Human Genome Epidemiology Literature Finder
|
Records 1 - 18 (of 18 Records) |
| Query Trace: Syndrome and CEBPA[original query] |
|---|
| CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin's lymphoma. Blood cells, molecules & diseases 0 40 (3): 401-5. Fuchs Ota, Provaznikova Dana, Kocova Marcela, Kostecka Arnost, Cvekova Pavla, Neuwirtova Radana, Kobylka Petr, Cermak Jaroslav, Brezinova Jana, Schwarz Jiri, Markova Jana, Salaj Peter, Klamova Hana, Maaloufova Jacqueline, Lemez Petr, Novakova Ludmila, Benesova Kateri |
| The impact on outcome of the addition of all-trans retinoic acid to intensive chemotherapy in younger patients with nonacute promyelocytic acute myeloid leukemia: overall results and results in genotypic subgroups defined by mutations in NPM1, FLT3, and CEBPA. Blood 2010 Feb 115 (5): 948-56. Burnett Alan K, Hills Robert K, Green Claire, Jenkinson Sarah, Koo Kenneth, Patel Yashma, Guy Carol, Gilkes Amanda, Milligan Donald W, Goldstone Anthony H, Prentice Archibald G, Wheatley Keith, Linch David C, Gale Rosemary |
| AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterations. Blood 2009 Dec 114 (26): 5352-61. Tang Jih-Luh, Hou Hsin-An, Chen Chien-Yuan, Liu Chieh-Yu, Chou Wen-Chien, Tseng Mei-Hsuan, Huang Chi-Fei, Lee Fen-Yu, Liu Ming-Chih, Yao Ming, Huang Shang-Yi, Ko Bor-Sheng, Hsu Szu-Chun, Wu Shang-Ju, Tsay Woei, Chen Yao-Chang, Lin Liang-In, Tien Hwei-Fa |
| CCAAT/enhancer-binding protein alpha (CEBPA) polymorphisms and mutations in healthy individuals and in patients with peripheral artery disease, ischaemic heart disease and hyperlipidaemia. Folia biologica 2010 56 (2): 51-7. Fuchs O, Kostecka A, Provazníková D, Krásná B, Kotlín R, Stanková M, Kobylka P, Dostálová G, Zeman M, Chochola |
| A gene variation (rs12691) in the CCAT/enhancer binding protein a modulates glucose metabolism in metabolic syndrome. Nutrition, metabolism, and cardiovascular diseases : NMCD 2013 May 23 (5): 417-23. Delgado-Lista J, Perez-Martinez P, Garcia-Rios A, Phillips C M, Hall W, Gjelstad I M F, Lairon D, Saris W, Kie?-Wilk B, Karlström B, Drevon C A, Defoort C, Blaak E E, Dembinska-Kie? A, Risérus U, Lovegrove J A, Roche H M, Lopez-Miranda |
| Clonal leukemic evolution in myelodysplastic syndromes with TET2 and IDH1/2 mutations. Haematologica 2014 Jan 99 (1): 28-36. Lin Tung-Liang, Nagata Yasunobu, Kao Hsiao-Wen, Sanada Masashi, Okuno Yusuke, Huang Chein-Fuang, Liang Der-Cherng, Kuo Ming-Chung, Lai Chang-Liang, Lee En-Hui, Shih Yu-Shu, Tanaka Hiroko, Shiraishi Yuichi, Chiba Kenichi, Lin Tung-Huei, Wu Jin-Hou, Miyano Satoru, Ogawa Seishi, Shih Lee-Yu |
| Top single nucleotide polymorphisms affecting carbohydrate metabolism in metabolic syndrome: from the LIPGENE study. The Journal of clinical endocrinology and metabolism 2014 Feb 99 (2): E384-9. Delgado-Lista Javier, Perez-Martinez Pablo, Solivera Juan, Garcia-Rios Antonio, Perez-Caballero A I, Lovegrove Julie A, Drevon Christian A, Defoort Catherine, Blaak Ellen E, Dembinska-Kie? Aldona, Risérus Ulf, Herruzo-Gomez Ezequiel, Camargo Antonio, Ordovas Jose M, Roche Helen, Lopez-Miranda Jo |
| CEBPA methylation and mutation in myelodysplastic syndrome. Medical oncology (Northwood, London, England) 2015 Jul 32 (7): 192. Wen Xiang-mei, Hu Jia-bo, Yang Jing, Qian Wei, Yao Dong-ming, Deng Zhao-qun, Zhang Ying-ying, Zhu Xiao-wen, Guo Hong, Lin Jiang, Qian J |
| The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes. British journal of haematology 2016 Mar . Olsson Linda, Zettermark Sofia, Biloglav Andrea, Castor Anders, Behrendtz Mikael, Forestier Erik, Paulsson Kajsa, Johansson Bert |
| Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignancies. Blood advances 2018 01 2 (2): 146-150. Drazer Michael W, Kadri Sabah, Sukhanova Madina, Patil Sushant A, West Allison H, Feurstein Simone, Calderon Dalein A, Jones Matthew F, Weipert Caroline M, Daugherty Christopher K, Ceballos-López Adrián A, Raca Gordana, Lingen Mark W, Li Zejuan, Segal Jeremy P, Churpek Jane E, Godley Lucy |
| Analytical validation and performance characteristics of a 48-gene next-generation sequencing panel for detecting potentially actionable genomic alterations in myeloid neoplasms. PloS one 2021 4 16 (4): e0243683. Rosenthal Sun Hee, Gerasimova Anna, Ma Charles, Li Hai-Rong, Grupe Andrew, Chong Hansook, Acab Allan, Smolgovsky Alla, Owen Renius, Elzinga Christopher, Chen Rebecca, Sugganth Daniel, Freitas Tracey, Graham Jennifer, Champion Kristen, Bhattacharya Anindya, Racke Frederick, Lacbawan Felicit |
| The genetic landscape of germline DDX41 variants predisposing to myeloid neoplasms. Blood 2022 6 140 (7): 716-755. Li Peng, Brown Sara, Williams Margaret, White Thomas, Xie Wei, Cui Wei, Peker Deniz, Lei Li, Kunder Christian A, Wang Huan-You, Murray Sarah S, Vagher Jennie, Kovacsovics Tibor, Patel Jay |
| [Analysis of Gene Mutation Characteristics and Prognosis of Elderly Patients with Acute Myeloid Leukemia]. Zhongguo shi yan xue ye xue za zhi 2022 Jun 30 (3): 755-759. Zhou Nai-Cen, Li Guo-Hui, Qin Wei-Wei, Wang Wen-Qing, Guo Huai-Peng, Liu Cong, Liu |
| Genetic Characteristics According to Subgroup of Acute Myeloid Leukemia with Myelodysplasia-Related Changes. Journal of clinical medicine 2022 5 11 (9): . Kang Dain, Jung Jin, Park Silvia, Cho Byung-Sik, Kim Hee-Je, Kim Yeojae, Lee Jong-Mi, Kim Hoon Seok, Ahn Ari, Kim Myungshin, Kim Yongg |
| UBTF tandem duplications are rare but recurrent alterations in adult AML and associated with younger age, myelodysplasia, and inferior outcome. Blood cancer journal 2023 5 13 (1): 88. Julia-Annabell Georgi, Sebastian Stasik, Jan-Niklas Eckardt, Sven Zukunft, Marita Hartwig, Christoph Röllig, Jan Moritz Middeke, Uta Oelschlägel, Utz Krug, Tim Sauer, Sebastian Scholl, Andreas Hochhaus, Tim H Brümmendorf, Ralph Naumann, Björn Steffen, Hermann Einsele, Markus Schaich, Andreas Burchert, Andreas Neubauer, Kerstin Schäfer-Eckart, Christoph Schliemann, Stefan W Krause, Mathias Hänel, Richard Noppeney, Ulrich Kaiser, Claudia D Baldus, Martin Kaufmann, Carsten Müller-Tidow, Uwe Platzbecker, Wolfgang E Berdel, Hubert Serve, Gerhard Ehninger, Martin Bornhäuser, Johannes Schetelig, Frank Kroschinsky, Christian Thiede, |
| Gene mutation analysis using next-generation sequencing and its clinical significance in patients with myeloid neoplasm: A multi-center study from China. Cancer medicine 2023 2 . Li Junnan, Pei Li, Liang Simin, Xu Shuangnian, Wang Yi, Wang Xiao, Liao Yi, Zhan Qian, Cheng Wei, Yang Zesong, Tang Xiaoqiong, Zhang Hongbin, Xiao Qing, Chen Jianbin, Liu Lin, Wang |
| Analysis of CSF3R mutations in atypical chronic myeloid leukemia and other myeloid malignancies. Annals of diagnostic pathology 2024 4 71 152317. Seon Young Kim, Ik-Chan Song, Jimyung Kim, Gye Cheol Kw |
| [Analysis of Gene Mutation and Clinical Characteristics Related to Myelodysplastic Syndrome]. Zhongguo shi yan xue ye xue za zhi 2025 1 32 (6): 1798-1806. Yu-Feng Wang, Yan-Li Yang, Ying-Hua Ge |
- Page last reviewed:Feb 1, 2024
- Content source: