Published in Chromosoma on October 21, 2015
FANCJ at the FORK. Mutat Res (2016) 0.76
Cohesin Removal along the Chromosome Arms during the First Meiotic Division Depends on a NEK1-PP1γ-WAPL Axis in the Mouse. Cell Rep (2016) 0.75
Getting Ready for the Dance: FANCJ Irons Out DNA Wrinkles. Genes (Basel) (2016) 0.75
Dearth and Delayed Maturation of Testicular Germ Cells in Fanconi Anemia E Mutant Male Mice. PLoS One (2016) 0.75
Special issue on "recent advances in meiotic chromosome structure, recombination and segregation". Chromosoma (2016) 0.75
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet (2006) 7.72
BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures. Genes Dev (2000) 7.29
Recombinational DNA double-strand breaks in mice precede synapsis. Nat Genet (2001) 6.91
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nat Genet (1996) 6.06
BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function. Cell (2001) 5.05
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nat Genet (2005) 4.92
The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair. Science (2009) 4.85
MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair. Genes Dev (1995) 3.88
Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice. Genes Dev (2003) 3.58
AN AIR-DRYING METHOD FOR MEIOTIC PREPARATIONS FROM MAMMALIAN TESTES. Cytogenetics (1964) 3.56
Mutation of a meiosis-specific MutS homolog decreases crossing over but not mismatch correction. Cell (1994) 3.54
BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ. Cancer Cell (2005) 3.44
Meiotic pachytene arrest in MLH1-deficient mice. Cell (1996) 3.18
FANCJ helicase defective in Fanconia anemia and breast cancer unwinds G-quadruplex DNA to defend genomic stability. Mol Cell Biol (2008) 2.88
Mammalian MutS homologue 5 is required for chromosome pairing in meiosis. Nat Genet (1999) 2.62
Proliferation and migration of primordial germ cells during compensatory growth in mouse embryos. J Embryol Exp Morphol (1981) 2.55
Clonal analysis of the origin of primordial germ cells in the mouse. Ciba Found Symp (1994) 2.50
MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice. Genes Dev (2000) 2.49
Meiotic arrest and aneuploidy in MLH3-deficient mice. Nat Genet (2002) 2.39
Functional specificity of MutL homologs in yeast: evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction. Proc Natl Acad Sci U S A (1999) 2.25
Meiotic recombination in mammals: localization and regulation. Nat Rev Genet (2013) 2.00
Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene. Blood (1996) 1.99
Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis. Genes Dev (1999) 1.95
Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome. EMBO J (2011) 1.95
The FANCJ/MutLalpha interaction is required for correction of the cross-link response in FA-J cells. EMBO J (2007) 1.86
DNA interstrand crosslink repair in mammalian cells: step by step. Crit Rev Biochem Mol Biol (2010) 1.82
Mutagenic capacity of endogenous G4 DNA underlies genome instability in FANCJ-defective C. elegans. Curr Biol (2008) 1.80
MUS81 generates a subset of MLH1-MLH3-independent crossovers in mammalian meiosis. PLoS Genet (2008) 1.76
Activation of BRCA1/BRCA2-associated helicase BACH1 is required for timely progression through S phase. Mol Cell Biol (2007) 1.72
RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination. Mol Cell (2008) 1.68
BACH1/FANCJ acts with TopBP1 and participates early in DNA replication checkpoint control. Mol Cell (2010) 1.65
Targeted disruption of the murine Fanconi anemia gene, Fancg/Xrcc9. Blood (2001) 1.64
Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis. Mol Cell (2008) 1.61
Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia. Hum Mol Genet (2003) 1.60
The role of AtMUS81 in interference-insensitive crossovers in A. thaliana. PLoS Genet (2007) 1.57
Mice with a targeted disruption of the Fanconi anemia homolog Fanca. Hum Mol Genet (2000) 1.56
