Publications by authors named "Forrest Z Bowling"

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Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.
Michele Nicastro, Alexa M C Vermeer, Pieter G Postema, Rafik Tadros, Forrest Z Bowling

Am J Hum Genet· July 2025

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Biallelic variants in cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.
Michele Nicastro, Alexa M C Vermeer, Pieter G Postema, Rafik Tadros, Forrest Z Bowling

medRxiv· July 2024

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Defining the proximal interaction networks of Arf GTPases reveals a mechanism for the regulation of PLD1 and PI4KB.
Fu-Long Li, Zhengming Wu, Yong-Qi Gao, Forrest Z Bowling, J Matthew Franklin

EMBO J· September 2022

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Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy.
Najim Lahrouchi, Alex V Postma, Christian M Salazar, Daniel M De Laughter, Fleur Tjong, Forrest Z Bowling

J Clin Invest· March 2021

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Structure and regulation of human phospholipase D.
Forrest Z Bowling, Michael A Frohman, Michael V Airola

Adv Biol Regul· January 2021

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Crystal structure of human PLD1 provides insight into activation by PI(4,5)P and RhoA.
Forrest Z Bowling, Christian M Salazar, Justin A Bell, Tahrima S Huq, Michael A Frohman

Nat Chem Biol· April 2020

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