(Q47367787)

14 January 2018

title

Cryptic insertion of MLL gene into 9p22 leads to MLL-MLLT3 (AF9) fusion in a case of acute myelogenous leukemia (English)

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14 January 2018

Suzanne Kamel-Reid

3

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author name string

Mary Shago

1

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14 January 2018

Derek Bouman

2

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14 January 2018

Mark Minden

4

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14 January 2018

Kathy Chun

5

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14 January 2018

publication date

1 August 2004

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14 January 2018

Genes, Chromosomes and Cancer

published in

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14 January 2018

volume

40

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14 January 2018

issue

4

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14 January 2018

page(s)

349-354

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14 January 2018

The structure of the human ALL-1/MLL/HRX gene.

cites work

1 reference

Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins

21 January 2018

1 reference

7 January 2021

An ins(X;11)(q24;q23) fuses the MLL and the Septin 6/KIAA0128 gene in an infant with AML-M2.

1 reference

7 January 2021

Occurrence of an MLL/LAF4 fusion gene caused by the insertion ins(11;2)(q23;q11.2q11.2) in an infant with acute lymphoblastic leukemia

1 reference

7 January 2021

Exon scrambling of MLL transcripts occur commonly and mimic partial genomic duplication of the gene

1 reference

7 January 2021

Mouse Af9 is a controller of embryo patterning, like Mll, whose human homologue fuses with Af9 after chromosomal translocation in leukemia

1 reference

7 January 2021

An Mll-AF9 fusion gene made by homologous recombination causes acute leukemia in chimeric mice: a method to create fusion oncogenes

1 reference

7 January 2021

Insertion of MLL sequences into chromosome band 5q31 results in an MLL-AF5Q31 fusion and is a rare but recurrent abnormality associated with infant leukemia

1 reference

7 January 2021

A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias

1 reference

7 January 2021

The mll-AF9 gene fusion in mice controls myeloproliferation and specifies acute myeloid leukaemogenesis

1 reference

7 January 2021

Detection of cryptic MLL insertions using a commercial dual-color fluorescence in situ hybridization probe

1 reference

7 January 2021

The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemia

1 reference

7 January 2021

Cryptic chromosomal aberrations leading to an AML1/ETO rearrangement are frequently caused by small insertions

1 reference

7 January 2021

The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 gene

1 reference

7 January 2021

Hematological malignancies with a deletion of 11q23: cytogenetic and clinical aspects. European 11q23 Workshop participants

1 reference

7 January 2021

Prognostic importance of cytogenetic subgroups in de novo pediatric acute nonlymphocytic leukemia.

1 reference

7 January 2021

Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization

1 reference

7 January 2021

Abnormalities of chromosome band 11q23 and the MLL gene in pediatric myelomonocytic and monoblastic leukemias. Identification of the t(9;11) as an indicator of long survival

1 reference

7 January 2021

Two acute monocytic leukemia (AML-M5a) cell lines (MOLM-13 and MOLM-14) with interclonal phenotypic heterogeneity showing MLL-AF9 fusion resulting from an occult chromosome insertion, ins(11;9)(q23;p22p23).

1 reference

7 January 2021

The human MLL gene: nucleotide sequence, homology to the Drosophila trx zinc-finger domain, and alternative splicing.

1 reference

7 January 2021

Genes on chromosomes 4, 9, and 19 involved in 11q23 abnormalities in acute leukemia share sequence homology and/or common motifs

1 reference

7 January 2021

Exon/intron structure of the human ALL-1 (MLL) gene involved in translocations to chromosomal region 11q23 and acute leukaemias

1 reference

7 January 2021

Prognostic factors in infants with acute myeloid leukemia

1 reference

7 January 2021

The critical role of chromosome translocations in human leukemias.

1 reference

7 January 2021

Attitudes of terminally ill cancer patients about euthanasia and assisted suicide: predominance of psychosocial determinants and beliefs over symptom distress and subsequent survival.

1 reference

7 January 2021

MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisom

1 reference

7 January 2021

Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia

1 reference

7 January 2021

Hematological malignancies with t(9;11)(p21-22;q23)--a laboratory and clinical study of 125 cases. European 11q23 Workshop participants

1 reference

7 January 2021

Rearrangement of the MLL gene in acute lymphoblastic and acute myeloid leukemias with 11q23 chromosomal translocations

1 reference

7 January 2021

Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias

1 reference

7 January 2021

Molecular cytogenetic analysis of 10;11 rearrangements in acute myeloid leukemia

1 reference

7 January 2021

Insertion of the 5' part of BCR within the ABL gene at 9q34 in a Philadelphia-negative chronic myeloid leukemia

1 reference

7 January 2021

Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.20045

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14 January 2018

PubMed ID

15188459

1 reference

14 January 2018