Citations (46)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (1)
Santiago Haase, María Belén Garcia-Fabiani, Stephen Carney, David Altshuler, Felipe J. Núñez, Flor M. Méndez, Fernando Núñez, Pedro R. Lowenstein & Maria G. Castro. (2018) Mutant ATRX: uncovering a new therapeutic target for glioma. Expert Opinion on Therapeutic Targets 22:7, pages 599-613.
Read now
Read now
Articles from other publishers (45)
Michael R. van Gerven, Linda Schild, Jennemiek van Arkel, Bianca Koopmans, Luuk A. Broeils, Loes A. M. Meijs, Romy van Oosterhout, Max M. van Noesel, Jan Koster, Sander R. van Hooff, Jan J. Molenaar & Marlinde L. van den Boogaard. (2023) Two opposing gene expression patterns within ATRX aberrant neuroblastoma. PLOS ONE 18:8, pages e0289084.
Crossref
Crossref
Romana T Pop, Alessandra Pisante, Dorka Nagy, Patrick C N Martin, Liudmila A Mikheeva, Ateequllah Hayat, Gabriella Ficz & Nicolae Radu Zabet. (2023) Identification of mammalian transcription factors that bind to inaccessible chromatin. Nucleic Acids Research.
Crossref
Crossref
Dmitry Umerenkov, Alan Herbert, Dmitrii Konovalov, Anna Danilova, Nazar Beknazarov, Vladimir Kokh, Aleksandr Fedorov & Maria Poptsova. (2023) Z-flipon variants reveal the many roles of Z-DNA and Z-RNA in health and disease. Life Science Alliance 6:7, pages e202301962.
Crossref
Crossref
Giovanni Spirito, Michele Filosi, Enrico Domenici, Damiano Mangoni, Stefano Gustincich & Remo Sanges. (2023) Exploratory analysis of L1 retrotransposons expression in autism. Molecular Autism 14:1.
Crossref
Crossref
Maria Eugenia Marques da Costa, Robin Droit, Pierre Khneisser, Anne Gomez-Brouchet, Tiphaine Adam-de-Beaumais, Marie Nolla, Nicolas Signolles, Jacob Torrejon, Bérangère Lombard, Damarys Loew, Olivier Ayrault, Jean-Yves Scoazec, Birgit Geoerger, Gilles Vassal, Antonin Marchais & Nathalie Gaspar. (2023) Longitudinal characterization of primary osteosarcoma and derived subcutaneous and orthotopic relapsed patient-derived xenograft models. Frontiers in Oncology 13.
Crossref
Crossref
Danielle D. Dang, Jared S. Rosenblum, Ashish H. Shah, Zhengping Zhuang & Tara T. Doucet-O’Hare. (2023) Epigenetic Regulation in Primary CNS Tumors: An Opportunity to Bridge Old and New WHO Classifications. Cancers 15:9, pages 2511.
Crossref
Crossref
Ying Pang, Xu Chen, Tongjie Ji, Meng Cheng, Rui Wang, Chunyu Zhang, Min Liu, Jing Zhang & Chunlong Zhong. (2023) The Chromatin Remodeler ATRX: Role and Mechanism in Biology and Cancer. Cancers 15:8, pages 2228.
Crossref
Crossref
Zhenlin Huang, Xiang Li, Bo Tang, Hao Li, Jianong Zhang, Rui Sun, Jian Ma, Yunqian Pan, Binyuan Yan, Yingke Zhou, Donglin Ding, Yuqian Yan, Rafael Jimenez, Jacob J. Orme, Xin Jin, Jinjian Yang, Haojie Huang & Zhankui Jia. (2023) SETDB1 Modulates Degradation of Phosphorylated RB and Anticancer Efficacy of CDK4/6 Inhibitors. Cancer Research 83:6, pages 875-889.
Crossref
Crossref
Rossella Alfano, Esmée Bijnens, Sabine A S Langie, Tim S Nawrot, Brigitte Reimann, Kenneth Vanbrabant, Congrong Wang & Michelle Plusquin. (2023) Epigenome-wide analysis of maternal exposure to green space during gestation and cord blood DNA methylation in the ENVIRONAGE cohort. Environmental Research 216, pages 114828.
Crossref
Crossref
Sevilhan Artan & Ali Arslantas. 2023. Cancer Epigenetics. Cancer Epigenetics
245
273
.
Laura M. Woods, Fahad R. Ali, Roshna Gomez, Igor Chernukhin, Daniel Marcos, Lydia M. Parkinson, Ahmad N. Abou Tayoun, Jason S. Carroll & Anna Philpott. (2022) Elevated ASCL1 activity creates de novo regulatory elements associated with neuronal differentiation. BMC Genomics 23:1.
Crossref
Crossref
Julia Truch, Damien J. Downes, Caroline Scott, E. Ravza Gür, Jelena M. Telenius, Emmanouela Repapi, Ron Schwessinger, Matthew Gosden, Jill M. Brown, Stephen Taylor, Pak Leng Cheong, Jim R. Hughes, Douglas R. Higgs & Richard J. Gibbons. (2022) The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin. Nature Communications 13:1.
Crossref
Crossref
Tamara Casteels, Simon Bajew, Jiří Reiniš, Lennart Enders, Michael Schuster, Frédéric Fontaine, André C. Müller, Bridget K. Wagner, Christoph Bock & Stefan Kubicek. (2022) SMNDC1 links chromatin remodeling and splicing to regulate pancreatic hormone expression. Cell Reports 40:9, pages 111288.
Crossref
Crossref
Ragini Bhargava, Michelle Lee Lynskey & Roderick J. O’Sullivan. (2022) New twists to the ALTernative endings at telomeres. DNA Repair 115, pages 103342.
Crossref
Crossref
Michael R. van Gerven, Eva Bozsaky, Yvette A. H. Matser, Julian Vosseberg, Sabine Taschner‐Mandl, Jan Koster, Godelieve A. M. Tytgat, Jan J. Molenaar & Marlinde van den Boogaard. (2022)
Mutational spectrum of
ATRX
aberrations in neuroblastoma and associated patient and tumor characteristics
. Cancer Science 113:6, pages 2167-2178.
Crossref
Crossref
Chengchen Hu, Kimberly Wang, Ceylan Damon, Yi Fu, Tengjiao Ma, Lisa Kratz, Bachchu Lal, Mingyao Ying, Shuli Xia, Daniel P Cahill, Christopher M Jackson, Michael Lim, John Laterra & Yunqing Li. (2022) ATRX loss promotes immunosuppressive mechanisms in IDH1 mutant glioma. Neuro-Oncology 24:6, pages 888-900.
Crossref
Crossref
Amandine Barral, Gabrielle Pozo, Lucas Ducrot, Giorgio L. Papadopoulos, Sandrine Sauzet, Andrew J. Oldfield, Giacomo Cavalli & Jérôme Déjardin. (2022) SETDB1/NSD-dependent H3K9me3/H3K36me3 dual heterochromatin maintains gene expression profiles by bookmarking poised enhancers. Molecular Cell 82:4, pages 816-832.e12.
Crossref
Crossref
Tingting Qin, Brendan Mullan, Ramya Ravindran, Dana Messinger, Ruby Siada, Jessica R. Cummings, Micah Harris, Ashwath Muruganand, Kalyani Pyaram, Zachary Miklja, Mary Reiber, Taylor Garcia, Dustin Tran, Carla Danussi, Jacqueline Brosnan-Cashman, Drew Pratt, Xinyi Zhao, Alnawaz Rehemtulla, Maureen A. Sartor, Sriram Venneti, Alan K. Meeker, Jason T. Huse, Meredith A. Morgan, Pedro R. Lowenstein, Maria G. Castro, Viveka Nand Yadav & Carl Koschmann. (2022) ATRX loss in glioma results in dysregulation of cell-cycle phase transition and ATM inhibitor radio-sensitization. Cell Reports 38:2, pages 110216.
Crossref
Crossref
Laura V Glaser, Mara Steiger, Alisa Fuchs, Alena van Bömmel, Edda Einfeldt, Ho-Ryun Chung, Martin Vingron & Sebastiaan H Meijsing. (2021) Assessing genome-wide dynamic changes in enhancer activity during early mESC differentiation by FAIRE-STARR-seq. Nucleic Acids Research 49:21, pages 12178-12195.
