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Items: 1 to 20 of 26

1.
Transcription factor ATMIN facilitates chemoresistance in nasopharyngeal carcinoma
Xue-Liang Fang, Qing-Jie Li, Jia-Yi Lin, Cheng-Long Huang, Sheng-Yan Huang, Xi-Rong Tan, Shi-Wei He, Xun-Hua Zhu, Jun-Yan Li, Sha Gong, Han Qiao, Ying-Qin Li, Na Liu, Jun Ma, Yin Zhao, Ling-Long Tang
Cell Death Dis. 2024 Feb; 15(2): 112. Published online 2024 Feb 6. doi: 10.1038/s41419-024-06496-x
PMCID:
PMC10847093
AbstractArticlePDF–5.1M
2.
ATMIN is a tumor suppressor gene in lung adenocarcinoma
Hanna Foster, E. Josue Ruiz, Christopher Moore, Gordon W. Stamp, Emma L. Nye, Ningning Li, Yihang Pan, Yulong He, Julian Downward, Axel Behrens
Cancer Res. Author manuscript; available in PMC 2020 Apr 15.
Published in final edited form as: Cancer Res. 2019 Sep 3; 79(20): 5159–5166. Published online 2019 Sep 3. doi: 10.1158/0008-5472.CAN-19-0647
PMCID:
PMC6797498
AbstractArticlePDF–1.5M
3.
ASCIZ/ATMIN is dispensable for ATM signaling in response to replication stress
Rui Liu, Ashleigh King, Nicolas C. Hoch, Catherine Chang, Gemma L. Kelly, Andrew J. Deans, Jörg Heierhorst
DNA Repair (Amst) 2017 Sep; 57: 29–34. doi: 10.1016/j.dnarep.2017.06.022
PMCID:
PMC5576915
AbstractArticle
4.
ATMIN defines an NBS1-independent pathway of ATM signalling
Nnennaya Kanu, Axel Behrens
EMBO J. 2007 Jun 20; 26(12): 2933–2941. Published online 2007 May 24. doi: 10.1038/sj.emboj.7601733
PMCID:
PMC1894771
AbstractArticlePDF–319K
5.
MicroRNA-361-5p slows down gliomas development through regulating UBR5 to elevate ATMIN protein expression
Jiaoying Jia, Zhu Ouyang, Ming Wang, Wenjia Ma, Min Liu, Mingming Zhang, Mengqiang Yu
Cell Death Dis. 2021 Aug; 12(8): 746. Published online 2021 Jul 28. doi: 10.1038/s41419-021-04010-1
PMCID:
PMC8319180
AbstractArticlePDF–3.6M
6.
Mechanisms and consequences of ATMIN repression in hypoxic conditions: roles for p53 and HIF-1
Katarzyna B. Leszczynska, Eva-Leonne Göttgens, Deborah Biasoli, Monica M. Olcina, Jonathan Ient, Selvakumar Anbalagan, Stephan Bernhardt, Amato J. Giaccia, Ester M. Hammond
Sci Rep. 2016; 6: 21698. Published online 2016 Feb 15. doi: 10.1038/srep21698
PMCID:
PMC4753685
AbstractArticlePDF–1.0M
7.
ATMIN is required for the ATM-mediated signaling and recruitment of 53BP1 to DNA damage sites upon replication stress
Luisa Schmidt, Marc Wiedner, Georgia Velimezi, Jana Prochazkova, Michel Owusu, Sabine Bauer, Joanna I. Loizou
DNA Repair (Amst) 2014 Dec; 24: 122–130. doi: 10.1016/j.dnarep.2014.09.001
PMCID:
PMC4251980
AbstractArticle
8.
Atmin modulates Pkhd1 expression and may mediate Autosomal Recessive Polycystic Kidney Disease (ARPKD) through altered non-canonical Wnt/Planar Cell Polarity (PCP) signalling
Taylor Richards, Kavindiya Modarage, Charlotte Dean, Aidan McCarthy-Boxer, Helen Hilton, Chris Esapa, Jill Norman, Patricia Wilson, Paraskevi Goggolidou
Biochim Biophys Acta Mol Basis Dis. 2019 Feb 1; 1865(2): 378–390. doi: 10.1016/j.bbadis.2018.11.003
PMCID:
PMC6335440
AbstractArticle
9.
