The Fanconi Anemia Group C Protein Interacts with Uncoordinated 5A and Delays Apoptosis

Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia

(2013) Massimo Bogliolo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia

(2013) Kazuya Kashiyama et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Fanconi anemia proteins interact with CtBP1 and modulate the expression of the Wnt antagonist Dickkopf-1

(2013) C. C. Huard et al.   BLOOD

Netrins: versatile extracellular cues with diverse functions

(2011) K. L. W. Sun et al.   DEVELOPMENT

The Fanconi anaemia pathway orchestrates incisions at sites of crosslinked DNA

(2011) Gerry P Crossan et al.   JOURNAL OF PATHOLOGY

The Dependence Receptor UNC5H2/B Triggers Apoptosis via PP2A-Mediated Dephosphorylation of DAP Kinase

(2010) Céline Guenebeaud et al.   MOLECULAR CELL

Fanconi anemia and its diagnosis

(2009) Arleen D. Auerbach   MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS

HES1 is a novel interactor of the Fanconi anemia core complex

(2008) C. S. Tremblay et al.   BLOOD

Inherited aplastic anaemias/bone marrow failure syndromes

(2008) Inderjeet Dokal et al.   BLOOD REVIEWS