Fanconi Anemia
|
0.600 |
AlteredExpression
|
disease |
LHGDN |
Deficiency in incisions produced by XPF at the site of a DNA interstrand cross-link in Fanconi anemia cells.
|
18020456 |
2007 |
Fanconi Anemia
|
0.600 |
Biomarker
|
disease |
BEFREE |
XPF-ERCC1 participates in the Fanconi anemia pathway of cross-link repair.
|
19805513 |
2009 |
Fanconi Anemia
|
0.600 |
Biomarker
|
disease |
BEFREE |
Cells defective in the FA pathway or other factors involved in ICL processing, such as XPF and DNA Polζ, are all hypersensitive to killing by 6-TG/UVA-consistent with a significant contribution of photochemical ICLs to the cytotoxicity of this treatment.
|
21723207 |
2011 |
Fanconi Anemia
|
0.600 |
GermlineCausalMutation
|
disease |
ORPHANET |
Further biochemical and functional analysis demonstrated that the identified FA-causing ERCC4 mutations strongly disrupt the function of XPF in DNA ICL repair without severely compromising nucleotide excision repair.
|
23623386 |
2013 |
Fanconi Anemia
|
0.600 |
GeneticVariation
|
disease |
BEFREE |
Further biochemical and functional analysis demonstrated that the identified FA-causing ERCC4 mutations strongly disrupt the function of XPF in DNA ICL repair without severely compromising nucleotide excision repair.
|
23623386 |
2013 |
Fanconi Anemia
|
0.600 |
GeneticVariation
|
disease |
BEFREE |
Our results, together with those from Bogliolo et al., who describe XPF alterations resulting in FA alone, indicate a multifunctional role for XPF.
|
23623389 |
2013 |
Fanconi Anemia
|
0.600 |
GeneticVariation
|
disease |
BEFREE |
Finally, we identified additional bone-fide FA ERCC4 mutations specifically disrupting interstrand cross-link repair.
|
24027083 |
2013 |
Fanconi Anemia
|
0.600 |
GeneticVariation
|
disease |
BEFREE |
Given that, mutations in XPF can also lead to Fanconi anemia, we propose collaborations between Fanconi anemia, NER, and MMR are necessary to initiate checkpoint activation in replicating human cells to limit genomic instability.
|
24351291 |
2014 |
Fanconi Anemia
|
0.600 |
GeneticVariation
|
disease |
BEFREE |
Different cancer syndromes such as a subtype of Xeroderma pigmentosum, XPF, and recently a subtype of Fanconi Anemia, FA-Q, have been attributed to biallelic ERCC4 gene mutations.
|
24465539 |
2014 |
Fanconi Anemia
|
0.600 |
GeneticVariation
|
disease |
BEFREE |
The immunoprecipitation assay of cell extracts revealed that those XPF mutations, except XPF(C236R), located in the SLX4-interacting region cause instability of XPF protein, which could be the reason for the FA, progeria and/or CS phenotypes.
|
26453996 |
2015 |
Fanconi Anemia
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Germline Genetic Predisposition to Hematologic Malignancy.
|
28297620 |
2017 |
Fanconi Anemia
|
0.600 |
Biomarker
|
disease |
BEFREE |
However, mutated XPF/ERCC4/FANCQ protein in our patient's cells, as in the two other patients with FA-Q, was detectable on chromatin, in contrast to XP-F cells, where missense-mutant protein failed to properly translocate to the nucleus.
|
29325523 |
2018 |
Fanconi Anemia
|
0.600 |
GeneticVariation
|
disease |
BEFREE |
ERCC4 mutations have been known to cause xeroderma pigmentosum complementation group F (XP-F), Cockayne syndrome, and Fanconi anemia phenotypes.
|
29403087 |
2018 |