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Results: 1 to 20 of 97

Similar articles for PubMed (Select 24005565)

1.

Human DNA helicase HELQ participates in DNA interstrand crosslink tolerance with ATR and RAD51 paralogs.

Takata K, Reh S, Tomida J, Person MD, Wood RD.

Nat Commun. 2013;4:2338. doi: 10.1038/ncomms3338.

2.

HELQ promotes RAD51 paralogue-dependent repair to avert germ cell loss and tumorigenesis.

Adelman CA, Lolo RL, Birkbak NJ, Murina O, Matsuzaki K, Horejsi Z, Parmar K, Borel V, Skehel JM, Stamp G, D'Andrea A, Sartori AA, Swanton C, Boulton SJ.

Nature. 2013 Oct 17;502(7471):381-4. doi: 10.1038/nature12565. Epub 2013 Sep 4.

3.

Werner syndrome helicase has a critical role in DNA damage responses in the absence of a functional fanconi anemia pathway.

Aggarwal M, Banerjee T, Sommers JA, Iannascoli C, Pichierri P, Shoemaker RH, Brosh RM Jr.

Cancer Res. 2013 Sep 1;73(17):5497-507. doi: 10.1158/0008-5472.CAN-12-2975. Epub 2013 Jul 18.

4.

Mammalian Rad51C contributes to DNA cross-link resistance, sister chromatid cohesion and genomic stability.

Godthelp BC, Wiegant WW, van Duijn-Goedhart A, Schärer OD, van Buul PP, Kanaar R, Zdzienicka MZ.

Nucleic Acids Res. 2002 May 15;30(10):2172-82.

5.

Activation of the S phase DNA damage checkpoint by mitomycin C.

Mladenov E, Tsaneva I, Anachkova B.

J Cell Physiol. 2007 May;211(2):468-76.

PMID:
17167777
6.

Mcm8 and Mcm9 form a complex that functions in homologous recombination repair induced by DNA interstrand crosslinks.

Nishimura K, Ishiai M, Horikawa K, Fukagawa T, Takata M, Takisawa H, Kanemaki MT.

Mol Cell. 2012 Aug 24;47(4):511-22. doi: 10.1016/j.molcel.2012.05.047. Epub 2012 Jul 5.

7.

Checkpoint signaling from a single DNA interstrand crosslink.

Ben-Yehoyada M, Wang LC, Kozekov ID, Rizzo CJ, Gottesman ME, Gautier J.

Mol Cell. 2009 Sep 11;35(5):704-15. doi: 10.1016/j.molcel.2009.08.014.

8.

Helq acts in parallel to Fancc to suppress replication-associated genome instability.

Luebben SW, Kawabata T, Akre MK, Lee WL, Johnson CS, O'Sullivan MG, Shima N.

Nucleic Acids Res. 2013 Dec;41(22):10283-97. doi: 10.1093/nar/gkt676. Epub 2013 Sep 4.

9.

Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.

Hussain S, Witt E, Huber PA, Medhurst AL, Ashworth A, Mathew CG.

Hum Mol Genet. 2003 Oct 1;12(19):2503-10. Epub 2003 Aug 5.

11.

Recombination repair pathway in the maintenance of chromosomal integrity against DNA interstrand crosslinks.

Sasaki MS, Takata M, Sonoda E, Tachibana A, Takeda S.

Cytogenet Genome Res. 2004;104(1-4):28-34.

PMID:
15162012
12.
13.

ATR-dependent phosphorylation of FANCM at serine 1045 is essential for FANCM functions.

Singh TR, Ali AM, Paramasivam M, Pradhan A, Wahengbam K, Seidman MM, Meetei AR.

Cancer Res. 2013 Jul 15;73(14):4300-10. doi: 10.1158/0008-5472.CAN-12-3976. Epub 2013 May 22.

14.

Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents.

Hemphill AW, Akkari Y, Newell AH, Schultz RA, Grompe M, North PS, Hickson ID, Jakobs PM, Rennie S, Pauw D, Hejna J, Olson SB, Moses RE.

Cytogenet Genome Res. 2009;125(3):165-75. doi: 10.1159/000230001. Epub 2009 Sep 4.

15.

Inhibition of the Nedd8 system sensitizes cells to DNA interstrand cross-linking agents.

Kee Y, Huang M, Chang S, Moreau LA, Park E, Smith PG, D'Andrea AD.

Mol Cancer Res. 2012 Mar;10(3):369-77. doi: 10.1158/1541-7786.MCR-11-0497. Epub 2012 Jan 4.

16.

EGFR-activating mutations correlate with a Fanconi anemia-like cellular phenotype that includes PARP inhibitor sensitivity.

Pfäffle HN, Wang M, Gheorghiu L, Ferraiolo N, Greninger P, Borgmann K, Settleman J, Benes CH, Sequist LV, Zou L, Willers H.

Cancer Res. 2013 Oct 15;73(20):6254-63. doi: 10.1158/0008-5472.CAN-13-0044. Epub 2013 Aug 21.

17.
18.

The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair.

Bridge WL, Vandenberg CJ, Franklin RJ, Hiom K.

Nat Genet. 2005 Sep;37(9):953-7. Epub 2005 Aug 21.

PMID:
16116421
19.

Loss of CHK1 function impedes DNA damage-induced FANCD2 monoubiquitination but normalizes the abnormal G2 arrest in Fanconi anemia.

Guervilly JH, Macé-Aimé G, Rosselli F.

Hum Mol Genet. 2008 Mar 1;17(5):679-89. Epub 2007 Nov 20.

20.

Werner syndrome protein participates in a complex with RAD51, RAD54, RAD54B and ATR in response to ICL-induced replication arrest.

Otterlei M, Bruheim P, Ahn B, Bussen W, Karmakar P, Baynton K, Bohr VA.

J Cell Sci. 2006 Dec 15;119(Pt 24):5137-46. Epub 2006 Nov 21. Erratum in: J Cell Sci. 2006 Dec 15;119(Pt 24):5215.

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