(Q38825562)

6 September 2017

1 reference

title

The Fanconi anaemia pathway: new players and new functions (English)

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6 September 2017

Raphael Ceccaldi

1

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6 September 2017

Prabha Sarangi

series ordinal

2

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6 September 2017

Alan D D'Andrea

series ordinal

3

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6 September 2017

publication date

5 May 2016

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Nature Reviews Molecular Cell Biology

6 September 2017

published in

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6 September 2017

volume

17

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6 September 2017

issue

6

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6 September 2017

page(s)

337-349

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https://scigraph.springernature.com/pub.10.1038/nrm.2016.48

6 September 2017

exact match

0 references

cites work

The resurgence of platinum-based cancer chemotherapy

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https://api.crossref.org/works/10.1038%2FNRM.2016.48

Biallelic inactivation of BRCA2 in Fanconi anemia

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRM.2016.48

Mechanism and regulation of incisions during DNA interstrand cross-link repair

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRM.2016.48

The DNA translocase FANCM/MHF promotes replication traverse of DNA interstrand crosslinks

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRM.2016.48

Interstrand DNA cross-links induced by alpha,beta-unsaturated aldehydes derived from lipid peroxidation and environmental sources.

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRM.2016.48

Fancd2 counteracts the toxic effects of naturally produced aldehydes in mice

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRM.2016.48

Genotoxic consequences of endogenous aldehydes on mouse haematopoietic stem cell function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

DNA interstrand crosslink repair and cancer

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

DNA interstrand cross-link repair requires replication-fork convergence.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Fanconi anaemia and the repair of Watson and Crick DNA crosslinks

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCI Regulates Recruitment of the FA Core Complex at Sites of DNA Damage Independently of FANCD2

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

ATR couples FANCD2 monoubiquitination to the DNA-damage response

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The Fanconi Anemia DNA Repair Pathway Is Regulated by an Interaction between Ubiquitin and the E2-like Fold Domain of FANCL

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Functional interaction between the Fanconi Anemia D2 protein and proliferating cell nuclear antigen (PCNA) via a conserved putative PCNA interaction motif

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

RAD18-mediated ubiquitination of PCNA activates the Fanconi anemia DNA repair network

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The E3 ubiquitin ligase RAD18 regulates ubiquitylation and chromatin loading of FANCD2 and FANCI

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Rad18-mediated Translesion Synthesis of Bulky DNA Adducts Is Coupled to Activation of the Fanconi Anemia DNA Repair Pathway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The deubiquitinating enzyme USP1 regulates the Fanconi anemia pathway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

A UAF1-containing multisubunit protein complex regulates the Fanconi anemia pathway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Ubiquitin-like protein UBL5 promotes the functional integrity of the Fanconi anemia pathway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Ubiquitin-SUMO circuitry controls activated fanconi anemia ID complex dosage in response to DNA damage

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Fanconi anemia proteins FANCD2 and FANCI exhibit different DNA damage responses during S-phase

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

UHRF1 is a sensor for DNA interstrand crosslinks and recruits FANCD2 to initiate the Fanconi anemia pathway.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

UHRF1 contributes to DNA damage repair as a lesion recognition factor and nuclease scaffold

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

BRCA1 promotes unloading of the CMG helicase from a stalled DNA replication fork

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The ubiquitin-selective segregase VCP/p97 orchestrates the response to DNA double-strand breaks.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCD2 binds MCM proteins and controls replisome function upon activation of s phase checkpoint signaling.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Involvement of SLX4 in interstrand cross-link repair is regulated by the Fanconi anemia pathway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Mouse SLX4 is a tumor suppressor that stimulates the activity of the nuclease XPF-ERCC1 in DNA crosslink repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

XPF-ERCC1 acts in Unhooking DNA interstrand crosslinks in cooperation with FANCD2 and FANCP/SLX4

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Homology-directed Fanconi anemia pathway cross-link repair is dependent on DNA replication

