SLX4 wt Allele

Known as: KIAA1784, FANCP, BTB (POZ) Domain Containing 12 Gene 
Human SLX4 wild-type allele is located in the vicinity of 16p13.3 and is approximately 30 kb in length. This allele, which encodes structure-specific… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

2011-2015
01220112015

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Loss of function of DNA repair (DNAR) genes is associated with genomic instability and cancer predisposition; it also makes… (More)
Is this relevant?
2015
2015
Acute lymphoblastic leukemia (ALL) is the most common pediatric cancer. While the multi-step model of pediatric leukemogenesis… (More)
  • figure 1
  • figure 2
  • table 1
  • table 2
Is this relevant?
Highly Cited
2013
Highly Cited
2013
SLX4, the newly identified Fanconi anemia protein, FANCP, is implicated in repairing DNA damage induced by DNA interstrand cross… (More)
Is this relevant?
2012
2012
The recessive genetic disorder Fanconi anemia (FA) is clinically characterized by congenital defects, bone marrow failure and an… (More)
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
Highly Cited
2011
Highly Cited
2011
Fanconi anemia is a rare recessive disorder characterized by genome instability, congenital malformations, progressive bone… (More)
  • figure 1
  • figure 3
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2011
2011
SLX4, a coordinator of structure-specific endo-nucleases, is mutated in a new Fanconi anemia subtype Stoepker et al. (2011… (More)
Is this relevant?