Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway. - Wikidata - wikimedia - TriplyDB

Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

http://www.wikidata.org/entity/Q33480974

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S6K1 plays a critical role in early adipocyte differentiation Pushing the envelope in the mTOR pathway: the second generation of inhibitors Endoplasmic reticulum stress and the inflammatory basis of metabolic disease mTOR: from growth signal integration to cancer, diabetes and ageing mTOR signaling in growth control and disease Characterization of Rictor phosphorylation sites reveals direct regulation of mTOR complex 2 by S6K1 Sirolimus and Everolimus Pathway: Reviewing Candidate Genes Influencing Their Intracellular Effects Regulation of mTORC1 by PI3K signaling mTOR Signaling in Protein Translation Regulation: Implications in Cancer Genesis and Therapeutic Interventions Nutrient sensing, metabolism, and cell growth control Excessive Leucine-mTORC1-Signalling of Cow Milk-Based Infant Formula: The Missing Link to Understand Early Childhood Obesity BSTA promotes mTORC2-mediated phosphorylation of Akt1 to suppress expression of FoxC2 and stimulate adipocyte differentiation Spatial control of the TSC complex integrates insulin and nutrient regulation of mTORC1 at the lysosome Fermented blueberry juice extract and its specific fractions have an anti-adipogenic effect in 3 T3-L1 cells Nitazoxanide stimulates autophagy and inhibits mTORC1 signaling and intracellular proliferation of Mycobacterium tuberculosis Rapamycin regulates stearoyl CoA desaturase 1 expression in breast cancer Anti-diabetic effects of Caulerpa lentillifera: stimulation of insulin secretion in pancreatic β-cells and enhancement of glucose uptake in adipocytes.Mammalian target of rapamycin complex 1 suppresses lipolysis, stimulates lipogenesis, and promotes fat storage.Loss of MyoD Promotes Fate Transdifferentiation of Myoblasts Into Brown Adipocytes.The molecular mechanism of leptin secretion and expression induced by aristolochic acid in kidney fibroblast Decreased osteoclastogenesis and high bone mass in mice with impaired insulin clearance due to liver-specific inactivation to CEACAM1 Annual Wormwood Leaf Inhibits the Adipogenesis of 3T3-L1 and Obesity in High-Fat Diet-Induced Obese Rats.Tuberous sclerosis complex-1 deficiency attenuates diet-induced hepatic lipid accumulation.Akt- and Erk-mediated regulation of proliferation and differentiation during PDGFRβ-induced MSC self-renewal Coprinus comatus cap inhibits adipocyte differentiation via regulation of PPARγ and Akt signaling pathway Inhibition of adipogenesis and induction of apoptosis and lipolysis by stem bromelain in 3T3-L1 adipocytes Novel polysome messages and changes in translational activity appear after induction of adipogenesis in 3T3-L1 cells Citrus aurantium flavonoids inhibit adipogenesis through the Akt signaling pathway in 3T3-L1 cells Inhibition of Adipogenesis by Oligonol through Akt-mTOR Inhibition in 3T3-L1 Adipocytes.DEPTOR cell-autonomously promotes adipogenesis, and its expression is associated with obesity.Experimentally induced gestational androgen excess disrupts glucoregulation in rhesus monkey dams and their female offspring.Regulation of mTORC1 and its impact on gene expression at a glance.15(S)-HETE-induced angiogenesis in adipose tissue is mediated through activation of PI3K/Akt/mTOR signaling pathway.Cytosolic malic enzyme 1 (ME1) mediates high fat diet-induced adiposity, endocrine profile, and gastrointestinal tract proliferation-associated biomarkers in male mice.Centipede grass exerts anti-adipogenic activity through inhibition of C/EBPβ, C/EBPα, and PPARγ expression and the AKT signaling pathway in 3T3-L1 adipocytes.Reverse differentiation as a gene filtering tool in genome expression profiling of adipogenesis for fat marker gene selection and their analysis.mTOR inhibition rescues osteopenia in mice with systemic sclerosis.ERK and Akt signaling pathways function through parallel mechanisms to promote mTORC1 signaling Rohitukine inhibits in vitro adipogenesis arresting mitotic clonal expansion and improves dyslipidemia in vivo.SRA regulates adipogenesis by modulating p38/JNK phosphorylation and stimulating insulin receptor gene expression and downstream signaling.

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P2860

Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

http://www.wikidata.org/entity/Q33480974

description

2009 nî lūn-bûn

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2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2009年の論文

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2009年論文

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2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

@ast

Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

@en

type

label

Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

@ast

Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

@en

prefLabel

Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

@ast

Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

@en

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JOURNAL.PONE.0006189

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Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

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Bernard Boback

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Brendan D Manning

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Chin-Lee Wu

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Hui H Zhang

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Jingxiang Huang

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Katrin Düvel

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Rachel M Squillace

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Shulin Wu

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P2860

Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex

PRAS40 is an insulin-regulated inhibitor of the mTORC1 protein kinase

PRAS40 is a target for mammalian target of rapamycin complex 1 and is required for signaling downstream of this complex

Activity of TSC2 is inhibited by AKT-mediated phosphorylation and membrane partitioning

Expression of a constitutively active Akt Ser/Thr kinase in 3T3-L1 adipocytes stimulates glucose uptake and glucose transporter 4 translocation

Identification of a proline-rich Akt substrate as a 14-3-3 binding partner

Regulation of mTOR function in response to hypoxia by REDD1 and the TSC1/TSC2 tumor suppressor complex

The proline-rich Akt substrate of 40 kDa (PRAS40) is a physiological substrate of mammalian target of rapamycin complex 1

A complex interplay between Akt, TSC2 and the two mTOR complexes

AKT/PKB signaling: navigating downstream

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10.1371/JOURNAL.PONE.0006189

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