Molecular genetic framework underlying pulmonary arterial hypertension

L Southgate, RD Machado, S Gräf… - Nature Reviews …, 2020 - nature.com
Pulmonary arterial hypertension (PAH) is a rare, progressive disorder typified by occlusion
of the pulmonary arterioles owing to endothelial dysfunction and uncontrolled proliferation of …

[HTML][HTML] TGF-β signaling in liver, pancreas, and gastrointestinal diseases and cancer

NR Gough, X Xiang, L Mishra - Gastroenterology, 2021 - Elsevier
Genetic alterations affecting transforming growth factor–β (TGF-β) signaling are
exceptionally common in diseases and cancers of the gastrointestinal system. As a regulator …

Bone morphogenetic proteins

T Katagiri, T Watabe - Cold Spring Harbor Perspectives …, 2016 - cshperspectives.cshlp.org
Bone morphogenetic proteins (BMPs), originally identified as osteoinductive components in
extracts derived from bone, are now known to play important roles in a wide array of …

TGFβ/BMP signaling pathway in cartilage homeostasis

NGM Thielen, PM van der Kraan, APM van Caam - Cells, 2019 - mdpi.com
Cartilage homeostasis is governed by articular chondrocytes via their ability to modulate
extracellular matrix production and degradation. In turn, chondrocyte activity is regulated by …

Selective enhancement of endothelial BMPR-II with BMP9 reverses pulmonary arterial hypertension

L Long, ML Ormiston, X Yang, M Southwood, S Gräf… - Nature medicine, 2015 - nature.com
Genetic evidence implicates the loss of bone morphogenetic protein type II receptor (BMPR-
II) signaling in the endothelium as an initiating factor in pulmonary arterial hypertension …

Endothelial progenitor cells stimulate neonatal lung angiogenesis through FOXF1-mediated activation of BMP9/ACVRL1 signaling

G Wang, B Wen, Z Deng, Y Zhang… - Nature …, 2022 - nature.com
Pulmonary endothelial progenitor cells (EPCs) are critical for neonatal lung angiogenesis
and represent a subset of general capillary cells (gCAPs). Molecular mechanisms through …

BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia

WL Wooderchak-Donahue, J McDonald… - The American Journal of …, 2013 - cell.com
Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder,
is caused by mutations in genes involved in the transforming growth factor beta (TGF-β) …

[HTML][HTML] ALK1 signaling inhibits angiogenesis by cooperating with the Notch pathway

B Larrivée, C Prahst, E Gordon, R del Toro, T Mathivet… - Developmental cell, 2012 - cell.com
Activin receptor-like kinase 1 (ALK1) is an endothelial-specific member of the TGF-β/BMP
receptor family that is inactivated in patients with hereditary hemorrhagic telangiectasia …

Influence of the TGF-β superfamily on osteoclasts/osteoblasts balance in physiological and pathological bone conditions

J Jann, S Gascon, S Roux, N Faucheux - International journal of …, 2020 - mdpi.com
The balance between bone forming cells (osteoblasts/osteocytes) and bone resorbing cells
(osteoclasts) plays a crucial role in tissue homeostasis and bone repair. Several hormones …

Tumor angiogenesis revisited: regulators and clinical implications

R Ronca, M Benkheil, S Mitola, S Struyf… - Medicinal research …, 2017 - Wiley Online Library
Abstract Since Judah Folkman hypothesized in 1971 that angiogenesis is required for solid
tumor growth, numerous studies have been conducted to unravel the angiogenesis process …