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Items: 17

1.
K63-linked ubiquitination regulates RIPK1 kinase activity to prevent cell death during embryogenesis and inflammation
Yong Tang, Hailin Tu, Jie Zhang, Xueqiang Zhao, Yini Wang, Jun Qin, Xin Lin
Nat Commun. 2019; 10: 4157. Published online 2019 Sep 13. doi: 10.1038/s41467-019-12033-8
PMCID:
PMC6744441
AbstractArticlePDF–7.9M
2.
Ubiquitination of RIPK1 suppresses programmed cell death by regulating RIPK1 kinase activation during embryogenesis
Xixi Zhang, Haiwei Zhang, Chengxian Xu, Xiaoming Li, Ming Li, Xiaoxia Wu, Wenjuan Pu, Bin Zhou, Haikun Wang, Dali Li, Qiurong Ding, Hao Ying, Hui Wang, Haibing Zhang
Nat Commun. 2019; 10: 4158. Published online 2019 Sep 13. doi: 10.1038/s41467-019-11839-w
PMCID:
PMC6744433
AbstractArticlePDF–5.4M
3.
RIPK3 mediates renal tubular epithelial cell apoptosis in endotoxin-induced acute kidney injury
Shu Zhang, Ruizhao Li, Wei Dong, Huan Yang, Li Zhang, Yuanhan Chen, Weidong Wang, Chunling Li, Yanhua Wu, Zhiming Ye, Xingchen Zhao, Zhilian Li, Mengxi Zhang, Shuangxin Liu, Xinling Liang
Mol Med Rep. 2019 Aug; 20(2): 1613–1620. Published online 2019 Jun 24. doi: 10.3892/mmr.2019.10416
PMCID:
PMC6625383
AbstractArticlePDF–903K
4.
Microarray analysis of Foxa2 mutant mouse embryos reveals novel gene expression and inductive roles for the gastrula organizer and its derivatives
Owen J Tamplin, Doris Kinzel, Brian J Cox, Christine E Bell, Janet Rossant, Heiko Lickert
BMC Genomics. 2008; 9: 511. Published online 2008 Oct 30. doi: 10.1186/1471-2164-9-511
PMCID:
PMC2605479
AbstractArticlePDF–1.7M
5.
Kinase RIP3 Is Dispensable for Normal NF-κBs, Signaling by the B-Cell and T-Cell Receptors, Tumor Necrosis Factor Receptor 1, and Toll-Like Receptors 2 and 4
Kim Newton, Xiaoqing Sun, Vishva M. Dixit
Mol Cell Biol. 2004 Feb; 24(4): 1464–1469. doi: 10.1128/MCB.24.4.1464-1469.2004
PMCID:
PMC344190
AbstractArticlePDF–291K
6.
Mouse Receptor Interacting Protein 3 Does Not Contain a Caspase-Recruiting or a Death Domain but Induces Apoptosis and Activates NF-κB
Nanette J. Pazdernik, David B. Donner, Mark G. Goebl, Maureen A. Harrington
Mol Cell Biol. 1999 Oct; 19(10): 6500–6508. doi: 10.1128/mcb.19.10.6500
PMCID:
PMC84620
AbstractArticlePDF–1.3M
7.
TRADD Mediates RIPK1-Independent Necroptosis Induced by Tumor Necrosis Factor
Lili Wang, Xixi Chang, Jinli Feng, Jiyun Yu, Guozhu Chen
Front Cell Dev Biol. 2019; 7: 393. Published online 2020 Jan 22. doi: 10.3389/fcell.2019.00393
PMCID:
PMC6987388
AbstractArticlePDF–3.6M
8.
Regulated necrosis-related molecule mRNA expression in humans and mice and in murine acute tissue injury and systemic autoimmunity leading to progressive organ damage, and progressive fibrosis
Mohsen Honarpisheh, Jyaysi Desai, Julian A. Marschner, Marc Weidenbusch, Maciej Lech, Volker Vielhauer, Hans-Joachim Anders, Shrikant R. Mulay
Biosci Rep. 2016 Dec; 36(6): e00425. Prepublished online 2016 Nov 3. Published online 2016 Dec 9. doi: 10.1042/BSR20160336
PMCID:
PMC5146826
AbstractArticlePDF–2.0M
9.
The necroptosis-inducing kinase RIPK3 dampens adipose tissue inflammation and glucose intolerance
Jérémie Gautheron, Mihael Vucur, Anne T. Schneider, Ilenia Severi, Christoph Roderburg, Sanchari Roy, Matthias Bartneck, Peter Schrammen, Mauricio Berriel Diaz, Josef Ehling, Felix Gremse, Felix Heymann, Christiane Koppe, Twan Lammers, Fabian Kiessling, Niels Van Best, Oliver Pabst, Gilles Courtois, Andreas Linkermann, Stefan Krautwald, Ulf P. Neumann, Frank Tacke, Christian Trautwein, Douglas R. Green, Thomas Longerich, Norbert Frey, Mark Luedde, Matthias Bluher, Stephan Herzig, Mathias Heikenwalder, Tom Luedde
Nat Commun. 2016; 7: 11869. Published online 2016 Jun 21. doi: 10.1038/ncomms11869
PMCID:
PMC4919522
AbstractArticlePDF–4.1M
10.
