Published in Mol Cell on March 26, 2010
The DNA damage response: making it safe to play with knives. Mol Cell (2010) 16.13
DNA interstrand crosslink repair and cancer. Nat Rev Cancer (2011) 4.29
Regulation of DNA cross-link repair by the Fanconi anemia/BRCA pathway. Genes Dev (2012) 3.42
Expanded roles of the Fanconi anemia pathway in preserving genomic stability. Genes Dev (2010) 3.33
Homologous recombination and its regulation. Nucleic Acids Res (2012) 2.44
Ubiquitin signalling in DNA replication and repair. Nat Rev Mol Cell Biol (2010) 2.41
ATR signalling: more than meeting at the fork. Biochem J (2011) 2.37
The centromere: chromatin foundation for the kinetochore machinery. Dev Cell (2014) 2.00
CENP-T-W-S-X forms a unique centromeric chromatin structure with a histone-like fold. Cell (2012) 1.85
Molecular pathogenesis and clinical management of Fanconi anemia. J Clin Invest (2012) 1.79
The ABCs of CENPs. Chromosoma (2011) 1.72
DNA helicases involved in DNA repair and their roles in cancer. Nat Rev Cancer (2013) 1.58
The RSF1 histone-remodelling factor facilitates DNA double-strand break repair by recruiting centromeric and Fanconi Anaemia proteins. PLoS Biol (2014) 1.47
Whole-proteome genetic analysis of dependencies in assembly of a vertebrate kinetochore. J Cell Biol (2015) 1.47
Functions of the centromere and kinetochore in chromosome segregation. Curr Opin Cell Biol (2013) 1.41
The FANCM/FAAP24 complex is required for the DNA interstrand crosslink-induced checkpoint response. Mol Cell (2010) 1.35
FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway. Blood (2012) 1.29
The fission yeast FANCM ortholog directs non-crossover recombination during meiosis. Science (2012) 1.26
The genetic and biochemical basis of FANCD2 monoubiquitination. Mol Cell (2014) 1.22
Ubiquitylation and the Fanconi anemia pathway. FEBS Lett (2011) 1.21
Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair. Oncogene (2013) 1.20
A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network. Mol Cell (2012) 1.19
Using synthetic DNA interstrand crosslinks to elucidate repair pathways and identify new therapeutic targets for cancer chemotherapy. Cell Mol Life Sci (2010) 1.12
Quantitative Proteomic Atlas of Ubiquitination and Acetylation in the DNA Damage Response. Mol Cell (2015) 1.12
Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models. Dis Model Mech (2013) 1.05
The centromere: epigenetic control of chromosome segregation during mitosis. Cold Spring Harb Perspect Biol (2014) 1.05
Restriction of replication fork regression activities by a conserved SMC complex. Mol Cell (2014) 1.04
What is the DNA repair defect underlying Fanconi anemia? Curr Opin Cell Biol (2015) 1.03
Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects. Elife (2014) 1.03
The structure of the FANCM-MHF complex reveals physical features for functional assembly. Nat Commun (2012) 1.03
Processing of DNA structures via DNA unwinding and branch migration by the S. cerevisiae Mph1 protein. DNA Repair (Amst) (2011) 1.01
FANCM and FAAP24 maintain genome stability via cooperative as well as unique functions. Mol Cell (2013) 1.00
Stress and DNA repair biology of the Fanconi anemia pathway. Blood (2014) 0.99
A new nuclease member of the FAN club. Nat Struct Mol Biol (2010) 0.98
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
The Fanconi anemia pathway: repairing the link between DNA damage and squamous cell carcinoma. Mutat Res (2013) 0.95
Rad5-dependent DNA repair functions of the Saccharomyces cerevisiae FANCM protein homolog Mph1. J Biol Chem (2012) 0.95
TNF-α signaling in Fanconi anemia. Blood Cells Mol Dis (2013) 0.94
Genetic and physical interactions between the yeast ELG1 gene and orthologs of the Fanconi anemia pathway. Cell Cycle (2013) 0.91
The Fanconi anaemia components UBE2T and FANCM are functionally linked to nucleotide excision repair. PLoS One (2012) 0.91
The centromeric nucleosome-like CENP-T-W-S-X complex induces positive supercoils into DNA. Nucleic Acids Res (2013) 0.91
Remodeling and spacing factor 1 (RSF1) deposits centromere proteins at DNA double-strand breaks to promote non-homologous end-joining. Cell Cycle (2013) 0.90
MHF1-2/CENP-S-X performs distinct roles in centromere metabolism and genetic recombination. Open Biol (2013) 0.88
