Mutation-induced LZTR1 polymerization provokes cardiac pathology in recessive Noonan syndrome
Alexandra Viktoria Busley(Universitätsmedizin Göttingen), Lukas Cyganek(Institute of Molecular Bioimaging and Physiology)
Cited by 13
Related Papers
Deep phenotyping of human induced pluripotent stem cell–derived atrial and ventricular cardiomyocytes
|JCI Insight|2018|298
Catecholamine-Dependent β-Adrenergic Signaling in a Pluripotent Stem Cell Model of Takotsubo Cardiomyopathy
|Journal of the American College of Cardiology|2017|164
Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis
|Human Genetics|2020|32
Deciphering the pathogenic role of a variant with uncertain significance for short QT and Brugada syndromes using gene‐edited human‐induced pluripotent stem cell‐derived cardiomyocytes and preclinical drug screening
|Clinical and Translational Medicine|2021|22
LZTR1 polymerization provokes cardiac pathology in recessive Noonan syndrome
|bioRxiv (Cold Spring Harbor Laboratory)|2023|2