1. Defective mitochondrial protease LonP1 can cause classical mitochondrial disease. (6th March 2018) Authors: Peter, Bradley; Waddington, Christie L; Oláhová, Monika; Sommerville, Ewen W; Hopton, Sila; Pyle, Angela; Champion, Michael; Ohlson, Monica; Siibak, Triinu; Chrzanowska-Lightowlers, Zofia M A; Taylor, Robert W; Falkenberg, Maria; Lightowlers, Robert N Journal: Human molecular genetics Issue: Volume 27:Number 10(2018:May 15) Page Start: 1743 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Corrigendum to: Structural basis for adPEO-causing mutations in the mitochondrial TWINKLE helicase. (14th January 2020) Authors: Peter, Bradley; Farge, Geraldine; Pardo-Hernandez, Carlos; Tångefjord, Stefan; Falkenberg, Maria Journal: Human molecular genetics Issue: Volume 29:Number 3(2020) Page Start: 528 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Ribonucleotides embedded in template DNA impair mitochondrial RNA polymerase progression. Issue 2 (8th January 2022) Authors: Singh, Meenakshi; Posse, Viktor; Peter, Bradley; Falkenberg, Maria; Gustafsson, Claes M Journal: Nucleic acids research Issue: Volume 50:Issue 2(2022) Page Start: 989 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Mammalian mitochondrial DNA replication and mechanisms of deletion formation. (1st November 2020) Authors: Falkenberg, Maria; Gustafsson, Claes M. Journal: Critical reviews in biochemistry and molecular biology Issue: Volume 55:Number 6(2020) Page Start: 509 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Two type I topoisomerases maintain DNA topology in human mitochondria. Issue 19 (10th October 2022) Authors: Menger, Katja E; Chapman, James; Díaz-Maldonado, Héctor; Khazeem, Mushtaq M; Deen, Dasha; Erdinc, Direnis; Casement, John W; Di Leo, Valeria; Pyle, Angela; Rodríguez-Luis, Alejandro; Cowell, Ian G; Falkenberg, Maria; Austin, Caroline A; Nicholls, Thomas J Journal: Nucleic acids research Issue: Volume 50:Issue 19(2022) Page Start: 11154 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study. Issue 9 (6th July 2022) Authors: Percetti, Marco; Franco, Giulia; Monfrini, Edoardo; Caporali, Leonardo; Minardi, Raffaella; La Morgia, Chiara; Valentino, Maria Lucia; Liguori, Rocco; Palmieri, Ilaria; Ottaviani, Donatella; Vizziello, Maria; Ronchi, Dario; Di Berardino, Federica; Cocco, Antoniangela; Macao, Bertil; Falkenberg, M... Journal: Movement disorders Issue: Volume 37:Issue 9(2022) Page Start: 1938 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mammalian RNase H1 directs RNA primer formation for mtDNA replication initiation and is also necessary for mtDNA replication completion. Issue 15 (10th August 2022) Authors: Misic, Jelena; Milenkovic, Dusanka; Al-Behadili, Ali; Xie, Xie; Jiang, Min; Jiang, Shan; Filograna, Roberta; Koolmeister, Camilla; Siira, Stefan J; Jenninger, Louise; Filipovska, Aleksandra; Clausen, Anders R; Caporali, Leonardo; Valentino, Maria Lucia; La Morgia, Chiara; Care... Journal: Nucleic acids research Issue: Volume 50:Issue 15(2022) Page Start: 8749 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing. (27th May 2021) Authors: Hedberg‐Oldfors, Carola; Lindgren, Ulrika; Basu, Swaraj; Visuttijai, Kittichate; Lindberg, Christopher; Falkenberg, Maria; Larsson Lekholm, Erik; Oldfors, Anders Journal: Brain pathology Issue: Volume 31:Number 3(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Correction to 'DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion'. Issue 18 (14th September 2021) Authors: Silva-Pinheiro, Pedro; Pardo-Hernández, Carlos; Reyes, Aurelio; Tilokani, Lisa; Mishra, Anup; Cerutti, Raffaele; Li, Shuaifeng; Rozsivalova, Dieu-Hien; Valenzuela, Sebastian; Dogan, Sukru A; Peter, Bradley; Fernández-Silva, Patricio; Trifunovic, Aleksandra; Prudent, Julien; Minczuk, Michal; Bindo... Journal: Nucleic acids research Issue: Volume 49:Issue 18(2021) Page Start: 10803 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. An Adaptable High-Throughput Technology Enabling the Identification of Specific Transcription Modulators. (April 2017) Authors: Bergbrede, Tim; Hoberg, Emily; Larsson, Nils-Göran; Falkenberg, Maria; Gustafsson, Claes M. Journal: SLAS discovery Issue: Volume 22:Number 4(2017) Page Start: 378 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