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Article

Transcript Map and Comparative Analysis of the 1.5-Mb Commonly Deleted Segment of Human 5q31 in Malignant Myeloid Diseases with a del(5q)

1 Jan 2001

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Share to Acute Myeloid Leukemia Research
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Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 11161817
DOI: 10.1006/geno.2000.6414

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Transcript Map and Comparative Analysis of the 1.5-Mb Commonly Deleted Segment of Human 5q31 in Malignant Myeloid Diseases with a del(5q)PMID 11161817Read ↗

Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases.Semantic proximity Read ↗

Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1–1.5 Mb and preparation of a PAC-based physical mapSemantic proximity Read ↗

Recurrent genetic defects on chromosome 5q in myeloid neoplasms.Semantic proximity Read ↗

Analysis of expressed sequence tags mapping to the critical region of the 5q syndromeSemantic proximity Read ↗

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Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31Semantic proximity Read ↗

Involvement of deleted chromosome 5 in complex chromosomal aberrations in newly diagnosed myelodysplastic syndromes (MDS) is correlated with extremely adverse prognosisSemantic proximity Read ↗

A novel nuclear protein, 5qNCA (LOC51780) is a candidate for the myeloid leukemia tumor suppressor gene on chromosome 5 band q31.Semantic proximity Read ↗

Deletion 5q in myelodysplastic syndrome: a paradigm for the study of hemizygous deletions in cancerSemantic proximity Read ↗

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Genomic gains and losses influence expression levels of genes located within the affected regions: a study on acute myeloid leukemias with trisomy 8, 11, or 13, monosomy 7, or deletion 5qSemantic proximity Read ↗

Pathophysiologic and clinical implications of molecular profiles resultant from deletion 5q.Semantic proximity Read ↗

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