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5q32

A chromosome band present on 5q
National Institutes of Health

Papers overview

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2005
2005
Chromosome segment 12q13→q15 recombines with many different chromosome bands in lipomas and at least ten recurrent translocations… Expand
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Highly Cited
2002
Highly Cited
2002
The 5q- syndrome is the most distinct of the myelodysplastic syndromes, and the molecular basis for this disorder remains unknown… Expand
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Highly Cited
2001
Highly Cited
2001
Improved molecular understanding of the pathogenesis of type 2 diabetes is essential if current therapeutic and preventative… Expand
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Highly Cited
2001
Highly Cited
2001
The Comèl-Netherton syndrome is an autosomal recessive multisystemic disorder characterized by localized or generalized… Expand
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Highly Cited
2000
Highly Cited
2000
Netherton syndrome (NS [MIM 256500]) is a rare and severe autosomal recessive disorder characterized by congenital ichthyosis, a… Expand
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Highly Cited
1998
Highly Cited
1998
Atopy, a clinical syndrome characterized by heightened IgE responsiveness, is largely determined by genetic factors. The disease… Expand
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Highly Cited
1997
Highly Cited
1997
To search for a mammalian homologue of ATX1, a human liver cDNA library was screened and a cDNA clone was isolated, which encodes… Expand
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1994
1994
A genomic clone encoding the human plasma glutathione peroxidase (PGPx), a major enzyme in reducing lipid hydroperoxide and… Expand
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Highly Cited
1990
Highly Cited
1990
The adrenergic receptors (ARs) (subtypes alpha 1, alpha 2, beta 1, and beta 2) are a prototypic family of guanine nucleotide… Expand
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Highly Cited
1985
Highly Cited
1985
Human granulocyte-macrophage colony-stimulating factor (GM-CSF) is a 22,000-dalton glycoprotein that stimulates the growth of… Expand
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