1-1-2008 Biomarkers and mechanisms of FANCD 2 function

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  2013

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• Fanconi Anemia

  2019influential reference
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  2005cited by this paper
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  2005cited by this paper
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  2005cited by this paper
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  2005cited by this paper
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• Fanconi anaemia proteins: major roles in cell protection against oxidative damage.

  2003influential reference
• Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice.

  2003cited by this paper
• Indicators of late normal tissue response after radiotherapy for head and neck cancer: fibroblasts, lymphocytes, genetics, DNA repair, and chromosome aberrations.

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• Convergence of the fanconi anemia and ataxia telangiectasia signaling pathways.

  2002cited by this paper
• ATM deficiency and oxidative stress: a new dimension of defective response to DNA damage.

  2002cited by this paper
• Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia.

  2002cited by this paper
• Histone H2AX Is Phosphorylated in an ATR-dependent Manner in Response to Replicational Stress*

  2001cited by this paper
• Positional cloning of a novel Fanconi anemia gene, FANCD2.

  2001cited by this paper
• Cellular function of the Fanconi anemia pathway

  2001cited by this paper
• The emerging genetic and molecular basis of Fanconi anaemia

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• Fanconi anemia group C protein prevents apoptosis in hematopoietic cells through redox regulation of GSTP1

  2001cited by this paper
• The Fanconi anemia complementation group C gene product: structural evidence of multifunctionality.

  2001cited by this paper
• Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway.

  2001cited by this paper
• Initiation of DNA Fragmentation during Apoptosis Induces Phosphorylation of H2AX Histone at Serine 139*

  2000cited by this paper
• Deregulated apoptosis is a hallmark of the Fanconi anemia syndrome.

  1997cited by this paper
• Fanconi anemia group A and D cell lines respond normally to inhibitors of cell cycle regulation

  1997cited by this paper
• Immortalization of four new fanconi anemia fibroblast cell lines by an improved procedure

  1996cited by this paper
• Increased formation of 8-hydroxydeoxyguanosine, an oxidative DNA damage, in lymphoblasts from Fanconi's anemia patients due to possible catalase deficiency.

  1993cited by this paper
• Hypersensitivity to oxygen is a uniform and secondary defect in Fanconi anemia cells.

  1993cited by this paper
• Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia

  1981cited by this paper

• No citing papers are available for this paper.