5q32

Chromosome segment 12q13→q15 recombines with many different chromosome bands in lipomas and at least ten recurrent translocations… Expand

The 5q- syndrome is the most distinct of the myelodysplastic syndromes, and the molecular basis for this disorder remains unknown… Expand

Improved molecular understanding of the pathogenesis of type 2 diabetes is essential if current therapeutic and preventative… Expand

The Comèl-Netherton syndrome is an autosomal recessive multisystemic disorder characterized by localized or generalized… Expand

Netherton syndrome (NS [MIM 256500]) is a rare and severe autosomal recessive disorder characterized by congenital ichthyosis, a… Expand

Atopy, a clinical syndrome characterized by heightened IgE responsiveness, is largely determined by genetic factors. The disease… Expand

To search for a mammalian homologue of ATX1, a human liver cDNA library was screened and a cDNA clone was isolated, which encodes… Expand

A genomic clone encoding the human plasma glutathione peroxidase (PGPx), a major enzyme in reducing lipid hydroperoxide and… Expand

The adrenergic receptors (ARs) (subtypes alpha 1, alpha 2, beta 1, and beta 2) are a prototypic family of guanine nucleotide… Expand

Human granulocyte-macrophage colony-stimulating factor (GM-CSF) is a 22,000-dalton glycoprotein that stimulates the growth of… Expand