Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 206,228,435 papers from all fields of science
Search
Sign In
Create Free Account
SLX4 wt Allele
Known as:
KIAA1784
, FANCP
, BTB (POZ) Domain Containing 12 Gene
Expand
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
Create Alert
Alert
Related topics
Related topics
3 relations
16p13.3
DNA Repair
Enzyme Induction
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.
F. Sousa
,
R. Matuo
,
+8 authors
Y. Pommier
DNA repair
2015
Corpus ID: 13778736
2015
2015
Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes
Jean-François Spinella
,
Jasmine Healy
,
+4 authors
D. Sinnett
BMC Cancer
2015
Corpus ID: 7463385
BackgroundAcute lymphoblastic leukemia (ALL) is the most common pediatric cancer. While the multi-step model of pediatric…
Expand
2015
2015
Chapter 3 Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX 4 / FANCP
Friedl
,
Birgit Gottwald-Mühlhauser
,
J. Winter
,
D. Schindler
2015
Corpus ID: 44188214
Highly Cited
2013
Highly Cited
2013
Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4.
Yonghwan Kim
,
Gabriella S. Spitz
,
Uma Veturi
,
Francis P Lach
,
A. Auerbach
,
A. Smogorzewska
Blood
2013
Corpus ID: 206913429
SLX4, the newly identified Fanconi anemia protein, FANCP, is implicated in repairing DNA damage induced by DNA interstrand cross…
Expand
2012
2012
The nuclease hSNM 1 B / Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP / SLX 4
Bastian Salewsky
,
M. Schmiester
,
D. Schindler
,
M. Digweed
,
I. Demuth
2012
Corpus ID: 3537630
The recessive genetic disorder Fanconi anemia (FA) is clinically characterized by congenital defects, bone marrow failure and an…
Expand
Highly Cited
2011
Highly Cited
2011
Mutations of the SLX4 gene in Fanconi anemia
Yonghwan Kim
,
Francis P Lach
,
R. Desetty
,
H. Hanenberg
,
A. Auerbach
,
A. Smogorzewska
Nature Genetics
2011
Corpus ID: 30971920
Fanconi anemia is a rare recessive disorder characterized by genome instability, congenital malformations, progressive bone…
Expand
Highly Cited
2011
Highly Cited
2011
Mammalian BTBD12 (SLX4) Protects against Genomic Instability during Mammalian Spermatogenesis
J. K. Holloway
,
S. Mohan
,
+6 authors
P. Cohen
PLoS genetics
2011
Corpus ID: 2722658
The mammalian ortholog of yeast Slx4, BTBD12, is an ATM substrate that functions as a scaffold for various DNA repair activities…
Expand
2011
2011
Cancel all Hollidays for SLX4 mutations: identification of a new Fanconi anemia subtype, FANCP
M. Kang
Clinical genetics
2011
Corpus ID: 38007184
SLX4, a coordinator of structure‐specific endo‐nucleases, is mutated in a new Fanconi anemia subtype
2011
2011
HotSpots Cancel all Hollidays for SLX 4 mutations : identification of a new Fanconi anemia subtype , FANCP
Mh Kang
2011
Corpus ID: 34035736
For the clinician, the two major challenges in correctly diagnosing Fanconi anemia (FA; OMIM# 227650) are its clinical…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
,
Terms of Service
, and
Dataset License
ACCEPT & CONTINUE