Deficiency of Axl aggravates pulmonary arterial hypertension via BMPR2.
Tatyana Novoyatleva,
Nabham Rai,
Baktybek Kojonazarov,
Swathi Veeroju,
Isabel Ben-Batalla,
Paola Caruso,
Mazen Shihan,
Nadine Presser,
Elsa Götz,
Carina Lepper,
Sebastian Herpel,
Grégoire Manaud,
Frédéric Perros,
Henning Gall,
Hossein Ardeschir Ghofrani,
Norbert Weissmann,
Friedrich Grimminger,
John Wharton,
Martin Wilkins,
Paul D Upton,
Sonja Loges,
Nicholas W Morrell,
Werner Seeger,
Ralph T Schermuly
Jan 28, 2022
Pulmonary arterial hypertension (PAH), is a fatal disease characterized by a pseudo-malignant phenotype. We investigated the expression and the role of the receptor tyrosine kinase Axl in experimental (i.e., monocrotaline and...