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Items: 8

1.

Telomere dysfunction results in enhanced organismal sensitivity to the alkylating agent N-methyl-N-nitrosourea.

González-Suárez E, Goytisolo FA, Flores JM, Blasco MA.

Cancer Res. 2003 Nov 1;63(21):7047-50.

2.

Many ways to telomere dysfunction: in vivo studies using mouse models.

Goytisolo FA, Blasco MA.

Oncogene. 2002 Jan 21;21(4):584-91. Review.

3.

Normal telomere length and chromosomal end capping in poly(ADP-ribose) polymerase-deficient mice and primary cells despite increased chromosomal instability.

Samper E, Goytisolo FA, Ménissier-de Murcia J, González-Suárez E, Cigudosa JC, de Murcia G, Blasco MA.

J Cell Biol. 2001 Jul 9;154(1):49-60.

5.

Mammalian Ku86 protein prevents telomeric fusions independently of the length of TTAGGG repeats and the G-strand overhang.

Samper E, Goytisolo FA, Slijepcevic P, van Buul PP, Blasco MA.

EMBO Rep. 2000 Sep;1(3):244-52.

6.

Short telomeres result in organismal hypersensitivity to ionizing radiation in mammals.

Goytisolo FA, Samper E, Martín-Caballero J, Finnon P, Herrera E, Flores JM, Bouffler SD, Blasco MA.

J Exp Med. 2000 Dec 4;192(11):1625-36.

7.

Photoaffinity labelling of a DNA-binding site on the globular domain of histone H5.

Goytisolo FA, Packman LC, Thomas JO.

Eur J Biochem. 1996 Dec 15;242(3):619-26.

8.

Identification of two DNA-binding sites on the globular domain of histone H5.

Goytisolo FA, Gerchman SE, Yu X, Rees C, Graziano V, Ramakrishnan V, Thomas JO.

EMBO J. 1996 Jul 1;15(13):3421-9.

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