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The SLX4 complex is a SUMO E3 ligase that impacts on replication stress outcome and genome stability

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FAN1 Acts with FANCI-FANCD2 to Promote DNA Interstrand Cross-Link Repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Structural insights into 5' flap DNA unwinding and incision by the human FAN1 dimer

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Human FAN1 promotes strand incision in 5'-flapped DNA complexed with RPA.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCD2-associated nuclease 1, but not exonuclease 1 or flap endonuclease 1, is able to unhook DNA interstrand cross-links in vitro

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Ubiquitinated Fancd2 recruits Fan1 to stalled replication forks to prevent genome instability

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Repair of intermediate structures produced at DNA interstrand cross-links in Saccharomyces cerevisiae

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

DNA interstrand crosslink repair during G1 involves nucleotide excision repair and DNA polymerase zeta

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

DNA polymerase zeta (pol zeta) in higher eukaryotes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Interaction of human DNA polymerase eta with monoubiquitinated PCNA: a possible mechanism for the polymerase switch in response to DNA damage

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Structure of the ubiquitin-binding zinc finger domain of human DNA Y-polymerase eta

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Structural Basis of Ubiquitin Recognition by Translesion Synthesis DNA Polymerase ι

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Structural Analysis of the Conserved Ubiquitin-binding Motifs (UBMs) of the Translesion Polymerase iota in Complex with Ubiquitin

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Regulation of the Rev1-pol ζ complex during bypass of a DNA interstrand cross-link

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Regulation of Rev1 by the Fanconi anemia core complex

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Biophysical characterization of the interaction between FAAP20-UBZ4 domain and Rev1-BRCT domain

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

REV1 and polymerase ζ facilitate homologous recombination repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Structural Basis of Rev1-mediated Assembly of a Quaternary Vertebrate Translesion Polymerase Complex Consisting of Rev1, Heterodimeric Polymerase (Pol) , and Pol

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

DNA polymerase eta reduces the gamma-H2AX response to psoralen interstrand crosslinks in human cells

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

DNA polymerase POLN participates in cross-link repair and homologous recombination

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Homologous recombination and human health: the roles of BRCA1, BRCA2, and associated proteins

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Mechanism of RAD51-dependent DNA interstrand cross-link repair.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

BOD1L Is Required to Suppress Deleterious Resection of Stressed Replication Forks

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The FANCJ/MutLalpha interaction is required for correction of the cross-link response in FA-J cells

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Targeting the FANCJ-BRCA1 interaction promotes a switch from recombination to poleta-dependent bypass

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The BRCT Domain Is a Phospho-Protein Binding Domain

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCJ localization by mismatch repair is vital to maintain genomic integrity after UV irradiation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCD2 and CtIP cooperate to repair DNA interstrand crosslinks

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCD2 binds CtIP and regulates DNA-end resection during DNA interstrand crosslink repair.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

CtIP mediates replication fork recovery in a FANCD2-regulated manner

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

MRE11-RAD50-NBS1 is a critical regulator of FANCD2 stability and function during DNA double-strand break repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Preventing over-resection by DNA2 helicase/nuclease suppresses repair defects in Fanconi anemia cells

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

DNA2 and EXO1 in replication-coupled, homology-directed repair and in the interplay between HDR and the FA/BRCA network

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Double-strand break repair-independent role for BRCA2 in blocking stalled replication fork degradation by MRE11.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaks

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

MAD2L2 controls DNA repair at telomeres and DNA breaks by inhibiting 5' end resection

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

REV7 counteracts DNA double-strand break resection and affects PARP inhibition

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

A distinct replication fork protection pathway connects Fanconi anemia tumor suppressors to RAD51-BRCA1/2.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The Fanconi Anemia Pathway Maintains Genome Stability by Coordinating Replication and Transcription

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The Fanconi Anemia Pathway Protects Genome Integrity from R-loops

