Published in Genes Dev on October 15, 2008
RecQ helicases: multifunctional genome caretakers. Nat Rev Cancer (2009) 3.63
All tangled up: how cells direct, manage and exploit topoisomerase function. Nat Rev Mol Cell Biol (2011) 2.66
Mus81 and Yen1 promote reciprocal exchange during mitotic recombination to maintain genome integrity in budding yeast. Mol Cell (2010) 2.49
Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase. Cell (2012) 2.36
Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome. EMBO J (2011) 1.95
The RecQ DNA helicases in DNA repair. Annu Rev Genet (2010) 1.85
HSSB1 and hSSB2 form similar multiprotein complexes that participate in DNA damage response. J Biol Chem (2009) 1.52
Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation. Mol Cell Biol (2010) 1.50
Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation. Nat Neurosci (2013) 1.46
Rif1 provides a new DNA-binding interface for the Bloom syndrome complex to maintain normal replication. EMBO J (2010) 1.36
Interactome analysis identifies a new paralogue of XRCC4 in non-homologous end joining DNA repair pathway. Nat Commun (2015) 1.32
Oligonucleotide/oligosaccharide-binding fold proteins: a growing family of genome guardians. Crit Rev Biochem Mol Biol (2010) 1.30
RecQ helicases: multiple structures for multiple functions? HFSP J (2009) 1.20
FANCD2 regulates BLM complex functions independently of FANCI to promote replication fork recovery. Nucleic Acids Res (2013) 1.18
More complexity to the Bloom's syndrome complex. Genes Dev (2008) 1.16
Arginine methylation facilitates the recruitment of TOP3B to chromatin to prevent R loop accumulation. Mol Cell (2014) 1.15
DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells. J Biol Chem (2014) 1.14
Decatenation of DNA by the S. cerevisiae Sgs1-Top3-Rmi1 and RPA complex: a mechanism for disentangling chromosomes. Mol Cell (2012) 1.11
PICH and BLM limit histone association with anaphase centromeric DNA threads and promote their resolution. EMBO J (2011) 1.11
TOPO3alpha influences antigenic variation by monitoring expression-site-associated VSG switching in Trypanosoma brucei. PLoS Pathog (2010) 1.11
Human topoisomerase IIIalpha is a single-stranded DNA decatenase that is stimulated by BLM and RMI1. J Biol Chem (2010) 1.10
Pathways for Holliday junction processing during homologous recombination in Saccharomyces cerevisiae. Mol Cell Biol (2011) 1.09
A protein-protein interaction map of trypanosome ~20S editosomes. J Biol Chem (2009) 1.08
Interplay between structure-specific endonucleases for crossover control during Caenorhabditis elegans meiosis. PLoS Genet (2013) 1.07
A fine-scale dissection of the DNA double-strand break repair machinery and its implications for breast cancer therapy. Nucleic Acids Res (2014) 1.05
Structure and cellular roles of the RMI core complex from the bloom syndrome dissolvasome. Structure (2010) 1.05
Distinct roles of RECQ1 in the maintenance of genomic stability. DNA Repair (Amst) (2010) 1.05
The dissolution of double Holliday junctions. Cold Spring Harb Perspect Biol (2014) 1.03
Holliday junction-containing DNA structures persist in cells lacking Sgs1 or Top3 following exposure to DNA damage. Proc Natl Acad Sci U S A (2011) 1.02
CtIP mediates replication fork recovery in a FANCD2-regulated manner. Hum Mol Genet (2014) 1.01
The G-quadruplex ligand telomestatin impairs binding of topoisomerase IIIalpha to G-quadruplex-forming oligonucleotides and uncaps telomeres in ALT cells. PLoS One (2009) 1.00
Fanconi anemia and Bloom's syndrome crosstalk through FANCJ-BLM helicase interaction. Trends Genet (2011) 1.00
FANCD2-controlled chromatin access of the Fanconi-associated nuclease FAN1 is crucial for the recovery of stalled replication forks. Mol Cell Biol (2014) 1.00
RECQL5 cooperates with Topoisomerase II alpha in DNA decatenation and cell cycle progression. Nucleic Acids Res (2011) 0.98
Structural and mechanistic insight into Holliday-junction dissolution by topoisomerase IIIα and RMI1. Nat Struct Mol Biol (2014) 0.97