Crossref
Crossref
Chuanle Wang, Zhou Songyang & Yan Huang. (2021) TRIM28 inhibits alternative lengthening of telomere phenotypes by protecting SETDB1 from degradation. Cell & Bioscience 11:1.
Crossref
Crossref
Martina Valenzuela, Roberta Amato, Antonella Sgura, Antonio Antoccia & Francesco Berardinelli. (2021) The Multiple Facets of ATRX Protein. Cancers 13:9, pages 2211.
Crossref
Crossref
Mariam Markouli, Dimitrios Strepkos, Sarantis Chlamydas & Christina Piperi. (2021) Histone lysine methyltransferase SETDB1 as a novel target for central nervous system diseases. Progress in Neurobiology 200, pages 101968.
Crossref
Crossref
Joseph M. Cabral, Camille H. Cushman, Catherine N. Sodroski & David M. Knipe. (2021) ATRX limits the accessibility of histone H3-occupied HSV genomes during lytic infection. PLOS Pathogens 17:4, pages e1009567.
Crossref
Crossref
Maéva Langouët, Dea Gorka, Clarisse Orniacki, Clémence M Dupont-Thibert, Michael S Chung, Heather R Glatt-Deeley, Noelle Germain, Leann J Crandall, Justin L Cotney, Christopher E Stoddard, Marc Lalande & Stormy J Chamberlain. (2020)
Specific ZNF274 binding interference at
SNORD116
activates the maternal transcripts in Prader-Willi syndrome neurons
. Human Molecular Genetics 29:19, pages 3285-3295.
Crossref
Crossref
Banaja P. Dash, Marcel Naumann, Jared Sterneckert & Andreas Hermann. (2020) Genome Wide Analysis Points towards Subtype-Specific Diseases in Different Genetic Forms of Amyotrophic Lateral Sclerosis. International Journal of Molecular Sciences 21:18, pages 6938.
Crossref
Crossref
Silvia Meyer-Nava, Victor E. Nieto-Caballero, Mario Zurita & Viviana Valadez-Graham. (2020) Insights into HP1a-Chromatin Interactions. Cells 9:8, pages 1866.
Crossref
Crossref
Yueyan Zhu, Daijing Sun, Mira Jakovcevski & Yan Jiang. (2020) Epigenetic mechanism of SETDB1 in brain: implications for neuropsychiatric disorders. Translational Psychiatry 10:1.
Crossref
Crossref
Lynn Petukhova, Aakash V. Patel, Rachel K. Rigo, Li Bian, Miguel Verbitsky, Simone Sanna‐Cherchi, Stephanie O. Erjavec, Alexa R. Abdelaziz, Jane E. Cerise, Ali Jabbari & Angela M. Christiano. (2019) Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy. Experimental Dermatology 29:3, pages 243-253.
Crossref
Crossref
Prim B. Singh & Andrew G. Newman. (2020) On the relations of phase separation and Hi-C maps to epigenetics. Royal Society Open Science 7:3, pages 191976.
Crossref
Crossref
Melania BrunoMohamed MahgoubTodd S. Macfarlan. (2019) The Arms Race Between KRAB–Zinc Finger Proteins and Endogenous Retroelements and Its Impact on Mammals. Annual Review of Genetics 53:1, pages 393-416.
Crossref
Crossref
Hui Shi, Ruslan Strogantsev, Nozomi Takahashi, Anastasiya Kazachenka, Matthew C. Lorincz, Myriam Hemberger & Anne C. Ferguson-Smith. (2019) ZFP57 regulation of transposable elements and gene expression within and beyond imprinted domains. Epigenetics & Chromatin 12:1.
Crossref
Crossref
Pengyu Ni & Zhengchang Su. (2019) Deciphering epigenomic code for cell differentiation using deep learning. BMC Genomics 20:1.
Crossref
Crossref
Zulekha A. Qadeer, David Valle-Garcia, Dan Hasson, Zhen Sun, April Cook, Christie Nguyen, Aroa Soriano, Anqi Ma, Lyra M. Griffiths, Maged Zeineldin, Dan Filipescu, Luz Jubierre, Asif Chowdhury, Orla Deevy, Xiang Chen, David B. Finkelstein, Armita Bahrami, Elizabeth Stewart, Sara Federico, Soledad Gallego, Fumiko Dekio, Mary Fowkes, David Meni, John M. Maris, William A. Weiss, Stephen S. Roberts, Nai-Kong V. Cheung, Jian Jin, Miguel F. Segura, Michael A. Dyer & Emily Bernstein. (2019) ATRX In-Frame Fusion Neuroblastoma Is Sensitive to EZH2 Inhibition via Modulation of Neuronal Gene Signatures. Cancer Cell 36:5, pages 512-527.e9.
