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Science (New York, N.Y.)|November 1, 2012
The Legionella effector RavZ inhibits host autophagy through irreversible Atg8 deconjugationAugustine Choy, Julia Dancourt, Brian Mugo, et al.
FEBS Letters|May 14, 2016
Small cargoes pass through synthetically glued Golgi stacksJulia Dancourt, Hong Zheng, Francesca Bottanelli, et al.
Communications Biology|May 17, 2023
Lack of involvement of CD63 and CD9 tetraspanins in the extracellular vesicle content delivery processMaria Laura Tognoli, Julia Dancourt, Emeline Bonsergent, et al.
Nature Cell Biology|April 22, 2014
Lipidation of the LC3/GABARAP family of autophagy proteins relies on a membrane-curvature-sensing domain in Atg3Sangeeta Nath, Julia Dancourt, Vladimir Shteyn, et al.
Pediatric Research|April 28, 2006
A new intronic mutation in the DPM1 gene is associated with a milder form of CDG Ie in two French siblingsJulia Dancourt, Sandrine Vuillaumier-Barrot, Helene Ogier de Baulny, et al.
Pediatric Research|November 14, 2018
Wide clinical spectrum in ALG8-CDG: clues from molecular findings suggest an explanation for a milder phenotype in the first-described patientSandrine Vuillaumier-Barrot, Manuel Schiff, Francesca Mattioli, et al.
The Journal of Biological Chemistry|May 2, 2002
Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferaseIsabelle Chantret, Thierry Dupré, Christophe Delenda, et al.
The Journal of Biological Chemistry|December 14, 2002
A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylationIsabelle Chantret, Julia Dancourt, Thierry Dupré, et al.
Aging Cell|November 6, 2020
FOXO3 targets are reprogrammed as Huntington's disease neural cells and striatal neurons face senescence with p16<sup>INK4a</sup> increaseJessica Voisin, Francesca Farina, Swati Naphade, et al.
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