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FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway

Blood, 2012-04, Vol.119 (14), p.3285-3294

2012

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Fancd2-deficient hematopoietic stem and progenitor cells depend on augmented mitochondrial translation for survival and proliferation

Stem cell research, 2019-10, Vol.40, p.101550-101550, Article 101550

2019

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Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M

Blood, 2009-07, Vol.114 (1), p.174-180

2009

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Human MutS and FANCM complexes function as redundant DNA damage sensors in the Fanconi Anemia pathway

DNA repair, 2011-12, Vol.10 (12), p.1203-1212

2011

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Instructive Role of MLL-Fusion Proteins Revealed by a Model of t(4;11) Pro-B Acute Lymphoblastic Leukemia

Cancer cell, 2016-11, Vol.30 (5), p.737-749

2016

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FANCD2 is required for the repression of germline transposable elements

Reproduction (Cambridge, England), 2020-06, Vol.159 (6), p.659-668

2020

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Remodeling of Interstrand Crosslink Proximal Replisomes Is Dependent on ATR, FANCM, and FANCD2

Cell reports (Cambridge), 2019-05, Vol.27 (6), p.1794-1808.e5

2019

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FANCB is essential in the male germline and regulates H3K9 methylation on the sex chromosomes during meiosis

Human molecular genetics, 2015-09, Vol.24 (18), p.5234-5249

2015

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MHF1-MHF2, a Histone-Fold-Containing Protein Complex, Participates in the Fanconi Anemia Pathway via FANCM

Molecular cell, 2010-03, Vol.37 (6), p.879-886

2010

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ATR-Dependent Phosphorylation of FANCM at Serine 1045 Is Essential for FANCM Functions

Cancer research (Chicago, Ill.), 2013-07, Vol.73 (14), p.4300-4310

2013

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BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome

Genes & development, 2008-10, Vol.22 (20), p.2856-2868

2008

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Fancd2 in vivo interaction network reveals a non-canonical role in mitochondrial function

Scientific reports, 2017-04, Vol.7 (1), p.45626-45626, Article 45626

2017

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A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

Nature genetics, 2005-09, Vol.37 (9), p.958-963

2005

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A novel ubiquitin ligase is deficient in Fanconi anemia

Nature genetics, 2003-10, Vol.35 (2), p.165-170

2003

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A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome

Molecular and Cellular Biology, 2003-05, Vol.23 (10), p.3417-3426

2003

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Rif1 provides a new DNA-binding interface for the Bloom syndrome complex to maintain normal replication

The EMBO journal, 2010-09, Vol.29 (18), p.3140-3155

2010

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Loss of Faap20 Causes Hematopoietic Stem and Progenitor Cell Depletion in Mice Under Genotoxic Stress

Stem cells (Dayton, Ohio), 2015-07, Vol.33 (7), p.2320-2330

2015

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FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway

The EMBO journal, 2007-04, Vol.26 (8), p.2104-2114

2007

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Evidence for subcomplexes in the Fanconi anemia pathway

Blood, 2006-09, Vol.108 (6), p.2072-2080

2006

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Crystal Structures of RMI1 and RMI2, Two OB-Fold Regulatory Subunits of the BLM Complex

Structure (London), 2010-09, Vol.18 (9), p.1159-1170

2010

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Identification and characterization of mutations in FANCL gene: A second case of Fanconi anemia belonging to FA-L complementation group

Human mutation, 2009-07, Vol.30 (7), p.E761-E770

2009

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Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair

Oncogene, 2014-10, Vol.33 (40), p.4803-4812

2014

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Identification of FAAP24, a Fanconi Anemia Core Complex Protein that Interacts with FANCM

Molecular cell, 2007-02, Vol.25 (3), p.331-343

2007

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FANCL Replaces BRCA1 as the Likely Ubiquitin Ligase Responsible for FANCD2 Monoubiquitination

Cell cycle (Georgetown, Tex.), 2004-02, Vol.3 (2), p.174-176

2004

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Fancb deficiency impairs hematopoietic stem cell function

Scientific reports, 2015-12, Vol.5 (1), p.18127-18127, Article 18127

2015

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FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway

Fancd2-deficient hematopoietic stem and progenitor cells depend on augmented mitochondrial translation for survival and proliferation

Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M

Human MutS and FANCM complexes function as redundant DNA damage sensors in the Fanconi Anemia pathway

Instructive Role of MLL-Fusion Proteins Revealed by a Model of t(4;11) Pro-B Acute Lymphoblastic Leukemia

FANCD2 is required for the repression of germline transposable elements

Remodeling of Interstrand Crosslink Proximal Replisomes Is Dependent on ATR, FANCM, and FANCD2

FANCB is essential in the male germline and regulates H3K9 methylation on the sex chromosomes during meiosis

MHF1-MHF2, a Histone-Fold-Containing Protein Complex, Participates in the Fanconi Anemia Pathway via FANCM

ATR-Dependent Phosphorylation of FANCM at Serine 1045 Is Essential for FANCM Functions

BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome

Fancd2 in vivo interaction network reveals a non-canonical role in mitochondrial function

A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

A novel ubiquitin ligase is deficient in Fanconi anemia

A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome

Rif1 provides a new DNA-binding interface for the Bloom syndrome complex to maintain normal replication

Loss of Faap20 Causes Hematopoietic Stem and Progenitor Cell Depletion in Mice Under Genotoxic Stress

FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway

Evidence for subcomplexes in the Fanconi anemia pathway

Crystal Structures of RMI1 and RMI2, Two OB-Fold Regulatory Subunits of the BLM Complex

Identification and characterization of mutations in FANCL gene: A second case of Fanconi anemia belonging to FA-L complementation group

Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair

Identification of FAAP24, a Fanconi Anemia Core Complex Protein that Interacts with FANCM

FANCL Replaces BRCA1 as the Likely Ubiquitin Ligase Responsible for FANCD2 Monoubiquitination

Fancb deficiency impairs hematopoietic stem cell function

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