(Q28571377)

31 January 2017

title

Hypoxia induces alteration of bone morphogenetic protein receptor signaling in pulmonary artery endothelial cell (English)

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31 January 2017

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Kunihiko Takahashi

1

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31 January 2017

Shigetoyo Kogaki

2

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31 January 2017

Tohru Matsushita

3

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31 January 2017

Sayaka Nasuno

4

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31 January 2017

Shunji Kurotobi

5

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31 January 2017

Keiichi Ozono

6

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31 January 2017

language of work or name

English

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publication date

1 April 2007

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31 January 2017

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31 January 2017

volume

61

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31 January 2017

issue

4

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31 January 2017

page(s)

392–397

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Clinical classification of pulmonary hypertension.

31 January 2017

cites work

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https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Smad-dependent and Smad-independent pathways in TGF-beta family signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Signaling molecules in nonfamilial pulmonary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

BMP type II receptor is required for gastrulation and early development of mouse embryos

21 January 2018

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https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

BMPR-II heterozygous mice have mild pulmonary hypertension and an impaired pulmonary vascular remodeling response to prolonged hypoxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Bone morphogenetic protein receptor type II is a receptor for growth differentiation factor-9

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Targets of transcriptional regulation by two distinct type I receptors for transforming growth factor-beta in human umbilical vein endothelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Pulmonary hypertension in transgenic mice expressing a dominant-negative BMPRII gene in smooth muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Endothelial dysfunction in pulmonary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Downregulation of type II bone morphogenetic protein receptor in hypoxic pulmonary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Stimulation of Id1 expression by bone morphogenetic protein is sufficient and necessary for bone morphogenetic protein-induced activation of endothelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Id1 regulates angiogenesis through transcriptional repression of thrombospondin-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Increased vascular endothelial growth factor production in the lungs of rats with hypoxia-induced pulmonary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Controlling the angiogenic switch: a balance between two distinct TGF-b receptor signaling pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Alterations in TGF-beta1 expression in lambs with increased pulmonary blood flow and pulmonary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180332CBA

10.1203/PDR.0B013E3180332CBA

21 January 2018

Identifiers

DOI

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Dimensions Publication ID

31 January 2017

1004604716

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