WARSAW BREAKAGE SYNDROME

Known as: WABS 
 
National Institutes of Health

Papers overview

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2019
2019
BACKGROUND Warsaw Breakage Syndrome (WABS) is an ultra rare cohesinopathy caused by biallelic mutation of DDX11 gene. It is… (More)
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2018
2018
Establishment of sister chromatid cohesion is coupled to DNA replication, but the underlying molecular mechanisms are… (More)
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2017
2017
We present two new cases of Warsaw Breakage Syndrome (WABS), an autosomal recessive cohesinopathy, in sisters aged 13 and 11… (More)
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2015
2015
We report a new case of Warsaw Breakage syndrome (WABS) with 2 confirmed mutations in DDX11. Like the previous reported cases… (More)
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2015
2015
DDX11 was recently identified as a cause of Warsaw breakage syndrome (WABS). However, the functional mechanism of DDX11 and the… (More)
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2015
2015
Warsaw breakage syndrome (WABS) is caused by defective DDX11, a DNA helicase that is essential for chromatid cohesion. Here, a… (More)
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Review
2014
Review
2014
In 2010, a new recessive cohesinopathy disorder, designated Warsaw breakage syndrome (WABS), was described. The individual with… (More)
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2013
2013
Mutations in the gene encoding the iron-sulfur-containing DNA helicase DDX11 (ChlR1) were recently identified as a cause of a new… (More)
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2010
2010
Fanconi anemia (FA) is a recessively inherited disease characterized by multiple symptoms including growth retardation, skeletal… (More)
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2010
2010
  • Angel R. Lopez-Sanchez, Cesar Esteban
  • 2010
Aims. We have performed a comprehensive multiwavelength analysis of a sample of 20 starburst galaxies that show a substantial… (More)
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