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Article

Identified hidden genomic changes in mantle cell lymphoma using high-resolution single nucleotide polymorphism genomic array.

Experimental hematology - 1 Aug 2009

Kawamata Norihiko, Ogawa Seishi, Gueller Saskia, Ross Samuel H, Huynh Thien, Chen John, Chang Andrew, Nabavi-Nouis Shayan, Megrabian Nairi, Siebert Reiner, Martinez-Climent Jose A, Koeffler H Phillip

Abstract excerpt

OBJECTIVE: Mantle cell lymphoma (MCL) is a lymphoma characterized by aberrant activation of CCND1/cyclin D1 followed by sequential genetic abnormalities. Genomic abnormalities in MCL have been extensively examined by classical cytogenetics and microarray-based comparative genomic hybridization techniques, pointing out a number of alterations in genomic regions that correlate with the neoplastic phenotype and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Loss of Heterozygosity

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Share to Oligonucleotide Array Sequence Analysis

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Source

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Identifiers

PMID: 19477219
DOI: 10.1016/j.exphem.2009.04.012
PMCID: PMC5892830

Genes

ATM
CCND1
MYC

Provenance

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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