日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

DNA methylation influences human centromere positioning and function.

DNA甲基化影响人类着丝粒的定位和功能。

Salinas-Luypaert Catalina, Dubocanin Danilo, Lee Rosa Jooyoung, Andrade Ruiz Lorena, Gamba Riccardo, Grison Marine, Velikovsky Leonid, Angrisani Annapaola, Scelfo Andrea, Xu Yuan, Dumont Marie, Barra Viviana, Wilhelm Therese, Velasco Guillaume, Losito Marialucrezia, Wardenaar René, Francastel Claire, Foijer Floris, Kops Geert J P L, Miga Karen H, Altemose Nicolas, Fachinetti Daniele

Small nucleolar RNAs promote the restoration of muscle differentiation defects in cells from myotonic dystrophy type 1.

小核仁RNA促进1型强直性肌营养不良细胞肌肉分化缺陷的恢复

Bogard Baptiste, Bonnet Hélène, Boyarchuk Ekaterina, Tellier Gilles, Furling Denis, Mouly Vincent, Francastel Claire, Hubé Florent

ZBTB24 is a conserved multifaceted transcription factor at genes and centromeres that governs the DNA methylation state and expression of satellite repeats

ZBTB24 是一种保守的多功能转录因子,存在于基因和着丝粒上,控制着 DNA 甲基化状态和卫星重复序列的表达。

Grillo, Giacomo; Boyarchuk, Ekaterina; Mihic, Seed; Ivkovic, Ivana; Bertrand, Mathilde; Jouneau, Alice; Dahlet, Thomas; Dumas, Michael; Weber, Michael; Velasco, Guillaume; Francastel, Claire

Tunable DNMT1 degradation reveals DNMT1/DNMT3B synergy in DNA methylation and genome organization

可调节的 DNMT1 降解揭示了 DNMT1/DNMT3B 在 DNA 甲基化和基因组组织中的协同作用

Andrea Scelfo, Viviana Barra #, Nezar Abdennur #, George Spracklin #, Florence Busato, Catalina Salinas-Luypaert, Elena Bonaiti, Guillaume Velasco, Frédéric Bonhomme, Anna Chipont, Andréa E Tijhuis, Diana C J Spierings, Coralie Guérin, Paola Arimondo, Claire Francastel, Floris Foijer, Jӧrg Tost, Leo

A Tool to Design Bridging Oligos Used to Detect Pseudouridylation Sites on RNA after CMC Treatment

设计用于检测 CMC 处理后 RNA 上的假尿苷化位点的桥接寡核苷酸的工具

Baptiste Bogard, Gilles Tellier, Claire Francastel, Florent Hubé

BRCA1 prevents R-loop-associated centromeric instability

BRCA1 可防止 R 环相关的着丝粒不稳定性

Racca, Carine; Britton, Sébastien; Hédouin, Sabrine; Francastel, Claire; Calsou, Patrick; Larminat, Florence

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders

评估DNA甲基化表观遗传特征在42种孟德尔遗传性神经发育障碍的诊断和表型相关性

Aref-Eshghi, Erfan; Kerkhof, Jennifer; Pedro, Victor P; France, Groupe DI; Barat-Houari, Mouna; Ruiz-Pallares, Nathalie; Andrau, Jean-Christophe; Lacombe, Didier; Van-Gils, Julien; Fergelot, Patricia; Dubourg, Christéle; Cormier-Daire, Valerie; Rondeau, Sophie; Lecoquierre, François; Saugier-Veber, Pascale; Nicolas, Gaël; Lesca, Gaetan; Chatron, Nicolas; Sanlaville, Damien; Vitobello, Antonio; Faivre, Laurence; Thauvin-Robinet, Christel; Laumonnier, Frederic; Raynaud, Martine; Alders, Mariëlle; Mannens, Marcel; Henneman, Peter; Hennekam, Raoul C; Velasco, Guillaume; Francastel, Claire; Ulveling, Damien; Ciolfi, Andrea; Pizzi, Simone; Tartaglia, Marco; Heide, Solveig; Héron, Delphine; Mignot, Cyril; Keren, Boris; Whalen, Sandra; Afenjar, Alexandra; Bienvenu, Thierry; Campeau, Philippe M; Rousseau, Justine; Levy, Michael A; Brick, Lauren; Kozenko, Mariya; Balci, Tugce B; Siu, Victoria Mok; Stuart, Alan; Kadour, Mike; Masters, Jennifer; Takano, Kyoko; Kleefstra, Tjitske; de Leeuw, Nicole; Field, Michael; Shaw, Marie; Gecz, Jozef; Ainsworth, Peter J; Lin, Hanxin; Rodenhiser, David I; Friez, Michael J; Tedder, Matt; Lee, Jennifer A; DuPont, Barbara R; Stevenson, Roger E; Skinner, Steven A; Schwartz, Charles E; Genevieve, David; Sadikovic, Bekim

Interplay between Histone and DNA Methylation Seen through Comparative Methylomes in Rare Mendelian Disorders

通过对罕见孟德尔遗传病中组蛋白甲基化组的比较研究,揭示组蛋白和DNA甲基化之间的相互作用

Velasco, Guillaume; Ulveling, Damien; Rondeau, Sophie; Marzin, Pauline; Unoki, Motoko; Cormier-Daire, Valérie; Francastel, Claire

Systematic Identification and Functional Validation of New snoRNAs in Human Muscle Progenitors

人类肌肉祖细胞中新 snoRNA 的系统鉴定和功能验证

Baptiste Bogard, Claire Francastel, Florent Hubé

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders

评估DNA甲基化表观遗传特征在42种孟德尔遗传性神经发育障碍的诊断和表型相关性

Aref-Eshghi, Erfan; Kerkhof, Jennifer; Pedro, Victor P; Barat-Houari, Mouna; Ruiz-Pallares, Nathalie; Andrau, Jean-Christophe; Lacombe, Didier; Van-Gils, Julien; Fergelot, Patricia; Dubourg, Christèle; Cormier-Daire, Valerie; Rondeau, Sophie; Lecoquierre, François; Saugier-Veber, Pascale; Nicolas, Gaël; Lesca, Gaetan; Chatron, Nicolas; Sanlaville, Damien; Vitobello, Antonio; Faivre, Laurence; Thauvin-Robinet, Christel; Laumonnier, Frederic; Raynaud, Martine; Alders, Mariëlle; Mannens, Marcel; Henneman, Peter; Hennekam, Raoul C; Velasco, Guillaume; Francastel, Claire; Ulveling, Damien; Ciolfi, Andrea; Pizzi, Simone; Tartaglia, Marco; Heide, Solveig; Héron, Delphine; Mignot, Cyril; Keren, Boris; Whalen, Sandra; Afenjar, Alexandra; Bienvenu, Thierry; Campeau, Philippe M; Rousseau, Justine; Levy, Michael A; Brick, Lauren; Kozenko, Mariya; Balci, Tugce B; Siu, Victoria Mok; Stuart, Alan; Kadour, Mike; Masters, Jennifer; Takano, Kyoko; Kleefstra, Tjitske; de Leeuw, Nicole; Field, Michael; Shaw, Marie; Gecz, Jozef; Ainsworth, Peter J; Lin, Hanxin; Rodenhiser, David I; Friez, Michael J; Tedder, Matt; Lee, Jennifer A; DuPont, Barbara R; Stevenson, Roger E; Skinner, Steven A; Schwartz, Charles E; Genevieve, David; Sadikovic, Bekim