Pierre-Emmanuel Gleizes
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Explore the profile of Pierre-Emmanuel Gleizes including associated specialties, affiliations and a list of published articles.
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60
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3055
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Recent Articles
1.
Karim E, Gatel C, Leforestier A, Balor S, Soldan V, Plisson-Chastang C, et al.
J Struct Biol
. 2025 Jan;
217(1):108169.
PMID: 39818354
Transmission electron microscopy, especially at cryogenic temperature, is largely used for studying biological macromolecular complexes. A main difficulty of TEM imaging of biological samples is the weak amplitude contrasts due...
2.
Brunello L, Polanowska J, Le Tareau L, Maghames C, Georget V, Guette C, et al.
EMBO J
. 2024 Dec;
44(3):801-823.
PMID: 39690241
The identification of pathways that control elimination of protein inclusions is essential to understand the cellular response to proteotoxicity, particularly in the nuclear compartment, for which our knowledge is limited....
3.
Tagneres S, Santo P, Radermecker J, Rinaldi D, Froment C, Provost Q, et al.
Nat Commun
. 2024 Sep;
15(1):8404.
PMID: 39333141
Cancer cells rely on high ribosome production to sustain their proliferation rate. Many chemotherapies impede ribosome production which is perceived by cells as "nucleolar stress" (NS), triggering p53-dependent and independent...
4.
Fellmann F, Saunders C, ODonohue M, Reid D, McFadden K, Montel-Lehry N, et al.
JCI Insight
. 2024 Aug;
9(17).
PMID: 39088281
Diamond-Blackfan anemia syndrome (DBA) is a ribosomopathy associated with loss-of-function variants in more than 20 ribosomal protein (RP) genes. Here, we report the genetic, functional, and biochemical dissection of 2...
5.
Wlodarski M, Vlachos A, Farrar J, Da Costa L, Kattamis A, Dianzani I, et al.
Lancet Haematol
. 2024 May;
11(5):e368-e382.
PMID: 38697731
Diamond-Blackfan anaemia (DBA), first described over 80 years ago, is a congenital disorder of erythropoiesis with a predilection for birth defects and cancer. Despite scientific advances, this chronic, debilitating, and...
6.
Da Costa L, Mohandas N, David-NGuyen L, Platon J, Marie I, ODonohue M, et al.
Blood Cells Mol Dis
. 2024 Feb;
106:102838.
PMID: 38413287
Diamond-Blackfan anemia (DBA) was the first ribosomopathy described in humans. DBA is a congenital hypoplastic anemia, characterized by macrocytic aregenerative anemia, manifesting by differentiation blockage between the BFU-e/CFU-e developmental erythroid...
7.
ODonohue M, Da Costa L, Lezzerini M, Unal S, Joret C, Bartels M, et al.
Blood
. 2022 Feb;
139(21):3111-3126.
PMID: 35213692
The congenital bone marrow failure syndrome Diamond-Blackfan anemia (DBA) is typically associated with variants in ribosomal protein (RP) genes impairing erythroid cell development. Here we report multiple individuals with biallelic...
8.
Lebaron S, ODonohue M, Smith S, Engleman K, Juusola J, Safina N, et al.
Hum Mutat
. 2021 Dec;
43(3):389-402.
PMID: 34961992
Diamond-Blackfan anemia is a rare genetic disease characterized by erythroblastopenia and a large spectrum of developmental anomalies. The vast majority of the cases genetically described are linked to heterozygous pathogenic...
9.
Plassart L, Shayan R, Montellese C, Rinaldi D, Larburu N, Pichereaux C, et al.
Elife
. 2021 Apr;
10.
PMID: 33908345
Preventing premature interaction of pre-ribosomes with the translation apparatus is essential for translational accuracy. Hence, the final maturation step releasing functional 40S ribosomal subunits, namely processing of the 18S ribosomal...
10.
Malecki J, ODonohue M, Kim Y, Jakobsson M, Gessa L, Pinto R, et al.
Nucleic Acids Res
. 2021 Mar;
49(6):3185-3203.
PMID: 33693809
Protein methylation occurs primarily on lysine and arginine, but also on some other residues, such as histidine. METTL18 is the last uncharacterized member of a group of human methyltransferases (MTases)...