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Potential of the TRPM7 channel as a novel therapeutic target for pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is an intractable vascular disease characterized by a progressive increase in pulmonary vascular resistance caused by pulmonary vascular remodeling, which ultimately leads to right-sided heart failure. PAH remains incurable, despite the development of PAH-target...

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Detalles Bibliográficos
Autores principales:	Hiraishi, Keizo, Kurahara, Lin Hai, Ishikawa, Kaori, Go, Tetsuhiko, Yokota, Naoya, Hu, Yaopeng, Fujita, Takayuki, Inoue, Ryuji, Hirano, Katsuya
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Japan Society of Smooth Muscle Research 2022
Materias:	Invited Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364263/ https://www.ncbi.nlm.nih.gov/pubmed/35944979 http://dx.doi.org/10.1540/jsmr.58.50

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