del(1p36)

Known as: 1p36 Deletion, Loss of Chromosome 1p36 
A chromosomal deletion involving the p36 band of chromosome 1. This deletion is associated with 1p36 deletion syndrome.
National Institutes of Health

Papers overview

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Review
2012
Review
2012
A broad range of human malignancies is associated with nonrandom 1p36 deletions, suggesting the existence of tumor suppressors… (More)
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Highly Cited
2010
Highly Cited
2010
Glioblastoma multiforme (GBM) is the most common and lethal primary brain cancer that is driven by aberrant signaling of growth… (More)
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Highly Cited
2008
Highly Cited
2008
OBJECTIVES Deletion 1p36 syndrome is a recently delineated disorder, considered to be the most common subtelomeric microdeletion… (More)
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Highly Cited
2008
Highly Cited
2008
MicroRNAs are small noncoding RNAs that have critical roles in regulating a number of cellular functions through transcriptional… (More)
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Review
2007
Review
2007
Monosomy 1p36 results from a heterozygous deletion of the most distal chromosomal band on the short arm of chromosome 1… (More)
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2007
2007
Chromosome 1p is frequently deleted in neuroblastoma (NB) tumours. The commonly deleted region has been narrowed down by loss of… (More)
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2007
2007
Tumor recurrence is the major clinical complication in meningiomas, and its prediction in histologically benign/grade I tumors… (More)
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2006
2006
Monosomy 1p36 is one of the most commonly observed mental retardation (MR) syndromes that results in a clinically recognizable… (More)
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2002
2002
Terminal deletions of 1p36 result in a specific and common syndrome characterised by the following: growth delay, distinctive… (More)
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1999
1999
The deletion of chromosome 1p36 is a newly recognized, relatively common contiguous gene deletion syndrome with a variable… (More)
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