ATR-dependent phosphorylation of FANCM at serine 1045 is essential for FANCM functions. Cancer Res (2013) 0.88
The differences between ICL repair during and outside of S phase. Trends Biochem Sci (2013) 0.88
The conserved Fanconi anemia nuclease Fan1 and the SUMO E3 ligase Pli1 act in two novel Pso2-independent pathways of DNA interstrand crosslink repair in yeast. DNA Repair (Amst) (2013) 0.88
Fanconi anemia core complex gene promoters harbor conserved transcription regulatory elements. PLoS One (2011) 0.88
FANCM-associated proteins MHF1 and MHF2, but not the other Fanconi anemia factors, limit meiotic crossovers. Nucleic Acids Res (2014) 0.87
Anarchic centromeres: deciphering order from apparent chaos. Curr Opin Cell Biol (2013) 0.87
The Fanconi anemia ID2 complex: dueling saxes at the crossroads. Cell Cycle (2014) 0.87
CtIP is required to initiate replication-dependent interstrand crosslink repair. PLoS Genet (2012) 0.86
Fanconi anemia and the cell cycle: new perspectives on aneuploidy. F1000Prime Rep (2014) 0.86
Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia. Blood Rev (2016) 0.84
Towards a molecular understanding of the fanconi anemia core complex. Anemia (2012) 0.84
Immune response profiling identifies autoantibodies specific to Moyamoya patients. Orphanet J Rare Dis (2013) 0.84
The Fanconi anemia pathway and DNA interstrand cross-link repair. Protein Cell (2011) 0.83
Stabilizing and remodeling the blocked DNA replication fork: anchoring FANCM and the Fanconi anemia damage response. Mol Cell (2010) 0.83
Functions and regulation of the multitasking FANCM family of DNA motor proteins. Genes Dev (2015) 0.82
Forkhead box F2 regulation of platelet-derived growth factor and myocardin/serum response factor signaling is essential for intestinal development. J Biol Chem (2015) 0.82
A CENP-S/X complex assembles at the centromere in S and G2 phases of the human cell cycle. Open Biol (2014) 0.82
Fanconi anemia proteins and their interacting partners: a molecular puzzle. Anemia (2012) 0.82
The MHF complex senses branched DNA by binding a pair of crossover DNA duplexes. Nat Commun (2014) 0.81
Fanconi-like crosslink repair in yeast. Genome Integr (2012) 0.81
Multiple interactions of the intrinsically disordered region between the helicase and nuclease domains of the archaeal Hef protein. J Biol Chem (2014) 0.81
Structural insights into the functions of the FANCM-FAAP24 complex in DNA repair. Nucleic Acids Res (2013) 0.80
The histone-fold complex MHF is remodeled by FANCM to recognize branched DNA and protect genome stability. Cell Res (2014) 0.80
Exploiting the Fanconi Anemia Pathway for Targeted Anti-Cancer Therapy. Mol Cells (2015) 0.80
A protein prioritization approach tailored for the FA/BRCA pathway. PLoS One (2013) 0.80
Cellular robustness conferred by genetic crosstalk underlies resistance against chemotherapeutic drug doxorubicin in fission yeast. PLoS One (2013) 0.80
A Molecular View of Kinetochore Assembly and Function. Biology (Basel) (2017) 0.79
Evolutionary Turnover of Kinetochore Proteins: A Ship of Theseus? Trends Cell Biol (2016) 0.79
Selective modulation of the functions of a conserved DNA motor by a histone fold complex. Genes Dev (2015) 0.79
DNA repair mechanisms in cancer development and therapy. Front Genet (2015) 0.78
MTE1 Functions with MPH1 in Double-Strand Break Repair. Genetics (2016) 0.78
How SUMOylation Fine-Tunes the Fanconi Anemia DNA Repair Pathway. Front Genet (2016) 0.78
FANCM interacts with PCNA to promote replication traverse of DNA interstrand crosslinks. Nucleic Acids Res (2016) 0.78
Lentiviral vector-mediated insertional mutagenesis screen identifies genes that influence androgen independent prostate cancer progression and predict clinical outcome. Mol Carcinog (2015) 0.78
Stepwise unfolding supports a subunit model for vertebrate kinetochores. Proc Natl Acad Sci U S A (2017) 0.77
Differential regulation of the anti-crossover and replication fork regression activities of Mph1 by Mte1. Genes Dev (2016) 0.77
Structure analysis of FAAP24 reveals single-stranded DNA-binding activity and domain functions in DNA damage response. Cell Res (2013) 0.77
FANCM, BRCA1, and BLM cooperatively resolve the replication stress at the ALT telomeres. Proc Natl Acad Sci U S A (2017) 0.76
