A Novel Fusion Between MOZ and the Nuclear Receptor Coactivator TIF2 in Acute Myeloid Leukemia
M Carapeti, RCT Aguiar, JM Goldman… - Blood, The Journal of …, 1998 - ashpublications.org
Chromosomal abnormalities of band 8p11 are associated with a distinct subtype of acute
myeloid leukemia with French-American-British M4/5 morphology and prominent …
myeloid leukemia with French-American-British M4/5 morphology and prominent …
A new gene, BCM, on chromosome 16 is fused to the interleukin 2 gene by at (4; 16)(q26; p13) translocation in a malignant T cell lymphoma.
Y Laabi, MP Gras, F Carbonnel, JC Brouet… - The EMBO …, 1992 - embopress.org
A t (4; 16)(q26; p13. 1) chromosome translocation found in tumour cells from a patient with a
T cell lymphoma was shown to rearrange the interleukin 2 gene, normally located on …
T cell lymphoma was shown to rearrange the interleukin 2 gene, normally located on …
The t(6;8)(q27;p11) Translocation in a Stem Cell Myeloproliferative Disorder Fuses a Novel Gene, FOP, to Fibroblast Growth Factor Receptor 1
C Popovici, B Zhang, MJ Grégoire… - Blood, The Journal …, 1999 - ashpublications.org
In patients with an atypical stem-cell myeloproliferative disorder with lymphoma (B or T cell),
myeloid hyperplasia, and eosinophilia, the chromosome 8p11-12 region is the site of a …
myeloid hyperplasia, and eosinophilia, the chromosome 8p11-12 region is the site of a …
FGFR1 is fused to the centrosome-associated proteinCEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33)
G Guasch, GJ Mack, C Popovici… - Blood, The Journal …, 2000 - ashpublications.org
The hallmark of the 8p12 stem cell myeloproliferative disorder (MPD) is the disruption of the
FGFR1 gene, which encodes a tyrosine kinase receptor for members of the fibroblast growth …
FGFR1 gene, which encodes a tyrosine kinase receptor for members of the fibroblast growth …
Pediatric acute myeloid leukemia with t (8; 16)(p11; p13), a distinct clinical and biological entity: a collaborative study by the International-Berlin-Frankfurt-Münster …
EA Coenen, CM Zwaan, D Reinhardt… - Blood, The Journal …, 2013 - ashpublications.org
In pediatric acute myeloid leukemia (AML), cytogenetic abnormalities are strong indicators of
prognosis. Some recurrent cytogenetic abnormalities, such as t (8; 16)(p11; p13), are so rare …
prognosis. Some recurrent cytogenetic abnormalities, such as t (8; 16)(p11; p13), are so rare …
AML with translocation t (8; 16)(p11; p13) demonstrates unique cytomorphological, cytogenetic, molecular and prognostic features
T Haferlach, A Kohlmann, HU Klein, C Ruckert… - Leukemia, 2009 - nature.com
Balanced chromosomal rearrangements define distinct entities in acute myeloid leukemia
(AML). Here, we present 13 AML cases with t (8; 16)(p11; p13) with observed low incidence …
(AML). Here, we present 13 AML cases with t (8; 16)(p11; p13) with observed low incidence …
A distinct subtype of M4/M5 acute myeloblastic leukemia (AML) associated with t (8: 16)(p11: p13), in a patient with the variant t (8: 19)(p11: q13)—case report and …
B Stark, P Resnitzky, M Jeison, D Luria, O Blau… - Leukemia research, 1995 - Elsevier
Acute myeloblastic leukemia (AML) with t (8: 16) or its variant t (8: V) has been rarely
reported. A high proportion of patients are infants and children, often with a bleeding …
reported. A high proportion of patients are infants and children, often with a bleeding …
Acute monocytic leukemia (French-American-British classification M5) does not have a worse prognosis than other subtypes of acute myeloid leukemia: a report from …
MS Tallman, HT Kim, E Paietta, JM Bennett… - Journal of clinical …, 2004 - ascopubs.org
Purpose Acute monocytic leukemia is a distinct subtype of acute myeloid leukemia (AML)
with characteristic biologic and clinical features. This study was designed to compare the …
with characteristic biologic and clinical features. This study was designed to compare the …
Acute myeloid leukaemia with 8p11 (MYST3) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogenetique …
C Gervais, A Murati, C Helias, S Struski, A Eischen… - Leukemia, 2008 - nature.com
Thirty cases of acute myeloid leukaemia (AML) with MYST histone acetyltransferase 3
(MYST3) rearrangement were collected in a retrospective study from 14 centres in France …
(MYST3) rearrangement were collected in a retrospective study from 14 centres in France …
Acute monoblastic leukemia with t (8; 16): a distinct clinicopathologic entity; report of a case and review of the literature
T Sun, E Wu - American journal of hematology, 2001 - Wiley Online Library
We report a case of acute monoblastic leukemia with t (8; 16) in a 71‐year‐old man who had
rapid rise of leukocyte counts from 20.3× 109/l to 62.7× 109/l in two weeks. The peripheral …
rapid rise of leukocyte counts from 20.3× 109/l to 62.7× 109/l in two weeks. The peripheral …