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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 17, 2024. (Total: 231532Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Trisomy and JAK2[original query]
Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome.
Lancet (London, England) 2008 Oct 372 (9648): 1484-92.
Bercovich Dani, Ganmore Ithamar, Scott Linda M, Wainreb Gilad, Birger Yehudit, Elimelech Arava, Shochat Chen, Cazzaniga Giovanni, Biondi Andrea, Basso Giuseppe, Cario Gunnar, Schrappe Martin, Stanulla Martin, Strehl Sabine, Haas Oskar A, Mann Georg, Binder Vera, Borkhardt Arndt, Kempski Helena, Trka Jan, Bielorei Bella, Avigad Smadar, Stark Batia, Smith Owen, Dastugue Nicole, Bourquin Jean-Pierre, Tal Nir Ben, Green Anthony R, Izraeli Sh
Association of JAK2 mutation status and cytogenetic abnormalities in myeloproliferative neoplasms and myelodysplastic/myeloproliferative neoplasms.
American journal of clinical pathology 2011 May 135 (5): 709-19.
Dunlap Jennifer, Kelemen Katalin, Leeborg Nicky, Braziel Rita, Olson Susan, Press Richard, Huang James, Gatter Ken, Loriaux Marc, Fan Gua
Secondary genetic lesions in acute myeloid leukemia with inv(16) or t(16;16): a study of the German-Austrian AML Study Group (AMLSG).
Blood 2013 Jan 121 (1): 170-7.
Paschka Peter, Du Juan, Schlenk Richard F, Gaidzik Verena I, Bullinger Lars, Corbacioglu Andrea, Späth Daniela, Kayser Sabine, Schlegelberger Brigitte, Krauter Jürgen, Ganser Arnold, Köhne Claus-Henning, Held Gerhard, von Lilienfeld-Toal Marie, Kirchen Heinz, Rummel Mathias, Götze Katharina, Horst Heinz-August, Ringhoffer Mark, Lübbert Michael, Wattad Mohammed, Salih Helmut R, Kündgen Andrea, Döhner Hartmut, Döhner Konstan
Dynamics of ASXL1 mutation and other associated genetic alterations during disease progression in patients with primary myelodysplastic syndrome.
Blood cancer journal 2014 4 e177.
Chen T-C, Hou H-A, Chou W-C, Tang J-L, Kuo Y-Y, Chen C-Y, Tseng M-H, Huang C-F, Lai Y-J, Chiang Y-C, Lee F-Y, Liu M-C, Liu C-W, Liu C-Y, Yao M, Huang S-Y, Ko B-S, Hsu S-C, Wu S-J, Tsay W, Chen Y-C, Tien H
Detection of CALR Mutation in Clonal and Nonclonal Hematologic Diseases Using Fragment Analysis and Next-Generation Sequencing.
American journal of clinical pathology 2016 Oct 146 (4): 448-55.
Gardner Juli-Anne, Peterson Jason D, Turner Scott A, Soares Barbara L, Lancor Courtney R, Dos Santos Luciana L, Kaur Prabhjot, Ornstein Deborah L, Tsongalis Gregory J, de Abreu Francine
High Frequency of Copy-Neutral Loss of Heterozygosity in Patients with Myelofibrosis.
Cytogenetic and genome research 2018 Mar .
Rego de Paula Junior Milton, Nonino Alexandre, Minuncio Nascimento Juliana, Bonadio Raphael S, Pic-Taylor Aline, de Oliveira Silviene F, Wellerson Pereira Rinaldo, do Couto Mascarenhas Cintia, Forte Mazzeu Julia
Somatically acquired mutations in primary myelofibrosis: A case report and meta-analysis.
Experimental and therapeutic medicine 2021 1 21 (3): 193.
Xia Yongming, Hong Qingxiao, Gao Zhibin, Wang Shijun, Duan Shiw
Triple-Negative Primary Myelofibrosis: A Bone Marrow Pathology Group Study.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2023 2 36 (3): 100016.
Al-Ghamdi Yahya A, Lake Jonathan, Bagg Adam, Thakral Beenu, Wang Sa A, Bueso-Ramos Carlos, Masarova Lucia, Verstovsek Srdan, Rogers Heesun J, Hsi Eric D, Gralewski Jonathon H, Chabot-Richards Devon, George Tracy I, Rets Anton, Hasserjian Robert P, Weinberg Olga K, Parilla Megan, Arber Daniel A, Padilla Osvaldo, Orazi Attilio, Tam Way
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