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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… Expand
National Institutes of Health

Papers overview

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2015
2015
Loss of function of DNA repair (DNAR) genes is associated with genomic instability and cancer predisposition; it also makes… Expand
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2015
2015
BackgroundAcute lymphoblastic leukemia (ALL) is the most common pediatric cancer. While the multi-step model of pediatric… Expand
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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… Expand
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2012
2012
The recessive genetic disorder Fanconi anemia (FA) is clinically characterized by congenital defects, bone marrow failure and an… Expand
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Highly Cited
2011
Highly Cited
2011
Fanconi anemia is a rare recessive disorder characterized by genome instability, congenital malformations, progressive bone… Expand
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2011
2011
The mammalian ortholog of yeast Slx4, BTBD12, is an ATM substrate that functions as a scaffold for various DNA repair activities… Expand
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2011
2011
SLX4, a coordinator of structure-specific endo-nucleases, is mutated in a new Fanconi anemia subtype Stoepker et al. (2011… Expand
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2011
2011
For the clinician, the two major challenges in correctly diagnosing Fanconi anemia (FA; OMIM# 227650) are its clinical… Expand
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