| scholarly article | Q13442814 |
| P2093 | author name string | Hoehn H | |
| Flentje M | |||
| Schindler D | |||
| Oppitz U | |||
| Rothfuss A | |||
| Djuzenova CS | |||
| Spelt G | |||
| P2860 | cites work | A simple technique for quantitation of low levels of DNA damage in individual cells | Q29014320 |
| DNA damage and repair in individual cells: applications of the comet assay in radiobiology | Q33637269 | ||
| Heterozygous manifestations in four autosomal recessive human cancer-prone syndromes: ataxia telangiectasia, xeroderma pigmentosum, Fanconi anemia, and Bloom syndrome. | Q35148328 | ||
| Chromatid damage after G2 phase x-irradiation of cells from cancer-prone individuals implicates deficiency in DNA repair | Q37348947 | ||
| Drug sensitivity spectra in Fanconi anemia lymphoblastoid cell lines of defined complementation groups | Q40922341 | ||
| Chromatin structure and cellular radiosensitivity: a comparison of two human tumour cell lines | Q41147641 | ||
| Fanconi's anemia and malignancies | Q41189229 | ||
| DNA repair in a fanconi's anemia fibroblast cell strain | Q41439790 | ||
| Levels of peripheral blood cell DNA damage in insulin dependent diabetes mellitus human subjects | Q42489285 | ||
| G2 chromosomal radiosensitivity in Fanconi's anemia | Q43754870 | ||
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| Polyamine-induced compaction and aggregation of DNA--a major factor in radioprotection of chromatin under physiological conditions. | Q46714171 | ||
| Is Fanconi anemia caused by a defect in the processing of DNA damage? | Q52184525 | ||
| Cellular sensitivity and low dose-rate recovery in Fanconi anaemia fibroblasts. | Q52216424 | ||
| Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia | Q59073358 | ||
| Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells | Q59080097 | ||
| Chromatin Compaction and the Efficiency of Formation of DNA-Protein Crosslinks in γ-Irradiated Mammalian Cells | Q67739924 | ||
| Radiosensitivity in Fanconi anemia: application to the conditioning for bone marrow transplantation | Q68614771 | ||
| Physical and laboratory characteristics of heterozygote carriers of the Fanconi aplasia gene | Q68644240 | ||
| In vitro chromosomal radiosensitivity in "chromosomal breakage syndromes" | Q69558534 | ||
| Radiosensitivity in Fanconi anaemia: application to the conditioning regimen for bone marrow transplantation | Q70261816 | ||
| The cell cycle of lymphocytes in Fanconi anemia | Q70578804 | ||
| Comet assay demonstrates a higher ultraviolet B sensitivity to DNA damage in dysplastic nevus cells than in common melanocytic nevus cells and foreskin melanocytes | Q71383603 | ||
| Response of lymphocytes from Fanconi's anemia patients and their heterozygous relatives to 8-methoxy-psoralene in a cloning survival test system | Q71826957 | ||
| The comet assay as a repair test for prenatal diagnosis of Xeroderma pigmentosum and trichothiodystrophy | Q73012068 | ||
| Impaired DNA repair as assessed by the "comet" assay in patients with thyroid tumors after a history of radiation therapy: a preliminary study | Q74434743 | ||
| Confounding factors in the diagnosis of Fanconi anaemia | Q77435996 | ||
| Analysis by alkaline comet assay of cancer patients with severe reactions to radiotherapy: defective rejoining of radioinduced DNA strand breaks in lymphocytes of breast cancer patients | Q78132603 | ||
| P433 | issue | 2 | |
| P921 | main subject | Fanconi anemia | Q845779 |
| heterozygosity | Q124059385 | ||
| homozygosity | Q114049690 | ||
| P304 | page(s) | 185-192 | |
| P577 | publication date | 2001-02-01 | |
| P1433 | published in | Laboratory Investigation | Q6467260 |
| P1476 | title | Response to X-irradiation of Fanconi anemia homozygous and heterozygous cells assessed by the single-cell gel electrophoresis (comet) assay. | |
| P478 | volume | 81 |
| Q41848878 | BRCA1, FANCD2 and Chk1 are potential molecular targets for the modulation of a radiation-induced DNA damage response in bystander cells. |
| Q42503804 | Biomarkers for genome instability in some genetic disorders: a pilot study |
| Q39485543 | Clinical vignette: early-onset head and neck cancer: beware of fanconi anaemia! |
| Q28207549 | Convergence of the fanconi anemia and ataxia telangiectasia signaling pathways |
| Q38449075 | Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia |
| Q44411742 | Differential diagnosis of Fanconi anemia by nitrogen mustard and diepoxybutane |
| Q35828191 | Fanconi anaemia and leukaemia - clinical and molecular aspects |
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| Q42421841 | Fanconi anemia gene variants in therapy-related myeloid neoplasms. |
| Q35532416 | GS-nitroxide (JP4-039)-mediated radioprotection of human Fanconi anemia cell lines |
| Q36030871 | Genetic and epigenetic features in radiation sensitivity. Part II: implications for clinical practice and radiation protection |
| Q53259285 | Heterozygous mutations in the PALB2 hereditary breast cancer predisposition gene impact on the three-dimensional nuclear organization of patient-derived cell lines. |
| Q36093174 | Human umbilical cord blood-derived mesenchymal stem cells undergo cellular senescence in response to oxidative stress |
| Q35768837 | Hypersensitivity to chemoradiation in FANCA carrier with cervical carcinoma-A case report and review of the literature. |
| Q47857337 | Mutations in Fanconi anemia genes and the risk of esophageal cancer |
| Q82521188 | Radiation-induced DNA damage and repair in peripheral blood mononuclear cells from Nijmegen breakage syndrome patients and carriers assessed by the Comet assay |
| Q41894983 | Radiosensitivity and repair kinetics of gamma-irradiated leukocytes from sporadic prostate cancer patients and healthy individuals assessed by alkaline comet assay |
| Q36614103 | Radiosensitivity in breast cancer assessed by the Comet and micronucleus assays |
| Q37578363 | Squamous cell carcinoma of base of tongue in a patient with Fanconi's anemia treated with radiation therapy: case report and review of literature |
| Q38498596 | Suppression of autophagy by FIP200 deletion impairs DNA damage repair and increases cell death upon treatments with anticancer agents |
| Q54856855 | Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype. |
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