The oncogene and developmental regulator EVI1: expression, biochemical properties, and biological functions
R Wieser - Gene, 2007 - Elsevier
The EVI1 gene codes for a zinc finger transcription factor with important roles both in normal
development and in leukemogenesis. Transcriptional activation of this gene through …
development and in leukemogenesis. Transcriptional activation of this gene through …
Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease
S Stein, MG Ott, S Schultze-Strasser, A Jauch… - Nature medicine, 2010 - nature.com
Gene-modified autologous hematopoietic stem cells (HSC) can provide ample clinical
benefits to subjects suffering from X-linked chronic granulomatous disease (X-CGD), a rare …
benefits to subjects suffering from X-linked chronic granulomatous disease (X-CGD), a rare …
Clinical, molecular, and prognostic significance of WHO type inv (3)(q21q26. 2)/t (3; 3)(q21; q26. 2) and various other 3q abnormalities in acute myeloid leukemia
S Lugthart, S Gröschel, HB Beverloo… - Journal of clinical …, 2010 - ascopubs.org
Purpose Acute myeloid leukemia (AML) with inv (3)(q21q26. 2)/t (3; 3)(q21; q26. 2)[inv (3)/t
(3; 3)] is recognized as a distinctive entity in the WHO classification. Risk assignment and …
(3; 3)] is recognized as a distinctive entity in the WHO classification. Risk assignment and …
Pretreatment cytogenetics add to other prognostic factors predicting complete remission and long-term outcome in patients 60 years of age or older with acute myeloid …
We investigated the relative prognostic significance of cytogenetics in 635 adult acute
myeloid leukemia (AML) patients 60 years of age or older treated on front-line protocols …
myeloid leukemia (AML) patients 60 years of age or older treated on front-line protocols …
3q26/EVI1 rearrangements in myeloid hemopathies: a cytogenetic review
M De Braekeleer, MJ Le Bris, E De Braekeleer… - Future …, 2015 - Taylor & Francis
The EVI1 gene, located in chromosomal band 3q26, is a transcription factor that has stem
cell-specific expression pattern and is essential for the regulation of self-renewal of …
cell-specific expression pattern and is essential for the regulation of self-renewal of …
Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study
H Hasle, TA Alonzo, A Auvrignon… - Blood, The Journal …, 2007 - ashpublications.org
Abstract Monosomy 7 (− 7) and deletion 7q\del (7q) are rare in childhood acute myeloid
leukemia (AML). We retrospectively collected data on 258 children with AML or refractory …
leukemia (AML). We retrospectively collected data on 258 children with AML or refractory …
Myelodysplasia after clonal hematopoiesis with APOBEC3-mediated CYBB inactivation in retroviral gene therapy for X-CGD
T Uchiyama, T Kawai, K Nakabayashi, Y Nakazawa… - Molecular Therapy, 2023 - cell.com
Stem cell gene therapy using the MFGS-gp91 phox retroviral vector was performed on a 27-
year-old patient with X-linked chronic granulomatous disease (X-CGD) in 2014. The …
year-old patient with X-linked chronic granulomatous disease (X-CGD) in 2014. The …
Expression and prognostic significance of different mRNA 5′‐end variants of the oncogene EVI1 in 266 patients with de novo AML: EVI1 and MDS1/EVI1 …
K Haas, M Kundi, WR Sperr… - Genes …, 2008 - Wiley Online Library
Rearrangements of chromosome band 3q26. 2 lead to overexpression of the EVI1 gene and
are associated with a poor prognosis in myeloid malignancies. EVI1 is also overexpressed …
are associated with a poor prognosis in myeloid malignancies. EVI1 is also overexpressed …
EVI1 is consistently expressed as principal transcript in common and rare recurrent 3q26 rearrangements
B Poppe, N Dastugue, J Vandesompele… - Genes …, 2006 - Wiley Online Library
In contrast to the well‐documented involvement of EVI1 in various 3q26 aberrations, the
transcriptional status of EVI1 in rare recurrent or sporadic 3q26 chromosomal defects has …
transcriptional status of EVI1 in rare recurrent or sporadic 3q26 chromosomal defects has …
Ring chromosomes in human neoplasias
E Gebhart - Cytogenetic and genome research, 2008 - karger.com
Though reported from a wide variety of human neoplasias, ring chromosomes, in general,
are a rare finding in these diseases. The majority were detected by chance when tumors …
are a rare finding in these diseases. The majority were detected by chance when tumors …