نتایج جستجو برای: insulin receptor substrate 1gene expression

تعداد نتایج: 1578901  

Journal: :The Journal of Cell Biology 1986
A L Jochen P Berhanu

To explore the possible role of proteolytic step(s) in receptor-mediated endocytosis of insulin, the effects of inhibitors of various classes of proteases on the internalization process were studied in isolated rat adipocytes. Intracellular accumulation of receptor-bound 125I-insulin at 37 degrees C was quantitated after rapidly dissociating surface-bound insulin with an acidic buffer (pH 3.0)....

Journal: :Keluwih 2021

Abstract--Insulin resistance underlies the pathogenesis of chronic disease, such as diabetes mellitus which has high morbidity and mortality rate. Insulin is a pathological condition when cells fail to respond normally insulin hormone, because signaling pathway disruption. Bound between insulin’s receptor cannot phosphorylate tyrosine activate substrate-1 (IRS-1). This failure decrease Glucose ...

Journal: :Cancer research 2006
Kathryn E O'Reilly Fredi Rojo Qing-Bai She David Solit Gordon B Mills Debra Smith Heidi Lane Francesco Hofmann Daniel J Hicklin Dale L Ludwig Jose Baselga Neal Rosen

Stimulation of the insulin and insulin-like growth factor I (IGF-I) receptor activates the phosphoinositide-3-kinase/Akt/mTOR pathway causing pleiotropic cellular effects including an mTOR-dependent loss in insulin receptor substrate-1 expression leading to feedback down-regulation of signaling through the pathway. In model systems, tumors exhibiting mutational activation of phosphoinositide-3-...

Journal: :Nihon Naibunpi Gakkai zasshi 1995
M Shichiri E Araki

IRS-1 (insulin receptor substrate-1) is a major substrate for the insulin receptor tyrosine kinase. After phosphorylation by the insulin receptor, IRS-1 binds to the specific molecules which possess SH2 (src homology 2) domain such as 85 kDa subunit of phosphatidylinositol 3 kinase and may mediate insulin signals. The regulation of IRS-1 has been analyzed in animal models of insulin resistance,...

Journal: :Diabetes 2000
A Krook M Björnholm D Galuska X J Jiang R Fahlman M G Myers H Wallberg-Henriksson J R Zierath

We characterized metabolic and mitogenic signaling pathways in isolated skeletal muscle from well-matched type 2 diabetic and control subjects. Time course studies of the insulin receptor, insulin receptor substrate (IRS)-1/2, and phosphatidylinositol (PI) 3-kinase revealed that signal transduction through this pathway was engaged between 4 and 40 min. Insulin-stimulated (0.6-60 nmol/l) tyrosin...

2002
Katrine Almind Laurent Delahaye Torben Hansen Emmanuel Van Obberghen Oluf Pedersen Ronald Kahn

Phosphatidylinositol 3-kinase is a key step in the metabolic actions of insulin. Two amino acid substitutions have been identified in the gene for the regulatory subunit of human p85 , Met-326Ile, and Asn-330Asp, and the former has been associated with alterations in glucose insulin homeostasis. When the four human p85 proteins were expressed in yeast, a 27% decrease occurred in the level of pr...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2012
Elena V Galkina Matthew Butcher Susanna R Keller Matthew Goff Anthony Bruce Hong Pei Ian J Sarembock John M Sanders Melissa H Nagelin Suseela Srinivasan Rohit N Kulkarni Catherine C Hedrick Frank A Lattanzio Anca D Dobrian Jerry L Nadler Klaus Ley

OBJECTIVE Prediabetic states are associated with accelerated atherosclerosis, but the availability of mouse models to study connections between these diseases has been limited. The aim of this study was to test the selective role of impaired insulin receptor/insulin receptor substrate-1 signaling on atherogenesis. METHODS AND RESULTS To address the effects of impaired insulin signaling associ...

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