Molecular Mechanisms of Pulmonary Vascular Remodeling in Pulmonary Arterial Hypertension (Q28067063)

microvasculature remodeling

inferred from title

pulmonary hypertension

3 references

22 March 2019

10 October 2019

14 November 2020

5 references

22 March 2019

10 October 2019

14 November 2020

24 January 2021

13 January 2024

1 reference

10 October 2019

1 reference

14 November 2020

1 reference

24 January 2021

Jane Leopold

1

1 reference

Bradley Maron

series ordinal

2

1 reference

International Journal of Molecular Sciences

language of work or name

1 reference

18 May 2016

6 references

22 March 2019

10 October 2019

14 November 2020

24 January 2021

13 January 2024

5 references

22 March 2019

10 October 2019

14 November 2020

24 January 2021

13 January 2024

17

1 reference

issue

5

1 reference

Creative Commons Attribution

page(s)

761

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copyright license

5 references

22 March 2019

10 October 2019

14 November 2020

24 January 2021

13 January 2024

0 references

on focus list of Wikimedia project

ScienceSource

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cites work

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Alterations of cellular bioenergetics in pulmonary artery endothelial cells

29 September 2017

1 reference

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Dichloroacetate prevents and reverses pulmonary hypertension by inducing pulmonary artery smooth muscle cell apoptosis

29 September 2017

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Microsatellite instability of endothelial cell growth and apoptosis genes within plexiform lesions in primary pulmonary hypertension

29 September 2017

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Monoclonal endothelial cell proliferation is present in primary but not secondary pulmonary hypertension

29 September 2017

1 reference

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Systems-level regulation of microRNA networks by miR-130/301 promotes pulmonary hypertension.

29 September 2017

1 reference

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2 June 2018

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Epigenetic attenuation of mitochondrial superoxide dismutase 2 in pulmonary arterial hypertension: a basis for excessive cell proliferation and a new therapeutic target.

2 June 2018

1 reference

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2 June 2018

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Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension

21 January 2018

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EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension.

21 January 2018

1 reference

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Early onset severe pulmonary arterial hypertension with 'two-hit' digenic mutations in both BMPR2 and KCNA5 genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

Role for DNA damage signaling in pulmonary arterial hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

Reduced microRNA-150 is associated with poor survival in pulmonary arterial hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

Plexiform vasculopathy of severe pulmonary arterial hypertension and microRNA expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

Downregulation of MicroRNA-126 Contributes to the Failing Right Ventricle in Pulmonary Arterial Hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

Dichloroacetate treatment partially regresses established pulmonary hypertension in mice with SM22alpha-targeted overexpression of the serotonin transporter.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

The zinc transporter ZIP12 regulates the pulmonary vascular response to chronic hypoxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

Chronic Hypoxia Increases Intracellular Ca(2 ) Concentration via Enhanced Ca(2 ) Entry Through Receptor-Operated Ca(2 ) Channels in Pulmonary Venous Smooth Muscle Cells

21 January 2018

1 reference

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Mature vascular endothelium can give rise to smooth muscle cells via endothelial-mesenchymal transdifferentiation: in vitro analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

Endothelial-to-mesenchymal transition in pulmonary hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

Endothelial to Mesenchymal Transition Contributes to Endothelial Dysfunction in Pulmonary Arterial Hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

Endothelial fate mapping in mice with pulmonary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.3390/IJMS17050761

A Role for miR-145 in Pulmonary Arterial Hypertension

21 January 2018

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12 December 2020

Familial and sporadic primary pulmonary hypertension is caused by BMPR2 gene mutations resulting in haploinsufficiency of the bone morphogenetic protein tùype II receptor

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12 December 2020

Histopathology of pulmonary hypertension

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Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33

1 reference

12 December 2020

Cell cycle--dependent expression of L- and T-type Ca2 currents in rat aortic smooth muscle cells in primary culture

1 reference

12 December 2020

Stretch-induced Ca2 signalling in vascular smooth muscle cells depends on Ca2 store segregation

1 reference

12 December 2020

Loss of bone morphogenetic protein receptor 2 is associated with abnormal DNA repair in pulmonary arterial hypertension

1 reference

12 December 2020