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ACVRL1 wt Allele
Known as:
ACVRL1
, ALK-1
, Activin A Receptor, Type II-Like Kinase 1 wt Allele
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Human ACVRL1 wild-type allele is located within 12q11-q14 and is approximately 14 kb in length. This allele, which encodes serine/threonine-protein…
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National Institutes of Health
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Related topics
Related topics
11 relations
12q11-q14
ACVRL1 protein, human
Hereditary hemorrhagic telangiectasia
Homo sapiens
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Broader (1)
ACVRL1 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2011
Review
2011
ALK1 as an emerging target for antiangiogenic therapy of cancer.
S. Cunha
,
K. Pietras
Blood
2011
Corpus ID: 206899142
Members of the TGF-β family act on many, if not all, cell types within the body, producing diverse and complex cellular outcomes…
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Review
2010
Review
2010
Signaling by members of the TGF-beta family in vascular morphogenesis and disease.
E. Pardali
,
M. Goumans
,
P. ten Dijke
Trends in Cell Biology
2010
Corpus ID: 1741050
Highly Cited
2008
Highly Cited
2008
ALK5- and TGFBR2-independent role of ALK1 in the pathogenesis of hereditary hemorrhagic telangiectasia type 2.
S. Park
,
Y. J. Lee
,
+9 authors
S. P. Oh
Blood
2008
Corpus ID: 35966192
ALK1 belongs to the type I receptor family for transforming growth factor-beta family ligands. Heterozygous ALK1 mutations cause…
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Highly Cited
2008
Highly Cited
2008
ALK1 Opposes ALK5/Smad3 Signaling and Expression of Extracellular Matrix Components in Human Chondrocytes
K. Finnson
,
W. Parker
,
P. ten Dijke
,
M. Thorikay
,
A. Philip
Journal of Bone and Mineral Research
2008
Corpus ID: 11496816
Introduction: TGF‐β is a multifunctional regulator of chondrocyte proliferation, differentiation, and extracellular matrix…
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Highly Cited
2007
Highly Cited
2007
Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers
C. Sabbà
,
G. Pasculli
,
+5 authors
G. Guanti
Journal of Thrombosis and Haemostasis
2007
Corpus ID: 38590485
Summary. Background: Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder characterized by epistaxis, mucocutaneous…
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Highly Cited
2003
Highly Cited
2003
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia
R. E. Harrison
,
J. A. Flanagan
,
+14 authors
R. Trembath
Journal of Medical Genetics
2003
Corpus ID: 11718926
Background: Mutations of the transforming growth factor β (TGFβ) receptor components ENDOGLIN and ALK-1 cause the autosomal…
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Highly Cited
2002
Highly Cited
2002
Targets of transcriptional regulation by two distinct type I receptors for transforming growth factor‐β in human umbilical vein endothelial cells
T. Ota
,
M. Fujii
,
+4 authors
K. Miyazono
Journal of Cellular Physiology
2002
Corpus ID: 45032138
Transforming growth factor‐β (TGF‐β) plays a crucial role in vascular development and homeostasis by regulating many…
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Highly Cited
1999
Highly Cited
1999
Roles of bone morphogenetic protein type I receptors and Smad proteins in osteoblast and chondroblast differentiation.
M. Fujii
,
K. Takeda
,
+7 authors
K. Miyazono
Molecular Biology of the Cell
1999
Corpus ID: 7464863
The biological effects of type I serine/threonine kinase receptors and Smad proteins were examined using an adenovirus-based…
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Highly Cited
1998
Highly Cited
1998
Genetic alterations of the transforming growth factor beta receptor genes in pancreatic and biliary adenocarcinomas.
M. Goggins
,
M. Shekher
,
Kenan K. Turnacioglu
,
C. Yeo
,
R. Hruban
,
S. Kern
Cancer Research
1998
Corpus ID: 32999047
Transforming growth factor beta (TGF-beta) is an extracellular ligand that binds to a heterodimeric receptor, initiating signals…
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Highly Cited
1993
Highly Cited
1993
Activin receptor-like kinases: a novel subclass of cell-surface receptors with predicted serine/threonine kinase activity.
P. tenDijke
,
H. Ichijo
,
+5 authors
K. Miyazono
Oncogene
1993
Corpus ID: 46434079
Human cDNA clones encoding four novel putative transmembrane protein serine/threonine kinases, denoted activin receptor-like…
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