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CCND1 gene

Known as: CCND1/PTH Fusion Gene, CCND1-PTH Fusion Gene, BCL1 
A fusion gene that results from a chromosomal translocation t(11;22)(q13;q11) which places the CCND1 gene on the 5' side of the immunoglobulin light… Expand
National Institutes of Health

Papers overview

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2018
2018
Background/Aims: The long noncoding RNA homeobox (HOX) transcript antisense intergenic RNA (HOTAIR) has been demonstrated to be a… Expand
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Highly Cited
2013
Highly Cited
2013
A number of specific chromosomal abnormalities define the subgroups of multiple myeloma. In a meta-analysis of two genome-wide… Expand
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Highly Cited
2012
Highly Cited
2012
Osteosarcoma, the most common primary tumor of the bones, causes many deaths due to its rapid proliferation and drug resistance… Expand
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Highly Cited
2012
Highly Cited
2012
The microRNA miR-138 is dysregulated in several human cancers, but the underlying mechanism remains largely unknown. Here, we… Expand
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Highly Cited
2012
Highly Cited
2012
Similar to other malignancies, urothelial carcinoma (UC) is characterized by specific recurrent chromosomal aberrations and gene… Expand
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Highly Cited
2008
Highly Cited
2008
IntroductionThe amplification event occurring at chromosome locus 11q13, reported in several different cancers, includes a number… Expand
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Highly Cited
2006
Highly Cited
2006
Chromosomal band 11q13 is frequently amplified in oral squamous cell carcinoma (OSCC) and assumed to be critically involved in… Expand
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Highly Cited
2003
Highly Cited
2003
Gene amplification is a common mechanism for oncogene overexpression. High-level amplifications at 11q13 have been repeatedly… Expand
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Highly Cited
2001
Highly Cited
2001
The roles of the MYC, ERBB2, and CCND1 genes in thyroid carcinogenesis are poorly known. We used real-time quantitative… Expand
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Highly Cited
1994
Highly Cited
1994
Rearrangement and overexpression of CCND1 (BCL1/PRAD1), a member of the cyclin G1 gene family, are consistent features of t(11q13… Expand
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