RAD18, WRNIP1 and ATMIN promote ATM signalling in response to replication stress
Nnennaya Kanu, Tianyi Zhang, Rebecca A. Burrell, Atanu Chakraborty, Janet Cronshaw, Clive Da Costa, Eva Grönroos, Helen N. Pemberton, Emma Anderton, Laure Gonzalez, Simone Sabbioneda, Helle D. Ulrich, Charles Swanton, Axel Behrens
Oncogene. Author manuscript; available in PMC 2016 Sep 22.
Published in final edited form as: Oncogene. 2016 Jul 28; 35(30): 4009–4019. Published online 2015 Nov 9. doi: 10.1038/onc.2015.427
Correction in:
Oncogene. 2016 Jul 28; 35(30): 4020.
PMCID:
PMC4842010
AbstractArticlePDF–2.0M
10.
ASCIZ regulates lesion-specific Rad51 focus formation and apoptosis after methylating DNA damage
Carolyn J McNees, Lindus A Conlan, Nora Tenis, Jörg Heierhorst
EMBO J. 2005 Jul 6; 24(13): 2447–2457. Published online 2005 Jun 2. doi: 10.1038/sj.emboj.7600704
PMCID:
PMC1173145
AbstractArticlePDF–509K
11.
UBR5-mediated ubiquitination of ATMIN is required for ionizing radiation-induced ATM signaling and function
Tianyi Zhang, Janet Cronshaw, Nnennaya Kanu, Ambrosius P. Snijders, Axel Behrens
Proc Natl Acad Sci U S A. 2014 Aug 19; 111(33): 12091–12096. Published online 2014 Aug 4. doi: 10.1073/pnas.1400230111
PMCID:
PMC4143036
AbstractArticlePDF–1.4M
12.
ATM Substrate Chk2-interacting Zn2+ Finger (ASCIZ) Is a Bi-functional Transcriptional Activator and Feedback Sensor in the Regulation of Dynein Light Chain (DYNLL1) Expression
Sabine Jurado, Lindus A. Conlan, Emma K. Baker, Jane-Lee Ng, Nora Tenis, Nicolas C. Hoch, Kimberly Gleeson, Monique Smeets, David Izon, Jörg Heierhorst
J Biol Chem. 2012 Jan 27; 287(5): 3156–3164. Published online 2011 Dec 13. doi: 10.1074/jbc.M111.306019
PMCID:
PMC3270970
AbstractArticlePDF–2.8M
13.
Dual Functions of ASCIZ in the DNA Base Damage Response and Pulmonary Organogenesis
Sabine Jurado, Ian Smyth, Bryce van Denderen, Nora Tenis, Andrew Hammet, Kimberly Hewitt, Jane-Lee Ng, Carolyn J. McNees, Sergei V. Kozlov, Hayato Oka, Masahiko Kobayashi, Lindus A. Conlan, Timothy J. Cole, Ken-ichi Yamamoto, Yoshihito Taniguchi, Shunichi Takeda, Martin F. Lavin, Jörg Heierhorst
PLoS Genet. 2010 Oct; 6(10): e1001170. Published online 2010 Oct 21. doi: 10.1371/journal.pgen.1001170
Correction in:
PLoS Genet. 2010 Nov; 6(11): 10.1371/annotation/bce92e15-60b4-493b-89de-28529386f4ac.
PMCID:
PMC2958817
AbstractArticlePDF–17M
14.
Interactome of the negative regulator of nuclear import BRCA1-binding protein 2
Shadma Fatima, Kylie M. Wagstaff, Kate L. Loveland, David A. Jans
Sci Rep. 2015; 5: 9459. Published online 2015 Mar 30. doi: 10.1038/srep09459
PMCID:
PMC4377634
AbstractArticlePDF–12M
15.
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects
Zari Dastani, Päivi Pajukanta, Michel Marcil, Nicholas Rudzicz, Isabelle Ruel, Swneke D Bailey, Jenny C Lee, Mathieu Lemire, Janet Faith, Jill Platko, John Rioux, Thomas J Hudson, Daniel Gaudet, James C Engert, Jacques Genest
Eur J Hum Genet. 2010 Mar; 18(3): 342–347. Published online 2009 Oct 21. doi: 10.1038/ejhg.2009.157
PMCID:
PMC2824775
AbstractArticlePDF–366K
16.
