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RTEL1 contributes to DNA replication and repair and telomere maintenance.

Uringa EJ, Lisaingo K, Pickett HA, Brind'Amour J, Rohde JH, Zelensky A, Essers J, Lansdorp PM.

Mol Biol Cell. 2012 Jul;23(14):2782-92. doi: 10.1091/mbc.E12-03-0179. Epub 2012 May 16.


Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.

Le Guen T, Jullien L, Touzot F, Schertzer M, Gaillard L, Perderiset M, Carpentier W, Nitschke P, Picard C, Couillault G, Soulier J, Fischer A, Callebaut I, Jabado N, Londono-Vallejo A, de Villartay JP, Revy P.

Hum Mol Genet. 2013 Aug 15;22(16):3239-49. doi: 10.1093/hmg/ddt178. Epub 2013 Apr 15.


The mINO80 chromatin remodeling complex is required for efficient telomere replication and maintenance of genome stability.

Min JN, Tian Y, Xiao Y, Wu L, Li L, Chang S.

Cell Res. 2013 Dec;23(12):1396-413. doi: 10.1038/cr.2013.113. Epub 2013 Aug 27.


RTEL1 is a replisome-associated helicase that promotes telomere and genome-wide replication.

Vannier JB, Sandhu S, Petalcorin MI, Wu X, Nabi Z, Ding H, Boulton SJ.

Science. 2013 Oct 11;342(6155):239-42. doi: 10.1126/science.1241779.


BLM has early and late functions in homologous recombination repair in mouse embryonic stem cells.

Chu WK, Hanada K, Kanaar R, Hickson ID.

Oncogene. 2010 Aug 19;29(33):4705-14. doi: 10.1038/onc.2010.214. Epub 2010 Jun 7.


Postreplicative joining of DNA double-strand breaks causes genomic instability in DNA-PKcs-deficient mouse embryonic fibroblasts.

Martín M, Genescà A, Latre L, Jaco I, Taccioli GE, Egozcue J, Blasco MA, Iliakis G, Tusell L.

Cancer Res. 2005 Nov 15;65(22):10223-32.


Protection against chromosome degradation at the telomeres.

Grandin N, Charbonneau M.

Biochimie. 2008 Jan;90(1):41-59. Epub 2007 Jul 24. Review.


On BLM helicase in recombination-mediated telomere maintenance.

Rezazadeh S.

Mol Biol Rep. 2013 Apr;40(4):3049-64. doi: 10.1007/s11033-012-2379-0. Epub 2012 Dec 26.


Telomeres: hallmarks of radiosensitivity.

Ayouaz A, Raynaud C, Heride C, Revaud D, Sabatier L.

Biochimie. 2008 Jan;90(1):60-72. Epub 2007 Sep 22. Review.


The Arabidopsis thaliana homolog of the helicase RTEL1 plays multiple roles in preserving genome stability.

Recker J, Knoll A, Puchta H.

Plant Cell. 2014 Dec;26(12):4889-902. doi: 10.1105/tpc.114.132472. Epub 2014 Dec 16.


The role of recombination in telomere length maintenance.

Royle NJ, Méndez-Bermúdez A, Gravani A, Novo C, Foxon J, Williams J, Cotton V, Hidalgo A.

Biochem Soc Trans. 2009 Jun;37(Pt 3):589-95. doi: 10.1042/BST0370589.


Murine Pif1 interacts with telomerase and is dispensable for telomere function in vivo.

Snow BE, Mateyak M, Paderova J, Wakeham A, Iorio C, Zakian V, Squire J, Harrington L.

Mol Cell Biol. 2007 Feb;27(3):1017-26. Epub 2006 Nov 27.


Pot1 deficiency initiates DNA damage checkpoint activation and aberrant homologous recombination at telomeres.

Wu L, Multani AS, He H, Cosme-Blanco W, Deng Y, Deng JM, Bachilo O, Pathak S, Tahara H, Bailey SM, Deng Y, Behringer RR, Chang S.

Cell. 2006 Jul 14;126(1):49-62.


Molecular insights into the heterogeneity of telomere reprogramming in induced pluripotent stem cells.

Wang F, Yin Y, Ye X, Liu K, Zhu H, Wang L, Chiourea M, Okuka M, Ji G, Dan J, Zuo B, Li M, Zhang Q, Liu N, Chen L, Pan X, Gagos S, Keefe DL, Liu L.

Cell Res. 2012 Apr;22(4):757-68. doi: 10.1038/cr.2011.201. Epub 2011 Dec 20.


Timeless Maintains Genomic Stability and Suppresses Sister Chromatid Exchange during Unperturbed DNA Replication.

Urtishak KA, Smith KD, Chanoux RA, Greenberg RA, Johnson FB, Brown EJ.

J Biol Chem. 2009 Mar 27;284(13):8777-85. doi: 10.1074/jbc.M806103200. Epub 2008 Dec 28.


RTEL1: an essential helicase for telomere maintenance and the regulation of homologous recombination.

Uringa EJ, Youds JL, Lisaingo K, Lansdorp PM, Boulton SJ.

Nucleic Acids Res. 2011 Mar;39(5):1647-55. doi: 10.1093/nar/gkq1045. Epub 2010 Nov 18. Review.


Fission yeast Taz1 and RPA are synergistically required to prevent rapid telomere loss.

Kibe T, Ono Y, Sato K, Ueno M.

Mol Biol Cell. 2007 Jun;18(6):2378-87. Epub 2007 Apr 11.


Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal-Hreidarsson syndrome.

Deng Z, Glousker G, Molczan A, Fox AJ, Lamm N, Dheekollu J, Weizman OE, Schertzer M, Wang Z, Vladimirova O, Schug J, Aker M, Londoño-Vallejo A, Kaestner KH, Lieberman PM, Tzfati Y.

Proc Natl Acad Sci U S A. 2013 Sep 3;110(36):E3408-16. doi: 10.1073/pnas.1300600110. Epub 2013 Aug 19.

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