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217 related items for PubMed ID: 11261779

  • 1. DNA damage and apoptosis in mononuclear cells from glucose-6-phosphate dehydrogenase-deficient patients (G6PD Aachen variant) after UV irradiation.
    Efferth T, Fabry U, Osieka R.
    J Leukoc Biol; 2001 Mar; 69(3):340-2. PubMed ID: 11261779
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  • 2. Evaluation of DNA damage in leukocytes of G6PD-deficient Iranian newborns (Mediterranean variant) using comet assay.
    Mesbah-Namin SA, Nemati A, Tiraihi T.
    Mutat Res; 2004 Dec 21; 568(2):179-85. PubMed ID: 15542105
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  • 3. Molecular characterization of a German variant of glucose-6-phosphate dehydrogenase deficiency (G6PD Aachen).
    Efferth T, Osieka R, Beutler E.
    Blood Cells Mol Dis; 2000 Feb 21; 26(1):101-4. PubMed ID: 10772881
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  • 4. Induction of apoptosis, depletion of glutathione, and DNA damage by extracorporeal photochemotherapy and psoralen with exposure to UV light in vitro.
    Efferth T, Fabry U, Osieka R.
    Anticancer Res; 2001 Feb 21; 21(4A):2777-83. PubMed ID: 11724354
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  • 5. Increased induction of apoptosis in mononuclear cells of a glucose-6-phosphate dehydrogenase deficient patient.
    Efferth T, Fabry U, Glatte P, Osieka R.
    J Mol Med (Berl); 1995 Jan 21; 73(1):47-9. PubMed ID: 7633942
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  • 9. G6PD deficiency from lyonization after hematopoietic stem cell transplantation from female heterozygous donors.
    Au WY, Pang A, Lam KK, Song YQ, Lee WM, So JC, Kwong YL.
    Bone Marrow Transplant; 2007 Oct 21; 40(7):677-81. PubMed ID: 17660836
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  • 11. Modification to reporting of qualitative fluorescent spot test results improves detection of glucose-6-phosphate dehydrogenase (G6PD)-deficient heterozygote female newborns.
    Nadarajan V, Shanmugam H, Sthaneshwar P, Jayaranee S, Sultan KS, Ang C, Arumugam S.
    Int J Lab Hematol; 2011 Oct 21; 33(5):463-70. PubMed ID: 21501392
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  • 13. Biochemical and cytochemical evaluation of heterozygote individuals with glucose-6-phosphate dehydrogenase deficiency.
    Gurbuz N, Aksu TA, Van Noorden CJ.
    Acta Histochem; 2005 Oct 21; 107(4):261-7. PubMed ID: 16139339
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  • 17. Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency.
    Pietrapertosa A, Palma A, Campanale D, Delios G, Vitucci A, Tannoia N.
    Haematologica; 2001 Jan 21; 86(1):30-5. PubMed ID: 11146567
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  • 18. DNA hypermethylation and X chromosome inactivation are major determinants of phenotypic variation in women heterozygous for G6PD mutations.
    Wang J, Xiao QZ, Chen YM, Yi S, Liu D, Liu YH, Zhang CM, Wei XF, Zhou YQ, Zhong XM, Zhao CY, Xiong F, Wei XC, Xu XM.
    Blood Cells Mol Dis; 2014 Dec 21; 53(4):241-5. PubMed ID: 24958328
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