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RECQL4 protein, human

Known as: RecQ protein-like 4 protein, human, RecQ4 protein, human, RecQ Protein Like 4 
ATP-dependent DNA helicase Q4 (1208 aa, ~133 kDa) is encoded by the human RECQL4 gene. This protein is involved in repair, replication and… Expand
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
RECQL4 is associated with Rothmund–Thomson Syndrome (RTS), a rare autosomal recessive disorder characterized by premature aging… Expand
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Review
2010
Review
2010
Rothmund-Thomson syndrome (RTS) is a genodermatosis presenting with a characteristic facial rash (poikiloderma) associated with… Expand
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Highly Cited
2009
Highly Cited
2009
In eukaryotes, the activation of the prereplicative complex and assembly of an active DNA unwinding complex are critical but… Expand
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Highly Cited
2009
Highly Cited
2009
Mutations in the RECQL4 gene can lead to three clinical phenotypes with overlapping features. All these syndromes, Rothmund… Expand
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Highly Cited
2006
Highly Cited
2006
Baller-Gerold syndrome (BGS) is a rare autosomal recessive condition with radial aplasia/hypoplasia and craniosynostosis (OMIM… Expand
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Highly Cited
2005
Highly Cited
2005
How the replication machinery is loaded at origins of DNA replication is poorly understood. Here, we implicate in this process… Expand
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Highly Cited
2005
Highly Cited
2005
Rothmund-Thomson syndrome (RTS) is a human genetic disorder characterized by genome instability, cancer susceptibility and… Expand
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Highly Cited
2003
Highly Cited
2003
The RECQL4 helicase gene is a member of the RECQL gene family, mutated in some Rothmund-Thomson syndrome (RTS) patients. Other… Expand
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Highly Cited
2003
Highly Cited
2003
BACKGROUND Rothmund-Thomson syndrome (RTS) is an autosomal recessive disorder associated with an increased predisposition to… Expand
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Highly Cited
1999
Highly Cited
1999
Rothmund-Thomson syndrome (RTS; also known as poikiloderma congenitale) is a rare, autosomal recessive genetic disorder… Expand
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