A nonsense mutation in the DNA repair factor Hebo causes mild bone marrow failure and microcephaly
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J. Soulier | P. Revy | I. Callebaut | B. Lopez | J. de Villartay | I. Rouvet | C. Pondarré | G. Pennarun | Gabriella Vera | Shu Zhang | P. Bertrand | H. Labussière-Wallet | Marie Chansel | Benoit France | Gaëlle Pennarun
[1] A. D’Andrea,et al. Fanconi anemia pathway , 2017, Current Biology.
[2] S. Savage,et al. Unraveling the pathogenesis of Hoyeraal–Hreidarsson syndrome, a complex telomere biology disorder , 2015, British journal of haematology.
[3] S. Gabriel,et al. Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia. , 2015, Cell reports.
[4] A. Jankowska,et al. AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia , 2015, Human molecular genetics.
[5] S. Miyano,et al. Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia. , 2015, American journal of human genetics.
[6] David A. Williams,et al. Exit from dormancy provokes DNA-damage-induced attrition in haematopoietic stem cells , 2015, Nature.
[7] A. Smogorzewska,et al. SnapShot: Fanconi Anemia and Associated Proteins , 2015, Cell.
[8] D. Ruggero,et al. Marrow failure: a window into ribosome biology. , 2014, Blood.
[9] Chen Li,et al. Hematopoietic stem cell dysfunction underlies the progressive lymphocytopenia in XLF/Cernunnos deficiency. , 2014, Blood.
[10] V. Plagnol,et al. ERCC6L2 mutations link a distinct bone-marrow-failure syndrome to DNA repair and mitochondrial function. , 2014, American journal of human genetics.
[11] J. Shendure,et al. A general framework for estimating the relative pathogenicity of human genetic variants , 2014, Nature Genetics.
[12] M. Hurles,et al. Extreme Growth Failure is a Common Presentation of Ligase IV Deficiency , 2013, Human mutation.
[13] David A. Scott,et al. Genome engineering using the CRISPR-Cas9 system , 2013, Nature Protocols.
[14] A. Fischer,et al. Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability. , 2013, Human molecular genetics.
[15] Guilhem Faure,et al. Identification of hidden relationships from the coupling of Hydrophobic Cluster Analysis and Domain Architecture information , 2013, Bioinform..
[16] D. Durocher,et al. 53BP1 is a reader of the DNA damage-induced H2A Lys15 ubiquitin mark , 2013, Nature.
[17] R. Brosh,et al. Disease-causing missense mutations in human DNA helicase disorders. , 2013, Mutation research.
[18] Yu Zhang,et al. Mechanisms of Programmed DNA Lesions and Genomic Instability in the Immune System , 2013, Cell.
[19] R. Greenberg,et al. Acetylation Limits 53BP1 Association with Damaged Chromatin to Promote Homologous Recombination , 2012, Nature Structural &Molecular Biology.
[20] J. Cheng,et al. PHF20 is an effector protein of p53 double lysine methylation that stabilizes and activates p53 , 2012, Nature Structural &Molecular Biology.
[21] J. Soulier,et al. Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells. , 2012, Cell stem cell.
[22] Frédérick A. Mallette,et al. RNF8‐ and RNF168‐dependent degradation of KDM4A/JMJD2A triggers 53BP1 recruitment to DNA damage sites , 2012, The EMBO journal.
[23] D. Reinberg,et al. Crystal Structure of TDRD3 and Methyl-Arginine Binding Characterization of TDRD3, SMN and SPF30 , 2012, PloS one.
[24] A. Fischer,et al. Heterogeneous telomere defects in patients with severe forms of dyskeratosis congenita. , 2012, The Journal of allergy and clinical immunology.
[25] D. Fessas,et al. Structural basis for dimethylarginine recognition by the Tudor domains of human SMN and SPF30 proteins , 2011, Nature Structural &Molecular Biology.
[26] W. Heyer,et al. Functions of the Snf2/Swi2 family Rad54 motor protein in homologous recombination. , 2011, Biochimica et biophysica acta.
