(Q44225835)

1 December 2017

Pulmonary veno-occlusive disease caused by an inherited mutation in bone morphogenetic protein receptor II. (English)

1 reference

1 December 2017

1 reference

8

John H Newman

1 reference

1 December 2017

James R Runo

1

1 reference

1 December 2017

Cindy L Vnencak-Jones

2

1 reference

1 December 2017

Melissa Prince

3

1 reference

1 December 2017

James E Loyd

4

1 reference

1 December 2017

Lisa Wheeler

5

1 reference

1 December 2017

Ivan M Robbins

6

1 reference

1 December 2017

Kirk B Lane

7

1 reference

1 December 2017

Joyce Johnson

9

1 reference

1 December 2017

William C Nichols

10

1 reference

1 December 2017

John A Phillips

11

1 reference

1 December 2017

language of work or name

English

0 references

publication date

21 November 2002

1 reference

American Journal of Respiratory and Critical Care Medicine

1 December 2017

1 reference

1 December 2017

167

1 reference

1 December 2017

889-894

1 reference

1 December 2017

6

1 reference

Pulmonary Veno-occlusive Disease

1 December 2017

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Pulmonary veno-occlusive disease: a case series and new observations

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

The pathology of pulmonary veno-occlusive disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Pulmonary arterial hypertension: thin-section CT predictors of epoprostenol therapy failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

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/10.1164%2FRCCM.200208-861OC

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Effects of continuous IV prostacyclin in a patient with pulmonary veno-occlusive disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Functional heterogeneity of bone morphogenetic protein receptor-II mutants found in patients with primary pulmonary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Pulmonary veno-occlusive disease. Morphological changes suggesting a viral cause

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Pulmonary veno-occlusive disease in a HIV-infected intravenous drug abuser.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Radiation-induced pulmonary veno-occlusive disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Pulmonary veno-occlusive disease after neoadjuvant mitomycin chemotherapy and surgery for lung carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Familial pulmonary veno-occlusive disease: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

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/10.1164%2FRCCM.200208-861OC

Mutation in the gene for bone morphogenetic protein receptor II as a cause of primary pulmonary hypertension in a large kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

TGF-beta signalling from cell membrane to nucleus through SMAD proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

Divergence and convergence of TGF-beta/BMP signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200208-861OC

10.1164/RCCM.200208-861OC

21 January 2018

Identifiers

DOI

1 reference

1 December 2017

1 reference