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Article

Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies.

Proceedings of the National Academy of Sciences of the United States of America - 11 May 2004

Li Juan, Bench Anthony J, Vassiliou George S, Fourouclas Nasios, Ferguson-Smith Anne C, Green Anthony R

Abstract excerpt

L3MBTL encodes a member of the Polycomb family of proteins, which, together with Trithorax group proteins, is responsible for the coordinated regulation of patterns of gene activity. Members of the Polycomb family also regulate self renewal of normal and malignant hematopoietic stem cells. L3MBTL lies in a region of chromosome 20, deletion of which is associated with myeloid malignancies and represents a good...

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Share to Chromosomes, Human, Pair 20
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 15123827
DOI: 10.1073/pnas.0308195101
PMCID: PMC409920

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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