[27] David J. Chen,et al. Congenital bone marrow failure in DNA-PKcs mutant mice associated with deficiencies in DNA repair , 2011, The Journal of cell biology.
[28] A. Fischer,et al. Function of Apollo (SNM1B) at telomere highlighted by a splice variant identified in a patient with Hoyeraal–Hreidarsson syndrome , 2010, Proceedings of the National Academy of Sciences.
[29] Veena S Patil,et al. Repression of Retroelements in Drosophila Germline via piRNA Pathway by the Tudor Domain Protein Tejas , 2010, Current Biology.
[30] A. D’Andrea,et al. How the fanconi anemia pathway guards the genome. , 2009, Annual review of genetics.
[31] A. Auerbach,et al. Fanconi anemia and its diagnosis. , 2009, Mutation research.
[32] A. D’Andrea,et al. Mouse models of Fanconi anemia. , 2009, Mutation research.
[33] J. Soulier,et al. Diagnosis of Fanconi anemia in patients with bone marrow failure , 2009, Haematologica.
[34] T. Vulliamy,et al. Inherited aplastic anaemias/bone marrow failure syndromes. , 2008, Blood reviews.
[35] D. Wigley,et al. Structure and mechanism of helicases and nucleic acid translocases. , 2007, Annual review of biochemistry.
[36] S. Elledge,et al. Identification of the FANCI Protein, a Monoubiquitinated FANCD2 Paralog Required for DNA Repair , 2007, Cell.
[37] Georges Mer,et al. Structural Basis for the Methylation State-Specific Recognition of Histone H4-K20 by 53BP1 and Crb2 in DNA Repair , 2006, Cell.
[38] A. Fischer,et al. Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly , 2006, Cell.
[39] Yunmei Ma,et al. Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV , 2006, European journal of immunology.
[40] Johannes Söding,et al. The HHpred interactive server for protein homology detection and structure prediction , 2005, Nucleic Acids Res..
[41] C. Körner,et al. X-Ray Structures of the Sulfolobus solfataricus SWI2/SNF2 ATPase Core and Its Complex with DNA , 2005, Cell.
[42] A. Alexeev,et al. Structure of the SWI2/SNF2 chromatin-remodeling domain of eukaryotic Rad54 , 2005, Nature Structural &Molecular Biology.
[43] R. Guérois,et al. The Tudor tandem of 53BP1: a new structural motif involved in DNA and RG-rich peptide binding. , 2004, Structure.
[44] A. Sancar,et al. Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints. , 2004, Annual review of biochemistry.
[45] A. Fischer,et al. The mechanisms of immune diversification and their disorders , 2003, Nature Reviews Immunology.
[46] Judith A. Goodship,et al. A splicing mutation affecting expression of ataxia–telangiectasia and Rad3–related protein (ATR) results in Seckel syndrome , 2003, Nature Genetics.
[47] J. Bartek,et al. Distinct spatiotemporal dynamics of mammalian checkpoint regulators induced by DNA damage , 2003, Nature Cell Biology.
[48] I. Hickson. RecQ helicases: caretakers of the genome , 2003, Nature Reviews Cancer.
[49] A. Sali,et al. Comparative protein structure modeling of genes and genomes. , 2000, Annual review of biophysics and biomolecular structure.
[50] S. Ganesan,et al. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. , 2001, Molecular cell.
[51] A. Shimamoto,et al. Human RecQ5β, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerases 3α and 3β , 2000 .
[52] E. Rogakou,et al. DNA Double-stranded Breaks Induce Histone H2AX Phosphorylation on Serine 139* , 1998, The Journal of Biological Chemistry.
[53] Thomas L. Madden,et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. , 1997, Nucleic acids research.
[54] G. Labesse,et al. Deciphering protein sequence information through hydrophobic cluster analysis (HCA): current status and perspectives , 1997, Cellular and Molecular Life Sciences CMLS.
[55] C Roskelley,et al. A biomarker that identifies senescent human cells in culture and in aging skin in vivo. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[56] M. Jasin,et al. Measuring recombination proficiency in mouse embryonic stem cells. , 2005, Methods in molecular biology.