EM Heath, SM Chan, MD Minden, T Murphy, LI Shlush… - Leukemia, 2017 - nature.com
Acute myeloid leukemia (AML) is characterized by accumulation of myeloid cells in the bone marrow because of impaired differentiation and proliferation, resulting in hematopoietic …
B Falini, MP Martelli, N Bolli… - Blood, The Journal …, 2011 - ashpublications.org
After the discovery of NPM1-mutated acute myeloid leukemia (AML) in 2005 and its subsequent inclusion as a provisional entity in the 2008 World Health Organization …
Nucleophosmin (NPM1) is a highly conserved nucleo-cytoplasmic shuttling protein that shows a restricted nucleolar localization. Mutations of NPM1 gene leading to aberrant …
R Rau, P Brown - Hematological oncology, 2009 - Wiley Online Library
Nucleophosmin (NPM) is a ubiquitously expressed chaperone protein that shuttles rapidly between the nucleus and cytoplasm, but predominantly resides in the nucleolus. It plays key …
C Haferlach, C Mecucci, S Schnittger… - Blood, The Journal …, 2009 - ashpublications.org
Acute myeloid leukemia (AML) with mutated NPM1 usually carries normal karyotype (NK), but it may harbor chromosomal aberrations whose significance remains unclear. We …
MP Martelli, P Sportoletti, E Tiacci, MF Martelli, B Falini - Blood reviews, 2013 - Elsevier
Acute myeloid leukemia (AML) is a molecularly heterogeneous disease. Based on cytogenetics and FISH, AML patients are stratified into three major risk categories …
B Falini - American journal of hematology, 2023 - Wiley Online Library
The nucleophosmin (NPM1) gene encodes for a multifunctional chaperone protein that is localized in the nucleolus but continuously shuttles between the nucleus and cytoplasm …
B Falini, K Macijewski, T Weiss… - Blood, The Journal …, 2010 - ashpublications.org
NPM1-mutated acute myeloid leukemia (AML) is a provisional entity in the 2008 World Health Organization (WHO) classification of myeloid neoplasms. The significance of …
B Falini, S Sciabolacci, L Falini, L Brunetti, MP Martelli - Leukemia, 2021 - nature.com
Mutations of Nucleophosmin (NPM1) are the most common genetic abnormalities in adult acute myeloid leukaemia (AML), accounting for about 30% of cases. NPM1-mutated AML …