Crossref
Crossref
Valerie Turcotte-Cardin, Kevin G. Young & David J. Picketts. 2019. Chromatin Signaling and Neurological Disorders. Chromatin Signaling and Neurological Disorders
235
257
.
Lukasz Huminiecki. (2018) Modelling of the breadth of expression from promoter architectures identifies pro-housekeeping transcription factors. PLOS ONE 13:6, pages e0198961.
Crossref
Crossref
Bo Han, Jinquan Cai, Weida Gao, Xiangqi Meng, Fei Gao, Pengfei Wu, Chunbin Duan, Ruijia Wang, Magafurov Dinislam, Lin Lin, Chunsheng Kang & Chuanlu Jiang. (2018) Loss of ATRX suppresses ATM dependent DNA damage repair by modulating H3K9me3 to enhance temozolomide sensitivity in glioma. Cancer Letters 419, pages 280-290.
Crossref
Crossref
Carla Danussi, Promita Bose, Prasanna T. Parthasarathy, Pedro C. Silberman, John S. Van Arnam, Mark Vitucci, Oliver Y. Tang, Adriana Heguy, Yuxiang Wang, Timothy A. Chan, Gregory J. Riggins, Erik P. Sulman, Frederick F. Lang, Chad J. Creighton, Benjamin Deneen, C. Ryan Miller, David J. Picketts, Kasthuri Kannan & Jason T. Huse. (2018) Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling. Nature Communications 9:1.
Crossref
Crossref
Maéva Langouët, Heather R Glatt-Deeley, Michael S Chung, Clémence M Dupont-Thibert, Elodie Mathieux, Erin C Banda, Christopher E Stoddard, Leann Crandall & Marc Lalande. (2018) Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons. Human Molecular Genetics 27:3, pages 505-515.
Crossref
Crossref
Yu Tao, Ming-Ren Yen, Tsotne Chitiashvili, Haruko Nakano, Rachel Kim, Linzi Hosohama, Yao Chang Tan, Atsushi Nakano, Pao-Yang Chen & Amander T. Clark. (2018) TRIM28-Regulated Transposon Repression Is Required for Human Germline Competency and Not Primed or Naive Human Pluripotency. Stem Cell Reports 10:1, pages 243-256.
Crossref
Crossref
Rebekka Mauser, Goran Kungulovski, Corinna Keup, Richard Reinhardt & Albert Jeltsch. (2017) Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state. Epigenetics & Chromatin 10:1.
Crossref
Crossref
Diu TT Nguyen, Hsiao Phin J Voon, Barbara Xella, Caroline Scott, David Clynes, Christian Babbs, Helena Ayyub, Jon Kerry, Jacqueline A Sharpe, Jackie A Sloane‐Stanley, Sue Butler, Chris A Fisher, Nicki E Gray, Thomas Jenuwein, Douglas R Higgs & Richard J Gibbons. (2017)
The chromatin remodelling factor
ATRX
suppresses R‐loops in transcribed telomeric repeats
. EMBO reports 18:6, pages 914-928.
Crossref
Crossref
Michael A. Dyer, Zulekha A. Qadeer, David Valle-Garcia & Emily Bernstein. (2017) ATRX and DAXX: Mechanisms and Mutations. Cold Spring Harbor Perspectives in Medicine 7:3, pages a026567.
Crossref
Crossref
Paul B. Talbert & Steven Henikoff. (2016) Histone variants on the move: substrates for chromatin dynamics. Nature Reviews Molecular Cell Biology 18:2, pages 115-126.
Crossref
Crossref
Prim B Singh. (2016) Heterochromatin and the molecular mechanisms of ‘parent-of-origin’ effects in animals. Journal of Biosciences 41:4, pages 759-786.
Crossref
Crossref
Kevin G Young & David J Picketts. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences
1
7
.