XPNPEP1 gene

OBJECTIVES Biliary atresia (BA) is a progressive fibroinflammatory cholangiopathy affecting the bile ducts of neonates. Although… (More)

Eukaryotic aminopeptidase P1 (APP1), also known as X-prolyl aminopeptidase (XPNPEP1) in human tissues, is a cytosolic… (More)

Cytosolic aminopeptidase P1 (APP1) is one of the three known mammalian aminopeptidase Ps (APPs) that cleave the N-terminal amino… (More)

The use of an appropriate reference gene to ensure accurate normalisation is crucial for the correct quantification of gene… (More)

Some upstream open reading frames (uORFs) regulate gene expression (i.e., they are functional) and can play key roles in keeping… (More)

Rovelet-Lecrux and colleagues’ demonstration that duplications of the amyloid precursor protein gene (APP) in French families… (More)

We use Global Positioning System (GPS) data from nine permanent GPS sites surrounding the epicentre of the December 26, 2004… (More)

Aminopeptidase P (APP) isoforms specifically remove the N-terminal amino acid from peptides that have a proline residue in the… (More)

BACKGROUND A wide pulse pressure (PP) can provide important risk assessment information about myocardial infarction, carotid… (More)

The authors examined the ultrastructural localization of amyloid beta protein precursor (APP) in normal human brains… (More)