Found: 25
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Type III Collagen Deficiency in a Family with Intracranial Aneurysms.
- Published in:
- Cerebrovascular Diseases, 2001, v. 11, n. 2, p. 92, doi. 10.1159/000047618
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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
Connecting Fanconi anemia to BRCA1.
- Published in:
- Nature Medicine, 2001, v. 7, n. 4, p. 406, doi. 10.1038/86458
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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
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
- Published in:
- 2005
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- Publication type:
- Letter
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.
- Published in:
- Nature Genetics, 1999, v. 22, n. 4, p. 379, doi. 10.1038/11956
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- Publication type:
- Article
Inherited susceptibility to bleomycin-induced chromatid breaks in cultured peripheral blood lymphocytes.
- Published in:
- 1999
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- Publication type:
- journal article
Characterization, expression and complex formation of the murine Fanconi anaemia gene product Fancg.
- Published in:
- 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
Fanconi DNA repair pathway is required for survival and long-term maintenance of neural progenitors.
- Published in:
- EMBO Journal, 2008, v. 27, n. 5, p. 770, doi. 10.1038/emboj.2008.14
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- Publication type:
- Article
Electrophoretic characterization of posttranslational modifications of human parotid salivary α-amylase.
- Published in:
- Electrophoresis, 1991, v. 12, n. 1, p. 74, doi. 10.1002/elps.1150120114
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- Publication type:
- Article
Impaired functionality and homing of Fancg-deficient hematopoietic stem cells.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 1, p. 121, doi. 10.1093/hmg/ddr447
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- Publication type:
- 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
Cloning and characterization of murine Fanconi anemia group A gene: Fanca protein is expressed in lymphoid tissues, testis, and ovary.
- Published in:
- Mammalian Genome, 2000, v. 11, n. 4, p. 326, doi. 10.1007/s003350010060
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- Publication type:
- Article
Phenotype correction of fanconi anemia group a hematopoietic stem cells using lentiviral vector
- Published in:
- Molecular Therapy, 2003, v. 8, n. 4, p. 600, doi. 10.1016/S1525-0016(03)00223-5
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- Publication type:
- Article
Clonally Related But Phenotypically Divergent Human Cancer Cell Lines Derived from a Single Follicular Thyroid Cancer Recurrence (TT2609).
- Published in:
- Thyroid, 2001, v. 11, n. 10, p. 909, doi. 10.1089/105072501753210966
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- Publication type:
- Article
Aberrant Fanconi anaemia protein profiles in acute myeloid leukaemia cells.
- Published in:
- 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
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
Evolutionary Clues to the Molecular Function of Fanconi Anemia Genes.
- Published in:
- Acta Haematologica, 2002, v. 108, n. 4, p. 231, doi. 10.1159/000065659
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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
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
Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia c gene, FAC.
- Published in:
- Human Mutation, 1996, v. 7, n. 3, p. 264, doi. 10.1002/(SICI)1098-1004(1996)7:3<264::AID-HUMU11>3.0.CO;2-0
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- Publication type:
- Article
Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 1, p. 151, doi. 10.1093/hmg/5.1.151
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- Publication type:
- Article
A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites.
- Published in:
- Anemia (20901267), 2012, p. 1, doi. 10.1155/2012/865170
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- Publication type:
- Article