Related references
Note: Only part of the references are listed.FancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in mice
Xianfei Sun et al.
CHROMOSOMA (2016)
Twenty years of the Italian Fanconi Anemia Registry: where we stand and what remains to be learned
Antonio M. Risitano et al.
HAEMATOLOGICA (2016)
Twenty years of the Italian Fanconi Anemia Registry: where we stand and what remains to be learned
Antonio M. Risitano et al.
HAEMATOLOGICA (2016)
Primary Ovarian Insufficiency Induced by Fanconi Anemia E Mutation in a Mouse Model
Chun Fu et al.
PLOS ONE (2016)
FANCB is essential in the male germline and regulates H3K9 methylation on the sex chromosomes during meiosis
Yasuko Kato et al.
HUMAN MOLECULAR GENETICS (2015)
Distinct but Concerted Roles of ATR, DNA-PK, and Chk1 in Countering Replication Stress during S Phase
Remi Buisson et al.
MOLECULAR CELL (2015)
Multiple facets of histone variant H2AX: a DNA double-strand-break marker with several biological functions
Valentina Turinetto et al.
NUCLEIC ACIDS RESEARCH (2015)
The Carboxyl Terminus of FANCE Recruits FANCD2 to the Fanconi Anemia (FA) E3 Ligase Complex to Promote the FA DNA Repair Pathway
David Polito et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Meiosis-Specific Cohesin Component, Stag3 Is Essential for Maintaining Centromere Chromatid Cohesion, and Required for DNA Repair and Synapsis between Homologous Chromosomes
Jessica Hopkins et al.
PLOS GENETICS (2014)
Meiosis-Specific Cohesin Component, Stag3 Is Essential for Maintaining Centromere Chromatid Cohesion, and Required for DNA Repair and Synapsis between Homologous Chromosomes
Jessica Hopkins et al.
PLOS GENETICS (2014)
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia
Massimo Bogliolo et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia
Kazuya Kashiyama et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models
Sietske T. Bakker et al.
DISEASE MODELS & MECHANISMS (2013)
Sequencing and characterization of the FVB/NJ mouse genome
Kim Wong et al.
GENOME BIOLOGY (2012)
Impaired immune function in children with Fanconi anaemia
Kasiani C. Myers et al.
BRITISH JOURNAL OF HAEMATOLOGY (2011)
Evidence for complete epistasis of null mutations in murine Fanconi anemia genes Fanca and Fancg
Henri J. van de Vrugt et al.
DNA REPAIR (2011)
Knockdown of Fanconi anemia genes in human embryonic stem cells reveals early developmental defects in the hematopoietic lineage
Asmin Tulpule et al.
BLOOD (2010)
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M
Sietske T. Bakker et al.
HUMAN MOLECULAR GENETICS (2009)
The Fanconi Anemia Pathway Promotes Replication-Dependent DNA Interstrand Cross-Link Repair
Puck Knipscheer et al.
SCIENCE (2009)
BRCA2 deficiency in mice leads to meiotic impairment and infertility
SK Sharan et al.
DEVELOPMENT (2004)
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
JCY Wong et al.
HUMAN MOLECULAR GENETICS (2003)
Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice
S Houghtaling et al.
GENES & DEVELOPMENT (2003)
A novel gene, Pog, is necessary for primordial germ cell proliferation in the mouse and underlies the germ cell deficient mutation, gcd
AI Agoulnik et al.
HUMAN MOLECULAR GENETICS (2002)
Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice
M Koomen et al.
HUMAN MOLECULAR GENETICS (2002)
Disease model: Fanconi anemia
JCY Wong et al.
TRENDS IN MOLECULAR MEDICINE (2002)
The Chinese hamster FANCG/XRCC9 mutant NM3 fails to express the monoubiquitinated form of the FANCD2 protein, is hypersensitive to a range of DNA damaging agents and exhibits a normal level of spontaneous sister chromatid exchange
JB Wilson et al.
CARCINOGENESIS (2001)
Interaction of the fanconi anemia proteins and BRCA1 in a common pathway
I Garcia-Higuera et al.
MOLECULAR CELL (2001)