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Experiment Name
Kaur et al.: No gene copy number changes in Dupuytren's contracture by array comparative genomic hybridization.
Accession
CG-EXP-52
Project
CMG Group Public
Authors
Kaur S, Forsman M, Ryhänen J, Knuutila S, Larramendy ML.
PubMed ID
18474290
Abstract
Dupuytren's contracture (DC), a benign disease of unknown origin, is characterized by abnormal fibroblast proliferation and matrix deposition within the palmar and plantar faciae, causing contracture of the digits. Conventional cytogenetic studies of cultured fibroblast cells from DC nodules have revealed nonrecurrent, but usually normal, clonal (mainly +7, +8, and -Y, plus structural changes) and sporadic (nonclonal) numerical/structural rearrangements. No unique cytogenetic features of DC are known so far. We used 44K oligonucleotide-based array comparative genomic hybridization to obtain a wide pattern of chromosomal imbalances in 18 patients with DC. The genome-wide analysis revealed no changes of DNA copy number sequences. Accordingly, gene amplifications or deletions are apparently not involved in the progression of abnormal fibroblast proliferation and matrix deposition that lead to DC.
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Contents
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Series:
Dupuytren's contracture
CG-SER-250
Data Files
CanGEM Generated
Gene calls.igv
(3.64 MB)
Gene frequencies.igv
(2.07 MB)
Created
2009-07-04 16:31:01 by
Ilari Scheinin
Last modified
2009-07-04 16:31:01 by
Ilari Scheinin
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GUID: {A2CB74B4-3B7F-4AB2-A412-DCAD6C1FAD32}
CanGEM
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CMG - Laboratory of Cytomolecular Genetics
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GIU - Genome Informatics Unit
session ID: 6cc721384b24013a5cb75ec6699df946