Methylation-dependent loss of RIP3 expression in cancer represses programmed necrosis in response to chemotherapeutics
Gi-Bang Koo, Michael J Morgan, Da-Gyum Lee, Woo-Jung Kim, Jung-Ho Yoon, Ja Seung Koo, Seung Il Kim, Soo Jung Kim, Mi Kwon Son, Soon Sun Hong, Jean M Mulcahy Levy, Daniel A Pollyea, Craig T Jordan, Pearlly Yan, David Frankhouser, Deedra Nicolet, Kati Maharry, Guido Marcucci, Kyeong Sook Choi, Hyeseong Cho, Andrew Thorburn, You-Sun Kim
Cell Res. 2015 Jun; 25(6): 707–725. Published online 2015 May 8. doi: 10.1038/cr.2015.56
PMCID:
PMC4456623
AbstractArticlePDF–1.7M
11.
Revisiting the Identification of Canonical Splice Isoforms through Integration of Functional Genomics and Proteomics Evidence
Hong-Dong Li, Rajasree Menon, Gilbert S. Omenn, Yuanfang Guan
Proteomics. Author manuscript; available in PMC 2015 Dec 1.
Published in final edited form as: Proteomics. 2014 Dec; 14(0): 2709–2718. Published online 2014 Nov 17. doi: 10.1002/pmic.201400170
PMCID:
PMC4372202
AbstractArticlePDF–503K
12.
Protease Activity of Procaspase-8 Is Essential for Cell Survival by Inhibiting Both Apoptotic and Nonapoptotic Cell Death Dependent on Receptor-interacting Protein Kinase 1 (RIP1) and RIP3
Mina Kikuchi, Shunsuke Kuroki, Mitsuhiro Kayama, Shota Sakaguchi, Kyung-Kwon Lee, Shin Yonehara
J Biol Chem. 2012 Nov 30; 287(49): 41165–41173. Published online 2012 Oct 15. doi: 10.1074/jbc.M112.419747
PMCID:
PMC3510816
AbstractArticlePDF–1.7M
13.
Suppression of Tumorigenicity-14, encoding matriptase, is a critical suppressor of colitis and colitis-associated colon carcinogenesis
Peter Kosa, Roman Szabo, Alfredo A. Molinolo, Thomas H. Bugge
Oncogene. Author manuscript; available in PMC 2013 Feb 9.
Published in final edited form as: Oncogene. 2012 Aug 9; 31(32): 3679–3695. Published online 2011 Dec 5. doi: 10.1038/onc.2011.545
PMCID:
PMC3299858
AbstractArticlePDF–3.1M
14.
Gene Profiling of Mta1 Identifies Novel Gene Targets and Functions
Krishna Sumanth Ghanta, Da-Qiang Li, Jeyanthy Eswaran, Rakesh Kumar
PLoS One. 2011; 6(2): e17135. Published online 2011 Feb 25. doi: 10.1371/journal.pone.0017135
PMCID:
PMC3045407
AbstractArticlePDF–1.0M
15.
Comparative Epigenomics of Human and Mouse Mammary Tumors
Berna Demircan, Lisa M. Dyer, Mallory Gerace, Edward K. Lobenhofer, Keith D. Robertson, Kevin D. Brown
Genes Chromosomes Cancer. Author manuscript; available in PMC 2010 Aug 30.
Published in final edited form as: Genes Chromosomes Cancer. 2009 Jan; 48(1): 83–97. doi: 10.1002/gcc.20620
PMCID:
PMC2929596
AbstractArticlePDF–1.9M
16.
Acetylation of p65 at lysine 314 is important for late NF-κB-dependent gene expression
Karin M Rothgiesser, Monika Fey, Michael O Hottiger
BMC Genomics. 2010; 11: 22. Published online 2010 Jan 11. doi: 10.1186/1471-2164-11-22
PMCID:
PMC2823688
AbstractArticlePDF–893K
17.
Microarray and comparative genomics-based identification of genes and gene regulatory regions of the mouse immune system
John J Hutton, Anil G Jegga, Sue Kong, Ashima Gupta, Catherine Ebert, Sarah Williams, Jonathan D Katz, Bruce J Aronow
BMC Genomics. 2004; 5: 82. Published online 2004 Oct 25. doi: 10.1186/1471-2164-5-82
PMCID:
PMC534115
AbstractArticlePDF–1.7M

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