Retinoblastoma protein functions as a molecular switch determining white versus brown adipocyte differentiation. - Wikidata - wikimedia - TriplyDB

Retinoblastoma protein functions as a molecular switch determining white versus brown adipocyte differentiation.

Retinoblastoma protein functions as a molecular switch determining white versus brown adipocyte differentiation.

http://www.wikidata.org/entity/Q37356575

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Rb induces a proliferative arrest and curtails Brn-2 expression in retinoblastoma cells Initiation of myoblast to brown fat switch by a PRDM16-C/EBP-beta transcriptional complex Emerging role of bone morphogenetic proteins in adipogenesis and energy metabolism PRDM16 controls a brown fat/skeletal muscle switch Retinoblastoma tumor suppressor functions shared by stem cell and cancer cell strategies Of mice and men: novel insights regarding constitutive and recruitable brown adipocytes Intricate Transcriptional Networks of Classical Brown and Beige Fat Cells The multiple connections between pRB and cell metabolism JDP2 suppresses adipocyte differentiation by regulating histone acetylation BRITER: a BMP responsive osteoblast reporter cell line The transcription factor GATA2 regulates differentiation of brown adipocytes Regulation of the brown and white fat gene programs through a PRDM16/CtBP transcriptional complex E2f4 is required for normal development of the airway epithelium Transcriptional control of brown fat determination by PRDM16 Proteomic analysis of pRb loss highlights a signature of decreased mitochondrial oxidative phosphorylation Adipocytes as regulators of energy balance and glucose homeostasis Brown adipose tissue: Recent insights into development, metabolic function and therapeutic potential Comparative expression analysis of isolated human adipocytes and the human adipose cell lines LiSa-2 and PAZ6.Attainment of brown adipocyte features in white adipocytes of hormone-sensitive lipase null mice.A genome scan for positive selection in thoroughbred horses.Dynamic regulation of genes involved in mitochondrial DNA replication and transcription during mouse brown fat cell differentiation and recruitment.The retinoblastoma tumor-suppressor gene, the exception that proves the rule Silencing of the small GTPase DIRAS3 induces cellular senescence in human white adipose stromal/progenitor cells UCP1 induction during recruitment of brown adipocytes in white adipose tissue is dependent on cyclooxygenase activity.Utility of transplantation in studying adipocyte biogenesis and function E2F4 cooperates with pRB in the development of extra-embryonic tissues.Cinnamon induces browning in subcutaneous adipocytes.Effects of Wnt signaling on brown adipocyte differentiation and metabolism mediated by PGC-1alpha.Cellular bioenergetics as a target for obesity therapy.Transcriptional regulatory program in wild-type and retinoblastoma gene-deficient mouse embryonic fibroblasts during adipocyte differentiation.Tailoring to RB: tumour suppressor status and therapeutic response.KSRP ablation enhances brown fat gene program in white adipose tissue through reduced miR-150 expression.Oxidative status of muscle is determined by p107 regulation of PGC-1alpha.Chronic peroxisome proliferator-activated receptor gamma (PPARgamma) activation of epididymally derived white adipocyte cultures reveals a population of thermogenically competent, UCP1-containing adipocytes molecularly distinct from classic brown ad Brown fat as a therapy for obesity and diabetes.Negative regulators of brown adipose tissue (BAT)-mediated thermogenesis Necdin controls proliferation of white adipocyte progenitor cells.Review: Epigenetic regulation of adipocyte differentiation and adipogenesis Transcriptional targets in adipocyte biology Nutritional regulation of bile acid metabolism is associated with improved pathological characteristics of the metabolic syndrome.

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Retinoblastoma protein functions as a molecular switch determining white versus brown adipocyte differentiation.

http://www.wikidata.org/entity/Q37356575

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 15 March 2004

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

@cs

name

Retinoblastoma protein functio ...... own adipocyte differentiation.

@en

Retinoblastoma protein functio ...... own adipocyte differentiation.

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type

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Retinoblastoma protein functio ...... own adipocyte differentiation.

@en

Retinoblastoma protein functio ...... own adipocyte differentiation.

@nl

prefLabel

Retinoblastoma protein functio ...... own adipocyte differentiation.

@en

Retinoblastoma protein functio ...... own adipocyte differentiation.

@nl

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PNAS.0301964101

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Proceedings of the National Academy of Sciences of the United States of America

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Retinoblastoma protein functio ...... rown adipocyte differentiation

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Claus Jørgensen

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Hans A Bøye

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Hein te Riele

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Karsten Kristiansen

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Natasa Petrovic

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Philip Hallenborg

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Rasmus K Petersen

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Saverio Cinti

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Sven Enerbäck

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P2860

A thyroid hormone receptor coactivator negatively regulated by the retinoblastoma protein

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Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1

PPAR gamma is required for the differentiation of adipose tissue in vivo and in vitro

Peroxisome proliferator-activated receptor gamma coactivator 1beta (PGC-1beta ), a novel PGC-1-related transcription coactivator associated with host cell factor

FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance

Nuclear receptor binding factor-1 (NRBF-1), a protein interacting with a wide spectrum of nuclear hormone receptors

Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators

Regulation of the uncoupling protein gene (Ucp) by beta 1, beta 2, and beta 3-adrenergic receptor subtypes in immortalized brown adipose cell lines

CREB regulates hepatic gluconeogenesis through the coactivator PGC-1

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4112-4117

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10.1073/PNAS.0301964101

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Rita De Matteis

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