The BLM dissolvasome in DNA replication and repair. Cell Mol Life Sci (2013) 0.97
Defining the molecular interface that connects the Fanconi anemia protein FANCM to the Bloom syndrome dissolvasome. Proc Natl Acad Sci U S A (2012) 0.96
Physical and functional interaction between yeast Pif1 helicase and Rim1 single-stranded DNA binding protein. Nucleic Acids Res (2012) 0.96
ETAA1 acts at stalled replication forks to maintain genome integrity. Nat Cell Biol (2016) 0.95
Multifaceted role of the Topo IIIα-RMI1-RMI2 complex and DNA2 in the BLM-dependent pathway of DNA break end resection. Nucleic Acids Res (2014) 0.94
Identification of Trypanosoma brucei RMI1/BLAP75 homologue and its roles in antigenic variation. PLoS One (2011) 0.94
Biochemical mechanism of DSB end resection and its regulation. DNA Repair (Amst) (2015) 0.94
Identification and analysis of new proteins involved in the DNA damage response network of Fanconi anemia and Bloom syndrome. Methods (2009) 0.93
The Werner syndrome protein is distinguished from the Bloom syndrome protein by its capacity to tightly bind diverse DNA structures. PLoS One (2012) 0.92
WRN helicase defective in the premature aging disorder Werner syndrome genetically interacts with topoisomerase 3 and restores the top3 slow growth phenotype of sgs1 top3. Aging (Albany NY) (2009) 0.92
Essential functions of C terminus of Drosophila Topoisomerase IIIα in double holliday junction dissolution. J Biol Chem (2012) 0.91
Human single-stranded DNA binding proteins are essential for maintaining genomic stability. BMC Mol Biol (2013) 0.91
Investigations of homologous recombination pathways and their regulation. Yale J Biol Med (2013) 0.90
Human RECQ1 helicase-driven DNA unwinding, annealing, and branch migration: insights from DNA complex structures. Proc Natl Acad Sci U S A (2015) 0.90
RMI1 promotes DNA replication fork progression and recovery from replication fork stress. Mol Cell Biol (2012) 0.89
Scaffolding protein SPIDR/KIAA0146 connects the Bloom syndrome helicase with homologous recombination repair. Proc Natl Acad Sci U S A (2013) 0.88
Human RECQ5 helicase promotes repair of DNA double-strand breaks by synthesis-dependent strand annealing. Nucleic Acids Res (2013) 0.87
Helicase-inactivating mutations as a basis for dominant negative phenotypes. Cell Cycle (2010) 0.86
Regulation of DNA pairing in homologous recombination. Cold Spring Harb Perspect Biol (2014) 0.86
Role of replication protein A in double holliday junction dissolution mediated by the BLM-Topo IIIα-RMI1-RMI2 protein complex. J Biol Chem (2013) 0.86
Resection activity of the Sgs1 helicase alters the affinity of DNA ends for homologous recombination proteins in Saccharomyces cerevisiae. Genetics (2013) 0.85
Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents. Cytogenet Genome Res (2009) 0.84
Bloom's syndrome: Why not premature aging?: A comparison of the BLM and WRN helicases. Ageing Res Rev (2016) 0.84
Defining the roles of the N-terminal region and the helicase activity of RECQ4A in DNA repair and homologous recombination in Arabidopsis. Nucleic Acids Res (2013) 0.83
Different functions for the domains of the Arabidopsis thaliana RMI1 protein in DNA cross-link repair, somatic and meiotic recombination. Nucleic Acids Res (2013) 0.83
BLM SUMOylation regulates ssDNA accumulation at stalled replication forks. Front Genet (2013) 0.83
Structure-specific endonucleases xpf and mus81 play overlapping but essential roles in DNA repair by homologous recombination. Cancer Res (2013) 0.83
Clostridium difficile TcdC protein binds four-stranded G-quadruplex structures. Nucleic Acids Res (2013) 0.82
Functions and regulation of the multitasking FANCM family of DNA motor proteins. Genes Dev (2015) 0.82
RMI1 attenuates tumor development and is essential for early embryonic survival. Mol Carcinog (2010) 0.79
Roles of DNA helicases in the mediation and regulation of homologous recombination. Adv Exp Med Biol (2013) 0.79
