HuGE Literature Finder
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| Clonal haematopoiesis of indeterminate potential-related mutations and outcome in dilated and ischaemic cardiomyopathy. ESC heart failure 2022 Aug . Wu Jasmine M F, Bekfani Tarek, Hinze Anna, Westphal Julian Georg, Steinacker Berit, Zeller Max, Hartmann Charlotte, Möbius-Winkler Sven, Hochhaus Andreas, Schulze P Christian, Ernst Thom |
| Comprehensive Analysis of Acquired Genetic Variants and Their Prognostic Impact in Systemic Mastocytosis. Cancers 2022 5 14 (10): . González-López Oscar, Muñoz-González Javier I, Orfao Alberto, Álvarez-Twose Iván, García-Montero Andrés |
| Otto Aufranc Award: Identification of Key Molecular Players in the Progression of Hip Osteoarthritis Through Transcriptomes and Epigenetics. The Journal of arthroplasty 2022 3 37 (7S): S391-S399. Pascual-Garrido Cecilia, Kamenaga Tomoyuki, Brophy Robert H, Shen Jie, O'Keefe Regis J, Clohisy John |
| Prevalence and prognostic significance of DNMT3A- and TET2- clonal haematopoiesis-driver mutations in patients presenting with ST-segment elevation myocardial infarction. EBioMedicine 2022 3 78 103964. Wang Shengfang, Hu Sining, Luo Xing, Bao Xiaoyi, Li Ji, Liu Minghao, Lv Ying, Zhao Chen, Zeng Ming, Chen Xi, Unsworth Amanda, Jones Sarah, Johnson Thomas W, White Stephen J, Jia Haibo, Yu |
| ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome. Blood advances 2021 9 6 (3): 793-807. West Robert R, Calvo Katherine R, Embree Lisa J, Wang Weixin, Tuschong Laura M, Bauer Thomas R, Tillo Desiree, Lack Justin, Droll Stephenie, Hsu Amy P, Holland Steven M, Hickstein Dennis |
| Excellent Prognosis of Low-Risk Myelodysplastic Syndromes (MDS) Without Detectable Myeloid-Related Mutations. Clinical lymphoma, myeloma & leukemia 2021 11 22 (5): e293-e299. Polprasert Chantana, Niparuck Pimjai, Rattanathammethee Thanawat, Chuncharunee Suporn, Kobbuaklee Sirorat, Songserm Kritanan, Suksusut Amornchai, Trithiphen Sasinipa, Lanamtieng Theerin, Kongkiatkamon Sunisa, Chanswangphuwana Chantiya, Lawasut Panisinee, Bunworasate Udomsak, Rojnuckarin Ponlap |
| Molecular Progression of Myeloproliferative and Myelodysplastic/Myeloproliferative Neoplasms: A Study on Sequential Bone Marrow Biopsies. Cancers 2021 11 13 (22): . Brune Magdalena M, Rau Achim, Overkamp Mathis, Flaadt Tim, Bonzheim Irina, Schürch Christian M, Federmann Birgit, Dirnhofer Stefan, Fend Falko, Tzankov Alexand |
| [Clinical Characteristics and Prognostic Significance of BCOR/BCORL1 Gene Mutation in Patients with Myelodysplastic Syndromes]. Zhongguo shi yan xue ye xue za zhi 2020 Dec 28 (6): 2004-2010. Cen Yan-Xia, Li Y |
| ASXL1 mutations, previous vascular complications and age at diagnosis predict survival in 85 WHO-defined polycythaemia vera patients. British journal of haematology 2020 Feb . Andréasson Björn, Pettersson Helna, Wasslavik Carina, Johansson Peter, Palmqvist Lars, Asp Jul |
