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Advances in Biological Regulation|January 26, 2021
Structure and regulation of human phospholipase DForrest Z Bowling, Michael A Frohman, Michael V Airola
Nature Chemical Biology|March 22, 2020
Crystal structure of human PLD1 provides insight into activation by PI(4,5)P<sub>2</sub> and RhoAForrest Z Bowling, Christian M Salazar, Justin A Bell, et al.
The Journal of Clinical Investigation|March 1, 2021
Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathyNajim Lahrouchi, Alex V Postma, Christian M Salazar, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
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