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ACVRL1 wt Allele

Known as: ACVRL1, ALK-1, Activin A Receptor, Type II-Like Kinase 1 wt Allele 
Human ACVRL1 wild-type allele is located within 12q11-q14 and is approximately 14 kb in length. This allele, which encodes serine/threonine-protein… 
National Institutes of Health

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11 relations
12q11-q14ACVRL1 protein, humanHereditary hemorrhagic telangiectasiaHomo sapiens

Broader (1)

ACVRL1 gene

Papers overview

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Review
2018
Review
2018
ALK-1 Positive Anaplastic Large Cell Lymphoma Presenting as Extensive and Exclusive Osseous Involvement: Report of a Rare Association and Review of Literature
2016
2016
Natural History of Epistaxis in a Spanish Population with Hereditary Haemorrhagic Telangiectasia ( HHT )
Objective: To describe the natural history of epistaxis in a cohort of Spanish patients with hereditary hemorrhagic… 
2016
2016
Genetics and its Associated Pathways of Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a devastating disease with significantly reduced survival. To date, no tested therapies… 
2015
2015
Hypertension: A new therapeutic strategy for PAH
Selective targeting of BMPR-II signalling using BMP9 could be a promising strategy for the treatment of pulmonary arterial… 
2012
2012
Kawasaki disease, Mycoplasma pneumoniae infection and anaplastic large cell lymphoma: An uncommon association
Kawasaki disease (KD) is an acute febrile systemic vasculitis occurring predominantly in young children less than 5 years of age… 
2009
2009
A Familial Case of Hereditary Hemorrhagic Telangiectasia
Hereditary hemorrhagic telangiectasia (HHT, also called Osler-Weber-Rendu Disease) is a rare systemic fibrovascular dysplasia… 
2007
2007
Gene expression profile of multiple myeloma cell line treated by arsenic trioxide
cDNA microarray was used to compare the gene expression profiles of multiple myeloma cell line RPMI8226 24 h before and after… 
2006
2006
A Novel Mutation in ALK-1 Causes Hereditary Hemorrhagic Telangiectasia Type 2
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal-dominant bleeding disorder and has two variants, HHT1 and HHT2… 
2001
2001
Die Hereditäre Hämorrhagische Teleangiektasie (Morbus Osler-Rendu-Weber) und ihre Manifestation an der Leber
M. Osler (Hereditary Hemorrhagic Telangiectasia, HHT) is an autosomal dominant inherited disease, with various vascular… 
1970
1970
Angiographic identification of enteric lesions. Guide to therapy in hereditary hemorrhagic telangiectasis.
Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome, HHT) is defined as a familial autosomal recessive disease… 
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