Protein degradation pathways regulate the functions of helicases in the DNA damage response and maintenance of genomic stability. Biomolecules (2015) 0.78
Escherichia coli RecG functionally suppresses human Bloom syndrome phenotypes. BMC Mol Biol (2012) 0.78
News from Arabidopsis on the meiotic roles of Blap75/Rmi1 and Top3alpha. PLoS Genet (2008) 0.77
Genome instability and embryonic developmental defects in RMI1 deficient mice. DNA Repair (Amst) (2013) 0.77
Separable Roles for a Caenorhabditis elegans RMI1 Homolog in Promoting and Antagonizing Meiotic Crossovers Ensure Faithful Chromosome Inheritance. PLoS Biol (2016) 0.77
Structural Motifs Critical for In Vivo Function and Stability of the RecQ-Mediated Genome Instability Protein Rmi1. PLoS One (2015) 0.76
Genomic Landscape of Primary Mediastinal B-Cell Lymphoma Cell Lines. PLoS One (2015) 0.76
Inching over hurdles: how DNA helicases move on crowded lattices. Cell Cycle (2010) 0.76
BLM and RMI1 alleviate RPA inhibition of TopoIIIα decatenase activity. PLoS One (2012) 0.76
Loss of RMI2 Increases Genome Instability and Causes a Bloom-Like Syndrome. PLoS Genet (2016) 0.75
The RTR Complex Partner RMI2 and the DNA Helicase RTEL1 Are Both Independently Involved in Preserving the Stability of 45S rDNA Repeats in Arabidopsis thaliana. PLoS Genet (2016) 0.75
Multimerization domains are associated with apparent strand exchange activity in BLM and WRN DNA helicases. DNA Repair (Amst) (2014) 0.75
Structural basis of the interaction between Topoisomerase IIIβ and the TDRD3 auxiliary factor. Sci Rep (2017) 0.75
Novel insight into the composition of human single-stranded DNA-binding protein 1 (hSSB1)-containing protein complexes. BMC Mol Biol (2016) 0.75
Bloom syndrome complex promotes FANCM recruitment to stalled replication forks and facilitates both repair and traverse of DNA interstrand crosslinks. Cell Discov (2016) 0.75
RMI1 and TOP3α limit meiotic CO formation through their C-terminal domains. Nucleic Acids Res (2016) 0.75
Type IA topoisomerases can be "magicians" for both DNA and RNA in all domains of life. RNA Biol (2017) 0.75
The Bloom's syndrome helicase suppresses crossing over during homologous recombination. Nature (2003) 8.68
BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures. Genes Dev (2000) 7.29
A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes. Proc Natl Acad Sci U S A (1974) 6.51
Bloom syndrome: a mendelian prototype of somatic mutational disease. Medicine (Baltimore) (1993) 4.89
The Bloom's syndrome gene product promotes branch migration of holliday junctions. Proc Natl Acad Sci U S A (2000) 4.67
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nat Genet (2005) 4.57
A dynamic model for replication protein A (RPA) function in DNA processing pathways. Nucleic Acids Res (2006) 4.49
Nucleic acid recognition by OB-fold proteins. Annu Rev Biophys Biomol Struct (2003) 4.13
A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome. Mol Cell Biol (2003) 3.85
The Bloom's syndrome gene product interacts with topoisomerase III. J Biol Chem (2000) 3.52
Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity. J Biol Chem (2000) 3.17
Potential role for the BLM helicase in recombinational repair via a conserved interaction with RAD51. J Biol Chem (2001) 3.05
BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates. Proc Natl Acad Sci U S A (2006) 3.00
Novel pro- and anti-recombination activities of the Bloom's syndrome helicase. Genes Dev (2007) 2.82
A double Holliday junction dissolvasome comprising BLM, topoisomerase IIIalpha, and BLAP75. J Biol Chem (2006) 2.69
The Bloom's syndrome helicase can promote the regression of a model replication fork. J Biol Chem (2006) 2.65
Binding and melting of D-loops by the Bloom syndrome helicase. Biochemistry (2000) 2.62
BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity. EMBO J (2005) 2.60
Yeast Rmi1/Nce4 controls genome stability as a subunit of the Sgs1-Top3 complex. Mol Cell Biol (2005) 2.49
Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase. Nucleic Acids Res (2006) 2.48