| Cytokine rs361525, rs1800750, rs1800629, rs1800896, rs1800872, rs1800795, rs1800470, and rs2430561 SNPs in relation with prognostic factors in acute myeloid leukemia. Cancer medicine 2019 Aug . B?nescu Claudia, Tripon Florin, Trifa Adrian P, Crauciuc Andrei G, Moldovan Valeriu G, Bogli? Alina, Benedek Istvan, Dima Delia, Cândea Marcela, Duicu Carmen, Iancu Mihae |
| DNMT1 and DNMT3B genetic polymorphisms affect the clinical course and outcome of melanoma patients. Melanoma research 2019 Apr . Maric Helena, Supic Gordana, Kandolf-Sekulovic Lidija, Maric Veljko, Mijuskovic Zeljko, Radevic Tatjana, Rajovic Milica, Magic Zvon |
| Impact of High-Molecular-Risk Mutations on Transplantation Outcomes in Patients with Myelofibrosis. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2019 1 25 (6): 1142-1151. Tamari Roni, Rapaport Franck, Zhang Nan, McNamara Caroline, Kuykendall Andrew, Sallman David A, Komrokji Rami, Arruda Andrea, Najfeld Vesna, Sandy Lonette, Medina Juan, Litvin Rivka, Famulare Christopher A, Patel Minal A, Maloy Molly, Castro-Malaspina Hugo, Giralt Sergio A, Weinberg Rona S, Mascarenhas John O, Mesa Ruben, Rondelli Damiano, Dueck Amylou C, Levine Ross L, Gupta Vikas, Hoffman Ronald, Rampal Raajit |
| Presence of copy number aberration and clinical prognostic factors in patients with acute myeloid leukemia: an analysis of effect modification. Polish archives of internal medicine 2019 12 . Banescu Claudia, Tripon Florin, Trifa Adrian P, Crauciuc Andrei G, Bogli? Alina, Lazar Erzsebet, Dima Delia, Macarie Ioan, Duicu Carmen, Iancu Mihae |
| Dynamics of DNMT3A mutation and prognostic relevance in patients with primary myelodysplastic syndrome. Clinical epigenetics 2018 4 10 42. Lin Ming-En, Hou Hsin-An, Tsai Cheng-Hong, Wu Shang-Ju, Kuo Yuan-Yeh, Tseng Mei-Hsuan, Liu Ming-Chih, Liu Chia-Wen, Chou Wen-Chien, Chen Chien-Yuan, Tang Jih-Luh, Yao Ming, Li Chi-Cheng, Huang Shang-Yi, Ko Bor-Sheng, Hsu Szu-Chun, Lin Chien-Ting, Tien Hwei-Fa |
| Evolution of Cytogenetically Normal Acute Myeloid Leukemia During Therapy and Relapse: An Exome Sequencing Study of 50 Patients. Clinical cancer research : an official journal of the American Association for Cancer Research 2018 1 24 (7): 1716-1726. Greif Philipp A, Hartmann Luise, Vosberg Sebastian, Stief Sophie M, Mattes Raphael, Hellmann Ines, Metzeler Klaus H, Herold Tobias, Bamopoulos Stefanos A, Kerbs Paul, Jurinovic Vindi, Schumacher Daniela, Pastore Friederike, Bräundl Kathrin, Zellmeier Evelyn, Ksienzyk Bianka, Konstandin Nikola P, Schneider Stephanie, Graf Alexander, Krebs Stefan, Blum Helmut, Neumann Martin, Baldus Claudia D, Bohlander Stefan K, Wolf Stephan, Görlich Dennis, Berdel Wolfgang E, Wörmann Bernhard J, Hiddemann Wolfgang, Spiekermann Karst |
| Expression profiling of chromatin-modifying enzymes and global DNA methylation in CD4+ T cells from patients with chronic HIV infection at different HIV control and progression states. Clinical epigenetics 2018 2 10 20. Bogoi Roberta Nicoleta, de Pablo Alicia, Valencia Eulalia, Martín-Carbonero Luz, Moreno Victoria, Vilchez-Rueda Helem Haydee, Asensi Victor, Rodriguez Rosa, Toledano Victor, Rodés Ber |
