Microarray analysis of thapsigargin-induced stress to the endoplasmic reticulum of mouse osteoblasts (Q42813233)

7 November 2017

title

Microarray analysis of thapsigargin-induced stress to the endoplasmic reticulum of mouse osteoblasts (English)

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7 November 2017

main subject

endoplasmic reticulum

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osteoblast

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author name string

Kazunori Hamamura

series ordinal

1

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7 November 2017

Yunlong Liu

series ordinal

2

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7 November 2017

Hiroki Yokota

series ordinal

3

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7 November 2017

publication date

11 May 2008

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Journal of Bone and Mineral Metabolism

7 November 2017

published in

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7 November 2017

volume

26

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7 November 2017

issue

3

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7 November 2017

page(s)

231-240

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Mediators of endoplasmic reticulum stress-induced apoptosis

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Hypoxia and hypoxia/reoxygenation activate p65PAK, p38 mitogen-activated protein kinase (MAPK), and stress-activated protein kinase (SAPK) in cultured rat cardiac myocytes

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CHOP induces death by promoting protein synthesis and oxidation in the stressed endoplasmic reticulum

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Activating transcription factor 4 is translationally regulated by hypoxic stress

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Stress to endoplasmic reticulum of mouse osteoblasts induces apoptosis and transcriptional activation for bone remodeling.

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Regulation of protein synthesis by hypoxia via activation of the endoplasmic reticulum kinase PERK and phosphorylation of the translation initiation factor eIF2alpha

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The bone morphogenetic protein family and osteogenesis

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Targeting homeostatic mechanisms of endoplasmic reticulum stress to increase susceptibility of cancer cells to fenretinide-induced apoptosis: the role of stress proteins ERdj5 and ERp57

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The novel zinc finger-containing transcription factor osterix is required for osteoblast differentiation and bone formation

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10.1007/S00774-007-0825-1

Identifiers

DOI

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Dimensions Publication ID

7 November 2017

1040946095

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