 2012 Mar 19; 196(6): 801–810. doi: 10.1083/jcb.201112098
PMCID:
PMC3308701
AbstractArticlePDF–1.6M
11.
Genome-wide CRISPR screens using isogenic cells reveal vulnerabilities conferred by loss of tumor suppressors
Xu Feng, Mengfan Tang, Merve Dede, Dan Su, Guangsheng Pei, Dadi Jiang, Chao Wang, Zhen Chen, Mi Li, Litong Nie, Yun Xiong, Siting Li, Jeong-Min Park, Huimin Zhang, Min Huang, Klaudia Szymonowicz, Zhongming Zhao, Traver Hart, Junjie Chen
Sci Adv. 2022 May; 8(19): eabm6638. Published online 2022 May 13. doi: 10.1126/sciadv.abm6638
PMCID:
PMC9106303
AbstractArticlePDF–918K
12.
Quantitative Lys-ϵ-Gly-Gly (diGly) Proteomics Coupled with Inducible RNAi Reveals Ubiquitin-mediated Proteolysis of DNA Damage-inducible Transcript 4 (DDIT4) by the E3 Ligase HUWE1
Joel W. Thompson, Jane Nagel, Sjouke Hoving, Bertran Gerrits, Andreas Bauer, Jason R. Thomas, Marc W. Kirschner, Markus Schirle, Sarah J. Luchansky
J Biol Chem. 2014 Oct 17; 289(42): 28942–28955. Published online 2014 Aug 21. doi: 10.1074/jbc.M114.573352
PMCID:
PMC4200252
AbstractArticlePDF–1.6M
13.
ARHGAP24 represses β-catenin transactivation-induced invasiveness in hepatocellular carcinoma mainly by acting as a GTPase-independent scaffold
Wenjing Yang, Beili Wang, Qian Yu, Te Liu, Tong Li, Tongtong Tian, Anli Jin, Lin Ding, Wei Chen, Hao Wang, Jingrong Xian, Baishen Pan, Jian Zhou, Jia Fan, Xinrong Yang, Wei Guo
Theranostics. 2022; 12(14): 6189–6206. Published online 2022 Aug 21. doi: 10.7150/thno.72134
PMCID:
PMC9475462
AbstractArticlePDF–4.6M
14.
Nuclear actin interactome analysis links actin to KAT14 histone acetyl transferase and mRNA splicing
Tiina Viita, Salla Kyheröinen, Bina Prajapati, Jori Virtanen, Mikko J. Frilander, Markku Varjosalo, Maria K. Vartiainen
J Cell Sci. 2019 Apr 15; 132(8): jcs226852. Published online 2019 Apr 17. doi: 10.1242/jcs.226852
PMCID:
PMC6503952
AbstractArticle
15.
New interaction partners for Nek4.1 and Nek4.2 isoforms: from the DNA damage response to RNA splicing
Fernanda Luisa Basei, Gabriela Vaz Meirelles, Germanna Lima Righetto, Deivid Lucas dos Santos Migueleti, Juliana Helena Costa Smetana, Jörg Kobarg
Proteome Sci. 2015; 13: 11. Published online 2015 Feb 26. doi: 10.1186/s12953-015-0065-6
PMCID:
PMC4367857
AbstractArticlePDF–3.1M
16.
Functional Proteomics Mapping of a Human Signaling Pathway
Frédéric Colland, Xavier Jacq, Virginie Trouplin, Christelle Mougin, Caroline Groizeleau, Alexandre Hamburger, Alain Meil, Jérôme Wojcik, Pierre Legrain, Jean-Michel Gauthier
Genome Res. 2004 Jul; 14(7): 1324–1332. doi: 10.1101/gr.2334104
PMCID:
PMC442148
AbstractArticlePDF–290K
17.
Large-scale characterization of HeLa cell nuclear phosphoproteins
Sean A. Beausoleil, Mark Jedrychowski, Daniel Schwartz, Joshua E. Elias, Judit Villén, Jiaxu Li, Martin A. Cohn, Lewis C. Cantley, Steven P. Gygi
Proc Natl Acad Sci U S A. 2004 Aug 17; 101(33): 12130–12135. Published online 2004 Aug 9. doi: 10.1073/pnas.0404720101
PMCID:
PMC514446
AbstractArticlePDF–475K
18.
Mammalian APE1 controls miRNA processing and its interactome is linked to cancer RNA metabolism
Giulia Antoniali, Fabrizio Serra, Lisa Lirussi, Mikiei Tanaka, Chiara D’Ambrosio, Shiheng Zhang, Slobodanka Radovic, Emiliano Dalla, Yari Ciani, Andrea Scaloni, Mengxia Li, Silvano Piazza, Gianluca Tell
Nat Commun. 2017; 8: 797. Published online 2017 Oct 6. doi: 10.1038/s41467-017-00842-8
PMCID:
PMC5630600
AbstractArticlePDF–2.3M
19.
N-Terminal Acetyltransferase Naa40p Whereabouts Put into N-Terminal Proteoform Perspective
Veronique Jonckheere, Petra Van Damme
Int J Mol Sci. 2021 Apr; 22(7): 3690. Published online 2021 Apr 1. doi: 10.3390/ijms22073690
PMCID:
PMC8037211
AbstractArticlePDF–6.5M
20.
Synthetic lethal and resistance interactions with BET bromodomain inhibitors in triple-negative breast cancer
Shaokun Shu, Hua-Jun Wu, Jennifer Y. Ge, Rhamy Zeid, Isaac S. Harris, Bojana Jovanović, Katherine Murphy, Binbin Wang, Xintao Qiu, Jennifer E. Endress, Jaime Reyes, Klothilda Lim, Alba Font-Tello, Sudeepa Syamala, Tengfei Xiao, Chandra Sekhar Reddy Chilamakuri, Evangelia K. Papachristou, Clive D’Santos, Jayati Anand, Kunihiko Hinohara, Wei Li, Thomas O. McDonald, Adrienne Luoma, Rebecca J. Modiste, Quang-De Nguyen, Brittany Michel, Paloma Cejas, Cigall Kadoch, Jacob D. Jaffe, Kai W. Wucherpfennig, Jun Qi, X. Shirley Liu, Henry Long, Myles Brown, Jason S. Carroll, Joan S. Brugge, James Bradner, Franziska Michor, Kornelia Polyak
Mol Cell. Author manuscript; available in PMC 2021 Jun 18.
Published in final edited form as: Mol Cell. 2020 Jun 18; 78(6): 1096–1113.e8. Published online 2020 May 15. doi: 10.1016/j.molcel.2020.04.027
PMCID:
PMC7306005
AbstractArticlePDF–3.2M

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