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Impaired DNA damage-induced nuclear Rad51 foci formation uniquely characterizes Fanconi anemia group D1.
- Published in:
- Oncogene, 2002, v. 21, n. 32, p. 5002, doi. 10.1038/sj.onc.1205656
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- Publication type:
- Article
A "late-but-fitter revertant cell" explains the high frequency of revertant mosaicism in epidermolysis bullosa.
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- PLoS ONE, 2018, v. 13, n. 2, p. 1, doi. 10.1371/journal.pone.0192994
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- Publication type:
- Article
THE EMERGING GENETIC AND MOLECULAR BASIS OF FANCONI ANAEMIA.
- Published in:
- Nature Reviews Genetics, 2001, v. 2, n. 6, p. 446, doi. 10.1038/35076590
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- Article
Biological consequences of DNA damage introduced in bacteriophage PM2 DNA by hydrogen peroxide-mediated free radial reactions.
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- Carcinogenesis, 1996, v. 17, n. 1, p. 5, doi. 10.1093/carcin/17.1.5
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- Article
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M.
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- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3484, doi. 10.1093/hmg/ddp297
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- Publication type:
- Article
Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway.
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- Human Molecular Genetics, 2004, v. 13, n. 24, p. 3127, doi. 10.1093/hmg/ddh335
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- Publication type:
- Article
A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51.
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- Nature Communications, 2015, v. 6, n. 12, p. 8829, doi. 10.1038/ncomms9829
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- Article
Evolutionary Clues to the Molecular Function of Fanconi Anemia Genes.
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- Acta Haematologica, 2002, v. 108, n. 4, p. 231, doi. 10.1159/000065659
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- Article
A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/ BRCA2 mutations.
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- Genes, Chromosomes & Cancer, 2005, v. 42, n. 4, p. 404, doi. 10.1002/gcc.20153
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- Article
Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma.
- Published in:
- Genes, Chromosomes & Cancer, 1996, v. 15, n. 1, p. 1, doi. 10.1002/(SICI)1098-2264(199601)15:1<1::AID-GCC1>3.0.CO;2-8
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- Publication type:
- Article
Metabolism: Alcohol, DNA and disease.
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- Nature, 2011, v. 475, n. 7354, p. 45, doi. 10.1038/475045a
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- Publication type:
- Article
Clinical and Molecular Characteristics of Squamous Cell Carcinomas From Fanconi Anemia Patients.
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- JNCI: Journal of the National Cancer Institute, 2008, v. 100, n. 22, p. 1649, doi. 10.1093/jnci/djn366
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- Article
Re: Human Papillomavirus DNA and p53 Polymorphisms in Squamous Cell Carcinomas From Fanconi Anemia Patients.
- Published in:
- 2004
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- Publication type:
- Letter
Identification, developmental expression and regulation of the Xenopus ortholog of human FANCG/XRCC9.
- Published in:
- Genes to Cells, 2007, v. 12, n. 7, p. 841, doi. 10.1111/j.1365-2443.2007.01096.x
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- Article
Characterization, expression and complex formation of the murine Fanconi anaemia gene product Fancg.
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- Genes to Cells, 2002, v. 7, n. 3, p. 333, doi. 10.1046/j.1365-2443.2002.00518.x
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- Publication type:
- Article
Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing.
- Published in:
- Anemia (20901267), 2012, p. 1, doi. 10.1155/2012/603253
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- Publication type:
- Article
Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis.
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- Anemia (20901267), 2012, p. 1, doi. 10.1155/2012/238731
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- Publication type:
- Article
Diagnosis of Fanconi Anemia: Mutation Analysis by Next-Generation Sequencing.
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- Anemia (20901267), 2012, p. 1, doi. 10.1155/2012/132856
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- Publication type:
- Article
Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome.
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- Anemia (20901267), 2010, p. 1, doi. 10.1155/2010/565268
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- Publication type:
- Article
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.
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- European Journal of Human Genetics, 2000, v. 8, n. 11, p. 861, doi. 10.1038/sj.ejhg.5200552
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- Publication type:
- Article
Localisation of a Fanconi anaemia gene to chromosome 9p.
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- European Journal of Human Genetics, 1998, v. 6, n. 5, p. 501, doi. 10.1038/sj.ejhg.5200241
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- Article
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype.
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- Nature Genetics, 2011, v. 43, n. 2, p. 138, doi. 10.1038/ng.751
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- Article
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.
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- Nature Genetics, 2007, v. 39, n. 2, p. 159, doi. 10.1038/ng1942
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- Publication type:
- Article
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
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- 2005
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- Publication type:
- Letter
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.
- Published in:
- 2005
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- Publication type:
- Letter
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion.
- Published in:
- Nature Genetics, 2005, v. 37, n. 5, p. 468, doi. 10.1038/ng1548
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- Publication type:
- Article
X-linked inheritance of Fanconi anemia complementation group B.
