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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… 
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… 
Highly Cited
2001
Highly Cited
2001
Improved molecular understanding of the pathogenesis of type 2 diabetes is essential if current therapeutic and preventative… 
Highly Cited
2001
Highly Cited
2001
The Comèl-Netherton syndrome is an autosomal recessive multisystemic disorder characterized by localized or generalized… 
Highly Cited
2000
Highly Cited
2000
Netherton syndrome (NS [MIM 256500]) is a rare and severe autosomal recessive disorder characterized by congenital ichthyosis, a… 
Highly Cited
1998
Highly Cited
1998
Atopy, a clinical syndrome characterized by heightened IgE responsiveness, is largely determined by genetic factors. The disease… 
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… 
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… 
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…