Interaction of FANCD2 and NBS1 in the DNA damage response

Author:

Nakanishi Koji,Taniguchi Toshiyasu,Ranganathan Velvizhi,New Helen V.,Moreau Lisa A.,Stotsky Maria,Mathew Christopher G.,Kastan Michael B.,Weaver David T.,D'Andrea Alan D.

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology

Reference38 articles.

1. Khanna, K. K. et al. Cellular responses to DNA Damage and the Human Chromosome Instability Syndromes (Humana, San Diego 1998).

2. Joenje, H. & Patel, K. J. The emerging genetic and molecular basis of fanconi anaemia. Nature Rev. Genet. 2, 446–459 (2001).

3. Weemaes, C. M. et al. A new chromosomal instability disorder: the Nijmegen breakage syndrome. Acta Paediatr. Scand. 70, 557–564 (1981).

4. Weemaes, C. M., Smeets, D. F., Horstink, M. Haraldsson, A. & Bakkeren J. A. Variants of Nijmegen breakage syndrome and ataxia telangiectasia. Immunodeficiency 4, 109–111 (1993).

5. Stewart, G. S. et al. The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder. Cell 99, 577–587 (1999).

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