Publications by authors named "Pierre-Emmanuel Gleizes"

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The 3'-5' exoribonuclease ISG20L2 contributes to 3' terminus maturation of 18S and 28S ribosomal RNAs.
Maxime Aubert, Hélène Zuber, Marine Mommert-Tripon, Sarah Le Page, Nathalie Montel-Lehry, Pierre-Emmanuel Gleizes

Nucleic Acids Res· November 2025

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VEXAS anemia is a mosaic erythroblastopenia.
Francois Rodrigues, Giulia Hardouin, Sara El Hoss, Aya Ghoul, Emilie-Fleur Gautier, Pierre-Emmanuel Gleizes

Blood· September 2025

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Off-axis electron holography of unstained bacteriophages: Towards electrostatic potential measurement of biological samples.
Elio Karim, Christophe Gatel, Amélie Leforestier, Stéphanie Balor, Vanessa Soldan, Pierre-Emmanuel Gleizes

J Struct Biol· March 2025

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A nuclear protein quality control system for elimination of nucleolus-related inclusions.
Lorène Brunello, Jolanta Polanowska, Léo Le Tareau, Chantal Maghames, Virginie Georget, Pierre-Emmanuel Gleizes

EMBO J· February 2025

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SURF2 is a MDM2 antagonist in triggering the nucleolar stress response.
Sophie Tagnères, Paulo Espirito Santo, Julie Radermecker, Dana Rinaldi, Carine Froment, Pierre-Emmanuel Gleizes

Nat Commun· September 2024

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An atypical form of 60S ribosomal subunit in Diamond-Blackfan anemia linked to RPL17 variants.
Florence Fellmann, Carol Saunders, Marie-Françoise O'Donohue, David W Reid, Kelsey A McFadden, Pierre-Emmanuel Gleizes

JCI Insight· August 2024

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Diamond-Blackfan anemia, the archetype of ribosomopathy: How distinct is it from the other constitutional ribosomopathies?
L Da Costa, Narla Mohandas, Ludivine David-NGuyen, Jessica Platon, Isabelle Marie, Pierre-Emmanuel Gleizes

Blood Cells Mol Dis· May 2024

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Diagnosis, treatment, and surveillance of Diamond-Blackfan anaemia syndrome: international consensus statement.
Marcin W Wlodarski, Adrianna Vlachos, Jason E Farrar, Lydie M Da Costa, Antonis Kattamis, Pierre-Emmanuel Gleizes

Lancet Haematol· May 2024

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HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia.
Marie-Françoise O'Donohue, Lydie Da Costa, Marco Lezzerini, Sule Unal, Clément Joret, Pierre-Emmanuel Gleizes

Blood· May 2022

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Functionally impaired RPL8 variants associated with Diamond-Blackfan anemia and a Diamond-Blackfan anemia-like phenotype.
Simon Lebaron, Marie-Françoise O'Donohue, Scott C Smith, Kendra L Engleman, Jane Juusola, Pierre-Emmanuel Gleizes

Hum Mutat· March 2022

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Human METTL18 is a histidine-specific methyltransferase that targets RPL3 and affects ribosome biogenesis and function.
Jędrzej M Małecki, Marie-Francoise Odonohue, Yeji Kim, Magnus E Jakobsson, Luca Gessa, Pierre-Emmanuel Gleizes

Nucleic Acids Res· April 2021

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The final step of 40S ribosomal subunit maturation is controlled by a dual key lock.
Laura Plassart, Ramtin Shayan, Christian Montellese, Dana Rinaldi, Natacha Larburu, Pierre-Emmanuel Gleizes

Elife· April 2021

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p53 activation during ribosome biogenesis regulates normal erythroid differentiation.
Salomé Le Goff, Ismael Boussaid, Celia Floquet, Anna Raimbault, Isabelle Hatin, Pierre-Emmanuel Gleizes

Blood· January 2021

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NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal-Hreidarsson syndrome.
Maname Benyelles, Marie-Françoise O'Donohue, Laëtitia Kermasson, Elodie Lainey, Raphael Borie, Pierre-Emmanuel Gleizes

Hum Mol Genet· April 2020

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Good Vibrations: Structural Remodeling of Maturing Yeast Pre-40S Ribosomal Particles Followed by Cryo-Electron Microscopy.
Ramtin Shayan, Dana Rinaldi, Natacha Larburu, Laura Plassart, Stéphanie Balor, Pierre-Emmanuel Gleizes

Molecules· March 2020

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The human methyltransferase ZCCHC4 catalyses N6-methyladenosine modification of 28S ribosomal RNA.
Rita Pinto, Cathrine B Vågbø, Magnus E Jakobsson, Yeji Kim, Marijke P Baltissen, Pierre-Emmanuel Gleizes

Nucleic Acids Res· January 2020

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Ribosomal protein gene RPL9 variants can differentially impair ribosome function and cellular metabolism.
Marco Lezzerini, Marianna Penzo, Marie-Françoise O'Donohue, Carolina Marques Dos Santos Vieira, Manon Saby, Pierre-Emmanuel Gleizes

Nucleic Acids Res· January 2020

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RPL13 Variants Cause Spondyloepimetaphyseal Dysplasia with Severe Short Stature.
Cedric Le Caignec, Benjamin Ory, François Lamoureux, Marie-Francoise O'Donohue, Emilien Orgebin, Pierre-Emmanuel Gleizes

Am J Hum Genet· November 2019

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Impaired telomere integrity and rRNA biogenesis in PARN-deficient patients and knock-out models.
Maname Benyelles, Harikleia Episkopou, Marie-Françoise O'Donohue, Laëtitia Kermasson, Pierre Frange, Pierre-Emmanuel Gleizes

EMBO Mol Med· July 2019

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Conformational proofreading of distant 40S ribosomal subunit maturation events by a long-range communication mechanism.
Valentin Mitterer, Ramtin Shayan, Sébastien Ferreira-Cerca, Guillaume Murat, Tanja Enne, Pierre-Emmanuel Gleizes

Nat Commun· June 2019

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Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation.
Amy E O'Connell, Maxim V Gerashchenko, Marie-Francoise O'Donohue, Samantha M Rosen, Eric Huntzinger, Pierre-Emmanuel Gleizes

PLoS Genet· February 2019

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The Genetic Landscape of Diamond-Blackfan Anemia.
Jacob C Ulirsch, Jeffrey M Verboon, Shideh Kazerounian, Michael H Guo, Daniel Yuan, Pierre-Emmanuel Gleizes

Am J Hum Genet· February 2019

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Maturation of pre-40S particles in yeast and humans.
Emilie Cerezo, Célia Plisson-Chastang, Anthony K Henras, Simon Lebaron, Pierre-Emmanuel Gleizes

Wiley Interdiscip Rev RNA· January 2019

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The path of pre-ribosomes through the nuclear pore complex revealed by electron tomography.
Franck Delavoie, Vanessa Soldan, Dana Rinaldi, Jean-Yves Dauxois, Pierre-Emmanuel Gleizes

Nat Commun· January 2019

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The Genetic Landscape of Diamond-Blackfan Anemia.
Jacob C Ulirsch, Jeffrey M Verboon, Shideh Kazerounian, Michael H Guo, Daniel Yuan, Pierre-Emmanuel Gleizes

Am J Hum Genet· December 2018

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