Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Poor outcomes in carriers of the RNF213 variant (p.Arg4810Lys) with pulmonary arterial hypertension

2 Sept 2019

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Moyamoya disease diagnosis and treatment
Share to Pulmonary Hypertension Research and Treatments
Share to Vascular Anomalies and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 31542298
DOI: 10.1016/j.healun.2019.08.022

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Poor outcomes in carriers of the RNF213 variant (p.Arg4810Lys) with pulmonary arterial hypertensionPMID 31542298Read ↗

Role of RNF213 p.4810K variant in the development of intracranial arterial disease in patients treated with nilotinib.Semantic proximity Read ↗

Prevalence and Clinical Characteristics of Heterozygous RNF213 p.Arg4810Lys Variant Carriers Diagnosed With Chronic Thromboembolic Pulmonary Hypertension.Semantic proximity Read ↗

Nonsyndromic Peripheral Pulmonary Artery Stenosis Is Associated With Homozygosity of RNF213 p.Arg4810Lys Regardless of Co-occurrence of Moyamoya Disease.Semantic proximity Read ↗

Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in CaucasiansSemantic proximity Read ↗

Genomic Comparison With Supercentenarians Identifies RNF213 as a Risk Gene for Pulmonary Arterial HypertensionSemantic proximity Read ↗

Channelopathy Genes in Pulmonary Arterial Hypertension.Semantic proximity Read ↗

A CELSR1 variant in a patient with pulmonary arterial hypertension.Semantic proximity Read ↗

In silico explanation for the causalities of deleterious RNF213 SNPs in Moyamoya disease and insulin resistance.Semantic proximity Read ↗

Editors' Note: D313Y Variant in Fabry Disease: A Systematic Review and Meta-analysis.Semantic proximity Read ↗

SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial HypertensionSemantic proximity Read ↗

Author Response: D313Y Variant in Fabry Disease: A Systematic Review and Meta-analysis.Semantic proximity Read ↗

Rare RNF213 variants and the risk of intracranial artery stenosis/occlusion disease in Chinese population: a case-control studySemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.