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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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- Article
Identification of multiple nuclear export sequences in Fanconi anemia group A protein that contribute to CRM1-dependent nuclear export.
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- Human Molecular Genetics, 2005, v. 14, n. 10, p. 1271, doi. 10.1093/hmg/ddi138
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- Article
Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways.
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- Human Molecular Genetics, 2004, v. 13, n. 12, p. 1241, doi. 10.1093/hmg/ddh135
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- 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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- 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.
- Published in:
- Genes, Chromosomes & Cancer, 2005, v. 42, n. 4, p. 404, doi. 10.1002/gcc.20153
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- Article
Growth inhibition by anti-estrogens and progestins in TGF-β-resistant and -sensitive breast-tumor cells.
- Published in:
- International Journal of Cancer, 1996, v. 65, n. 5, p. 682, doi. 10.1002/(SICI)1097-0215(19960301)65:5<682::AID-IJC20>3.0.CO;2-8
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- 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
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
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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- 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.
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- 2005
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- Publication type:
- Letter
X-linked inheritance of Fanconi anemia complementation group B.
- Published in:
- Nature Genetics, 2004, v. 36, n. 11, p. 1219, doi. 10.1038/ng1458
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- 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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- 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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- 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
Molecular diagnosis of Fanconi anemia with next-generation sequencing in a case with subtle signs and a negative chromosomal breakage test.
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- Turkish Journal of Pediatrics, 2015, v. 57, n. 3, p. 282
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- Article
Chemosensitizing tumor cells by targeting the Fanconi anemia pathway with an adenovirus overexpressing dominant-negative FANCA.
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- Cancer Gene Therapy, 2004, v. 11, n. 8, p. 539, doi. 10.1038/sj.cgt.7700734
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- 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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- Article
Fancf-deficient mice are prone to develop ovarian tumours.
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- Journal of Pathology, 2012, v. 226, n. 1, p. 28, doi. 10.1002/path.2992
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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.
- Published in:
- Nature Genetics, 1998, v. 20, n. 3, p. 281, doi. 10.1038/3093
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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
Analysis of baseline and cisplatin-inducible gene expression in Fanconi anemia cells using oligonucleotide-based microarrays.
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- BMC Blood Disorders, 2002, v. 2, p. 5
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- 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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- Article
Fanconi anemia A due to a novel frameshift mutation in hotspot motifs: Lack of FANCA protein.
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- 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
Whole Exome Sequencing Reveals Uncommon Mutations in the Recently Identified Fanconi Anemia Gene SLX 4/ FANCP.
- Published in:
- Human Mutation, 2013, v. 34, n. 1, p. 93, doi. 10.1002/humu.22221
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- Publication type:
- Article
Analysis of the Novel Fanconi Anemia Gene SLX4/ FANCP in Familial Breast Cancer Cases.
- Published in:
- Human Mutation, 2013, v. 34, n. 1, p. 70, doi. 10.1002/humu.22206
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- Publication type:
- Article
DPC4 (SMAD4) mediates transforming growth factor-β1 (TGF-β1) induced growth inhibition and transcriptional response in breast tumour cells.
- Published in:
- Oncogene, 1997, v. 14, n. 16, p. 1891, doi. 10.1038/sj.onc.1201017
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- Article