AbstractInsulin-degrading enzyme (IDE) is implicated in the pathogenesis of type 2 diabetes mellitus (DM2) and Alzheimer’s disease (AD). Here we provide genetic evidence that Drosophila Ide (dIde) antagonizes the insulin signaling pathway and human Aβ-induced neurotoxicity in Drosophila. In this study, we also generated a dIde knockout mutant (dIdeKO) by gene targeting, and found that loss of IDE increases the content of the major insect blood sugar, trehalose, thus suggesting a conserved role of IDE in sugar metabolism. Using dIdeKO as a model, further investigations into the biological functions of IDE and its role in the pathogenesis of DM2 and AD can be made
<div><p>Insulin is a major regulator of metabolism in metazoans, including the fruit fly <i>Drosophi...
G4C2 repeat expansions within the C9orf72 gene are the most common genetic cause of amyotrophic late...
Insulin-degrading enzyme (IDE) is a ubiquitous zinc peptidase of the inverzincin family, which has b...
AbstractInsulin-degrading enzyme (IDE) is implicated in the pathogenesis of type 2 diabetes mellitus...
Mammalian insulin-degrading enzyme (IDE) cleaves insulin, among other peptidic substrates, but its f...
ABSTRACT Mammalian insulin-degrading enzyme (IDE) cleaves insulin, among other pep-tidic substrates,...
The precise mechanism by which insulin is degraded in mammalian cells is not presently known. Severa...
SUMMARY Insulin-resistant, ‘type 2’ diabetes (T2D) results from a complex interplay between genes an...
International audienceIn multicellular organisms, insulin/IGF signaling (IIS) plays a central role i...
Insulin is a major regulator of metabolism in metazoans, including the fruit fly Drosophila melanoga...
<div><p>In multicellular organisms, insulin/IGF signaling (IIS) plays a central role in matching ene...
SummarySpecific neurosecretory cells of the Drosophila brain express insulin-like peptides (dilps), ...
Insulin Degrading Enzyme (IDE) is an endopeptidase that degrades insulin and glucagon. Ide gene has ...
OBJECTIVE—Type 2 diabetes is the most common form of diabetes worldwide. Some of its complications, ...
Abstract The insulin-degrading enzyme (IDE) is an evolutionarily conserved zinc-dependent metallopep...
<div><p>Insulin is a major regulator of metabolism in metazoans, including the fruit fly <i>Drosophi...
G4C2 repeat expansions within the C9orf72 gene are the most common genetic cause of amyotrophic late...
Insulin-degrading enzyme (IDE) is a ubiquitous zinc peptidase of the inverzincin family, which has b...
AbstractInsulin-degrading enzyme (IDE) is implicated in the pathogenesis of type 2 diabetes mellitus...
Mammalian insulin-degrading enzyme (IDE) cleaves insulin, among other peptidic substrates, but its f...
ABSTRACT Mammalian insulin-degrading enzyme (IDE) cleaves insulin, among other pep-tidic substrates,...
The precise mechanism by which insulin is degraded in mammalian cells is not presently known. Severa...
SUMMARY Insulin-resistant, ‘type 2’ diabetes (T2D) results from a complex interplay between genes an...
International audienceIn multicellular organisms, insulin/IGF signaling (IIS) plays a central role i...
Insulin is a major regulator of metabolism in metazoans, including the fruit fly Drosophila melanoga...
<div><p>In multicellular organisms, insulin/IGF signaling (IIS) plays a central role in matching ene...
SummarySpecific neurosecretory cells of the Drosophila brain express insulin-like peptides (dilps), ...
Insulin Degrading Enzyme (IDE) is an endopeptidase that degrades insulin and glucagon. Ide gene has ...
OBJECTIVE—Type 2 diabetes is the most common form of diabetes worldwide. Some of its complications, ...
Abstract The insulin-degrading enzyme (IDE) is an evolutionarily conserved zinc-dependent metallopep...
<div><p>Insulin is a major regulator of metabolism in metazoans, including the fruit fly <i>Drosophi...
G4C2 repeat expansions within the C9orf72 gene are the most common genetic cause of amyotrophic late...
Insulin-degrading enzyme (IDE) is a ubiquitous zinc peptidase of the inverzincin family, which has b...