The Fanconi anemia DNA repair pathway: structural and functional insights into a complex disorder. Annu Rev Biophys (2014) 1.55
Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I. J Cell Biol (2005) 1.38
Meiotic recombination intermediates and mismatch repair proteins. Cytogenet Genome Res (2004) 1.37
Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice. Hum Mol Genet (2002) 1.29
Expression and functional analysis of AtMUS81 in Arabidopsis meiosis reveals a role in the second pathway of crossing-over. Plant J (2008) 1.25
Mouse germ cell development: from specification to sex determination. Mol Cell Endocrinol (2009) 1.24
A novel gene, Pog, is necessary for primordial germ cell proliferation in the mouse and underlies the germ cell deficient mutation, gcd. Hum Mol Genet (2002) 1.24
The DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombination. Hum Mol Genet (2002) 1.23
Expression and nuclear localization of BLM, a chromosome stability protein mutated in Bloom's syndrome, suggest a role in recombination during meiotic prophase. J Cell Sci (2000) 1.23
Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene. Genomics (1997) 1.21
Bloom's syndrome protein, BLM, colocalizes with replication protein A in meiotic prophase nuclei of mammalian spermatocytes. Proc Natl Acad Sci U S A (1999) 1.16
FANCJ: solving problems in DNA replication. DNA Repair (Amst) (2010) 1.10
Mammalian BTBD12 (SLX4) protects against genomic instability during mammalian spermatogenesis. PLoS Genet (2011) 1.07
Molecular basis of BACH1/FANCJ recognition by TopBP1 in DNA replication checkpoint control. J Biol Chem (2010) 1.06
AGO4 regulates entry into meiosis and influences silencing of sex chromosomes in the male mouse germline. Dev Cell (2012) 1.06
Mammalian BLM helicase is critical for integrating multiple pathways of meiotic recombination. J Cell Biol (2010) 1.06
Genetics of meiosis and recombination in mice. Int Rev Cell Mol Biol (2012) 1.05
New and old ways to control meiotic recombination. Trends Genet (2011) 1.04
Fanconi anemia group A and C double-mutant mice: functional evidence for a multi-protein Fanconi anemia complex. Exp Hematol (2002) 1.01
Fanconi anemia and Bloom's syndrome crosstalk through FANCJ-BLM helicase interaction. Trends Genet (2011) 1.00
Fanconi anemia proteins, DNA interstrand crosslink repair pathways, and cancer therapy. Curr Cancer Drug Targets (2009) 1.00
Functional and physical interaction between the mismatch repair and FA-BRCA pathways. Hum Mol Genet (2011) 0.97
Mouse GGN1 and GGN3, two germ cell-specific proteins from the single gene Ggn, interact with mouse POG and play a role in spermatogenesis. J Biol Chem (2003) 0.96
Antagonistic roles of ubiquitin ligase HEI10 and SUMO ligase RNF212 regulate meiotic recombination. Nat Genet (2014) 0.95
Control of meiotic recombination in Arabidopsis: role of the MutL and MutS homologues. Biochem Soc Trans (2006) 0.92
hMSH4-hMSH5 adenosine nucleotide processing and interactions with homologous recombination machinery. J Biol Chem (2007) 0.91
Crosstalk between BRCA-Fanconi anemia and mismatch repair pathways prevents MSH2-dependent aberrant DNA damage responses. EMBO J (2014) 0.90
The Fanconi anemia pathway and the DNA interstrand cross-links repair. Biochimie (2003) 0.87
Assessing the link between BACH1/FANCJ and MLH1 in DNA crosslink repair. Environ Mol Mutagen (2010) 0.84
Mammalian CNTD1 is critical for meiotic crossover maturation and deselection of excess precrossover sites. J Cell Biol (2014) 0.84
Hypersensitivity of primordial germ cells to compromised replication-associated DNA repair involves ATM-p53-p21 signaling. PLoS Genet (2014) 0.84
Premature separation of sister chromatids in human male meiosis. Hum Reprod (2008) 0.80
BRCA1 and FancJ cooperatively promote interstrand crosslinker induced centrosome amplification through the activation of polo-like kinase 1. Cell Cycle (2014) 0.77
hMSH5 Facilitates the Repair of Camptothecin-induced Double-strand Breaks through an Interaction with FANCJ. J Biol Chem (2015) 0.77