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Arthritis and Rheumatism|July 11, 2013
Endothelial injury in a transforming growth factor β-dependent mouse model of scleroderma induces pulmonary arterial hypertensionEmma C Derrett-Smith, Audrey Dooley, Adrian J Gilbane, et al.
American Journal of Respiratory and Critical Care Medicine|August 27, 2011
A novel murine model of severe pulmonary arterial hypertensionLoredana Ciuclan, Olivier Bonneau, Martin Hussey, et al.
The International Journal of Biochemistry & Cell Biology|March 4, 2021
Selective deletion of connective tissue growth factor attenuates experimentally-induced pulmonary fibrosis and pulmonary arterial hypertensionAngela Y Y Tam, Amy L Horwell, Sarah L Trinder, et al.
The American Journal of Pathology|January 1, 2009
Activin-like kinase 5 (ALK5) mediates abnormal proliferation of vascular smooth muscle cells from patients with familial pulmonary arterial hypertension and is involved in the progression of experimental pulmonary arterial hypertension induced by monocrotalineMatthew Thomas, Cerys Docx, Alan M Holmes, et al.
Arthritis and Rheumatism|July 1, 2009
Pivotal role of connective tissue growth factor in lung fibrosis: MAPK-dependent transcriptional activation of type I collagenMarkella Ponticos, Alan M Holmes, Xu Shi-wen, et al.
Circulation|August 18, 2010
Elevated levels of inflammatory cytokines predict survival in idiopathic and familial pulmonary arterial hypertensionElaine Soon, Alan M Holmes, Carmen M Treacy, et al.
The New England Journal of Medicine|September 21, 2007
A polymorphism in the CTGF promoter region associated with systemic sclerosisCarmen Fonseca, Gisela E Lindahl, Markella Ponticos, et al.
The American Journal of Pathology|June 14, 2013
Assessment of Brd4 inhibition in idiopathic pulmonary fibrosis lung fibroblasts and in vivo models of lung fibrosisXiaoyan Tang, Ruoqi Peng, Jonathan E Phillips, et al.
Circulation Research|December 17, 2013
Evidence for the involvement of type I interferon in pulmonary arterial hypertensionPeter M George, Eduardo Oliver, Peter Dorfmuller, et al.
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