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

Small molecules restore mutant mitochondrial DNA polymerase activity

小分子可恢复突变线粒体DNA聚合酶活性

Sebastian Valenzuela ,Xuefeng Zhu ,Bertil Macao ,Mattias Stamgren ,Carol Geukens ,Paul S Charifson ,Gunther Kern ,Emily Hoberg ,Louise Jenninger ,Anja V Gruszczyk ,Seoeun Lee ,Katarina A S Johansson ,Javier Miralles Fusté ,Yonghong Shi ,S Jordan Kerns ,Laleh Arabanian ,Gabriel Martinez Botella ,Sofie Ekström ,Jeremy Green ,Andrew M Griffin ,Carlos Pardo-Hernández ,Thomas A Keating ,Barbara Küppers-Munther ,Nils-Göran Larsson ,Cindy Phan ,Viktor Posse ,Juli E Jones ,Xie Xie ,Simon Giroux ,Claes M Gustafsson ,Maria Falkenberg

The mutation R107Q alters mtSSB ssDNA compaction ability and binding dynamics

突变 R107Q 改变了 mtSSB ssDNA 压缩能力和结合动力学

Martial Martucci, Amandine Moretton, Aleix Tarrés-Solé, Virginie Ropars, Louise Lambert, Patrick Vernet, Maria Solà, Maria Falkenberg, Geraldine Farge, Siet van den Wildenberg

Mechanistic basis of atypical TERT promoter mutations

非典型 TERT 启动子突变的机制基础

Kerryn Elliott, Vinod Kumar Singh, Alan Bäckerholm, Linnea Ögren, Markus Lindberg, Katarzyna M Soczek, Emily Hoberg, Tom Luijts, Jimmy Van den Eynden, Maria Falkenberg, Jennifer Doudna, Anders Ståhlberg, Erik Larsson

Two type I topoisomerases maintain DNA topology in human mitochondria

两种I型拓扑异构酶维持人类线粒体中的DNA拓扑结构

Katja E Menger ,James Chapman ,Héctor Díaz-Maldonado ,Mushtaq M Khazeem ,Dasha Deen ,Direnis Erdinc ,John W Casement ,Valeria Di Leo ,Angela Pyle ,Alejandro Rodríguez-Luis ,Ian G Cowell ,Maria Falkenberg ,Caroline A Austin ,Thomas J Nicholls

The human mitochondrial genome contains a second light strand promoter

人类线粒体基因组含有第二个轻链启动子

Benedict G Tan, Christian D Mutti, Yonghong Shi, Xie Xie, Xuefeng Zhu, Pedro Silva-Pinheiro, Katja E Menger, Héctor Díaz-Maldonado, Wei Wei, Thomas J Nicholls, Patrick F Chinnery, Michal Minczuk, Maria Falkenberg, Claes M Gustafsson

DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion

损害全酶稳定性的DNA聚合酶γ突变会导致催化亚基耗竭。

Pedro Silva-Pinheiro ,Carlos Pardo-Hernández ,Aurelio Reyes ,Lisa Tilokani ,Anup Mishra ,Raffaele Cerutti ,Shuaifeng Li ,Dieu-Hien Rozsivalova ,Sebastian Valenzuela ,Sukru A Dogan ,Bradley Peter ,Patricio Fernández-Silva ,Aleksandra Trifunovic ,Julien Prudent ,Michal Minczuk ,Laurence Bindoff ,Bertil Macao ,Massimo Zeviani ,Maria Falkenberg ,Carlo Viscomi

Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing

以深度测序为特征的包涵体肌炎线粒体 DNA 变异

Carola Hedberg-Oldfors, Ulrika Lindgren, Swaraj Basu, Kittichate Visuttijai, Christopher Lindberg, Maria Falkenberg, Erik Larsson Lekholm, Anders Oldfors

Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions

线粒体 L 链合成过程中的复制选择重组导致 DNA 缺失

Örjan Persson, Yazh Muthukumar, Swaraj Basu, Louise Jenninger, Jay P Uhler, Anna-Karin Berglund, Robert McFarland, Robert W Taylor, Claes M Gustafsson, Erik Larsson, Maria Falkenberg

Dinucleotide Degradation by REXO2 Maintains Promoter Specificity in Mammalian Mitochondria

REXO2介导的二核苷酸降解维持哺乳动物线粒体启动子的特异性

Thomas J Nicholls ,Henrik Spåhr ,Shan Jiang ,Stefan J Siira ,Camilla Koolmeister ,Sushma Sharma ,Johanna H K Kauppila ,Min Jiang ,Volkhard Kaever ,Oliver Rackham ,Andrei Chabes ,Maria Falkenberg ,Aleksandra Filipovska ,Nils-Göran Larsson ,Claes M Gustafsson

A two-nuclease pathway involving RNase H1 is required for primer removal at human mitochondrial OriL

人类线粒体 OriL 的引物去除需要 RNase H1 参与的双核酸酶途径

Ali Al-Behadili, Jay P Uhler, Anna-Karin Berglund, Bradley Peter, Mara Doimo, Aurelio Reyes, Sjoerd Wanrooij, Massimo Zeviani, Maria Falkenberg