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Items: 1 to 20 of 55

1.
Roles of the histone acetyltransferase monocytic leukemia zinc finger protein in normal and malignant hematopoiesis
Takuo Katsumoto, Naomi Yoshida, Issay Kitabayashi
Cancer Sci. 2008 Aug; 99(8): 1523–1527. Published online 2008 Aug 14. doi: 10.1111/j.1349-7006.2008.00865.x
PMCID:
PMC11158476
AbstractArticlePDF–244K
2.
Acute Monoblastic Leukemia with Erythrophagocytosis and Absence of KAT6A Rearrangement
Carlos De Miguel Sánchez, Diego Robles de Castro, Ana Vega González de Viñaspre, Ariane Unamunzaga Zilaurren, Arantza Mendizábal Abad, José María Guinea de Castro
Turk J Haematol. 2020 Dec; 37(4): 282–283. Published online 2020 Nov 19. doi: 10.4274/tjh.galenos.2020.2020.0237
PMCID:
PMC7702662
ArticlePDF–243K
3.
KAT6A amplifications are associated with shorter progression-free survival and overall survival in patients with endometrial serous carcinoma
Ozlen Saglam, Zhenya Tang, Guilin Tang, L. Jeffrey Medeiros, Gokce A. Toruner
PLoS One. 2020; 15(9): e0238477. Published online 2020 Sep 2. doi: 10.1371/journal.pone.0238477
PMCID:
PMC7467277
AbstractArticlePDF–2.8M
4.
Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum
Roser Urreizti, Estrella Lopez-Martin, Antonio Martinez-Monseny, Montse Pujadas, Laura Castilla-Vallmanya, Luis Alberto Pérez-Jurado, Mercedes Serrano, Daniel Natera-de Benito, Beatriz Martínez-Delgado, Manuel Posada-de-la-Paz, Javier Alonso, Purificación Marin-Reina, Mar O’Callaghan, Daniel Grinberg, Eva Bermejo-Sánchez, Susanna Balcells
Orphanet J Rare Dis. 2020; 15: 44. Published online 2020 Feb 10. doi: 10.1186/s13023-020-1317-9
PMCID:
PMC7011274
AbstractArticlePDF–1.9M
5.
KAT6A Syndrome: Genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants
Joanna Kennedy, David Goudie, Edward Blair, Kate Chandler, Shelagh Joss, Victoria McKay, Andrew Green, Ruth Armstrong, Melissa Lees, Benjamin Kamien, Bruce Hopper, Tiong Yang Tan, Patrick Yap, Zornitza Stark, Nobuhiko Okamoto, Noriko Miyake, Naomichi Matsumoto, Ellen Macnamara, Jennifer L. Murphy, Elizabeth McCormick, Hakon Hakonarson, Marni J. Falk, Dong Li, Patrick Blackburn, Eric Klee, Dusica Babovic-Vuksanovic, Susan Schelley, Louanne Hudgins, Sarina Kant, Bertrand Isidor, Benjamin Cogne, Kimberley Bradbury, Mark Williams, Chirag Patel, Helen Heussler, Celia Duff-Farrier, Phillis Lakeman, Ingrid Scurr, Usha Kini, Mariet Elting, Margot Reijnders, Janneke Schuurs-Hoeijmakers, Mohamed Wafik, Anne Blomhoff, Claudia A.L. Ruivenkamp, Esther Nibbeling, Alexander J.M. Dingemans, Emilie D. Douine, Stanley F. Nelson, The DDD Study, Valerie A. Arboleda, Ruth Newbury-Ecob
Genet Med. Author manuscript; available in PMC 2019 Oct 1.
Published in final edited form as: Genet Med. 2019 Apr; 21(4): 850–860. Published online 2018 Sep 24. doi: 10.1038/s41436-018-0259-2
Correction in:
Genet Med. 2020 Aug 19
PMCID:
PMC6634310
AbstractArticlePDF–801K
6.
De Novo Nonsense Mutations in KAT6A, a Lysine Acetyl-Transferase Gene, Cause a Syndrome Including Microcephaly and Global Developmental Delay
Valerie A. Arboleda, Hane Lee, Naghmeh Dorrani, Neda Zadeh, Mary Willis, Colleen Forsyth Macmurdo, Melanie A. Manning, Andrea Kwan, Louanne Hudgins, Florian Barthelemy, M. Carrie Miceli, Fabiola Quintero-Rivera, Sibel Kantarci, Samuel P. Strom, Joshua L. Deignan, UCLA Clinical Genomics Center, Wayne W. Grody, Eric Vilain, Stanley F. Nelson
Am J Hum Genet. 2015 Mar 5; 96(3): 498–506. doi: 10.1016/j.ajhg.2015.01.017
PMCID:
PMC4375619
AbstractArticlePDF–790K
7.
Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features
Emma Tham, Anna Lindstrand, Avni Santani, Helena Malmgren, Addie Nesbitt, Holly A. Dubbs, Elaine H. Zackai, Michael J. Parker, Francisca Millan, Kenneth Rosenbaum, Golder N. Wilson, Ann Nordgren
Am J Hum Genet. 2015 Mar 5; 96(3): 507–513. doi: 10.1016/j.ajhg.2015.01.016
PMCID:
PMC4375419
AbstractArticlePDF–912K
8.
The MYSTerious MOZ, a histone acetyltransferase with a key role in haematopoiesis
Flor M Perez-Campo, Guilherme Costa, Michael Lie-a-Ling, Valerie Kouskoff, Georges Lacaud
Immunology. 2013 Jun; 139(2): 161–165. Published online 2013 Apr 23. doi: 10.1111/imm.12072
PMCID:
PMC3647182
AbstractArticlePDF–273K
9.
KAT6A mutations in Arboleda-Tham syndrome drive epigenetic regulation of posterior HOXC cluster
Meghna Singh, Sarah J. Spendlove, Angela Wei, Leroy M. Bondhus, Aileen A. Nava, Francisca N. de L. Vitorino, Seth Amano, Jacob Lee, Gesenia Echeverria, Dianne Gomez, Benjamin A. Garcia, Valerie A. Arboleda
Hum Genet. 2023; 142(12): 1705–1720. Published online 2023 Oct 20. doi: 10.1007/s00439-023-02608-3
PMCID:
PMC10676314
AbstractArticlePDF–4.2M
10.
KAT6A and ENL form an epigenetic transcriptional control module to drive critical leukemogenic gene expression programs
Fangxue Yan, Jinyang Li, Jelena Milosevic, Ricardo Petroni, Suying Liu, Zhennan Shi, Salina Yuan, Janice M. Reynaga, Yuwei Qi, Joshua Rico, Sixiang Yu, Yiman Liu, Susumu Rokudai, Neil Palmisiano, Sara E. Meyer, Pamela J Sung, Liling Wan, Fei Lan, Benjamin A. Garcia, Ben Z. Stanger, David B. Sykes, M. Andrés Blanco
Cancer Discov. Author manuscript; available in PMC 2022 Sep 1.
Published in final edited form as: Cancer Discov. 2022 Mar 1; 12(3): 792–811. doi: 10.1158/2159-8290.CD-20-1459
PMCID:
PMC8916037
AbstractArticlePDF–2.6M
11.
Identification of MYST3 as a novel epigenetic activator of ERα frequently amplified in breast cancer
L Yu, Y Liang, X Cao, X Wang, H Gao, S-Y Lin, R Schiff, X-S Wang, K Li
Oncogene. 2017 May 18; 36(20): 2910–2918. Published online 2016 Nov 28. doi: 10.1038/onc.2016.433
PMCID:
PMC5436938
AbstractArticlePDF–2.9M
12.
Regulation of KAT6 Acetyltransferases and Their Roles in Cell Cycle Progression, Stem Cell Maintenance, and Human Disease
Fu Huang, Susan M. Abmayr, Jerry L. Workman
Mol Cell Biol. 2016 Jul 15; 36(14): 1900–1907. Prepublished online 2016 May 16. Published online 2016 Jun 29. doi: 10.1128/MCB.00055-16
PMCID:
PMC4936061
AbstractArticlePDF–1.6M
13.
KAT6A, a Chromatin Modifier from the 8p11-p12 Amplicon is a Candidate Oncogene in Luminal Breast Cancer
Brittany Turner-Ivey, Stephen T. Guest, Jonathan C. Irish, Christiana S. Kappler, Elizabeth Garrett-Mayer, Robert C. Wilson, Stephen P. Ethier
Neoplasia. 2014 Aug; 16(8): 644–655. Published online 2014 Sep 10. doi: 10.1016/j.neo.2014.07.007
PMCID:
PMC4234874
AbstractArticlePDF–1.3M
14.
