Results 11 to 20 of about 4,377,369 (241)

AML with inv(16)/t(16;16) and high-risk cytogenetic abnormalities: atypical features and unfavorable outcome [PDF]

open access: yesHematology, 2022
Objectives Acute myeloid leukemia (AML) with inv(16)/t(16;16) is among the most frequent AML subtypes. It is recognized by the detection of the CBFB-MYH11 fusion which confers a favorable prognosis, irrespective of the presence of secondary cytogenetic ...
Nada Assaf   +10 more
doaj   +2 more sources

Addiction of t(8;21) and inv(16) Acute Myeloid Leukemia to Native RUNX1 [PDF]

open access: yesCell Reports, 2013
The t(8;21) and inv(16) chromosomal aberrations generate the oncoproteins AML1-ETO (A-E) and CBFβ-SMMHC (C-S). The role of these oncoproteins in acute myeloid leukemia (AML) etiology has been well studied.
Oren Ben-Ami   +8 more
doaj   +2 more sources

Acute Myeloid Leukemia With Inv(16)(p13q22) Associated With Hidden Systemic Mastocytosis: Case Report and Review of Literature [PDF]

open access: yesClinical Medicine Insights: Blood Disorders, 2017
Systemic mastocytosis (SM) is a condition associated with clonal neoplastic proliferation of mast cells. In up to 40% of systemic mastocytosis cases, an associated clonal hematological disease of non–mast cell lineage, such as acute myeloid leukemia (AML)
Feryal Abbas Ibrahim Hilmi   +6 more
doaj   +2 more sources

Secondary cytogenetic abnormalities in core-binding factor AML harboring inv(16) vs t(8;21). [PDF]

open access: yesBlood Adv, 2021
Patients with core-binding factor (CBF) acute myeloid leukemia (AML), caused by either t(8;21)(q22;q22) or inv(16)(p13q22)/t(16;16)(p13;q22), have higher complete remission rates and longer survival than patients with other subtypes of AML. However, ∼40%
Han SY   +46 more
europepmc   +4 more sources

Abnormal eosinophils with immature eosinophilic granules in chronic myeloid leukemia in accelerated phase

open access: yesClinical Case Reports, 2021
Abnormal eosinophils with immature eosinophilic granules are typically observed in acute myeloid leukemia with inv (16) (p13.1q22) or t (16;16) (p13.1;q22) but can also be seen in chronic myeloid leukemia without inv (16) or t (16;16).
Jennifer Cai   +3 more
doaj   +1 more source

inv(16) and NPM1mut AMLs engraft human cytokine knock-in mice.

open access: yesBlood, 2016
Favorable-risk human acute myeloid leukemia (AML) engrafts poorly in currently used immunodeficient mice, possibly because of insufficient environmental support of these leukemic entities.
Ellegast JM   +15 more
europepmc   +2 more sources

HDAC8 Inhibition Specifically Targets Inv(16) Acute Myeloid Leukemic Stem Cells by Restoring p53 Acetylation. [PDF]

open access: yesCell Stem Cell, 2015
SummaryAcute myeloid leukemia (AML) is driven and sustained by leukemia stem cells (LSCs) with unlimited self-renewal capacity and resistance to chemotherapy.
Qi J   +14 more
europepmc   +2 more sources

Comprehensive Mutation Profile in Acute Myeloid Leukemia Patients with RUNX1-RUNX1T1 or CBFB-MYH11 Fusions

open access: yesTurkish Journal of Hematology, 2022
Objective: This study was undertaken with the aim of better understanding the genomic landscape of core-binding factor (CBF) acute myeloid leukemia (AML).
Wei Qin   +6 more
doaj   +1 more source

Clinical characteristics and prognostic factors analysis of core binding factor acute myeloid leukemia in real world

open access: yesCancer Medicine, 2023
Background Chromosomal translocations involving core binding factor (CBF) genes account for 15% of adult acute myeloid leukemia (AML) cases in China. Despite being classified as favorable‐risk by European Leukemia Net (ELN), CBF‐AML patients have a 40 ...
Yamei Zhai   +12 more
doaj   +1 more source

inv(16)(p13q24) CBFA2T3/GLIS2 [PDF]

open access: yes, 2013
Review on inv(16)(p13q24) CBFA2T3/GLIS2, with data on clinics, and the genes ...
Huret, JL
core   +1 more source

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