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Items: 1 to 20 of 160

1.
Molecular basis of non-deletional HPFH in Thailand and identification of two novel mutations at the binding sites of CCAAT and GATA-1 transcription factors
Kritsada Singha, Anupong Pansuwan, Mattanee Chewasateanchai, Goonnapa Fucharoen, Supan Fucharoen
Sci Rep. 2023; 13: 11926. Published online 2023 Jul 24. doi: 10.1038/s41598-023-39173-8
PMCID:
PMC10366219
AbstractArticlePDF–1.8M
2.
Multidimensional profiling reveals GATA1-modulated stage-specific chromatin states and functional associations during human erythropoiesis
Dong Li, Xin-Ying Zhao, Shuo Zhou, Qi Hu, Fan Wu, Hsiang-Ying Lee
Nucleic Acids Res. 2023 Jul 21; 51(13): 6634–6653. Published online 2023 May 31. doi: 10.1093/nar/gkad468
PMCID:
PMC10359633
AbstractArticlePDF–5.2M
3.
A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger
José M. Bastida, Stefano Malvestiti, Doris Boeckelmann, Verónica Palma-Barqueros, Mira Wolter, María L. Lozano, Hannah Glonnegger, Rocío Benito, Carlo Zaninetti, Felix Sobotta, Freimut H. Schilling, Neil V. Morgan, Kathleen Freson, José Rivera, Barbara Zieger
Cells. 2022 Oct; 11(20): 3223. Published online 2022 Oct 14. doi: 10.3390/cells11203223
PMCID:
PMC9600848
AbstractArticlePDF–2.1M
4.
Germline GATA1s-generating mutations predispose to leukemia with acquired trisomy 21 and Down syndrome-like phenotype
Henrik Hasle, Ronald M. Kline, Eigil Kjeldsen, Nik F. Nik-Abdul-Rashid, Deepa Bhojwani, Jeffrey M. Verboon, Stephanie P. DiTroia, Katherine R. Chao, Klas Raaschou-Jensen, Josefine Palle, C. Michel Zwaan, Charlotte Guldborg Nyvold, Vijay G. Sankaran, Alan B. Cantor
Blood. 2022 May 26; 139(21): 3159–3165. doi: 10.1182/blood.2021011463
PMCID:
PMC9136882
AbstractArticle
5.
Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1
Leif S. Ludwig, Caleb A. Lareau, Erik L. Bao, Nan Liu, Taiju Utsugisawa, Alex M. Tseng, Samuel A. Myers, Jeffrey M. Verboon, Jacob C. Ulirsch, Wendy Luo, Christoph Muus, Claudia Fiorini, Meagan E. Olive, Christopher M. Vockley, Mathias Munschauer, Abigail Hunter, Hiromi Ogura, Toshiyuki Yamamoto, Hiroko Inada, Shinichiro Nakagawa, Shuichi Ohzono, Vidya Subramanian, Roberto Chiarle, Bertil Glader, Steven A. Carr, Martin J. Aryee, Anshul Kundaje, Stuart H. Orkin, Aviv Regev, Timothy L. McCavit, Hitoshi Kanno, Vijay G. Sankaran
Blood. 2022 Apr 21; 139(16): 2534–2546. doi: 10.1182/blood.2021013753
Correction in:
Blood. 2023 Mar 2; 141(9): 1094.
PMCID:
PMC9029090
AbstractArticle
6.
GATA-1 Defects in Diamond–Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of Disease
Birgit van Dooijeweert, Sima Kheradmand Kia, Niklas Dahl, Odile Fenneteau, Roos Leguit, Edward Nieuwenhuis, Wouter van Solinge, Richard van Wijk, Lydie Da Costa, Marije Bartels
Genes (Basel) 2022 Mar; 13(3): 447. Published online 2022 Feb 28. doi: 10.3390/genes13030447
PMCID:
PMC8949872
AbstractArticlePDF–1.7M
7.
