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Expert Review of Hematology Volume 9, 2016 - Issue 12
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Review

Myelodysplastic syndromes and acute leukemia with genetic predispositions: a new challenge for hematologists

Nicolas DuployezLaboratory of Hematology, CHU Lille, Lille, France;INSERM, UMR-S 1172, Lille, FranceView further author information
,
Sophie LejeuneDepartment of Clinical Genetics, CHU Lille, Lille, FranceView further author information
,
Aline RennevilleLaboratory of Hematology, CHU Lille, Lille, France;INSERM, UMR-S 1172, Lille, FranceView further author information
&
Claude PreudhommeLaboratory of Hematology, CHU Lille, Lille, France;INSERM, UMR-S 1172, Lille, FranceCorrespondence[email protected]
View further author information
Pages 1189-1202 | Received 15 Sep 2016, Accepted 31 Oct 2016, Published online: 21 Nov 2016

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Mingmin He, Yongqin Jia, Yan Wang & Xiongwei Cai. (2022) Dysregulated MAPK signaling pathway in acute myeloid leukemia with RUNX1 mutations. Expert Review of Hematology 15:8, pages 769-779.
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Nicolas Duployez & Laurène Fenwarth. (2020) Controversies about germline RUNX1 missense variants. Leukemia & Lymphoma 61:2, pages 497-499.
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Articles from other publishers (15)

Cheng-Yu Tsai, Huey-Jiun Ko, Shean-Jaw Chiou, Xin-Yi Lin, Tsung-Hsien Chuang, Jiin-Tsuey Cheng, Yu-Feng Su, Joon-Khim Loh & Yi-Ren Hong. (2023) GSKIP modulates cell aggregation through EMT/MET signaling rather than differentiation in SH-SY5Y human neuroblastoma cells. Journal of Cell Communication and Signaling 17:3, pages 1039-1054.
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Cheng-Yu Tsai, Shean-Jaw Chiou, Huey-Jiun Ko, Yu-Fan Cheng, Sin-Yi Lin, Yun-Ling Lai, Chen-Yen Lin, Chihuei Wang, Jiin-Tsuey Cheng, Hsin-Fu Liu, Aij-Li Kwan, Joon-Khim Loh & Yi-Ren Hong. (2022) Deciphering the evolution of composite-type GSKIP in mitochondria and Wnt signaling pathways. PLOS ONE 17:1, pages e0262138.
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Cristina Andrés‐Zayas, Julia Suárez‐González, Gabriela Rodríguez‐Macías, Nieves Dorado, Santiago Osorio, Patricia Font, Diego Carbonell, María Chicano, Paula Muñiz, Mariana Bastos, Mi Kwon, José Luis Díez‐Martín, Ismael Buño & Carolina Martínez‐Laperche. (2021) Clinical utility of targeted next‐generation sequencing for the diagnosis of myeloid neoplasms with germline predisposition. Molecular Oncology 15:9, pages 2273-2284.
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Rashmi Kanagal-Shamanna. (2021) The Emerging Role of Hematopathologists and Molecular Pathologists in Detection, Monitoring, and Management of Myeloid Neoplasms with Germline Predisposition. Current Hematologic Malignancy Reports.
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Joseph H. Oved, Michele P. Lambert, M. Anna Kowalska, Mortimer Poncz & Konrad J. Karczewski. (2021) Population based frequency of naturally occurring loss‐of‐function variants in genes associated with platelet disorders. Journal of Thrombosis and Haemostasis 19:1, pages 248-254.
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M. P. T. Ernst & M. H. G. P. Raaijmakers. 2021. Acute Myeloid Leukemia. Acute Myeloid Leukemia 55 70 .
Naval Daver, Andrew H. Wei, Daniel A. Pollyea, Amir T. Fathi, Paresh Vyas & Courtney D. DiNardo. (2020) New directions for emerging therapies in acute myeloid leukemia: the next chapter. Blood Cancer Journal 10:10.
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Elise Fournier, Camille Debord, Valérie Soenen, Nathalie Trillot, Fanny Gonzales, Véronique Tintiller, Louis Terriou, Coralie Derrieux, Wadih Abou Chahla, Camille Paris, Céline Berthon, Thomas Boyer, Anne Lambilliotte, Pierre Boisseau, Soraya Wuillème, Marc Fouassier, Sophie Susen, Claude Preudhomme & Nicolas Duployez. (2020) Baseline dysmegakaryopoiesis in inherited thrombocytopenia/platelet disorder with predisposition to haematological malignancies. British Journal of Haematology 189:4.
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Nicolas Duployez, Laure Goursaud, Laurène Fenwarth, Claire Bories, Alice Marceau-Renaut, Thomas Boyer, Elise Fournier, Olivier Nibourel, Catherine Roche-Lestienne, Guillemette Huet, David Beauvais, Céline Berthon, Nathalie Cambier, Bruno Quesnel & Claude Preudhomme. (2019) Familial myeloid malignancies with germline TET2 mutation. Leukemia 34:5, pages 1450-1453.
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Shinya Rai, J. Luis Espinoza, Yasuyoshi Morita, Hirokazu Tanaka & Itaru Matsumura. (2019) Severe Eosinophilia in Myelodysplastic Syndrome With a Defined and Rare Cytogenetic Abnormality. Frontiers in Immunology 9.
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Mujahed I Mustafa, Zainab O Mohammed, Naseem S Murshed, Nafisa M Elfadol, Abdelrahman H Abdelmoneim & Mohamed A Hassan. (2019) In Silico Genetics Revealing 5 Mutations in CEBPA Gene Associated With Acute Myeloid Leukemia . Cancer Informatics 18, pages 117693511987081.
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Elisabeth F. Heuston, Cheryl A. Keller, Jens Lichtenberg, Belinda Giardine, Stacie M. Anderson, Ross C. Hardison & David M. Bodine. (2018) Establishment of regulatory elements during erythro-megakaryopoiesis identifies hematopoietic lineage-commitment points. Epigenetics & Chromatin 11:1.
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Chia-Hua Chou, Ming-Chang Yang, Bo-Xiu Hsiao, Yin-Hsuan Wang, Hsin-Fu Liu, Shean-Jaw Chiou, Yu-Chung Chuang, Chia-Ning Yang, Ann-Shung Lieu, Joon-Khim Loh, Shen-Long Howng, An-Kuo Chou, Chao-Neng Tseng, Jiin-Tsuey Cheng & Yi-Ren Hong. (2018) The origin of GSKIP, a multifaceted regulatory factor in the mammalian Wnt pathway. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 1865:8, pages 1046-1059.
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Attila Péter Király, Krisztián Kállay, Ambrus Gángó, Ádám Kellner, Miklós Egyed, Anita Szőke, Richárd Kiss, István Vályi-Nagy, Judit Csomor, András Matolcsy & Csaba Bödör. (2017) Familial Acute Myeloid Leukemia and Myelodysplasia in Hungary. Pathology & Oncology Research 24:1, pages 83-88.
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Jyotinder Nain Punia, Sa A. Wang & M. Tarek Elghetany. 2018. Diagnosis of Blood and Bone Marrow Disorders. Diagnosis of Blood and Bone Marrow Disorders 81 117 .

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