RecQ helicases: guardian angels of the DNA replication fork. Chromosoma (2008) 2.43
DNA helicases required for homologous recombination and repair of damaged replication forks. Annu Rev Genet (2006) 2.43
RMI1/NCE4, a suppressor of genome instability, encodes a member of the RecQ helicase/Topo III complex. EMBO J (2005) 2.34
Regulation and localization of the Bloom syndrome protein in response to DNA damage. J Cell Biol (2001) 2.30
BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome. Genes Dev (2008) 2.29
Evidence for BLM and Topoisomerase IIIalpha interaction in genomic stability. Hum Mol Genet (2001) 1.85
Topoisomerase IIIalpha and Bloom's helicase can resolve a mobile double Holliday junction substrate through convergent branch migration. Proc Natl Acad Sci U S A (2006) 1.83
Possible association of BLM in decreasing DNA double strand breaks during DNA replication. EMBO J (2000) 1.78
Holliday junction processing activity of the BLM-Topo IIIalpha-BLAP75 complex. J Biol Chem (2007) 1.59
Functional relationships of FANCC to homologous recombination, translesion synthesis, and BLM. EMBO J (2004) 1.56
Binding and activation of DNA topoisomerase III by the Rmi1 subunit. J Biol Chem (2007) 1.54
Cell cycle regulation of the endogenous wild type Bloom's syndrome DNA helicase. Oncogene (2000) 1.53
Functional role of BLAP75 in BLM-topoisomerase IIIalpha-dependent holliday junction processing. J Biol Chem (2008) 1.43
Bloom helicase and DNA topoisomerase IIIalpha are involved in the dissolution of sister chromatids. Mol Cell Biol (2006) 1.41
MPS1-dependent mitotic BLM phosphorylation is important for chromosome stability. Proc Natl Acad Sci U S A (2006) 1.28
The role for zinc in replication protein A. J Biol Chem (2000) 1.26
ATR and ATM-dependent movement of BLM helicase during replication stress ensures optimal ATM activation and 53BP1 focus formation. Cell Cycle (2004) 1.15
DNA binding by the substrate specificity (wedge) domain of RecG helicase suggests a role in processivity. J Biol Chem (2005) 1.06
Embryonic stem cells deficient for Brca2 or Blm exhibit divergent genotoxic profiles that support opposing activities during homologous recombination. Mutat Res (2006) 0.96
Chromosomal instability in B-lymphoblasotoid cell lines from Werner and Bloom syndrome patients. Mutat Res (2002) 0.95
Genetic variant of the human homologous recombination-associated gene RMI1 (S455N) impacts the risk of AML/MDS and malignant melanoma. Cancer Lett (2007) 0.92
Functional interactions between BLM and XRCC3 in the cell. J Cell Biol (2007) 0.85
Global mapping of the yeast genetic interaction network. Science (2004) 21.34
Functional dissection of protein complexes involved in yeast chromosome biology using a genetic interaction map. Nature (2007) 9.25
The Bloom's syndrome helicase suppresses crossing over during homologous recombination. Nature (2003) 8.68
Integration of chemical-genetic and genetic interaction data links bioactive compounds to cellular target pathways. Nat Biotechnol (2003) 5.60
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Nat Genet (2006) 4.98
A novel ubiquitin ligase is deficient in Fanconi anemia. Nat Genet (2003) 4.79
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nat Genet (2005) 4.57
Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM. Mol Cell (2007) 4.28
Replication stress induces sister-chromatid bridging at fragile site loci in mitosis. Nat Cell Biol (2009) 4.15
Superoxide flashes in single mitochondria. Cell (2008) 4.08
A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome. Mol Cell Biol (2003) 3.85
RecQ helicases: suppressors of tumorigenesis and premature aging. Biochem J (2003) 3.71
RecQ helicases: multifunctional genome caretakers. Nat Rev Cancer (2009) 3.63
Ubc9- and mms21-mediated sumoylation counteracts recombinogenic events at damaged replication forks. Cell (2006) 3.60
The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies. Proc Natl Acad Sci U S A (2003) 3.52