Defective FANCI binding by a fanconi anemia-related FANCD2 mutant. PLoS One (2014) 0.76
miR146a-mediated targeting of FANCM during inflammation compromises genome integrity. Oncotarget (2016) 0.75
A new histone at the centromere? Cell (2012) 0.75
Forkhead transcription factor FoxF1 interacts with Fanconi anemia protein complexes to promote DNA damage response. Oncotarget (2016) 0.75
FoxF1 and FoxF2 transcription factors synergistically promote rhabdomyosarcoma carcinogenesis by repressing transcription of p21(Cip1) CDK inhibitor. Oncogene (2016) 0.75
Mechanism and disease association of E2-conjugating enzymes: lessons from UBE2T and UBE2L3. Biochem J (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
CENPT bridges adjacent CENPA nucleosomes on young human α-satellite dimers. Genome Res (2016) 0.75
DNA damage response and cancer therapeutics through the lens of the Fanconi Anemia DNA repair pathway. Cell Commun Signal (2017) 0.75
The human CENP-A centromeric nucleosome-associated complex. Nat Cell Biol (2006) 6.85
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
Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24. Blood (2008) 2.83
The Fanconi anemia protein FANCM can promote branch migration of Holliday junctions and replication forks. Mol Cell (2008) 2.68
The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway. Nat Struct Mol Biol (2005) 2.55
The genetic and molecular basis of Fanconi anemia. Mutat Res (2008) 2.45
Yeast Mph1 helicase dissociates Rad51-made D-loops: implications for crossover control in mitotic recombination. Genes Dev (2009) 2.43
The histone fold: a ubiquitous architectural motif utilized in DNA compaction and protein dimerization. Proc Natl Acad Sci U S A (1995) 2.40
Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M. Blood (2009) 2.33
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
Remodeling of DNA replication structures by the branch point translocase FANCM. Proc Natl Acad Sci U S A (2008) 2.20
The FANCM ortholog Fml1 promotes recombination at stalled replication forks and limits crossing over during DNA double-strand break repair. Mol Cell (2008) 2.19
FANCM and FAAP24 function in ATR-mediated checkpoint signaling independently of the Fanconi anemia core complex. Mol Cell (2008) 2.14
Regulated interaction of the Fanconi anemia protein, FANCD2, with chromatin. Blood (2004) 2.08
The CENP-S complex is essential for the stable assembly of outer kinetochore structure. J Cell Biol (2009) 1.99
Cellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insights. Mutat Res (2009) 1.80
The Walker B motif in avian FANCM is required to limit sister chromatid exchanges but is dispensable for DNA crosslink repair. Nucleic Acids Res (2009) 1.65
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M. Hum Mol Genet (2009) 1.47
A novel 1p36.2 located gene, APITD1, with tumour-suppressive properties and a putative p53-binding domain, shows low expression in neuroblastoma tumours. Br J Cancer (2004) 1.04
FANCM-FAAP24 and FANCJ: FA proteins that metabolize DNA. Mutat Res (2009) 0.99
Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group. Hum Mutat (2009) 0.95
Mechanism of eukaryotic homologous recombination. Annu Rev Biochem (2008) 8.86
DNA helicase Srs2 disrupts the Rad51 presynaptic filament. Nature (2003) 5.66
Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM. Mol Cell (2007) 4.28
RECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filaments. Genes Dev (2007) 4.16
Crosstalk between SUMO and ubiquitin on PCNA is mediated by recruitment of the helicase Srs2p. Mol Cell (2005) 4.02
Genetic steps of mammalian homologous repair with distinct mutagenic consequences. Mol Cell Biol (2004) 3.96
Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair. Proc Natl Acad Sci U S A (2005) 3.93
Design of stable alpha-helical arrays from an idealized TPR motif. Structure (2003) 3.17
Mechanism of the ATP-dependent DNA end-resection machinery from Saccharomyces cerevisiae. Nature (2010) 2.79
A double Holliday junction dissolvasome comprising BLM, topoisomerase IIIalpha, and BLAP75. J Biol Chem (2006) 2.69
BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity. EMBO J (2005) 2.60
Structure of a prokaryotic virtual proton pump at 3.2 A resolution. Nature (2009) 2.53
