(Q34518952)

2 August 2017

title

High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9. (English)

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2 August 2017

8

Rob Pieters

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2 August 2017

Anne R M von Bergh

1

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2 August 2017

Ellen van Drunen

2

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2 August 2017

Elisabeth R van Wering

3

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2 August 2017

Laura J C M van Zutven

4

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2 August 2017

Ina Hainmann

5

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2 August 2017

Gudmar Lönnerholm

6

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2 August 2017

Jules P Meijerink

7

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2 August 2017

H Berna Beverloo

9

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2 August 2017

publication date

1 August 2006

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Genes, Chromosomes and Cancer

2 August 2017

published in

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2 August 2017

volume

45

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2 August 2017

issue

8

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2 August 2017

page(s)

731-739

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A novel method to compensate for different amplification efficiencies between patient DNA samples in quantitative real-time PCR.

2 August 2017

cites work

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ETV6: a versatile player in leukemogenesis.

21 January 2018

1 reference

7 January 2021

ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia

1 reference

7 January 2021

Evidence for position effects as a variant ETV6-mediated leukemogenic mechanism in myeloid leukemias with a t(4;12)(q11-q12;p13) or t(5;12)(q31;p13).

1 reference

7 January 2021

An investigation of the t(12;21) rearrangement in children with B-precursor acute lymphoblastic leukaemia using cytogenetic and molecular methods

1 reference

7 January 2021

A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly

1 reference

7 January 2021

TEL/AML1-positive pediatric leukemia: prognostic significance and therapeutic approaches

1 reference

7 January 2021

Activation of HLXB9 by juxtaposition with MYB via formation of t(6;7)(q23;q36) in an AML-M4 cell line (GDM-1).

1 reference

7 January 2021

HLXB9 activates IL6 in Hodgkin lymphoma cell lines and is regulated by PI3K signalling involving E2F3.

1 reference

7 January 2021

Ectopic expression of the homeobox gene Cdx2 is the transforming event in a mouse model of t(12;13)(p13;q12) acute myeloid leukemia

1 reference

7 January 2021

Chromosome abnormalities and MLL rearrangements in acute myeloid leukemia of infants

1 reference

7 January 2021

Cytogenetic and molecular heterogeneity of 7q36/12p13 rearrangements in childhood AML

1 reference

7 January 2021

Identification of NOM1, a nucleolar, eIF4A binding protein encoded within the chromosome 7q36 breakpoint region targeted in cases of pediatric acute myeloid leukemia

1 reference

7 January 2021

t(7;12)(q36;p13) and t(7;12)(q32;p13)--translocations involving ETV6 in children 18 months of age or younger with myeloid disorders

1 reference

7 January 2021

Differential mRNA expression of Ara-C-metabolizing enzymes explains Ara-C sensitivity in MLL gene-rearranged infant acute lymphoblastic leukemia

1 reference

7 January 2021

Incidence of additional genetic changes in the TEL and AML1 genes in DCOG and COALL-treated t(12;21)-positive pediatric ALL, and their relation with drug sensitivity and clinical outcome

1 reference

7 January 2021

Expression levels of TEL, AML1, and the fusion products TEL-AML1 and AML1-TEL versus drug sensitivity and clinical outcome in t(12;21)-positive pediatric acute lymphoblastic leukemia

1 reference

7 January 2021

t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia

1 reference

7 January 2021

Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.20335

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2 August 2017

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