Chromosomes, Human, Pair 12

Known as: 12 chromosome, Chromosome 12 
The designation for each member of the twelfth largest human autosomal chromosome pair. Chromosome 12 spans about 143 million base pairs and… (More)
National Institutes of Health

Papers overview

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Review
2012
Review
2012
Maternally expressed gene 3 (MEG3) is an imprinted gene belonging to the imprinted DLK1-MEG3 locus located at chromosome 14q32.3… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Lowering low-density lipoprotein cholesterol with statin therapy results in substantial reductions in cardiovascular… (More)
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Highly Cited
2003
Highly Cited
2003
Genomic imprinting causes parental origin–specific gene expression. Cis-acting regulatory elements that control imprinting are… (More)
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Highly Cited
2002
Highly Cited
2002
The cytidine (C) to uridine (U) editing of apolipoprotein (apo) B mRNA is mediated by tissue-specific, RNA-binding cytidine… (More)
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Highly Cited
1997
Highly Cited
1997
The potential contribution of maturity-onset diabetes of the young (MODY) genes to NIDDM susceptibility in African-American and… (More)
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Highly Cited
1997
Highly Cited
1997
Holt-Oram syndrome is a developmental disorder affecting the heart and upper limb, the gene for which was mapped to chromosome 12… (More)
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Highly Cited
1997
Highly Cited
1997
Estrogen receptor beta (ER beta) is a novel steroid receptor that is expressed in rat prostate and ovary. We have cloned the… (More)
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Highly Cited
1996
Highly Cited
1996
Hereditary haemorrhagic telangiectasia, or Osler–Rendu–Weber (ORW) syndrome, is an autosomal dominant vascular dysplasia. So far… (More)
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Highly Cited
1991
Highly Cited
1991
The development and maintenance of the vertebrate nervous system depends upon neuronal survival proteins known as neurotrophic… (More)
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Highly Cited
1990
Highly Cited
1990
The Myf-6 gene, a novel member of the human gene family of muscle determination factors has been detected by its highly conserved… (More)
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