FAQ

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

Related topics

Related topics

3 relations
16p13.3DNA RepairEnzyme Induction

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
SLX4 wt Allele
DNA Repair
Enzyme Induction
16p13.3

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Alterations of DNA repair genes in the NCI-60 cell lines and their predictive value for anticancer drug activity.
Loss of function of DNA repair (DNAR) genes is associated with genomic instability and cancer predisposition; it also makes… (More)
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2015
2015
Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes
Acute lymphoblastic leukemia (ALL) is the most common pediatric cancer. While the multi-step model of pediatric leukemogenesis… (More)
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Highly Cited
2013
Highly Cited
2013
Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4.
SLX4, the newly identified Fanconi anemia protein, FANCP, is implicated in repairing DNA damage induced by DNA interstrand cross… (More)
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2012
2012
The nuclease hSNM1B/Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP/SLX4.
The recessive genetic disorder Fanconi anemia (FA) is clinically characterized by congenital defects, bone marrow failure and an… (More)
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Highly Cited
2011
Highly Cited
2011
Mutations of the SLX4 gene in Fanconi anemia
Fanconi anemia is a rare recessive disorder characterized by genome instability, congenital malformations, progressive bone… (More)
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2011
2011
Cancel all Hollidays for SLX4 mutations: identification of a new Fanconi anemia subtype, FANCP.
SLX4, a coordinator of structure-specific endo-nucleases, is mutated in a new Fanconi anemia subtype Stoepker et al. (2011… (More)
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