A genome-wide screen for methyl methanesulfonate-sensitive mutants reveals genes required for S phase progression in the presence of DNA damage. Proc Natl Acad Sci U S A (2002) 3.46
The structure-specific endonuclease Mus81 contributes to replication restart by generating double-strand DNA breaks. Nat Struct Mol Biol (2007) 3.38
BLM is required for faithful chromosome segregation and its localization defines a class of ultrafine anaphase bridges. EMBO J (2007) 3.22
Functional targeting of DNA damage to a nuclear pore-associated SUMO-dependent ubiquitin ligase. Science (2008) 3.09
The synthetic genetic interaction spectrum of essential genes. Nat Genet (2005) 3.06
BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates. Proc Natl Acad Sci U S A (2006) 3.00
Regulation of fibroblastic growth factor 23 expression but not degradation by PHEX. J Biol Chem (2003) 2.91
X-linked inheritance of Fanconi anemia complementation group B. Nat Genet (2004) 2.86
PBAF chromatin-remodeling complex requires a novel specificity subunit, BAF200, to regulate expression of selective interferon-responsive genes. Genes Dev (2005) 2.70
Quantitative analysis of fitness and genetic interactions in yeast on a genome scale. Nat Methods (2010) 2.67
The Bloom's syndrome helicase can promote the regression of a model replication fork. J Biol Chem (2006) 2.65
BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity. EMBO J (2005) 2.60
Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases. J Biol Chem (2002) 2.53
Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase. Nucleic Acids Res (2006) 2.48
RecQ helicases: guardian angels of the DNA replication fork. Chromosoma (2008) 2.43
DNA helicases required for homologous recombination and repair of damaged replication forks. Annu Rev Genet (2006) 2.43
Dissecting DNA damage response pathways by analysing protein localization and abundance changes during DNA replication stress. Nat Cell Biol (2012) 2.40
A histone-fold complex and FANCM form a conserved DNA-remodeling complex to maintain genome stability. Mol Cell (2010) 2.36
RMI1/NCE4, a suppressor of genome instability, encodes a member of the RecQ helicase/Topo III complex. EMBO J (2005) 2.34
Identification of protein complexes required for efficient sister chromatid cohesion. Mol Biol Cell (2004) 2.34
Uncovering early response of gene regulatory networks in ESCs by systematic induction of transcription factors. Cell Stem Cell (2009) 2.32
Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function. Proc Natl Acad Sci U S A (2009) 2.30
Loss of BRG1/BRM in human lung cancer cell lines and primary lung cancers: correlation with poor prognosis. Cancer Res (2003) 2.28
Genome-wide association study dissects the genetic architecture of oil biosynthesis in maize kernels. Nat Genet (2012) 2.25
Phosphorylation of the Bloom's syndrome helicase and its role in recovery from S-phase arrest. Mol Cell Biol (2004) 2.20
A FancD2-monoubiquitin fusion reveals hidden functions of Fanconi anemia core complex in DNA repair. Mol Cell (2005) 2.15
Contemporary volume-outcome relationships for percutaneous nephrolithotomy: results from the Nationwide Inpatient Sample. J Endourol (2013) 2.04
Elg1 forms an alternative RFC complex important for DNA replication and genome integrity. EMBO J (2003) 2.03
Role for BLM in replication-fork restart and suppression of origin firing after replicative stress. Nat Struct Mol Biol (2007) 2.03
BAF250B-associated SWI/SNF chromatin-remodeling complex is required to maintain undifferentiated mouse embryonic stem cells. Stem Cells (2008) 2.02
Extracellular signal-regulated kinase 5 SUMOylation antagonizes shear stress-induced antiinflammatory response and endothelial nitric oxide synthase expression in endothelial cells. Circ Res (2008) 2.01
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway. EMBO J (2007) 2.00
Specific targeting and constitutive association of histone deacetylase complexes during transcriptional repression. Genes Dev (2002) 1.99
Isolation of a small molecule inhibitor of DNA base excision repair. Nucleic Acids Res (2005) 1.98
