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3p21

A chromosome band present on 3p
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
BACKGROUND Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases… Expand
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Highly Cited
2013
Highly Cited
2013
Purpose: To investigate the impact of newly identified chromosome 3p21 epigenetic tumor suppressors PBRM1, SETD2, and BAP1 on… Expand
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Highly Cited
2007
Highly Cited
2007
Background— Brugada syndrome is a rare, autosomal-dominant, male-predominant form of idiopathic ventricular fibrillation… Expand
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Highly Cited
2004
Highly Cited
2004
Nasopharyngeal carcinoma (NPC) poses one of the serious health problems in southern Chinese, with an incidence rate ranging from… Expand
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Highly Cited
2000
Highly Cited
2000
Allelic loss at the short arm of chromosome 3 is one of the most common and earliest events in the pathogenesis of lung cancer… Expand
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Highly Cited
1996
Highly Cited
1996
The chemokine receptor 5 (CKR5) protein serves as a secondary receptor on CD4+ T lymphocytes for certain strains of human… Expand
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Highly Cited
1996
Highly Cited
1996
To determine the role of the FHIT gene, which encompasses the fragile site at 3p14.2, we analyzed 59 tumors of the small cell and… Expand
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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… Expand
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Highly Cited
1994
Highly Cited
1994
THE human DNA mismatch repair gene homologue, hMSH2, on chromosome 2p is involved in hereditary non-polyposis colon cancer (HNPCC… Expand
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Highly Cited
1994
Highly Cited
1994
Some cases of hereditary nonpolyposis colorectal cancer (HNPCC) are due to alterations in a mutS-related mismatch repair gene. A… Expand
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