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Items: 17


Genome stability: What we have learned from cohesinopathies.

Cucco F, Musio A.

Am J Med Genet C Semin Med Genet. 2016 Jun;172(2):171-8. doi: 10.1002/ajmg.c.31492. Epub 2016 Apr 19. Review.


Tim/Timeless, a member of the replication fork protection complex, operates with the Warsaw breakage syndrome DNA helicase DDX11 in the same fork recovery pathway.

Calì F, Bharti SK, Di Perna R, Brosh RM Jr, Pisani FM.

Nucleic Acids Res. 2016 Jan 29;44(2):705-17. doi: 10.1093/nar/gkv1112. Epub 2015 Oct 25.


The Q Motif Is Involved in DNA Binding but Not ATP Binding in ChlR1 Helicase.

Ding H, Guo M, Vidhyasagar V, Talwar T, Wu Y.

PLoS One. 2015 Oct 16;10(10):e0140755. doi: 10.1371/journal.pone.0140755. eCollection 2015.


Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function.

de Lange J, Faramarz A, Oostra AB, de Menezes RX, van der Meulen IH, Rooimans MA, Rockx DA, Brakenhoff RH, van Beusechem VW, King RW, de Winter JP, Wolthuis RM.

Nat Commun. 2015 Oct 1;6:8399. doi: 10.1038/ncomms9399.


The Warsaw breakage syndrome-related protein DDX11 is required for ribosomal RNA synthesis and embryonic development.

Sun X, Chen H, Deng Z, Hu B, Luo H, Zeng X, Han L, Cai G, Ma L.

Hum Mol Genet. 2015 Sep 1;24(17):4901-15. doi: 10.1093/hmg/ddv213. Epub 2015 Jun 18.


Warsaw Breakage Syndrome--A further report, emphasising cutaneous findings.

Bailey C, Fryer AE, Greenslade M.

Eur J Med Genet. 2015 Apr;58(4):235-7. doi: 10.1016/j.ejmg.2015.02.001. Epub 2015 Feb 19.


DNA helicases FANCM and DDX11 are determinants of PARP inhibitor sensitivity.

Stoepker C, Faramarz A, Rooimans MA, van Mil SE, Balk JA, Velleuer E, Ameziane N, Te Riele H, de Winter JP.

DNA Repair (Amst). 2015 Feb;26:54-64. doi: 10.1016/j.dnarep.2014.12.003. Epub 2014 Dec 24.


A distinct triplex DNA unwinding activity of ChlR1 helicase.

Guo M, Hundseth K, Ding H, Vidhyasagar V, Inoue A, Nguyen CH, Zain R, Lee JS, Wu Y.

J Biol Chem. 2015 Feb 20;290(8):5174-89. doi: 10.1074/jbc.M114.634923. Epub 2015 Jan 5.


Molecular functions and cellular roles of the ChlR1 (DDX11) helicase defective in the rare cohesinopathy Warsaw breakage syndrome.

Bharti SK, Khan I, Banerjee T, Sommers JA, Wu Y, Brosh RM Jr.

Cell Mol Life Sci. 2014 Jul;71(14):2625-39. doi: 10.1007/s00018-014-1569-4. Epub 2014 Feb 1. Review.


Specialization among iron-sulfur cluster helicases to resolve G-quadruplex DNA structures that threaten genomic stability.

Bharti SK, Sommers JA, George F, Kuper J, Hamon F, Shin-ya K, Teulade-Fichou MP, Kisker C, Brosh RM Jr.

J Biol Chem. 2013 Sep 27;288(39):28217-29. doi: 10.1074/jbc.M113.496463. Epub 2013 Aug 9.


Roles of ChlR1 DNA helicase in replication recovery from DNA damage.

Shah N, Inoue A, Woo Lee S, Beishline K, Lahti JM, Noguchi E.

Exp Cell Res. 2013 Aug 15;319(14):2244-53. doi: 10.1016/j.yexcr.2013.06.005. Epub 2013 Jun 22.


Disease-causing missense mutations in human DNA helicase disorders.

Suhasini AN, Brosh RM Jr.

Mutat Res. 2013 Apr-Jun;752(2):138-52. doi: 10.1016/j.mrrev.2012.12.004. Epub 2012 Dec 28. Review.


DNA helicases associated with genetic instability, cancer, and aging.

Suhasini AN, Brosh RM Jr.

Adv Exp Med Biol. 2013;767:123-44. doi: 10.1007/978-1-4614-5037-5_6.


Identification and biochemical characterization of a novel mutation in DDX11 causing Warsaw breakage syndrome.

Capo-Chichi JM, Bharti SK, Sommers JA, Yammine T, Chouery E, Patry L, Rouleau GA, Samuels ME, Hamdan FF, Michaud JL, Brosh RM Jr, MĂ©garbane A, Kibar Z.

Hum Mutat. 2013 Jan;34(1):103-7. doi: 10.1002/humu.22226. Epub 2012 Oct 17.


Biochemical characterization of Warsaw breakage syndrome helicase.

Wu Y, Sommers JA, Khan I, de Winter JP, Brosh RM Jr.

J Biol Chem. 2012 Jan 6;287(2):1007-21. doi: 10.1074/jbc.M111.276022. Epub 2011 Nov 18.


Mammalian ChlR1 has a role in heterochromatin organization.

Inoue A, Hyle J, Lechner MS, Lahti JM.

Exp Cell Res. 2011 Oct 15;317(17):2522-35. doi: 10.1016/j.yexcr.2011.08.006. Epub 2011 Aug 11.


Warsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1.

van der Lelij P, Chrzanowska KH, Godthelp BC, Rooimans MA, Oostra AB, Stumm M, Zdzienicka MZ, Joenje H, de Winter JP.

Am J Hum Genet. 2010 Feb 12;86(2):262-6. doi: 10.1016/j.ajhg.2010.01.008. Epub 2010 Feb 4.

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