Ask about this productRelated genes to: ACVRL1 antibody
- Gene:
- ACVRL1 NIH gene
- Name:
- activin A receptor like type 1
- Previous symbol:
- ACVRLK1, ORW2
- Synonyms:
- HHT2, ALK1, HHT
- Chromosome:
- 12q13.13
- Locus Type:
- gene with protein product
- Date approved:
- 1994-12-12
- Date modifiied:
- 2019-04-23
Related products to: ACVRL1 antibody
Related articles to: ACVRL1 antibody
- HER2-positive breast cancer comprises 14%-20% of breast cancer cases and was previously linked with aggressive progression. Trastuzumab and its biosimilars have improved survival significantly, but their pulmonary toxicities remain underrecognized. While left ventricular dysfunction is a well-documented adverse effect, pulmonary hypertension, pulmonary arterial hypertension (PAH), and right heart failure are rarely reported. - Source: PubMed
Publication date: 2026/05/04
Ojo TimiCablay KoryEmara NeveenMeyer Armin - To diagnose undiagnosed heritable thoracic aortic disease (HTAD) using targeted next-generation sequencing technology on human aorta tissue obtained from a single-centre biobank. - Source: PubMed
Lee HaKim YoonjungKim Myeong SuLee Kyung-ASong Suk-Won - Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant vascular disorder characterized by multisystem arteriovenous malformations (AVMs). Still, the influence of demographic factors and specific pathogenic variants on systemic and cerebrovascular involvement remains incompletely defined. - Source: PubMed
Publication date: 2026/04/16
Palermo MatteoCocilovo FedericoTrevisi GianlucaLucci Cordisco EmanuelaDi Martino LuigiSonnini ElenaAlbanese AlessioDoglietto FrancescoOlivi AlessandroPola RobertoGaetani EleonoraSturiale Carmelo Lucio
- Source: PubMed
- Hereditary Hemorrhagic Telangiectasia (HHT) exhibits marked phenotypic heterogeneity. Although gene-organ associations are well established for visceral involvement, predictors of cerebrovascular malformations (CVMs), particularly brain arteriovenous malformations (bAVMs), remain incompletely defined. This study aimed to investigate genotype-phenotype correlations and identify predictors of bAVMs in a genetically confirmed HHT cohort. - Source: PubMed
Publication date: 2026/03/31
Sturiale Carmelo LucioCocilovo FedericoTrevisi GianlucaPalermo MatteoCordisco Emanuela LucciDi Martino LuigiSonnini ElenaAlbanese AlessioDoglietto FrancescoPola RobertoGaetani Eleonora