Several articles were published 2021/2022

Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects. 

Laëtitia Kermasson, Dmitri Churikov, Aya Awad, Riham Smoom, Elodie Lainey, Lauréline Roger et al..

Blood, American Society of Hematology, 2022

 

Mechanisms and Regulation of Cellular Senescence

Lauréline Roger, Fanny Tomas, Véronique Gire

International Journal of Molecular Sciences, MDPI, 2021, 22 (23), pp.13173.

 

Nucleosome Positioning on Large Tandem DNA Repeats of the ‘601’ Sequence Engineered in Saccharomyces cerevisiae

Astrid Lancrey, Alexandra Joubert, Evelyne Duvernois-Berthet, Etienne Routhier, Saurabh Raj, Agnès Thierry, Marta Sigarteu, Loic Ponger, Vincent Croquette, Julien Mozziconacci and Jean-Baptiste Boulé

Journal of molécular biology, 15 April 2022

 

Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue

Richa Sharma , Sushree S Sahoo , Masayoshi Honda , Sophie L Granger , Charnise Goodings , Louis Sanchez , Axel Künstner , Hauke Busch, Fabian Beier, Shondra M Pruett-Miller , Marcus B Valentine , Alfonso G Fernandez , Ti-Cheng Chang, Vincent Géli , Dmitri Churikov , Sandrine Hirschi , Victor B Pastor , Melanie Boerries , Melchior Lauten , Charikleia Kelaidi , Megan A Cooper, Sarah Nicholas , Jill A Rosenfeld, Sophia Polychronopoulou , Caroline Kannengiesser, Carole Saintomé , Charlotte M Niemeyer, Patrick Revy, Marc S Wold , Maria Spies , Miriam Erlacher , Stéphane Coulon , Marcin W Wlodarski 

Blood, 2022 Feb 17;139(7):1039-1051. doi: 10.1182/blood.2021011980.

 

The meiosis-specific MEIOB–SPATA22 complex cooperates with RPA to form a compacted mixed MEIOB/SPATA22/RPA/ssDNA complex

JonathanRibeiro, PaulineDupaigne, CynthiaPetrillo, CécileDucrot, ClotildeDuquenne, XavierVeaute, CaroleSaintomé, 

DidierBusso, RaphaëlGuerois, EmmanuelleMartini, GabrielLivera

DNA Repair, june 2021

Published on: 29/09/2021 09:47 - Updated on: 12/04/2022 09:08