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- Nature Genetics, 2004, v. 36, n. 11, p. 1219, doi. 10.1038/ng1458
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- Publication type:
- Article
A novel ubiquitin ligase is deficient in Fanconi anemia.
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- 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.
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- Nature, 1981, v. 290, n. 5802, p. 142, doi. 10.1038/290142a0
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- Article
Sensitivity to chromosomal breakage as risk factor in young adults with oral squamous cell carcinoma.
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- 2016
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- Publication type:
- journal article
Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia.
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- British Journal of Haematology, 2006, v. 133, n. 3, p. 284, doi. 10.1111/j.1365-2141.2006.05985.x
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- Publication type:
- Article
Short Report Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia.
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- British Journal of Haematology, 2003, v. 123, n. 3, p. 469, doi. 10.1046/j.1365-2141.2003.04640.x
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- Publication type:
- Article
Aberrant Fanconi anaemia protein profiles in acute myeloid leukaemia cells.
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- British Journal of Haematology, 2000, v. 111, n. 4, p. 1057, doi. 10.1111/j.1365-2141.2000.02450.x
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- Publication type:
- Article
Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma.
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- Familial Cancer, 2012, v. 11, n. 4, p. 661, doi. 10.1007/s10689-012-9553-3
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- Publication type:
- Article
Increased Cytosolic pH in Multidrug-Resistant Human Lung Tumor Cells: Effect of Verapamil.
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- JNCI: Journal of the National Cancer Institute, 1989, v. 81, n. 9, p. 706
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- Publication type:
- Article
A Protein Prioritization Approach Tailored for the FA/BRCA Pathway.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062017
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- Publication type:
- Article
The Cellular Phenotype of Roberts Syndrome Fibroblasts as Revealed by Ectopic Expression of ESCO2.
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- PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0006936
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- Publication type:
- Article
FANCD2 protein is expressed in proliferating cells of human tissues that are cancer-prone in Fanconi anaemia.
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- Journal of Pathology, 2003, v. 201, n. 2, p. 198, doi. 10.1002/path.1450
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- Publication type:
- Article
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM.
- Published in:
- Nature Genetics, 2000, v. 24, n. 1, p. 15, doi. 10.1038/71626
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- Publication type:
- Article
Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.
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- Nature Genetics, 1999, v. 22, n. 4, p. 379, doi. 10.1038/11956
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- Publication type:
- Article
The Fanconi anaemia group G gene FANCG is identical with XRCC9.
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- Nature Genetics, 1998, v. 20, n. 3, p. 281, doi. 10.1038/3093
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- Publication type:
- Article
Mechanism of hyperoxia-induced chromosomal breakage in chinese hamster cells.
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- Environmental & Molecular Mutagenesis, 1993, v. 22, n. 4, p. 264, doi. 10.1002/em.2850220414
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- Publication type:
- Article
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway.
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- EMBO Journal, 2007, v. 26, n. 8, p. 2104, doi. 10.1038/sj.emboj.7601666
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- Publication type:
- Article
FANCE: the link between Fanconi anaemia complex assembly and activity.
- Published in:
- EMBO Journal, 2002, v. 21, n. 13, p. 3414, doi. 10.1093/emboj/cdf355
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- Publication type:
- Article
Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients.
- Published in:
- 2011
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- Publication type:
- journal article
Analysis of baseline and cisplatin-inducible gene expression in Fanconi anemia cells using oligonucleotide-based microarrays.
- Published in:
- BMC Blood Disorders, 2002, v. 2, p. 5
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- Publication type:
- Article
Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
- Published in:
- Human Mutation, 2008, v. 29, n. 1, p. 159, doi. 10.1002/humu.20625
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- Publication type:
- Article
Spectrum of FANCA mutations in Italian Fanconi anemia patients: Identification of six novel alleles and phenotypic characterization of the S858R variant<FN ID="fn1">Communicated by Mark H. Paalman</FN><FN ID="fn2">Online Citation: Human Mutation, Mutation in Brief #651 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/651.pdf</FN>
- Published in:
- Human Mutation, 2003, v. 22, n. 4, p. 338, doi. 10.1002/humu.9180
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- Publication type:
- Article
Fanconi anemia A due to a novel frameshift mutation in hotspot motifs: Lack of FANCA protein.
- Published in:
- Human Mutation, 2000, v. 15, n. 6, p. 578, doi. 10.1002/1098-1004(200006)15:6<578::AID-HUMU12>3.0.CO;2-Q
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- Publication type:
- Article
Exon 6 skipping in the fanconi anemia C gene associated with a nonsense/missense mutation (775C→T) in exon 5: The first example of a nonsense mutation in one exon causing skipping of another downstream.
- Published in:
- Human Mutation, 1998, v. 11, p. S25, doi. 10.1002/humu.1380110109
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- Publication type:
- Article