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Molecular and Cellular Biology|July 31, 2013
Erythropoietic defect associated with reduced cell proliferation in mice lacking the 26S proteasome shuttling factor Rad23bSteven Bergink, Arjan F Theil, Wendy Toussaint, et al.Nature|December 22, 2006
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axisLaura J Niedernhofer, George A Garinis, Anja Raams, et al.Molecular Cell|March 10, 2022
Active DNA damage eviction by HLTF stimulates nucleotide excision repairMarvin van Toorn, Yasemin Turkyilmaz, Sueji Han, et al.Human Molecular Genetics|October 4, 2017
Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissueArjan F Theil, Imke K Mandemaker, Emile van den Akker, et al.EMBO Molecular Medicine|October 6, 2023
Trichothiodystrophy-associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiationArjan F Theil, Alex Pines, Tuğba Kalayci, et al.Science (New York, N.Y.)|October 30, 2025
FIGNL1 inhibits homologous recombination in BRCA2 deficient cells by dissociating RAD51 filamentsRaviprasad Kuthethur, Safa Nasrin Vz, Satheesh Kumar Sengodan, et al.Human Molecular Genetics|April 28, 2021
Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophyElena Botta, Arjan F Theil, Anja Raams, et al.American Journal of Human Genetics|August 3, 2019
Bi-allelic TARS Mutations Are Associated with Brittle Hair PhenotypeArjan F Theil, Elena Botta, Anja Raams, et al.Research Square|October 27, 2023
DDA1, a novel factor in transcription-coupled repair, modulates CRL4CSA dynamics at DNA damage-stalled RNA polymerase IIDiana Llerena Schiffmacher, Shun-Hsiao Lee, Katarzyna W Kliza, et al.Nature Communications|July 29, 2024
The small CRL4CSA ubiquitin ligase component DDA1 regulates transcription-coupled repair dynamicsDiana A Llerena Schiffmacher, Shun-Hsiao Lee, Katarzyna W Kliza, et al.Pageof 5