Publications by authors named "Maxime Boutry"

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SEPTIN9 locally activates the RhoGEF ARHGEF18 to promote early stages of mitochondrial fission.
Rachel Shannon, Yadu Balachandran, Xindi Wang, Maxime Boutry, Hong Xie

J Cell Biol· October 2025

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ROS transfer at peroxisome-mitochondria contact regulates mitochondrial redox.
Laura F DiGiovanni, Prabhsimran K Khroud, Ruth E Carmichael, Tina A Schrader, Shivneet K Gill, Maxime Boutry

Science· July 2025

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Acutely Modifying Phosphatidylinositol Phosphates on Endolysosomes Using Chemically Inducible Dimerization Systems.
Wei Sheng Yap, Peter K Kim, Maxime Boutry

Bio Protoc· October 2024

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Spatacsin regulates directionality of lysosome trafficking by promoting the degradation of its partner AP5Z1.
Alexandre Pierga, Raphaël Matusiak, Margaux Cauhapé, Julien Branchu, Lydia Danglot, Maxime Boutry

PLoS Biol· October 2023

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Arf1-PI4KIIIβ positive vesicles regulate PI(3)P signaling to facilitate lysosomal tubule fission.
Maxime Boutry, Laura F DiGiovanni, Nicholas Demers, Aaron Fountain, Sami Mamand

J Cell Biol· September 2023

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ORP1L mediated PI(4)P signaling at ER-lysosome-mitochondrion three-way contact contributes to mitochondrial division.
Maxime Boutry, Peter K Kim

Nat Commun· September 2021

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Loss of spatacsin impairs cholesterol trafficking and calcium homeostasis.
Maxime Boutry, Alexandre Pierga, Raphaël Matusiak, Julien Branchu, Marc Houllegatte

Commun Biol· April 2020

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Update on the Genetics of Spastic Paraplegias.
Maxime Boutry, Sara Morais, Giovanni Stevanin

Curr Neurol Neurosci Rep· February 2019

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Inhibition of Lysosome Membrane Recycling Causes Accumulation of Gangliosides that Contribute to Neurodegeneration.
Maxime Boutry, Julien Branchu, Céline Lustremant, Claire Pujol, Julie Pernelle

Cell Rep· June 2018

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Loss of spatacsin function alters lysosomal lipid clearance leading to upper and lower motor neuron degeneration.
Julien Branchu, Maxime Boutry, Laura Sourd, Marine Depp, Céline Leone

Neurobiol Dis· June 2017

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Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.
Typhaine Esteves, Alexandra Durr, Emeline Mundwiller, José L Loureiro, Maxime Boutry

Am J Hum Genet· February 2014

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