Sjoerd Wanrooij
Umeå University(SE)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, DNA Repair Mechanisms, Advanced biosensing and bioanalysis techniques, DNA and Nucleic Acid Chemistry
Most-Cited Works
- → Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria(2001)880 cited
- → What causes mitochondrial DNA deletions in human cells?(2008)380 cited
- → Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice(2005)329 cited
- → Mitochondrial RNA Polymerase Is Needed for Activation of the Origin of Light-Strand DNA Replication(2010)216 cited
- → Mammalian transcription factor A is a core component of the mitochondrial transcription machinery(2012)186 cited
- → Human mitochondrial RNA polymerase primes lagging-strand DNA synthesis in vitro(2008)177 cited
- → Alterations to the expression level of mitochondrial transcription factor A, TFAM, modify the mode of mitochondrial DNA replication in cultured human cells(2006)166 cited
- → Expression of catalytic mutants of the mtDNA helicase Twinkle and polymerase POLG causes distinct replication stalling phenotypes(2007)146 cited
- → In Vivo Occupancy of Mitochondrial Single-Stranded DNA Binding Protein Supports the Strand Displacement Mode of DNA Replication(2014)140 cited
- → Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling(2008)136 cited