Identification of a conserved family of Meis1-related homeobox genes (Q28304621)

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J J Moskow

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K Muzynski

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C North

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T Druck

5

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J C Montgomery

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K Huebner

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I O Daar

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A M Buchberg

A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif

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language of work or name

English

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publication date

February 1997

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published in

Genome Research

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volume

7

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issue

2

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page(s)

142-56

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cites work

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Homeodomain-DNA recognition

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A new homeobox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL

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E2A-Pbx1, the t(1;19) translocation protein of human pre-B-cell acute lymphocytic leukemia, causes acute myeloid leukemia in mice

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Expression of Hox-2.4 homeobox gene directed by proviral insertion in a myeloid leukemia.

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An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

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Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7

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Analysis of the murine All-1 gene reveals conserved domains with human ALL-1 and identifies a motif shared with DNA methyltransferases

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A direct repeat in the cellular retinol-binding protein type II gene confers differential regulation by RXR and RAR

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A conserved DNA sequence in homoeotic genes of the Drosophila Antennapedia and bithorax complexes

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PBX2 and PBX3, new homeobox genes with extensive homology to the human proto-oncogene PBX1

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Meis1, a PBX1-related homeobox gene involved in myeloid leukemia in BXH-2 mice

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Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor

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Correlation of cytogenetic analysis and loss of heterozygosity studies in human diffuse astrocytomas and mixed oligo‐astrocytomas

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Structural relationships among genes that control development: sequence homology between the Antennapedia, Ultrabithorax, and fushi tarazu loci of Drosophila

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Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia

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