(Q44360290)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24292273%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

title

EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension (English)

1 reference

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2 March 2020

2

1 reference

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2 March 2020

Peter Dorfmuller

10

1 reference

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2 March 2020

Christine Lonjou

6

1 reference

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2 March 2020

Olivier Sitbon

12

1 reference

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2 March 2020

David-Alexandre Trégouët

14

1 reference

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2 March 2020

Marc Humbert

15

1 reference

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2 March 2020

13

Gérald Simonneau

1 reference

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2 March 2020

3

Barbara Girerd

1 reference

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2 March 2020

11

Elie Fadel

1 reference

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2 March 2020

1

Mélanie Eyries

1 reference

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2 March 2020

8

Florence Coulet

1 reference

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2 March 2020

16

Florent Soubrier

1 reference

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2 March 2020

9

Damien Bonnet

1 reference

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2 March 2020

author name string

Claire Perret

4

1 reference

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2 March 2020

Anne Leroy

5

1 reference

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2 March 2020

Nadjim Chelghoum

7

1 reference

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2 March 2020

language of work or name

English

0 references

publication date

1 December 2013

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2 March 2020

1 reference

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2 March 2020

volume

46

1 reference

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2 March 2020

issue

1

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2 March 2020

page(s)

65-69

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https://scigraph.springernature.com/pub.10.1038/ng.2844

2 March 2020

exact match

0 references

cites work

Pulmonary Veno-occlusive Disease

1 reference

Pulmonary veno-occlusive disease

21 January 2018

1 reference

Updated clinical classification of pulmonary hypertension.

21 January 2018

1 reference

Pulmonary veno-occlusive disease: clinical, functional, radiologic, and hemodynamic characteristics and outcome of 24 cases confirmed by histology.

21 January 2018

1 reference

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

21 January 2018

1 reference

Clinical outcomes of pulmonary arterial hypertension in patients carrying an ACVRL1 (ALK1) mutation

21 January 2018

1 reference

Genetics and genomics of pulmonary arterial hypertension

21 January 2018

1 reference

Familial pulmonary veno-occlusive disease: a case report

21 January 2018

1 reference

Longitudinal analysis casts doubt on the presence of genetic anticipation in heritable pulmonary arterial hypertension.

21 January 2018

1 reference

The eIF2α kinases: their structures and functions

21 January 2018

1 reference

Preservation of liver protein synthesis during dietary leucine deprivation occurs at the expense of skeletal muscle mass in mice deleted for eIF2 kinase GCN2.

21 January 2018

1 reference

Identification of GCN2 as new redox regulator for oxidative stress prevention in vivo

21 January 2018

1 reference

Hyperoxia synergizes with mutant bone morphogenic protein receptor 2 to cause metabolic stress, oxidant injury, and pulmonary hypertension.

21 January 2018

1 reference

BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension

21 January 2018

1 reference

High-throughput mapping of a dynamic signaling network in mammalian cells

21 January 2018

1 reference

Amino acid availability controls TRB3 transcription in liver through the GCN2/eIF2α/ATF4 pathway

21 January 2018

1 reference

A novel regulatory mechanism of the bone morphogenetic protein (BMP) signaling pathway involving the carboxyl-terminal tail domain of BMP type II receptor

21 January 2018

1 reference

BMP type II receptor deficiency confers resistance to growth inhibition by TGF-β in pulmonary artery smooth muscle cells: role of proinflammatory cytokines

21 January 2018

1 reference

Separate domains in GCN1 for binding protein kinase GCN2 and ribosomes are required for GCN2 activation in amino acid-starved cells

21 January 2018

1 reference

Pulmonary arterial hypertension in France: results from a national registry

21 January 2018

1 reference

Long-term response to calcium channel blockers in idiopathic pulmonary arterial hypertension.

21 January 2018

1 reference

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

21 January 2018

1 reference

ACVRL1 germinal mosaic with two mutant alleles in hereditary hemorrhagic telangiectasia associated with pulmonary arterial hypertension.

21 January 2018

1 reference

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

1 reference

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 January 2018

1 reference

Allele-sharing models: LOD scores and accurate linkage tests

21 January 2018

1 reference

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

The Sequence Alignment/Map format and SAMtools

21 January 2018

1 reference

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

21 January 2018

1 reference

Familial pulmonary capillary hemangiomatosis resulting in primary pulmonary hypertension

21 January 2018

1 reference

12 December 2020

Intrapulmonary veno-occlusive disease

1 reference

12 December 2020

Pulmonary veno-occlusive disease in siblings: case reports and morphometric study

1 reference

12 December 2020

Pulmonary veno-occlusive disease

1 reference

12 December 2020

Pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis: a clinicopathologic study of 35 cases

1 reference

12 December 2020

Pulmonary edema complicating continuous intravenous prostacyclin in pulmonary capillary hemangiomatosis

1 reference

12 December 2020