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Human RECQL5beta stimulates flap endonuclease 1.
Speina E, Dawut L, Hedayati M, Wang Z, May A, Schwendener S, Janscak P, Croteau DL, Bohr VA. Speina E, et al. Among authors: may a. Nucleic Acids Res. 2010 May;38(9):2904-16. doi: 10.1093/nar/gkp1217. Epub 2010 Jan 16. Nucleic Acids Res. 2010. PMID: 20081208 Free PMC article.
Human RECQL5 is a member of the RecQ helicase family which is implicated in genome maintenance. Five human members of the family have been identified; three of them, BLM, WRN and RECQL4 are associated with elevated cancer risk. ...Our findings, together with the previous l …
Human RECQL5 is a member of the RecQ helicase family which is implicated in genome maintenance. Five human members of the family have …
Human RECQL5 participates in the removal of endogenous DNA damage.
Tadokoro T, Ramamoorthy M, Popuri V, May A, Tian J, Sykora P, Rybanska I, Wilson DM 3rd, Croteau DL, Bohr VA. Tadokoro T, et al. Among authors: may a. Mol Biol Cell. 2012 Nov;23(21):4273-85. doi: 10.1091/mbc.E12-02-0110. Epub 2012 Sep 12. Mol Biol Cell. 2012. PMID: 22973052 Free PMC article.
The RecQ helicase RECQL5 participates in psoralen-induced interstrand cross-link repair.
Ramamoorthy M, May A, Tadokoro T, Popuri V, Seidman MM, Croteau DL, Bohr VA. Ramamoorthy M, et al. Among authors: may a. Carcinogenesis. 2013 Oct;34(10):2218-30. doi: 10.1093/carcin/bgt183. Epub 2013 May 28. Carcinogenesis. 2013. PMID: 23715498 Free PMC article.
In this report, we identify the role of RECQL5, a member of the RecQ family of helicases, in the repair of ICLs. Using laser-directed confocal microscopy, we demonstrate that RECQL5 is recruited to ICLs formed by trioxalen (a psoralen-derived compound) and ultraviol …
In this report, we identify the role of RECQL5, a member of the RecQ family of helicases, in the repair of ICLs. Using laser-directed …
Gene expression profiling in Werner syndrome closely resembles that of normal aging.
Kyng KJ, May A, Kølvraa S, Bohr VA. Kyng KJ, et al. Among authors: may a. Proc Natl Acad Sci U S A. 2003 Oct 14;100(21):12259-64. doi: 10.1073/pnas.2130723100. Epub 2003 Oct 3. Proc Natl Acad Sci U S A. 2003. PMID: 14527998 Free PMC article.
Werner syndrome (WS) is a premature aging disorder, displaying defects in DNA replication, recombination, repair, and transcription. It has been hypothesized that several WS phenotypes are secondary consequences of aberrant gene expression and that a transcription d …
Werner syndrome (WS) is a premature aging disorder, displaying defects in DNA replication, recombination, repair, and transcription. …
The involvement of human RECQL4 in DNA double-strand break repair.
Singh DK, Karmakar P, Aamann M, Schurman SH, May A, Croteau DL, Burks L, Plon SE, Bohr VA. Singh DK, et al. Among authors: may a. Aging Cell. 2010 Jun;9(3):358-71. doi: 10.1111/j.1474-9726.2010.00562.x. Epub 2010 Mar 6. Aging Cell. 2010. PMID: 20222902 Free PMC article.
2,579 results