11p15.5

A chromosome band present on 11p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1983-2018
0204019832018

Papers overview

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2009
2009
The 11p15.5 chromosomal region (2.8 Mb) is of particular interest as it encloses five genes (HRAS1, SIRT3, TH, INS and IGF2), the… (More)
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Highly Cited
2008
Highly Cited
2008
Systemic lupus erythematosus (SLE) is a common systemic autoimmune disease with complex etiology but strong clustering in… (More)
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Highly Cited
2003
Highly Cited
2003
Atrial fibrillation (AF) is a common cardiac arrhythmia whose molecular etiology is poorly understood. We studied a family with… (More)
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Highly Cited
2002
Highly Cited
2002
The SIR2 (silent information regulator 2) gene family has diverse functions in yeast including gene silencing, DNA repair, cell… (More)
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Highly Cited
1996
Highly Cited
1996
Loss of heterozygosity (LOH) was detected in morphologically normal lobules adjacent to breast cancers. The most frequent… (More)
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1996
1996
Four distinct genes that encode mucins have previously been mapped to chromosome 11p15.5. Three of these genes (MUC2, MUC5AC, and… (More)
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Highly Cited
1995
Highly Cited
1995
Long QT syndrome (LQT) is an inherited disorder that causes sudden death from cardiac arrhythmias, specifically torsade de… (More)
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Highly Cited
1995
Highly Cited
1995
The IDDM2 locus encoding susceptibility to type 1 diabetes was mapped previously to a 4.1–kb region spanning the insulin gene and… (More)
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Highly Cited
1995
Highly Cited
1995
Cyclin-dependent kinases (Cdks) are positive regulators of cell proliferation, whereas Cdk inhibitors (CKIs) inhibit… (More)
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Highly Cited
1993
Highly Cited
1993
Loss of heterozygosity in certain human embryonal tumours implicates a tumour-suppressor gene at chromosome 11p15.5 and selective… (More)
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