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RECQL4 gene

Known as: RecQ4, RECQ PROTEIN-LIKE 4, RecQ Protein-Like 4 Gene 
This gene is involved in the initiation of DNA replication and sister-chromatid cohesion.
National Institutes of Health

Papers overview

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Review
2014
Review
2014
RecQ helicases are an important family of genome surveillance proteins conserved from bacteria to humans. Each of the five human… Expand
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Review
2008
Review
2008
  • V. Bohr
  • Trends in biochemical sciences
  • 2008
  • Corpus ID: 13791528
The RecQ helicases are guardians of the genome. Members of this conserved family of proteins have a key role in protecting and… 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
S-phase cells overcome chromosome lesions through replication-coupled recombination processes that seem to be assisted by… 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
2004
Highly Cited
2004
ABSTRACT Bloom's syndrome (BS) is a human genetic disorder associated with cancer predisposition. The BS gene product, BLM, is a… 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
2001
Highly Cited
2001
Werner syndrome (WS) is an inherited disorder characterized by premature aging and genomic instability. The protein encoded by… 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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