A scale of “bad” co-mutations in NPM1-driven AML
Author:
Affiliation:
1. UNIVERSITY OF PERUGIA
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/130/17/1877/1403190/blood804062.pdf
Reference10 articles.
1. Molecular synergy underlies the co-occurrence patterns and phenotype of NPM1-mutant acute myeloid leukemia;Dovey;Blood,2017
2. Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype;Falini;N Engl J Med,2005
3. Acute myeloid leukemia with mutated nucleophosmin (NPM1): is it a distinct entity?;Falini;Blood,2011
4. Leukemia-associated somatic mutations drive distinct patterns of age-related clonal hemopoiesis;McKerrell;Cell Reports,2015
5. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia;Arber;Blood,2016
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2. A Curious Novel Combination of Nucleophosmin (NPM1) Gene Mutations Leading to Aberrant Cytoplasmic Dislocation of NPM1 in Acute Myeloid Leukemia (AML);Genes;2021-09-16
3. NPM1-Mutated Myeloid Neoplasms with <20% Blasts: A Really Distinct Clinico-Pathologic Entity?;International Journal of Molecular Sciences;2020-11-26
4. NPM1-mutated acute myeloid leukemia: from bench to bedside;Blood;2020-10-08
5. Structural insights into amyloid structures of the C-terminal region of nucleophosmin 1 in type A mutation of acute myeloid leukemia;Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics;2019-06
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