19p13.2

A chromosome band present on 19p
National Institutes of Health

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Highly Cited
2010
Highly Cited
2010
BACKGROUND Plasma levels of coagulation factors VII (FVII), VIII (FVIII), and von Willebrand factor (vWF) influence risk of… (More)
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Highly Cited
2009
Highly Cited
2009
e16504 Background: A proof of principle array-based comparative genomic hybridization (aCGH) analysis was performed in archival… (More)
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Highly Cited
2008
Highly Cited
2008
PURPOSE Early/initiating oncogenic mutations have been identified for many cancers, but such mutations remain unidentified in… (More)
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Highly Cited
2008
Highly Cited
2008
While circulating levels of soluble Intercellular Adhesion Molecule 1 (sICAM-1) have been associated with diverse conditions… (More)
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Highly Cited
2006
Highly Cited
2006
BACKGROUND Nuclear factor erythroid-2 related factor 2 (NRF2) is a redox-sensitive transcription factor that positively regulates… (More)
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Highly Cited
2005
Highly Cited
2005
Autosomal dominant centronuclear myopathy is a rare congenital myopathy characterized by delayed motor milestones and muscular… (More)
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Highly Cited
2005
Highly Cited
2005
We identified previously a region on chromosome 19p13.2 spanning the genes encoding the intercellular adhesion molecules (ICAM… (More)
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2004
2004
Late-onset familial Alzheimer disease (LOFAD) is a genetically heterogeneous and complex disease for which only one locus, APOE… (More)
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Highly Cited
2000
Highly Cited
2000
Mucolipidosis type IV (MLIV) is a developmental neurodegenerative disorder characterized by severe neurologic and ophthalmologic… (More)
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1996
1996
The HuR gene encodes a specific RNA binding protein that is a member of the human Elav-like gene family. This family of proteins… (More)
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