Related references
Note: Only part of the references are listed.SMARCAL1 Deficiency Predisposes to Non-Hodgkin Lymphoma and Hypersensitivity to Genotoxic Agents In Vivo
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AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2012)
Perturbed replication induced genome wide or at common fragile sites is differently managed in the absence of WRN
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Werner syndrome protein suppresses the formation of large deletions during the replication of human telomeric sequences
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SMARCAL1 catalyzes fork regression and Holliday junction migration to maintain genome stability during DNA replication
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GENES & DEVELOPMENT (2012)
ATR and ATM differently regulate WRN to prevent DSBs at stalled replication forks and promote replication fork recovery
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Maintaining genome stability at the replication fork
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NATURE REVIEWS MOLECULAR CELL BIOLOGY (2010)
The Caenorhabditis elegans Werner Syndrome Protein Functions Upstream of ATR and ATM in Response to DNA Replication Inhibition and Double-Strand DNA Breaks
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PLOS GENETICS (2010)
The annealing helicase HARP protects stalled replication forks
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GENES & DEVELOPMENT (2009)
The SIOD disorder protein SMARCAL1 is an RPA-interacting protein involved in replication fork restart
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GENES & DEVELOPMENT (2009)
The annealing helicase SMARCAL1 maintains genome integrity at stalled replication forks
Carol E. Bansbach et al.
GENES & DEVELOPMENT (2009)
The annealing helicase HARP is recruited to DNA repair sites via an interaction with RPA
Timur Yusufzai et al.
GENES & DEVELOPMENT (2009)
Identification of SMARCAL1 as a Component of the DNA Damage Response
Lisa Postow et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
RecQ helicases: multifunctional genome caretakers
Wai Kit Chu et al.
NATURE REVIEWS CANCER (2009)
Werner syndrome helicase activity is essential in maintaining fragile site stability
Livia Maria Pirzio et al.
JOURNAL OF CELL BIOLOGY (2008)
Replication fork stalling in WRN-deficient cells is overcome by prompt activation of a MUS81-dependent pathway
Annapaola Franchitto et al.
JOURNAL OF CELL BIOLOGY (2008)
ATR: an essential regulator of genome integrity
Karlene A. Cimprich et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2008)
HARP Is an ATP-Driven Annealing Helicase
Timur Yusufzai et al.
SCIENCE (2008)
Function of a conserved checkpoint recruitment domain in ATRIP proteins
Heather L. Ball et al.
MOLECULAR AND CELLULAR BIOLOGY (2007)
Replication fork stalling at natural impediments
Ekaterina V. Mirkin et al.
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS (2007)
The Werner and Bloom syndrome proteins catalyze regression of a model replication fork
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BIOCHEMISTRY (2006)
Identification of multiple distinct Snf2 subfamilies with conserved structural motifs
Andrew Flaus et al.
NUCLEIC ACIDS RESEARCH (2006)
Physical and functional mapping of the replication protein A interaction domain of the Werner and Bloom syndrome helicases
KM Doherty et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
ATRIP binding to replication protein A-single-stranded DNA promotes ATR-ATRIP localization but is dispensable for Chk1 phosphorylation
HL Ball et al.
MOLECULAR BIOLOGY OF THE CELL (2005)
The N-terminal domain of the large subunit of human replication protein A binds to Werner syndrome protein and stimulates helicase activity
JC Shen et al.
MECHANISMS OF AGEING AND DEVELOPMENT (2003)
Werner's syndrome protein is phosphorylated in an ATR/ATM-dependent manner following replication arrest and DNA damage induced during the S phase of the cell cycle
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ONCOGENE (2003)
Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation
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JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia
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NATURE GENETICS (2002)
Werner syndrome protein: biochemical properties and functional interactions
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EXPERIMENTAL GERONTOLOGY (2000)
Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest
A Constantinou et al.
EMBO REPORTS (2000)