Common Chromosomal Fragile Sites—Conserved Failure Stories

por Voutsinos, Vasileios, Munk, Sebastian H. N., Oestergaard, Vibe H.
Publicado 2018

Large Intronic Deletion of the Fragile Site Gene PRKN Dramatically Lowers Its Fragility Without Impacting Gene Expression

por Munk, Sebastian H. N., Voutsinos, Vasileios, Oestergaard, Vibe H.
Publicado 2021

Lamin A/C impairments cause mitochondrial dysfunction by attenuating PGC1α and the NAMPT-NAD(+) pathway

por Maynard, Scott, Hall, Arnaldur, Galanos, Panagiotis, Rizza, Salvatore, Yamamoto, Tatsuro, Gram, Helena Hagner, Munk, Sebastian H N, Shoaib, Muhammad, Sørensen, Claus Storgaard, Bohr, Vilhelm A, Lerdrup, Mads, Maya-Mendoza, Apolinar, Bartek, Jiri
Publicado 2022