Sensitive GATA1 mutation screening reliably identifies neonates with Down syndrome at risk for myeloid leukemia
Bianca F. Goemans, Sanne Noort, Marjolein Blink, Yong-Dong Wang, Susan T. C. J. Peters, Jacobus P. van Wouwe, Gertjan Kaspers, Valerie de Haas, Wouter J. Kollen, Vincent H. J. van der Velden, Tanja A. Gruber, Christian M. Zwaan
Leukemia. 2021; 35(8): 2403–2406. Published online 2021 Jan 22. doi: 10.1038/s41375-021-01128-1
PMCID:
PMC8324475
ArticlePDF–590K
8.
Pluripotent stem cell model of early hematopoiesis in Down syndrome reveals quantitative effects of short-form GATA1 protein on lineage specification
Shiori Matsuo, Yoko Nishinaka-Arai, Yasuhiro Kazuki, Mitsuo Oshimura, Tatsutoshi Nakahata, Akira Niwa, Megumu K. Saito
PLoS One. 2021; 16(3): e0247595. Published online 2021 Mar 29. doi: 10.1371/journal.pone.0247595
PMCID:
PMC8007000
AbstractArticlePDF–2.0M
9.
Down syndrome-related transient abnormal myelopoiesis is attributed to a specific erythro-megakaryocytic subpopulation with GATA1 mutation
Yoko Nishinaka-Arai, Akira Niwa, Shiori Matsuo, Yasuhiro Kazuki, Yuwna Yakura, Takehiko Hiroma, Tsutomu Toki, Tetsushi Sakuma, Takashi Yamamoto, Etsuro Ito, Mitsuo Oshimura, Tatsutoshi Nakahata, Megumu K. Saito
Haematologica. 2021 Feb 1; 106(2): 635–640. Published online 2020 Apr 30. doi: 10.3324/haematol.2019.242693
PMCID:
PMC7849752
ArticlePDF–1.8M
10.
GATA1 Mutations in Red Cell Disorders
Te Ling, John D. Crispino
IUBMB Life. Author manuscript; available in PMC 2021 Jan 1.
Published in final edited form as: IUBMB Life. 2020 Jan; 72(1): 106–118. Published online 2019 Oct 25. doi: 10.1002/iub.2177
PMCID:
PMC7323890
AbstractArticlePDF–647K
11.
GATA‐1 isoforms differently contribute to the production and compartmentation of reactive oxygen species in the myeloid leukemia cell line K562
Patrizia Riccio, Raffaele Sessa, Sergio de Nicola, Fara Petruzziello, Silvia Trombetti, Giuseppe Menna, Giampiero Pepe, Pasquale Maddalena, Paola Izzo, Michela Grosso
J Cell Physiol. 2019 Nov; 234(11): 20829–20846. Published online 2019 May 2. doi: 10.1002/jcp.28688
PMCID:
PMC6767011
AbstractArticlePDF–2.4M
12.
GATA1 epigenetic deregulation contributes to the development of AML with NPM1 and FLT3-ITD cooperating mutations
Paolo Sportoletti, Letizia Celani, Emanuela Varasano, Roberta Rossi, Daniele Sorcini, Chiara Rompietti, Francesca Strozzini, Beatrice Del Papa, Valerio Guarente, Giulio Spinozzi, Debora Cecchini, Oxana Bereshchenko, Torsten Haferlach, Maria Paola Martelli, Franca Falzetti, Brunangelo Falini
Leukemia. 2019; 33(7): 1827–1832. Published online 2019 Feb 12. doi: 10.1038/s41375-019-0399-7
PMCID:
PMC6756200
ArticlePDF–899K
13.
Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation
Nour J. Abdulhay, Claudia Fiorini, Jeffrey M. Verboon, Leif S. Ludwig, Jacob C. Ulirsch, Barbara Zieger, Caleb A. Lareau, Xiaoli Mi, Anindita Roy, Esther A. Obeng, Miriam Erlacher, Namrata Gupta, Stacey B. Gabriel, Benjamin L. Ebert, Charlotte M. Niemeyer, Rami N. Khoriaty, Philip Ancliff, Hanna T. Gazda, Marcin W. Wlodarski, Vijay G. Sankaran
J Exp Med. 2019 May 6; 216(5): 1050–1060. Published online 2019 Mar 26. doi: 10.1084/jem.20181625
PMCID:
PMC6504223
AbstractArticlePDF–2.5M
14.
GATA1 insufficiencies in primary myelofibrosis and other hematopoietic disorders: consequences for therapy
Te Ling, John D. Crispino, Maria Zingariello, Fabrizio Martelli, Anna Rita Migliaccio
Expert Rev Hematol. Author manuscript; available in PMC 2018 Aug 24.
Published in final edited form as: Expert Rev Hematol. 2018 Mar; 11(3): 169–184. Published online 2018 Feb 19. doi: 10.1080/17474086.2018.1436965
PMCID:
PMC6108178
AbstractArticlePDF–681K
15.
GATA1s exerts developmental stage-specific effects in human hematopoiesis
Sofia Gialesaki, Anna Katharina Mahnken, Lena Schmid, Maurice Labuhn, Raj Bhayadia, Dirk Heckl, Jan-Henning Klusmann
Haematologica. 2018 Aug; 103(8): e336–e340. doi: 10.3324/haematol.2018.191338
PMCID:
PMC6068023
ArticlePDF–1.4M
16.
A child with dyserythropoietic anemia and megakaryocyte dysplasia due to a novel 5′UTR GATA1s splice mutation
Jacob Zucker, Constance Temm, Magdalena Czader, Grzegorz Nalepa
Pediatr Blood Cancer. Author manuscript; available in PMC 2017 May 1.
Published in final edited form as: Pediatr Blood Cancer. 2016 May; 63(5): 917–921. Published online 2015 Dec 29. doi: 10.1002/pbc.25871
PMCID:
PMC5138049
AbstractArticlePDF–650K
17.
GATA1 mutations in a cohort of Malaysian children with Down syndrome-associated myeloid disorder
Su Han Lum, Soo Sin Choong, Shekhar Krishnan, Zulqarnain Mohamed, Hany Ariffin
Singapore Med J. 2016 Jun; 57(6): 320–324. doi: 10.11622/smedj.2016106
PMCID:
PMC4971451
AbstractArticlePDF–206K
18.
Loss of GATA-1 Full Length as a Cause of Diamond–Blackfan Anemia Phenotype
Sara Parrella, Anna Aspesi, Paola Quarello, Emanuela Garelli, Elisa Pavesi, Adriana Carando, Margherita Nardi, Steven R. Ellis, Ugo Ramenghi, Irma Dianzani
Pediatr Blood Cancer. Author manuscript; available in PMC 2015 Dec 18.
Published in final edited form as: Pediatr Blood Cancer. 2014 Jul; 61(7): 1319–1321. Published online 2014 Jan 22. doi: 10.1002/pbc.24944
PMCID:
PMC4684094
AbstractArticlePDF–276K
19.
Global transcriptome and chromatin occupancy analysis reveal the short isoform of GATA1 is deficient for erythroid specification and gene expression
Timothy M. Chlon, Maureen McNulty, Benjamin Goldenson, Alexander Rosinski, John D. Crispino
Haematologica. 2015 May; 100(5): 575–584. doi: 10.3324/haematol.2014.112714
PMCID:
PMC4420206
AbstractArticlePDF–1.6M
20.
GATA1 induces epithelial-mesenchymal transition in breast cancer cells through PAK5 oncogenic signaling
Yang Li, Qiang Ke, Yangguang Shao, Ge Zhu, Yanshu Li, Nanxi Geng, Feng Jin, Feng Li
Oncotarget. 2015 Feb; 6(6): 4345–4356. Published online 2015 Jan 21. doi: 10.18632/oncotarget.2999
PMCID:
PMC4414194
AbstractArticlePDF–3.0M

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