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C19orf40 wt Allele

Known as: FLJ46828, Fanconi Anemia-Associated Protein, 24kDa Gene, Chromosome 19 Open Reading Frame 40 wt Allele 
Human C19orf40 wild-type allele is located in the vicinity of 19q13.11 and is approximately 5 kb in length. This allele, which encodes Fanconi anemia… 
National Institutes of Health

Papers overview

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2018
2018
  • 2018
  • Corpus ID: 53598097
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure (BMF), clonal proliferation of hematopoietic stem… 
2016
2016
Hereditary defects in several genes have been shown to disturb the normal immune response to EBV and to give rise to severe EBV… 
2013
2013
Fanconi anemia (FA) is a genetically heterogeneous disorder associated with deficiencies in the FA complementation group network… 
2013
2013
To maintain the integrity of the genome, multiple DNA repair systems exist to repair damaged DNA. Recognition of altered DNA… 
Review
2009
Review
2009
Review
2009
The ATR signalling pathway coordinates the cellular response to replication stress, which is essential for the maintenance of… 
Review
2008
Review
2008
Proteins belonging to the XPF/MUS81 family play important roles in the repair of DNA lesions caused by UV-light or DNA cross… 
2008
2008
  • Weidong Wang
  • 2008
  • Corpus ID: 26607334
The Fanconi anemia pathway is part of the DNA-damage network including breast cancer–susceptibility proteins BRCA1 and BRCA2…