Recapitulation of Werner syndrome sensitivity to camptothecin by limited knockdown of the WRN helicase/exonuclease
WRN is a RecQ helicase with an associated exonuclease activity important in DNA metabolism, including DNA replication, repair and recombination. In humans, deficiencies in WRN function cause the segmental progeroid Werner syndrome (WS), in which patients show premature onset of many hallmarks of nor...
Κύριοι συγγραφείς: | Bird, J, Jennert-Burston, K, Bachler, M, Mason, P, Lowe, J, Heo, S, Campisi, J, Faragher, R, Cox, L |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2012
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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Recapitulation of Werner syndrome sensitivity to camptothecin by limited knockdown of the WRN helicase/exonuclease.
ανά: Bird, J, κ.ά.
Έκδοση: (2012) -
Characterisation of the interaction between WRN, the helicase/exonuclease defective in progeroid Werner's syndrome, and an essential replication factor, PCNA.
ανά: Rodríguez-López, A, κ.ά.
Έκδοση: (2003) -
Modeling Werner Syndrome in Drosophila melanogaster: hyper-recombination in flies lacking WRN-like exonuclease.
ανά: Cox, L, κ.ά.
Έκδοση: (2007) -
DmWRNexo is a 3'-5' exonuclease: phenotypic and biochemical characterization of mutants of the Drosophila orthologue of human WRN exonuclease.
ανά: Boubriak, I, κ.ά.
Έκδοση: (2009) -
A high-throughput screen to identify novel small molecule inhibitors of the Werner Syndrome Helicase-Nuclease (WRN).
ανά: Joshua A Sommers, κ.ά.
Έκδοση: (2019-01-01)