The RecQ helicase-topoisomerase III-Rmi1 complex: a DNA structure-specific 'dissolvasome'? Trends Biochem Sci (2007) 1.97
Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1-Top3. Nat Struct Mol Biol (2010) 1.95
Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome. EMBO J (2011) 1.95
FANCJ is a structure-specific DNA helicase associated with the maintenance of genomic G/C tracts. J Biol Chem (2008) 1.93
RecQ helicases: multiple roles in genome maintenance. Trends Cell Biol (2003) 1.91
Interobserver reproducibility of electroencephalogram interpretation in critically ill children. J Clin Neurophysiol (2011) 1.87
Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication. Mol Cell (2009) 1.85
The HRDC domain of BLM is required for the dissolution of double Holliday junctions. EMBO J (2005) 1.84
Fanconi anemia proteins are required to prevent accumulation of replication-associated DNA double-strand breaks. Mol Cell Biol (2006) 1.82
Autophosphorylation at serine 1987 is dispensable for murine Atm activation in vivo. Nature (2006) 1.82
Identification of a polymorphic, neuron-specific chromatin remodeling complex. Genes Dev (2002) 1.80
The Bloom's syndrome helicase promotes the annealing of complementary single-stranded DNA. Nucleic Acids Res (2005) 1.76
Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes. Blood (2003) 1.71
BAF60a mediates critical interactions between nuclear receptors and the BRG1 chromatin-remodeling complex for transactivation. Mol Cell Biol (2003) 1.69
Slx4 regulates DNA damage checkpoint-dependent phosphorylation of the BRCT domain protein Rtt107/Esc4. Mol Biol Cell (2005) 1.66
FANCM of the Fanconi anemia core complex is required for both monoubiquitination and DNA repair. Hum Mol Genet (2008) 1.65
A small interfering RNA screen of genes involved in DNA repair identifies tumor-specific radiosensitization by POLQ knockdown. Cancer Res (2010) 1.65
POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates. J Biol Chem (2005) 1.64
RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway. Hum Mol Genet (2004) 1.56
A central role of connexin 43 in hypoxic preconditioning. J Neurosci (2008) 1.56
Functional relationships of FANCC to homologous recombination, translesion synthesis, and BLM. EMBO J (2004) 1.56
Molecular mechanisms of antidiuretic effect of oxytocin. J Am Soc Nephrol (2007) 1.55
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder. Am J Hum Genet (2009) 1.54
Diversity of eukaryotic DNA replication origins revealed by genome-wide analysis of chromatin structure. PLoS Genet (2010) 1.54
HSSB1 and hSSB2 form similar multiprotein complexes that participate in DNA damage response. J Biol Chem (2009) 1.52
The Human RecQ helicases, BLM and RECQ1, display distinct DNA substrate specificities. J Biol Chem (2008) 1.52
Suppression of genomic instability by SLX5 and SLX8 in Saccharomyces cerevisiae. DNA Repair (Amst) (2005) 1.51
Structural basis for inhibition of the replication licensing factor Cdt1 by geminin. Nature (2004) 1.50
Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation. Mol Cell Biol (2010) 1.50
Inhibition of TGF-β1-receptor posttranslational core fucosylation attenuates rat renal interstitial fibrosis. Kidney Int (2013) 1.50
Ubc9 is essential for viability of higher eukaryotic cells. Exp Cell Res (2002) 1.49
The origin recognition complex links replication, sister chromatid cohesion and transcriptional silencing in Saccharomyces cerevisiae. Genetics (2004) 1.49
ODC1 is a critical determinant of MYCN oncogenesis and a therapeutic target in neuroblastoma. Cancer Res (2008) 1.47
Seven-year follow-up of allogeneic transplant using BCNU, etoposide, cytarabine and melphalan chemotherapy in patients with Hodgkin lymphoma after autograft failure: importance of minimal residual disease. Leuk Lymphoma (2013) 1.47
Increased error-prone non homologous DNA end-joining--a proposed mechanism of chromosomal instability in Bloom's syndrome. Oncogene (2002) 1.47
Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation. Nat Neurosci (2013) 1.46