| Two novel methods for rapid detection and quantification of DNMT3A R882 mutations in acute myeloid leukemia. The Journal of molecular diagnostics : JMD 2015 Mar 17 (2): 179-84. Mancini Melissa, Hasan Syed Khizer, Ottone Tiziana, Lavorgna Serena, Ciardi Claudia, Angelini Daniela F, Agostini Francesca, Venditti Adriano, Lo-Coco Frances |
| Hepatic stellate cell transdifferentiation involves genome-wide remodeling of the DNA methylation landscape. Journal of hepatology 2015 12 64 (3): 661-73. Page Agata, Paoli Pier, Moran Salvador Eva, White Steve, French Jeremy, Mann Jele |
| TP53 mutations in de novo acute myeloid leukemia patients: longitudinal follow-ups show the mutation is stable during disease evolution. Blood cancer journal 2015 5 e331. Hou H-A, Chou W-C, Kuo Y-Y, Liu C-Y, Lin L-I, Tseng M-H, Chiang Y-C, Liu M-C, Liu C-W, Tang J-L, Yao M, Li C-C, Huang S-Y, Ko B-S, Hsu S-C, Chen C-Y, Lin C-T, Wu S-J, Tsay W, Chen Y-C, Tien H |
| SF3B1 mutations in patients with myelodysplastic syndromes: the mutation is stable during disease evolution. American journal of hematology 2014 Aug 89 (8): E109-15. Lin Chien-Chin, Hou Hsin-An, Chou Wen-Chien, Kuo Yuan-Yeh, Wu Shang-Ju, Liu Chieh-Yu, Chen Chien-Yuan, Tseng Mei-Hsuan, Huang Chi-Fei, Lee Fen-Yu, Liu Ming-Chih, Liu Chia-Wen, Tang Jih-Luh, Yao Ming, Huang Shang-Yi, Hsu Szu-Chun, Ko Bor-Sheng, Tsay Woei, Chen Yao-Chang, Tien Hwei-Fa |
| IDH mutations are closely associated with mutations of DNMT3A, ASXL1 and SRSF2 in patients with myelodysplastic syndromes and are stable during disease evolution. American journal of hematology 2014 Feb 89 (2): 137-44. Lin Chien-Chin, Hou Hsin-An, Chou Wen-Chien, Kuo Yuan-Yeh, Liu Chieh-Yu, Chen Chien-Yuan, Lai Yan-Jun, Tseng Mei-Hsuan, Huang Chi-Fei, Chiang Ying-Chieh, Lee Fen-Yu, Liu Ming-Chih, Liu Chia-Wen, Tang Jih-Luh, Yao Ming, Huang Shang-Yi, Ko Bor-Sheng, Wu Shang-Ju, Tsay Woei, Chen Yao-Chang, Tien Hwei-Fa |
| Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes. Haematologica 2013 Dec 98 (12): 1856-64. Fernandez-Mercado Marta, Burns Adam, Pellagatti Andrea, Giagounidis Aristoteles, Germing Ulrich, Agirre Xabier, Prosper Felipe, Aul Carlo, Killick Sally, Wainscoat James S, Schuh Anna, Boultwood Jacqueli |
| Screening for mutation R882 in the DNMT3A gene in Chinese patients with hematological disease. International journal of hematology 2012 Aug 96 (2): 229-33. Li Yunlong, Zhang Deng-Feng, Zhang Shi-Wen, Zeng Yun, Yao Yong-Ga |
| Frequency, onset and clinical impact of somatic DNMT3A mutations in therapy-related and secondary acute myeloid leukemia. Haematologica 2012 Feb 97 (2): 246-50. Fried Isabella, Bodner Claudia, Pichler Monika M, Lind Karin, Beham-Schmid Christine, Quehenberger Franz, Sperr Wolfgang R, Linkesch Werner, Sill Heinz, Wölfler Albe |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 21, 2023
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