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注意：仅列出部分参考文献，下载原文获取全部文献信息。RECQL4, the Protein Mutated in Rothmund-Thomson Syndrome, Functions in Telomere Maintenance
Avik K. Ghosh et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
RECQL5 cooperates with Topoisomerase II alpha in DNA decatenation and cell cycle progression
Mahesh Ramamoorthy et al.
NUCLEIC ACIDS RESEARCH (2012)
The N-terminal region of RECQL4 lacking the helicase domain is both essential and sufficient for the viability of vertebrate cells Role of the N-terminal region of RECQL4 in cells
Takuya Abe et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2011)
Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome
Avvaru N. Suhasini et al.
EMBO JOURNAL (2011)
The involvement of human RECQL4 in DNA double-strand break repair
Dharmendra Kumar Singh et al.
AGING CELL (2010)
Conserved helicase domain of human RecQ4 is required for strand annealing-independent DNA unwinding
Marie L. Rossi et al.
DNA REPAIR (2010)
Rif1 provides a new DNA-binding interface for the Bloom syndrome complex to maintain normal replication
Dongyi Xu et al.
EMBO JOURNAL (2010)
Human RECQ1 and RECQ4 Helicases Play Distinct Roles in DNA Replication Initiation
Saravanabhavan Thangavel et al.
MOLECULAR AND CELLULAR BIOLOGY (2010)
RecQL5 Promotes Genome Stabilization through Two Parallel Mechanisms-Interacting with RNA Polymerase II and Acting as a Helicase
M. Nurul Islam et al.
MOLECULAR AND CELLULAR BIOLOGY (2010)
Roles of RECQ helicases in recombination based DNA repair, genomic stability and aging
Dharmendra Kumar Singh et al.
BIOGERONTOLOGY (2009)
MCM10 mediates RECQ4 association with MCM2-7 helicase complex during DNA replication
Xiaohua Xu et al.
EMBO JOURNAL (2009)
Dual DNA unwinding activities of the Rothmund-Thomson syndrome protein, RECQ4
Xiaohua Xu et al.
EMBO JOURNAL (2009)
FANCJ Helicase Uniquely Senses Oxidative Base Damage in Either Strand of Duplex DNA and Is Stimulated by Replication Protein A to Unwind the Damaged DNA Substrate in a Strand-specific Manner
Avvaru N. Suhasini et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
p300-mediated acetylation of the Rothmund-Thomson-syndrome gene product RECQL4 regulates its subcellular localization
Tobias Dietschy et al.
JOURNAL OF CELL SCIENCE (2009)
Assembly of the Cdc45-Mcm2-7-GINS complex in human cells requires the Ctf4/And-1, RecQL4, and Mcm10 proteins
Jun-Sub Im et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
RecQ helicases: multifunctional genome caretakers
Wai Kit Chu et al.
NATURE REVIEWS CANCER (2009)
A RECQ5-RNA polymerase II association identified by targeted proteomic analysis of human chromatin
Ozan Aygun et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Rising from the RecQ-age: the role of human RecQ helicases in genome maintenance
Vilhelm A. Bohr
TRENDS IN BIOCHEMICAL SCIENCES (2008)
Human RECQ1 Is a DNA Damage Responsive Protein Required for Genotoxic Stress Resistance and Suppression of Sister Chromatid Exchanges
Sudha Sharma et al.
PLOS ONE (2007)
RECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filaments
Yiduo Hu et al.
GENES & DEVELOPMENT (2007)
Werner syndrome protein participates in a complex with RAD51, RAD54, RAD54B and ATR in response to ICL-induced replication arrest
Marit Otterlei et al.
JOURNAL OF CELL SCIENCE (2006)
A positive involvement of RecQL4 in UV-induced S-phase arrest
Su-Jung Park et al.
DNA AND CELL BIOLOGY (2006)
Human RECQ5β helicase promotes strand exchange on synthetic DNA structures resembling a stalled replication fork
Radhakrishnan Kanagaraj et al.
NUCLEIC ACIDS RESEARCH (2006)
BLM is an early responder to DNA double-strand breaks
Parimal Karmakar et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
The N-terminal noncatalytic region of Xenopus RecQ4 is required for chromatin binding of DNA polymerase α in the initiation of DNA replication
Kumiko Matsuno et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase
Csanad Z. Bachrati et al.
NUCLEIC ACIDS RESEARCH (2006)
The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability
M Petkovic et al.
JOURNAL OF CELL SCIENCE (2005)
The HRDC domain of BLM is required for the dissolution of double Holliday junctions
L Wu et al.
EMBO JOURNAL (2005)
Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome
MN Sangrithi et al.
CELL (2005)
Recq15 and blm RecQ DNA helicases have nonredundant roles in suppressing crossovers
YD Hu et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome
MB Mann et al.
HUMAN MOLECULAR GENETICS (2005)
Human RECQ5β, a protein with DNA helicase and strand-annealing activities in a single polypeptide
PL Garcia et al.
EMBO JOURNAL (2004)
Functional relation among RecQ family Helicases RecQL1, RecQL5, and BLM in cell growth and sister chromatid exchange formation
WS Wang et al.
MOLECULAR AND CELLULAR BIOLOGY (2003)
Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases
PL Opresko et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
G4 DNA unwinding by BLM and Sgs1p: substrate specificity and substrate-specific inhibition
MD Huber et al.
NUCLEIC ACIDS RESEARCH (2002)
Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins
C von Kobbe et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases
P Mohaghegh et al.
NUCLEIC ACIDS RESEARCH (2001)
Potential role for the BLM helicase in recombinational repair via a conserved interaction with RAD51
L Wu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Characterization of the human and mouse WRN 3′→5′ exonuclease
SR Huang et al.
NUCLEIC ACIDS RESEARCH (2000)
The Bloom's syndrome gene product promotes branch migration of Holliday junctions
JK Karow et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase
S Dutertre et al.
ONCOGENE (2000)
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