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

2019 ◽  
Vol 15 (2) ◽  
pp. 205-210 ◽  
Author(s):  
Amitabh Biswas ◽  
Ali Raza ◽  
Soumi Das ◽  
Mitali Kapoor ◽  
Rijith Jayarajan ◽  
...  
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Thea Hyttel Hansen ◽  
Yannan Yan ◽  
Gustav Ahlberg ◽  
Oliver Bundgaard Vad ◽  
Lena Refsgaard ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (1) ◽  
pp. e86569 ◽  
Author(s):  
Jae-Hong Ko ◽  
Wanjun Gu ◽  
Inja Lim ◽  
Hyoweon Bang ◽  
Eun A. Ko ◽  
...  

2020 ◽  
Vol 118 (3) ◽  
pp. 569a
Author(s):  
Julie L. Han ◽  
Emilia Entcheva

2005 ◽  
Vol 387 (1) ◽  
pp. 211-219 ◽  
Author(s):  
Christopher P. PALMER ◽  
Ebru AYDAR ◽  
Mustafa B. A. DJAMGOZ

Ion channel genes have been discovered in many microbial organisms. We have investigated a microbial TRP (transient receptor potential) ion channel gene which has most similarity to polycystic-kidney-disease-related ion channel genes. We have shown that this gene (pkd2) is essential for cellular viability, and is involved in cell growth and cell wall synthesis. Expression of this gene increases following damage to the cell wall. This fission yeast pkd2 gene, orthologues of which are found in all eukaryotic cells, appears to be a key signalling component in the regulation of cell shape and cell wall synthesis in yeast through an interaction with a Rho1-GTPase. A model for the mode of action of this Schizosaccharomyces pombe protein in a Ca2+ signalling pathway is hypothesized.


2014 ◽  
Vol 34 (7) ◽  
pp. 2538-2543 ◽  
Author(s):  
V. Wolfram ◽  
T. D. Southall ◽  
C. Gunay ◽  
A. A. Prinz ◽  
A. H. Brand ◽  
...  

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