Cognitive functions like learning and memory, are natural abilities that humans are highly dependent on to function properly. Neurological disorders like dementia, ischemia, and substance-use disorder may all severely impair cognitive functions.
Stam, Frida
core +1 more source
Alzheimer's, angiotensin IV and an aminopeptidase
The angiotensin AT4 receptor was originally defined as the specific, high affinity binding site for the hexapeptide angiotensin IV (Ang IV). Subsequently, the peptide LVV-hemorphin 7 was also demonstrated to be a bioactive ligand of the AT4 receptor ...
G Peck (12148926) +4 more
core
The Discovery of New Inhibitors of Insulin-Regulated Aminopeptidase by a High-Throughput Screening of 400,000 Drug-like Compounds. [PDF]
Gising J +9 more
europepmc +1 more source
AKT and AMP-activated protein kinase regulate TBC1D1 through phosphorylation and its interaction with the cytosolic tail of insulin-regulated aminopeptidase IRAP. [PDF]
Mafakheri S +10 more
europepmc +1 more source
A PCR-RFLP method for detection of the LNPEP encoding human insulin-regulated aminopeptidase (IRAP) rs4869317 polymorphism. [PDF]
RamIrez-Expósito MJ +3 more
europepmc +1 more source
Porcine insulin-regulated aminopeptidase: Cloning and expression
Kristensen, Torsten +6 more
openaire +2 more sources
Identification and development of specific inhibitors for insulin-regulated aminopeptidase as a new class of cognitive enhancers. [PDF]
Albiston AL +10 more
europepmc +1 more source
Integrated analysis of the adipocyte plasma membrane proteome reveals KCC1 and PIT2 as novel insulin-responsive transporters. [PDF]
Zhang Y +16 more
europepmc +1 more source
Evexomostat (SDX-7320), a methionine aminopeptidase type 2 inhibitor, stimulates weight loss and inhibits obesity-accelerated tumor growth. [PDF]
Cornelius P +8 more
europepmc +1 more source
Canonical and Alternative Pathways (Insulin and Exercise) of GLUT4 Synthesis, Signaling, Intracellular Clustering, and Recruitment to the Plasma Membrane. [PDF]
Ramos-Jiménez A +8 more
europepmc +1 more source

