Items per page
Sort by

Send to:

Choose Destination

Results: 14

Cited In for PubMed (Select 17364146)


Immunodeficiency in a Child with Rapadilino Syndrome: A Case Report and Review of the Literature.

Vollebregt MM, Malfroot A, De Raedemaecker M, van der Burg M, van der Werff Ten Bosch JE.

Case Reports Immunol. 2015;2015:137368. doi: 10.1155/2015/137368. Epub 2015 May 6.


The helicase and ATPase activities of RECQL4 are compromised by mutations reported in three human patients.

Jensen MB, Dunn CA, Keijzers G, Kulikowicz T, Rasmussen LJ, Croteau DL, Bohr VA.

Aging (Albany NY). 2012 Nov;4(11):790-802.


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.

Mol Biol Cell. 2012 Nov;23(21):4273-85. doi: 10.1091/mbc.E12-02-0110. Epub 2012 Sep 12.


RecQL4 cytoplasmic localization: implications in mitochondrial DNA oxidative damage repair.

Chi Z, Nie L, Peng Z, Yang Q, Yang K, Tao J, Mi Y, Fang X, Balajee AS, Zhao Y.

Int J Biochem Cell Biol. 2012 Nov;44(11):1942-51. doi: 10.1016/j.biocel.2012.07.016. Epub 2012 Jul 21.


Identification of a coiled coil in werner syndrome protein that facilitates multimerization and promotes exonuclease processivity.

Perry JJ, Asaithamby A, Barnebey A, Kiamanesch F, Chen DJ, Han S, Tainer JA, Yannone SM.

J Biol Chem. 2010 Aug 13;285(33):25699-707. doi: 10.1074/jbc.M110.124941. Epub 2010 Jun 1.


Gene expression profiles of human glioblastomas are associated with both tumor cytogenetics and histopathology.

Vital AL, Tabernero MD, Castrillo A, Rebelo O, Tão H, Gomes F, Nieto AB, Resende Oliveira C, Lopes MC, Orfao A.

Neuro Oncol. 2010 Sep;12(9):991-1003. doi: 10.1093/neuonc/noq050. Epub 2010 May 18.


Conserved helicase domain of human RecQ4 is required for strand annealing-independent DNA unwinding.

Rossi ML, Ghosh AK, Kulikowicz T, Croteau DL, Bohr VA.

DNA Repair (Amst). 2010 Jul 1;9(7):796-804. doi: 10.1016/j.dnarep.2010.04.003. Epub 2010 May 6.


Rothmund-Thomson syndrome.

Larizza L, Roversi G, Volpi L.

Orphanet J Rare Dis. 2010 Jan 29;5:2. doi: 10.1186/1750-1172-5-2. Review.


Roles of Werner syndrome protein in protection of genome integrity.

Rossi ML, Ghosh AK, Bohr VA.

DNA Repair (Amst). 2010 Mar 2;9(3):331-44. doi: 10.1016/j.dnarep.2009.12.011. Epub 2010 Jan 13. Review.


Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation.

Thangavel S, Mendoza-Maldonado R, Tissino E, Sidorova JM, Yin J, Wang W, Monnat RJ Jr, Falaschi A, Vindigni A.

Mol Cell Biol. 2010 Mar;30(6):1382-96. doi: 10.1128/MCB.01290-09. Epub 2010 Jan 11.


dRecQ4 is required for DNA synthesis and essential for cell proliferation in Drosophila.

Xu Y, Lei Z, Huang H, Dui W, Liang X, Ma J, Jiao R.

PLoS One. 2009 Jul 2;4(7):e6107. doi: 10.1371/journal.pone.0006107.


Rising from the RecQ-age: the role of human RecQ helicases in genome maintenance.

Bohr VA.

Trends Biochem Sci. 2008 Dec;33(12):609-20. doi: 10.1016/j.tibs.2008.09.003. Epub 2008 Oct 14. Review.


Sensitivity of RECQL4-deficient fibroblasts from Rothmund-Thomson syndrome patients to genotoxic agents.

Jin W, Liu H, Zhang Y, Otta SK, Plon SE, Wang LL.

Hum Genet. 2008 Jul;123(6):643-53. doi: 10.1007/s00439-008-0518-4. Epub 2008 May 27.


Human premature aging, DNA repair and RecQ helicases.

Brosh RM Jr, Bohr VA.

Nucleic Acids Res. 2007;35(22):7527-44. Epub 2007 Nov 15. Review.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk