Peripheral lymphocytes of three Fanconi's anemia (FA) patients and of five heterozygotes have been tested for their susceptibility to chromosomal breakage and sister chromatid exchange (SCE) induction by diepoxybutane (DEB). As previously shown, DEB dramatically increases the chromosomal breakage level in both homozygotes and heterozygotes. Slightly, but significantly, reduced spontaneous levels of SCE were found in cultures from FA patients and FA gene carriers as compared with controls. SCE rates were not enhanced in lymphocytes grown in the presence of DEB, irrespective of the time at which it had been added to the culture, and were comparable in cells of FA patients and FA heterozygotes. This was in contrast with SCE rates in control ce...
The high sensitivity of Fanconi’s anemia (FA) cells to drug induced DNA interstrand crosslinks (ICL)...
Fanconi Anemia (FA) is a rare recessive disorder clinically characterized by progressive bone marrow...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
and G. Joksić (2013): Enhanced frequency of sister chromatid exchanges induced by diepoxybutane is s...
Fanconi anemia (FA) is a rare genetically heterogeneous disease characterized by developmental abnor...
Spontaneous and diepoxybutane (DEB)-induced sister-chromatid exchanges (SCEs) were examined in whole...
Spontaneous and diepoxybutane (DEB)-induced sister chromatid exchanges (SCEs) were examined in cultu...
Peripheral blood lymphocytes from a sample of 62 randomly selected donors were analysed for spontane...
'To whom correspondence should be addressed Peripheral blood lymphocytes from a sample of 62 ra...
ABSTRACT. The main feature of Fanconi anemia (FA) is the high sensitivity of the cells to the clasto...
Mutat Res. 2003 Apr 20;536(1-2):61-7. Role of haemoglobin in the protection of cultured lymphocyt...
Background/Aim. Fanconi anemia (FA) is a rare hereditary disease in a heterogeneous group of synd...
Diagnóstico citogenético e molecular da anemia de Fanconi hyper-pigmentation, kidney and urinary tra...
Abstract Fanconi Anemia (FA) is a rare genetic disorder, characterized by progressive bone marrow fa...
A number of inherited disorders are associated with bone marrow failure. Amongst them Fanconi's anae...
The high sensitivity of Fanconi’s anemia (FA) cells to drug induced DNA interstrand crosslinks (ICL)...
Fanconi Anemia (FA) is a rare recessive disorder clinically characterized by progressive bone marrow...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
and G. Joksić (2013): Enhanced frequency of sister chromatid exchanges induced by diepoxybutane is s...
Fanconi anemia (FA) is a rare genetically heterogeneous disease characterized by developmental abnor...
Spontaneous and diepoxybutane (DEB)-induced sister-chromatid exchanges (SCEs) were examined in whole...
Spontaneous and diepoxybutane (DEB)-induced sister chromatid exchanges (SCEs) were examined in cultu...
Peripheral blood lymphocytes from a sample of 62 randomly selected donors were analysed for spontane...
'To whom correspondence should be addressed Peripheral blood lymphocytes from a sample of 62 ra...
ABSTRACT. The main feature of Fanconi anemia (FA) is the high sensitivity of the cells to the clasto...
Mutat Res. 2003 Apr 20;536(1-2):61-7. Role of haemoglobin in the protection of cultured lymphocyt...
Background/Aim. Fanconi anemia (FA) is a rare hereditary disease in a heterogeneous group of synd...
Diagnóstico citogenético e molecular da anemia de Fanconi hyper-pigmentation, kidney and urinary tra...
Abstract Fanconi Anemia (FA) is a rare genetic disorder, characterized by progressive bone marrow fa...
A number of inherited disorders are associated with bone marrow failure. Amongst them Fanconi's anae...
The high sensitivity of Fanconi’s anemia (FA) cells to drug induced DNA interstrand crosslinks (ICL)...
Fanconi Anemia (FA) is a rare recessive disorder clinically characterized by progressive bone marrow...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...