Yeast Mph1 helicase dissociates Rad51-made D-loops: implications for crossover control in mitotic recombination. Genes Dev (2009) 2.43
Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M. Blood (2009) 2.33
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
Roles of ATP binding and ATP hydrolysis in human Rad51 recombinase function. DNA Repair (Amst) (2006) 2.28
Recruitment of the recombinational repair machinery to a DNA double-strand break in yeast. Mol Cell (2003) 2.17
Rad54p is a chromatin remodeling enzyme required for heteroduplex DNA joint formation with chromatin. J Biol Chem (2003) 2.15
The yeast Hex3.Slx8 heterodimer is a ubiquitin ligase stimulated by substrate sumoylation. J Biol Chem (2007) 2.14
Hypoxia-induced down-regulation of BRCA1 expression by E2Fs. Cancer Res (2005) 2.02
Recombination mediator and Rad51 targeting activities of a human BRCA2 polypeptide. J Biol Chem (2006) 2.01
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway. EMBO J (2007) 2.00
ATP hydrolysis by mammalian RAD51 has a key role during homology-directed DNA repair. J Biol Chem (2002) 1.97
Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome. DNA Repair (Amst) (2005) 1.88
Role of Dnl4-Lif1 in nonhomologous end-joining repair complex assembly and suppression of homologous recombination. Nat Struct Mol Biol (2007) 1.87
Homologous DNA pairing by human recombination factors Rad51 and Rad54. J Biol Chem (2002) 1.82
Crystal structure of a bulged RNA tetraplex at 1.1 a resolution: implications for a novel binding site in RNA tetraplex. Structure (2003) 1.77
Structure of a synaptic gammadelta resolvase tetramer covalently linked to two cleaved DNAs. Science (2005) 1.73
The crystal structure of yeast fatty acid synthase, a cellular machine with eight active sites working together. Cell (2007) 1.70
Human meiotic recombinase Dmc1 promotes ATP-dependent homologous DNA strand exchange. Nature (2004) 1.70
Saccharomyces cerevisiae MPH1 gene, required for homologous recombination-mediated mutation avoidance, encodes a 3' to 5' DNA helicase. J Biol Chem (2005) 1.69
Bipartite stimulatory action of the Hop2-Mnd1 complex on the Rad51 recombinase. Genes Dev (2007) 1.67
Zinc chelation inhibits HIV Vif activity and liberates antiviral function of the cytidine deaminase APOBEC3G. FASEB J (2006) 1.64
Differential contributions of mammalian Rad54 paralogs to recombination, DNA damage repair, and meiosis. Mol Cell Biol (2006) 1.63
Holliday junction processing activity of the BLM-Topo IIIalpha-BLAP75 complex. J Biol Chem (2007) 1.59
Structural and functional basis of CXCL12 (stromal cell-derived factor-1 alpha) binding to heparin. J Biol Chem (2007) 1.58
Structural insight into the human immunodeficiency virus Vif SOCS box and its role in human E3 ubiquitin ligase assembly. J Virol (2008) 1.57
Pif1 helicase and Polδ promote recombination-coupled DNA synthesis via bubble migration. Nature (2013) 1.56
Enhancement of RAD51 recombinase activity by the tumor suppressor PALB2. Nat Struct Mol Biol (2010) 1.55
Yeast xrs2 binds DNA and helps target rad50 and mre11 to DNA ends. J Biol Chem (2003) 1.55
Regulation of meiotic recombination via Mek1-mediated Rad54 phosphorylation. Mol Cell (2009) 1.51
Cell cycle regulation of DNA double-strand break end resection by Cdk1-dependent Dna2 phosphorylation. Nat Struct Mol Biol (2011) 1.50
Promotion of homologous recombination and genomic stability by RAD51AP1 via RAD51 recombinase enhancement. Mol Cell (2007) 1.49
Mechanism of allosteric activation of SAMHD1 by dGTP. Nat Struct Mol Biol (2013) 1.49
Genomic architecture and inheritance of human ribosomal RNA gene clusters. Genome Res (2007) 1.48
A comparative analysis of Dmc1 and Rad51 nucleoprotein filaments. Nucleic Acids Res (2008) 1.46
A PP4 phosphatase complex dephosphorylates RPA2 to facilitate DNA repair via homologous recombination. Nat Struct Mol Biol (2010) 1.45
53BP1, BRCA1, and the choice between recombination and end joining at DNA double-strand breaks. Mol Cell Biol (2014) 1.45
Interaction with Rad51 is indispensable for recombination mediator function of Rad52. J Biol Chem (2002) 1.45
Role of ATP hydrolysis in the antirecombinase function of Saccharomyces cerevisiae Srs2 protein. J Biol Chem (2004) 1.43
