Deficiency of Axl aggravates pulmonary arterial hypertension via BMPR2

Novoyatleva, T; Rai, N; Kojonazarov, B; Veeroju, S; Ben-Batalla, I; Caruso, P; Shihan, M; Presser, N; Gotz, E; Lepper, C; Herpel, S; Manaud, G; Perros, F; Gall, H; Ghofrani, HA; Weissmann, N; Grimminger, F; Wharton, J; Wilkins, M; Upton, PD; Loges, S; Morrell, NW; Seeger, W; Schermuly, RT

Novoyatleva, T; Schermuly, RT (corresponding author), Justus Liebig Univ Giessen, Excellence Cluster Cardio Pulm Syst ECCPS, Univ Giessen & Marburg Lung Ctr UGMLC, German Ctr Lung Res DZL, Giessen, Germany.

COMMUNICATIONS BIOLOGY, 2021; 4 (1):

Abstract

Pulmonary arterial hypertension (PAH), is a fatal disease characterized by a pseudo-malignant phenotype. We investigated the expression and the role o......

Full Text Link


Links

期刊讨论 | 中国SCI论文 | 期刊主页 | 投稿经验 | 杂志官网 | 投稿链接 | 作者需知 | PMC链接 | Pubmed全文检索