Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy

Published:2019-05-31 Issue:2 Volume:15 Page:205-210
ISSN:1573-9538
Container-title:Purinergic Signalling
language:en
Short-container-title:Purinergic Signalling

Author:

Biswas Amitabh,Raza Ali,Das Soumi,Kapoor Mitali,Jayarajan Rijith,Verma Ankit,Shamsudheen Karuthedath Vellarikkal,Murry Benrithung,Seth Sandeep,Bhargava Balram,Scaria Vinod,Sivasubbu Sridhar,Rao Vadlamudi Raghavendra

Funder

Department of Biotechnology, Government of India

Indian Council of Medical Research

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Cellular and Molecular Neuroscience,Molecular Biology

Link

http://link.springer.com/content/pdf/10.1007/s11302-019-09660-7.pdf

Reference18 articles.

1. Barth K, Pfleger C, Linge A, Sim J, Surprenant A, Steinbronn N, Strasser R, Kasper M (2010) Increased P2X7R expression in atrial cardiomyocytes of caveolin-1 deficient mice. Histochem Cell Biol 134:31–38

2. Bracey NA, Beck PL, Muruve DA, Hirota SA, Guo J, Jabagi H, Wright JR Jr et al (2013) The Nlrp3 inflammasome promotes myocardial dysfunction in structural cardiomyopathy through interleukin-1β. Exp Physiol 98(2):462–472

3. Chen Z, He L, Li L, Chen L (2018) The P2X7 purinergic receptor: an emerging therapeutic target in cardiovascular diseases. Clin Chim Acta 479:196–207

4. Erlinge D, Burnstock G (2008) P2 receptors in cardiovascular regulation and disease. Purinerg Signal 4(1):1–20

5. Franceschini A, Capece M, Chiozzi P, Falzoni S, Sanz JM, Sarti AC, Bonora M, Pinton P, Di Virgilio F (2015) The P2X7 receptor directly interacts with the NLRP3 inflammasome scaffold protein. FASEB J 29(6):2450–2461

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