نتایج جستجو برای: irs 1

تعداد نتایج: 2755481  

Journal: :The Journal of clinical investigation 1996
K Almind G Inoue O Pedersen C R Kahn

Insulin receptor substrates-1 (IRS-1) is the major cytoplasmic substrate of the insulin and IGF-1 receptors. Recent studies have identified multiple sequence variants of IRS-1, especially in patients with non-insulin-dependent diabetes mellitus. In the present study, we have examined insulin-stimulated processes in 32D(IR) cells, a myeloid progenitor cell stably overexpressing the insulin recep...

Journal: :Molecular endocrinology 1998
A M Valverde M Lorenzo S Pons M F White M Benito

In the present study we have investigated the contribution of the insulin receptor substrate proteins (IRS-1 and IRS-2) to the insulin/insulin like growth factor I (IGF-I)-signaling pathways in fetal rat brown adipocytes, a model that expresses both insulin and IGF-I receptors. Insulin/IGF-I rapidly stimulated IRS-1 and IRS-2 tyrosine phosphorylation, their association with p85alpha, and IRS-1-...

Journal: :The Journal of biological chemistry 1994
T Sasaoka B Draznin J W Leitner W J Langlois J M Olefsky

Insulin stimulates tyrosine phosphorylation of insulin receptor substrate-1 (IRS-1) and She in Rat1 fibroblasts overexpressing wild type insulin receptors. We investigated the relative role of IRS-1 and She in insulin activation of guanine nucleotide releasing factor (GNRF) and p21ras-GTP formation. The time course of insulin-stimulated tyrosine phosphorylation of IRS-1 was rapid, whereas Shc p...

Journal: :The Journal of biological chemistry 1997
M J Welham H Bone M Levings L Learmonth L M Wang K B Leslie J H Pierce J W Schrader

Insulin receptor substrate 1 (IRS-1), and its structural relative IRS-2, are both phosphorylated on tyrosine following treatment of cells with interleukin-4 (IL-4) and insulin. We have investigated whether both IRS-1 and IRS-2 are expressed in murine lymphohemopoietic cells. T and B lymphocytes and macrophages from primary cultures expressed only IRS-2, which became phosphorylated on tyrosine f...

Journal: :The Journal of biological chemistry 2002
Adam Lassak Luis Del Valle Francesca Peruzzi Jin Ying Wang Sahnila Enam Sidney Croul Kamel Khalili Krzysztof Reiss

Insulin receptor substrate 1 (IRS-1) is the major signaling molecule for the insulin and insulin-like growth factor I receptors, which transduces both metabolic and growth-promoting signals, and has transforming properties when overexpressed in the cells. Here we show that IRS-1 is translocated to the nucleus in the presence of the early viral protein-T-antigen of the human polyomavirus JC. Nuc...

2016
Marc A. Becker Yasir H. Ibrahim Annabell S. Oh Dedra H. Fagan Sara A. Byron Aaron L. Sarver Adrian V. Lee Leslie M. Shaw Cheng Fan Charles M. Perou Douglas Yee

Therapies targeting the type I insulin-like growth factor receptor (IGF-1R) have not been developed with predictive biomarkers to identify tumors with receptor activation. We have previously shown that the insulin receptor substrate (IRS) adaptor proteins are necessary for linking IGF1R to downstream signaling pathways and the malignant phenotype in breast cancer cells. The purpose of this stud...

Journal: :Molecular and cellular biology 1995
D Chen D J Van Horn M F White J M Backer

Insulin signals are mediated through tyrosine phosphorylation of specific proteins such as insulin receptor substrate 1 (IRS-1) and Shc by the activated insulin receptor (IR). Phosphorylation of both proteins is nearly abolished by an alanine substitution at Tyr-960 (A960) in the beta-subunit of the receptor. However, overexpression of IRS-1 in CHO cells expressing the mutant receptor (A960 cel...

Journal: :American journal of physiology. Endocrinology and metabolism 2001
A Suryawan H V Nguyen J A Bush T A Davis

In neonatal animals, feeding stimulates skeletal muscle protein synthesis, a response that declines with development. Both the magnitude of the feeding response and its developmental decline can be reproduced by insulin infusion, suggesting that an altered responsiveness to insulin is a primary determinant of the developmental decline in the stimulation of protein synthesis by feeding. In this ...

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