Found: 17
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Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3484, doi. 10.1093/hmg/ddp297
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- Publication type:
- Article
A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51.
- Published in:
- Nature Communications, 2015, v. 6, n. 12, p. 8829, doi. 10.1038/ncomms9829
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- Publication type:
- Article
Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function.
- Published in:
- Nature Communications, 2015, v. 6, n. 10, p. 8399, doi. 10.1038/ncomms9399
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- Publication type:
- Article
A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/ BRCA2 mutations.
- Published in:
- Genes, Chromosomes & Cancer, 2005, v. 42, n. 4, p. 404, doi. 10.1002/gcc.20153
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- Publication type:
- Article
Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis.
- Published in:
- Anemia (20901267), 2012, p. 1, doi. 10.1155/2012/238731
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- Publication type:
- Article
Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome.
- Published in:
- Anemia (20901267), 2010, p. 1, doi. 10.1155/2010/565268
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- Publication type:
- Article
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype.
- Published in:
- Nature Genetics, 2011, v. 43, n. 2, p. 138, doi. 10.1038/ng.751
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- Publication type:
- Article
A novel ubiquitin ligase is deficient in Fanconi anemia.
- Published in:
- Nature Genetics, 2003, v. 35, n. 2, p. 165, doi. 10.1038/ng1241
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- Publication type:
- Article
Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia.
- Published in:
- Nature, 1981, v. 290, n. 5802, p. 142, doi. 10.1038/290142a0
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- Publication type:
- Article
Sensitivity to chromosomal breakage as risk factor in young adults with oral squamous cell carcinoma.
- Published in:
- 2016
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- Publication type:
- journal article
Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18066-8
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- Publication type:
- Article
The Cellular Phenotype of Roberts Syndrome Fibroblasts as Revealed by Ectopic Expression of ESCO2.
- Published in:
- PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0006936
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- Publication type:
- Article
Fancf-deficient mice are prone to develop ovarian tumours.
- Published in:
- Journal of Pathology, 2012, v. 226, n. 1, p. 28, doi. 10.1002/path.2992
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- Publication type:
- Article
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway.
- Published in:
- EMBO Journal, 2007, v. 26, n. 8, p. 2104, doi. 10.1038/sj.emboj.7601666
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- Publication type:
- Article
Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2.
- Published in:
- PLoS ONE, 2020, v. 15, n. 1, p. 1, doi. 10.1371/journal.pone.0220348
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- Publication type:
- Article
Reduced fertility and hypersensitivityto mitomycin C characterize Fancg/Xrcc9 nullmice.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 3, p. 273, doi. 10.1093/hmg/11.3.273
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- Publication type:
- Article
Mice with a targeted disruption of the Fanconi anemia homolog Fanca.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 12, p. 1805, doi. 10.1093/hmg/9.12.1805
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- Publication type:
- Article