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ACVRL1 encodes a type I cell-surface receptor for the TGF-beta superfamily of ligands. Additionally we are shipping ACVRL1 Antibodies (159) and ACVRL1 Kits (26) and many more products for this protein.
Showing 10 out of 23 products:
Results show that ALK5 (show TGFBR1 Proteins) and ALK1 play antagonistic roles in TGF-beta (show TGFB1 Proteins)-induced podosome formation in aortic endothelial cells.
ALK1 and ALK5 are both essential for correct regulation of VEGF, and that disruption of either pathway leads to disease.
alk1 loss has no effect on arterial endothelial cell proliferation but alters arterial endothelial cell migration within lumenized vessels.
Control of Notch (show NOTCH1 Proteins) targets in arterial endothelium is context-dependent, with gene-specific and region-specific requirements for Notch (show NOTCH1 Proteins) and Alk1
Blood flow is required not only for alk1 expression but also for Alk1 activity.
Study demonstrate that alk1 expression requires blood flow, and despite normal levels of shear stress, some flow-responsive genes are dysregulated in alk1 mutant arterial endothelial cells.
vbg encodes activin receptor-like kinase 1 (acvrl1), a TGFbeta (show TGFB1 Proteins) type I receptor that is expressed predominantly in the endothelium of the vessels that become dilated in vbg mutants.
Study showed that rs706819, rs2293094, and rs11169953 polymorphisms in the ACVRL1 gene are associated with higher susceptibility to brain arteriovenous malformations.
c.1027C > T(p.Gln343) mutation within the ACVRL1 gene in family with hereditary hemorrhagic telangiectasia
Bone morphogenetic protein (BMP)9 (show GDF2 Proteins) and BMP10 (show BMP10 Proteins) are high affinity ligands for activin receptor-like kinase 1 (ALK1).
Activin receptor-like kinase (ALK)1 is a transforming growth factor beta (TGF-beta) type I receptor (show TGFBR1 Proteins) predominantly expressed in actively proliferating endothelial cells (ECs).
Two novel missense mutations and two recurrent mutations in the ACVRL1 gene are associated with pulmonary arterial hypertension in in Chinese families.
ALK1 expression and microvessel density are increased in oral lichen planus , particularly in atrophic/erosive OLP type.
The genetic-interactions among BMPR-2 (show BMPR2 Proteins), ALK-1, and 5-HTT (show SLC6A4 Proteins) polymorphisms, elevated BMP-2 (show BMP2 Proteins) and 5-HT (show DDC Proteins) levels and differential gene expression substantiated the strong genetic contribution in high altitude pulmonary edema pathophysiology.
Study of four patients with pulmonary arterial hypertension associated with human immunodeficiency virus infection found predisposing mutations in the BMPR2 (show BMPR2 Proteins), ACVRL1 and ENG (show ENG Proteins) genes.
The preponderance of ACVRL1 mutations was due to founder mutations, specifically, c.830C>A (p.Thr277Lys), which was found in 24 families from the same geographical area of Norway.
Report interaction between ALK1 signaling and connexin40 in the development of arteriovenous malformations.
These data indicate that both Itgb8 and Alk1 are important in maintaining normal cerebral angiogenesis in response to VEGF (show VEGFA Proteins). Itgb8 deficiency enhances the formation of dysplastic vessels and hemorrhage in Alk1 (+/-) mice.
these studies characterize an accessory TGF-beta (show TGFB1 Proteins)-stimulated BMP R-Smad (show SMAD1 Proteins) signaling mechanism in interstitial cells of the developing lung.
this study demonstrates that ACVRL1 signaling plays a pivotal role whereby it suppresses plasmacytoid dendritic cell development while enhancing that of CD8alpha(+) dendritic cells, thus contributing to DC diversity development.
CD109 (show CD109 Proteins) differentially regulates TGF-beta (show TGFB1 Proteins)-induced ALK1-Smad1 (show SMAD1 Proteins)/5 versus ALK5 (show TGFBR1 Proteins)-Smad2 (show SMAD2 Proteins)/3 pathways, leading to decreased extracellular matrix production in the skin; epidermal CD109 (show CD109 Proteins) expression regulates dermal function through a paracrine mechanism
he results of the present study demonstrated that BMP9 promoted the osteoclast differentiation of osteoclast precursors via binding to the ALK1 receptor on the cell surface, and inhibiting the ERK1/2 signaling pathways in the cell
Conclude that the ALK-1 receptor is involved in the control of arterial pressure. High AP of Alk1(+/-) mice is explained mainly by the sympathetic overactivation, which is probably related to the decreased number of cholinergic neurons.
In vascular sprouting, neuropilin-1 (show NRP1 Proteins) suppresses the stalk-cell phenotype by limiting Smad2 (show SMAD2 Proteins)/3 activation through Alk1 and Alk5 (show TGFBR1 Proteins). Notch (show NOTCH1 Proteins) downregulates Nrp1 (show NRP1 Proteins), thus relieving the inhibition of Alk1 and Alk5 (show TGFBR1 Proteins), thereby driving stalk-cell behaviour.
BMP9 (show GDF2 Proteins)/ALK1 augmented vasculogenesis and angiogenesis, and thereby enhanced neovascularization. Thus, we suggest that BMP9 (show GDF2 Proteins)/ALK1 may improve the efficacy of EPC (show TCF21 Proteins)-based therapies for treating ischemic diseases.
BMP-9 (show GDF2 Proteins) induces vascular smooth muscle cell osteogenic differentiation and calcification via ALK1, Smad (show SMAD1 Proteins) and ALP (show CCL21A Proteins) dependent mechanisms.
This gene encodes a type I cell-surface receptor for the TGF-beta superfamily of ligands. It shares with other type I receptors a high degree of similarity in serine-threonine kinase subdomains, a glycine- and serine-rich region (called the GS domain) preceding the kinase domain, and a short C-terminal tail. The encoded protein, sometimes termed ALK1, shares similar domain structures with other closely related ALK or activin receptor-like kinase proteins that form a subfamily of receptor serine/threonine kinases. Mutations in this gene are associated with hemorrhagic telangiectasia type 2, also known as Rendu-Osler-Weber syndrome 2.
activin A receptor type II-like 1
, serine/threonine-protein kinase receptor R3
, serine/threonine-protein kinase receptor R3-like
, activin receptor-like kinase 1
, violet beauregarde
, TGF-B superfamily receptor type I
, activin A receptor, type II-like kinase 1
, Activin receptor like kinase 1
, activin receptor-like kinase-1