Cytoskeleton alterations of erythrocytes from patients with Fanconi's anemia
Open Access
- 22 February 2000
- journal article
- research article
- Published by Wiley in FEBS Letters
- Vol. 468 (2-3) , 125-128
- https://doi.org/10.1016/s0014-5793(00)01187-x
Abstract
Fanconi's anemia (FA) is a very rare genetically heterogeneous disease which has been hypothesized to be defective in the detoxification of reactive oxygen species. In this work we report the results...Keywords
This publication has 17 references indexed in Scilit:
- Congenital disorders sharing oxidative stress and cancer proneness as phenotypic hallmarks: prospects for joint research in pharmacologyMedical Hypotheses, 1998
- Exploring the Role of Oxygen in Fanconi’s AnemiaPublished by Springer Nature ,1997
- Increased formation of 8-hydroxydeoxyguanosine, an oxidative DNA damage, in lymphoblasts from Fanconi's anemia patients due to possible catalase deficiencyCarcinogenesis: Integrative Cancer Research, 1993
- A new, striking morphologic feature for the human erythrocyte in hereditary spherocytosis: the blebbing pattern [letter]Blood, 1993
- Cytoskeleton as a target in menadione‐induced oxidative stress in cultured mammalian cells. I. Biochemical and immunocytochemical featuresJournal of Cellular Physiology, 1990
- [75] Measurement of oxidant stress in VivoPublished by Elsevier ,1990
- Spectrin oxidation correlates with membrane vesiculation in stored RBCsBlood, 1987
- Sickle cell membranes and oxidative damageBiochemical Journal, 1986
- [13] Catalase in vitroPublished by Elsevier ,1984
- Red Blood Cell Fatty Acid Composition in a Sample of Italian Middle-Aged Men on Free DietAnnals of Nutrition and Metabolism, 1980