Lista de obras -

A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome ⬇️

artículo científico publicado el 1 de mayo de 2003

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

artículo científico publicado en 2005

A novel interplay between the Fanconi anemia core complex and ATR-ATRIP kinase during DNA cross-link repair

artículo científico publicado en 2013

A novel ubiquitin ligase is deficient in Fanconi anemia

artículo científico publicado en 2003

ATR-dependent phosphorylation of FANCM at serine 1045 is essential for FANCM functions.

artículo científico publicado en 2013

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

artículo científico publicado en 2008

BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity

artículo científico publicado en 2005

Crystal structures of RMI1 and RMI2, two OB-fold regulatory subunits of the BLM complex

artículo científico publicado en 2010

DEK is required for homologous recombination repair of DNA breaks

artículo científico publicado en 2017

Evidence for subcomplexes in the Fanconi anemia pathway

artículo científico publicado en 2006

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

artículo científico publicado en 2007

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

artículo científico publicado en 2012

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

artículo científico publicado en 2015

FANCL replaces BRCA1 as the likely ubiquitin ligase responsible for FANCD2 monoubiquitination.

artículo científico publicado en 2004

FANCM-FAAP24 and FANCJ: FA proteins that metabolize DNA.

artículo científico publicado en 2009

Fancb deficiency impairs hematopoietic stem cell function

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Fancd2 is required for the repression of germline transposable elements

scientific article published on 01 March 2020

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

scientific article published on 23 August 2019

Functional role of BLAP75 in BLM-topoisomerase IIIalpha-dependent holliday junction processing

artículo científico publicado en 2008

Generation of Multiple Site-Specific Mutations by Polymerase Chain Reaction ⬇️

artículo científico publicado el 1 de enero de 2002

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

artículo científico publicado en 2011

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

artículo científico publicado en 2009

Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.

artículo científico publicado en 2007

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

artículo científico publicado en 2009

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

artículo científico publicado en 2016

Involvement of protein kinase A in the phosphorylation of spermatidal protein TP2 and its effect on DNA condensation

artículo científico publicado en 2002

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

artículo científico publicado en 2015

MHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCM

artículo científico publicado en 2010

Monopolar spindle 1 (MPS1) protein-dependent phosphorylation of RecQ-mediated genome instability protein 2 (RMI2) at serine 112 is essential for BLM-Topo III α-RMI1-RMI2 (BTR) protein complex function upon spindle assembly checkpoint (SAC) activatio

artículo científico publicado en 2013

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

artículo científico publicado en 2019

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

artículo científico publicado en 2010

The MHF complex senses branched DNA by binding a pair of crossover DNA duplexes

artículo científico publicado en 2014

The nuclear DEK interactome supports multi-functionality.

artículo científico publicado en 2017

X-linked inheritance of Fanconi anemia complementation group B

artículo científico publicado en 2004

Lista de obras de

A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome ⬇️

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

A novel interplay between the Fanconi anemia core complex and ATR-ATRIP kinase during DNA cross-link repair

A novel ubiquitin ligase is deficient in Fanconi anemia

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

BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity

Crystal structures of RMI1 and RMI2, two OB-fold regulatory subunits of the BLM complex

DEK is required for homologous recombination repair of DNA breaks

Evidence for subcomplexes in the Fanconi anemia pathway

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

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

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

FANCL replaces BRCA1 as the likely ubiquitin ligase responsible for FANCD2 monoubiquitination.

FANCM-FAAP24 and FANCJ: FA proteins that metabolize DNA.

Fancb deficiency impairs hematopoietic stem cell function

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

Fancd2 is required for the repression of germline transposable elements

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

Functional role of BLAP75 in BLM-topoisomerase IIIalpha-dependent holliday junction processing

Generation of Multiple Site-Specific Mutations by Polymerase Chain Reaction ⬇️

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

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

Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.

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

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

Involvement of protein kinase A in the phosphorylation of spermatidal protein TP2 and its effect on DNA condensation

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

MHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCM

Monopolar spindle 1 (MPS1) protein-dependent phosphorylation of RecQ-mediated genome instability protein 2 (RMI2) at serine 112 is essential for BLM-Topo III α-RMI1-RMI2 (BTR) protein complex function upon spindle assembly checkpoint (SAC) activatio

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

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

The MHF complex senses branched DNA by binding a pair of crossover DNA duplexes

The nuclear DEK interactome supports multi-functionality.

X-linked inheritance of Fanconi anemia complementation group B