The double PHD finger domain of MOZ/MYST3 induces α-helical structure of the histone H3 tail to facilitate acetylation and methylation sampling and modification
Ingrid Dreveny, Sian E. Deeves, Joel Fulton, Baigong Yue, Marie Messmer, Amit Bhattacharya, Hilary M. Collins, David M. Heery
Nucleic Acids Res. 2014 Jan; 42(2): 822–835. Published online 2013 Oct 21. doi: 10.1093/nar/gkt931
PMCID:
PMC3902925
AbstractArticlePDF–9.6M
15.
Transcriptional regulation of the human MIP-1α promoter by RUNX1 and MOZ
Claire A. P. Bristow, Paul Shore
Nucleic Acids Res. 2003 Jun 1; 31(11): 2735–2744. doi: 10.1093/nar/gkg401
PMCID:
PMC156734
AbstractArticlePDF–332K
16.
MORF and MOZ acetyltransferases target unmethylated CpG islands through the winged helix domain
Dustin C. Becht, Brianna J. Klein, Akinori Kanai, Suk Min Jang, Khan L. Cox, Bing-Rui Zhou, Sabrina K. Phanor, Yi Zhang, Ruo-Wen Chen, Christopher C. Ebmeier, Catherine Lachance, Maxime Galloy, Amelie Fradet-Turcotte, Martha L. Bulyk, Yawen Bai, Michael G. Poirier, Jacques Côté, Akihiko Yokoyama, Tatiana G. Kutateladze
Nat Commun. 2023; 14: 697. Published online 2023 Feb 8. doi: 10.1038/s41467-023-36368-5
PMCID:
PMC9908889
AbstractArticlePDF–12M
17.
NEAT1-TFE3 and KAT6A-TFE3 renal cell carcinomas, new members of MiT family translocation renal cell carcinoma
Jianming Pei, Harry Cooper, Douglas B. Flieder, Jacqueline N. Talarchek, Tahseen Al-Saleem, Robert G. Uzzo, Essel Dulaimi, Arthur S. Patchefsky, Joseph R. Testa, Shuanzeng Wei
Mod Pathol. Author manuscript; available in PMC 2019 Jul 8.
Published in final edited form as: Mod Pathol. 2019 May; 32(5): 710–716. Published online 2019 Jan 8. doi: 10.1038/s41379-018-0191-7
PMCID:
PMC6486435
AbstractArticlePDF–860K
18.
Selective Recognition of Histone Crotonylation by Double PHD Fingers of MOZ and DPF2
Xiaozhe Xiong, Tatyana Panchenko, Shuang Yang, Shuai Zhao, Peiqiang Yan, Wenhao Zhang, Wei Xie, Yuanyuan Li, Yingming Zhao, C David Allis, Haitao Li
Nat Chem Biol. Author manuscript; available in PMC 2017 Jan 23.
Published in final edited form as: Nat Chem Biol. 2016 Dec; 12(12): 1111–1118. Published online 2016 Oct 24. doi: 10.1038/nchembio.2218
PMCID:
PMC5253430
AbstractArticlePDF–2.3M
19.
Tandem PHD fingers of MORF/MOZ acetyltransferases display selectivity for acetylated histone H3 and are required for the association with chromatin
Muzaffar Ali, Kezhi Yan, Marie-Eve Lalonde, Cindy Degerny, Scott B. Rothbart, Brian D. Strahl, Jacques Côté, Xiang-Jiao Yang, Tatiana G. Kutateladze
J Mol Biol. Author manuscript; available in PMC 2013 Dec 14.
Published in final edited form as: J Mol Biol. 2012 Dec 14; 424(5): 328–338. Published online 2012 Oct 12. doi: 10.1016/j.jmb.2012.10.004
PMCID:
PMC3502708
AbstractArticlePDF–2.6M
20.
Combinatorial readout of unmodified H3R2 and acetylated H3K14 by the tandem PHD finger of MOZ reveals a regulatory mechanism for HOXA9 transcription
Yu Qiu, Lei Liu, Chen Zhao, Chuanchun Han, Fudong Li, Jiahai Zhang, Yan Wang, Guohong Li, Yide Mei, Mian Wu, Jihui Wu, Yunyu Shi
Genes Dev. 2012 Jun 15; 26(12): 1376–1391. doi: 10.1101/gad.188359.112
PMCID:
PMC3387664
AbstractArticlePDF–3.9M

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