PPARγ Interaction with UBR5/ATMIN Promotes DNA Repairto Maintain Endothelial Homeostasis
Caiyun G. Li, Cathal Mahon, Nathaly M. Sweeney, Erik Verschueren, Vivek Kantamani, Dan Li, Jan K. Hennigs, David P. Marciano, Isabel Diebold, Ossama Abu-Halawa, Matthew Elliott, Silin Sa, Feng Guo, Lingli Wang, Aiqin Cao, Christophe Guignabert, Julie Sollier, Nils P. Nickel, Mark Kaschwich, Karlene A. Cimprich, Marlene Rabinovitch
Cell Rep. Author manuscript; available in PMC 2019 Mar 27.
Published in final edited form as: Cell Rep. 2019 Jan 29; 26(5): 1333–1343.e7. doi: 10.1016/j.celrep.2019.01.013
PMCID:
PMC6436616
AbstractArticlePDF–1.9M
17.
Global analysis of host-pathogen interactions that regulate early stage HIV-1 replication
Renate König, Yingyao Zhou, Daniel Elleder, Tracy L. Diamond, Ghislain M.C. Bonamy, Jeffrey T. Irelan, Chih-yuan Chiang, Buu P. Tu, Paul D. De Jesus, Caroline E. Lilley, Shannon Seidel, Amanda M. Opaluch, Jeremy S. Caldwell, Matthew D. Weitzman, Kelli L. Kuhen, Sourav Bandyopadhyay, Trey Ideker, Anthony P. Orth, Loren J. Miraglia, Frederic D. Bushman, John A. Young, Sumit K. Chanda
Cell. Author manuscript; available in PMC 2009 Oct 3.
Published in final edited form as: Cell. 2008 Oct 3; 135(1): 49–60. doi: 10.1016/j.cell.2008.07.032
PMCID:
PMC2628946
AbstractArticlePDF–3.4M
18.
A dual-activity topoisomerase complex regulates mRNA translation and turnover
Shuaikun Su, Yutong Xue, Alexei Sharov, Yongqing Zhang, Seung Kyu Lee, Jennifer L Martindale, Wen Li, Wai Lim Ku, Keji Zhao, Supriyo De, Weiping Shen, Payel Sen, Myriam Gorospe, Dongyi Xu, Weidong Wang
Nucleic Acids Res. 2022 Jul 8; 50(12): 7013–7033. Published online 2022 Jun 24. doi: 10.1093/nar/gkac538
PMCID:
PMC9262614
AbstractArticlePDF–3.6M
19.
Systematic mapping of genetic interactions for de novo fatty acid synthesis identifies C12orf49 as a regulator of lipid metabolism
Michael Aregger, Keith A. Lawson, Maximillian Billmann, Michael Costanzo, Amy H. Y. Tong, Katherine Chan, Mahfuzur Rahman, Kevin R. Brown, Catherine Ross, Matej Usaj, Lucy Nedyalkova, Olga Sizova, Andrea Habsid, Judy Pawling, Zhen-Yuan Lin, Hala Abdouni, Cassandra J. Wong, Alexander Weiss, Patricia Mero, James W. Dennis, Anne-Claude Gingras, Chad L. Myers, Brenda J. Andrews, Charles Boone, Jason Moffat
Nat Metab. Author manuscript; available in PMC 2020 Dec 1.
Published in final edited form as: Nat Metab. 2020 Jun; 2(6): 499–513. Published online 2020 Jun 1. doi: 10.1038/s42255-020-0211-z
PMCID:
PMC7566881
AbstractArticlePDF–4.8M
20.
Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing
Teng Fei, Yiwen Chen, Tengfei Xiao, Wei Li, Laura Cato, Peng Zhang, Maura B. Cotter, Michaela Bowden, Rosina T. Lis, Shuang G. Zhao, Qiu Wu, Felix Y. Feng, Massimo Loda, Housheng Hansen He, X. Shirley Liu, Myles Brown
Proc Natl Acad Sci U S A. 2017 Jun 27; 114(26): E5207–E5215. Published online 2017 Jun 13. doi: 10.1073/pnas.1617467114
PMCID:
PMC5495225
AbstractArticlePDF–1.3M

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