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

A concomitant loss of dormant origins and FANCC exacerbates genome instability by impairing DNA replication fork progression.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

ATR-mediated phosphorylation of FANCI regulates dormant origin firing in response to replication stress.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

A histone-fold complex and FANCM form a conserved DNA-remodeling complex to maintain genome stability

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Rad51 protects nascent DNA from Mre11-dependent degradation and promotes continuous DNA synthesis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

BRCA1 functions independently of homologous recombination in DNA interstrand crosslink repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCD2-controlled chromatin access of the Fanconi-associated nuclease FAN1 is crucial for the recovery of stalled replication forks

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCD2, FANCJ and BRCA2 cooperate to promote replication fork recovery independently of the Fanconi Anemia core complex

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

FANCD2 regulates BLM complex functions independently of FANCI to promote replication fork recovery

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Replication stress induces sister-chromatid bridging at fragile site loci in mitosis.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The FANC pathway and BLM collaborate during mitosis to prevent micro-nucleation and chromosome abnormalities

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Fanconi anemia signaling network regulates the spindle assembly checkpoint

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Crosstalk between translesion synthesis, Fanconi anemia network, and homologous recombination repair pathways in interstrand DNA crosslink repair and development of chemoresistance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Preventing nonhomologous end joining suppresses DNA repair defects of Fanconi anemia.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Ku70 corrupts DNA repair in the absence of the Fanconi anemia pathway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

DNA damage response factors from diverse pathways, including DNA crosslink repair, mediate alternative end joining

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Repair Pathway Choices and Consequences at the Double-Strand Break

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

RAD18 and poly(ADP-ribose) polymerase independently suppress the access of nonhomologous end joining to double-strand breaks and facilitate homologous recombination-mediated repair.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Impaired TIP60-mediated H4K16 acetylation accounts for the aberrant chromatin accumulation of 53BP1 and RAP80 in Fanconi anemia pathway-deficient cells

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Acetylation limits 53BP1 association with damaged chromatin to promote homologous recombination

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Modernizing the nonhomologous end-joining repertoire: alternative and classical NHEJ share the stage.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Fanca deficiency reduces A/T transitions in somatic hypermutation and alters class switch recombination junctions in mouse B cells.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Homologous-recombination-deficient tumours are dependent on Polθ-mediated repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Effect of the anti-neoplastic drug doxorubicin on XPD-mutated DNA repair-deficient human cells

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The ERCC1 and ERCC4 (XPF) genes and gene products

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Recruitment of DNA polymerase eta by FANCD2 in the early response to DNA damage

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Xeroderma pigmentosum variant and error-prone DNA polymerases

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

BRCA1 is required for postreplication repair after UV-induced DNA damage

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The Fanconi anaemia components UBE2T and FANCM are functionally linked to nucleotide excision repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

CtIP is required to initiate replication-dependent interstrand crosslink repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The Fanconi anemia proteins FANCD2 and FANCJ interact and regulate each other's chromatin localization

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

The FANCM/FAAP24 complex is required for the DNA interstrand crosslink-induced checkpoint response

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Pathophysiology and management of inherited bone marrow failure syndromes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Genotype-phenotype correlations in Fanconi anemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Cancer incidence in persons with Fanconi anemia.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Integrated genomic analyses of ovarian carcinoma

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Selective accumulation of virus-specific CD8+ T cells within the peripheral blood stem cell compartment.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Inactivation of Uaf1 causes defective homologous recombination and early embryonic lethality in mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Inactivation of murine Usp1 results in genomic instability and a Fanconi anemia phenotype.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Fanconi anemia: a model disease for studies on human genetics and advanced therapeutics

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Synthetic lethality and cancer therapy: lessons learned from the development of PARP inhibitors

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

Mammalian polymerase θ promotes alternative NHEJ and suppresses recombination

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRM.2016.48

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

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27145721

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRM.2016.48

1 reference

Dimensions Publication ID

6 September 2017

1017711392

0 references

1 reference