De Novo CNV Formation in Mouse Embryonic Stem Cells Occurs in the Absence of Xrcc4-Dependent Nonhomologous End Joining

por Arlt, Martin F., Rajendran, Sountharia, Birkeland, Shanda R., Wilson, Thomas E., Glover, Thomas W.
Publicado 2012

Genomic Structure, Evolutionary Origins, and Reproductive Function of a Large Amplified Intrinsically Disordered Protein-Coding Gene on the X Chromosome (Laidx) in Mice

por Arlt, Martin F., Brogley, Michele A., Stark-Dykema, Evan R., Hu, Yueh-Chiang, Mueller, Jacob L.
Publicado 2020

Large transcription units unify copy number variants and common fragile sites arising under replication stress

por Wilson, Thomas E., Arlt, Martin F., Park, So Hae, Rajendran, Sountharia, Paulsen, Michelle, Ljungman, Mats, Glover, Thomas W.
Publicado 2015

Locus-specific transcription silencing at the FHIT gene suppresses replication stress-induced copy number variant formation and associated replication delay

por Park, So Hae, Bennett-Baker, Pamela, Ahmed, Samreen, Arlt, Martin F, Ljungman, Mats, Glover, Thomas W, Wilson, Thomas E
Publicado 2021

A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome

por Bar, Daniel Z, Arlt, Martin F, Brazier, Joan F, Norris, Wendy E, Campbell, Susan E, Chines, Peter, Larrieu, Delphine, Jackson, Stephen P, Collins, Francis S, Glover, Thomas W, Gordon, Leslie B
Publicado 2017