Glucocorticoids inhibit osteoblast proliferation via transcriptional upregulation of MKP-1: A prime target for the development of novel osteo-anabolic agents

Glucocorticoids inhibit osteoblast proliferation via transcriptional upregulation of MKP-1: A prime target for the development of novel osteo-anabolic agents

Xehetasun bibliografikoak
Egile Nagusiak:	Hulley, P, Horsch, K, De Wet, H, Conradie, M, Langeveldt, C, Hough, F
Formatua:	Conference item
Argitaratua:	2003

Antzeko izenburuak

Rapid inhibitory effects of glucocorticoids on ERK activity and osteoblast proliferation occur via transcriptional upregulation of MKP-1
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Argitaratua: (2004)

Rapid inhibitory effects of glucocorticoids on ERK activity and osteoblast proliferation occur via transcriptional upregulation of MKP-1
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Vanadate protects osteoblasts in vitro and in vivo from glucocorticoid impairment of proliferation
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MKP-1 knockout does not prevent glucocorticoid-induced bone disease in mice.
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Mitogen-activated protein kinase phosphatase 1/dual specificity phosphatase 1 mediates glucocorticoid inhibition of osteoblast proliferation.
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Corrigendum: Glucocorticoid transiently upregulates mitochondrial biogenesis in the osteoblast
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Cynarin attenuates LPS-induced endothelial inflammation via upregulation of the negative regulator MKP-3
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Scoparone attenuates PD-L1 expression in human breast cancer cells by MKP-3 upregulation
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MECHANISMS OF OSTEOBLAST INHIBITION BY STEROIDS
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Bim is transcriptionally regulated during induction of apoptosis by growth factor withdrawal in osteoblasts
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Comparison of the Anabolic Effects of Reported Osteogenic Compounds on Human Mesenchymal Progenitor-derived Osteoblasts
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Prenatal dexamethasone exposure reduces osteoprogenitor proliferation in mice via histone modifications at the Mkp-1 gene locus
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TBX3 regulates the transcription of VEGFA to promote osteoblasts proliferation and microvascular regeneration
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