Role of the nuclease activity of Saccharomyces cerevisiae Mre11 in repair of DNA double-strand breaks in mitotic cells. Genetics (2004) 1.43
Functional role of BLAP75 in BLM-topoisomerase IIIalpha-dependent holliday junction processing. J Biol Chem (2008) 1.43
Evidence for subcomplexes in the Fanconi anemia pathway. Blood (2006) 1.43
Structural basis of cooperative ligand binding by the glycine riboswitch. Chem Biol (2011) 1.43
Structural basis of evasion of cellular adaptive immunity by HIV-1 Nef. Nat Struct Mol Biol (2012) 1.42
A DNA-translocating Snf2 molecular motor: Saccharomyces cerevisiae Rdh54 displays processive translocation and extrudes DNA loops. J Mol Biol (2007) 1.41
Structural insight into the mechanisms of enveloped virus tethering by tetherin. Proc Natl Acad Sci U S A (2010) 1.39
Crystal structures of the Bacillus stearothermophilus CCA-adding enzyme and its complexes with ATP or CTP. Cell (2002) 1.38
A single amino acid difference in human APOBEC3H variants determines HIV-1 Vif sensitivity. J Virol (2009) 1.38
Rif1 provides a new DNA-binding interface for the Bloom syndrome complex to maintain normal replication. EMBO J (2010) 1.36
Protein-induced photophysical changes to the amyloid indicator dye thioflavin T. Proc Natl Acad Sci U S A (2010) 1.35
The E3 ubiquitin ligase RAD18 regulates ubiquitylation and chromatin loading of FANCD2 and FANCI. Blood (2011) 1.30
Hed1 regulates Rad51-mediated recombination via a novel mechanism. Genes Dev (2008) 1.30
Localization of recombination proteins and Srs2 reveals anti-recombinase function in vivo. J Cell Biol (2009) 1.29
Physical and functional interaction between the XPF/ERCC1 endonuclease and hRad52. J Biol Chem (2004) 1.29
FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway. Blood (2012) 1.29
Yeast recombination factor Rdh54 functionally interacts with the Rad51 recombinase and catalyzes Rad51 removal from DNA. J Biol Chem (2006) 1.29
FBH1 promotes DNA double-strand breakage and apoptosis in response to DNA replication stress. J Cell Biol (2013) 1.28
Multiple interactions with the Rad51 recombinase govern the homologous recombination function of Rad54. J Biol Chem (2004) 1.28
Human rRNA gene clusters are recombinational hotspots in cancer. Cancer Res (2009) 1.27
Characterization of a novel Cullin5 binding domain in HIV-1 Vif. J Mol Biol (2007) 1.27
FANCI binds branched DNA and is monoubiquitinated by UBE2T-FANCL. J Biol Chem (2009) 1.27
Functional cross-talk among Rad51, Rad54, and replication protein A in heteroduplex DNA joint formation. J Biol Chem (2002) 1.25
Functional significance of the Rad51-Srs2 complex in Rad51 presynaptic filament disruption. Nucleic Acids Res (2009) 1.21
Physical interaction of RECQ5 helicase with RAD51 facilitates its anti-recombinase activity. J Biol Chem (2010) 1.19
Nucleosome dynamics regulates DNA processing. Nat Struct Mol Biol (2013) 1.19
Direct and indirect roles of RECQL4 in modulating base excision repair capacity. Hum Mol Genet (2009) 1.18
Role for proteasome activator PA200 and postglutamyl proteasome activity in genomic stability. Proc Natl Acad Sci U S A (2008) 1.18
Molecular anatomy of the recombination mediator function of Saccharomyces cerevisiae Rad52. J Biol Chem (2008) 1.18
Loss of 26S proteasome function leads to increased cell size and decreased cell number in Arabidopsis shoot organs. Plant Physiol (2009) 1.17
The Rad50 coiled-coil domain is indispensable for Mre11 complex functions. Nat Struct Mol Biol (2011) 1.16
ATPase and DNA helicase activities of the Saccharomyces cerevisiae anti-recombinase Srs2. J Biol Chem (2003) 1.16
Variant XRCC3 implicated in cancer is functional in homology-directed repair of double-strand breaks. Oncogene (2002) 1.15
Interaction with RPA is necessary for Rad52 repair center formation and for its mediator activity. J Biol Chem (2008) 1.15
Rad52 SUMOylation affects the efficiency of the DNA repair. Nucleic Acids Res (2010) 1.14
Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients. Mol Vis (2007) 1.14
Overcoming natural replication barriers: differential helicase requirements. Nucleic Acids Res (2011) 1.14
The splicing-factor related protein SFPQ/PSF interacts with RAD51D and is necessary for homology-directed repair and sister chromatid cohesion. Nucleic Acids Res (2010) 1.12