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1. 4-Hydroxynonenal, a lipid peroxidation product of dietary polyunsaturated fatty acids, has anticarcinogenic properties in colon carcinoma cell lines through the inhibition of telomerase activity

2. PPARγ ligands inhibit telomerase activity and hTERT expression through modulation of the Myc/Mad/Max network in colon cancer cells

3. Choline and phosphatidylcholine fluorescent derivatives localization in carcinoma cells studied by laser scanning confocal fluorescence microscopy

4. Regulation of Mouse p45 NF-E2 Transcription by an Erythroid-specific GATA-dependent Intronic Alternative Promoter

5. Contents, Vol. 95, 1996

6. Erythroid-Specific Activation of the Distal (Testis) Promoter of GATA1 during Differentiation of Purified Normal Murine Hematopoietic Stem Cells

7. Immortalization of multipotent growth-factor dependent hemopoietic progenitors from mice transgenic for GATA-1 driven SV40 tsA58 gene

8. Regulation of ?-Globin Expression in Hereditary Persistence of Fetal Hemoglobin

9. 4-Hydroxynonenal inhibits telomerase activity and hTERT expression in human leukemic cell lines

10. 4-Hydroxynonenal affects pRb/E2F pathway in HL-60 human leukemic cells

12. Tumorigenic activity of a rearranged c-myc gene from a human T-cell leukemia line

13. Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23

14. An erythroid specific enhancer upstream to the gene encodin the cell-type specific transcription factor GATA-1

15. Subject Index Vol. 95, 1996

16. Editors’/Publisher’s Disclaimer

17. A frequent A?-persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with ?-thalassemia

18. Biosynthesis of globin chains in fetal liver and adult marrow cultures

19. A gene controlling fetal hemoglobin expression in adults is not linked to the non-alpha globin cluster

20. Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced by his) carriers

21. beta-Like Globin RNA Sequences in Hemoglobin Lepore Disease

22. The same nuclear proteins bind the proximal CACCC box of the human β-globin promoter and a similar sequence in the enhancer

23. Preferential induction of fetal versus embryonic globin chains in human leukemic cell lines

24. δβ-Thalassemia is due to a gene deletion

25. A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemia

26. A Model for Hemoglobin F Synthesis in Adult Life: Evidence for Regulation at the Level of Erythroblasts

27. Heterogeneity of ?, ?-Thalassemia and Hereditary Persistence of Hb F in the Mediterranean Area

28. Transcriptional and Post-transcriptional Defects in beta0-Thalassaemia

29. Gγ and Aγ globin chains separation and quantitation by isoelectric focusing

30. Direct demonstration of β-globin mRNA in homozygous Ferrara β0-thalassaemia patients

31. Globin gene deletion in HPFH, δ°β° thalassaemia and Hb Lepore disease

32. DNA Sequences Regulating Human Globin Gene Transcription in Nondeletional Hereditary Persistence of Fetal Hemoglobin

33. Dissociation of Single Ribosomes as a Preliminary Step for Their Participation in Protein Synthesis

34. Globin RNA sequences in human leukaemic peripheral blood

35. The beta-globin gene in Sardinian delta beta 0-thalassemia carries a C--T nonsense mutation at codon 39

36. Globin α-Chain Synthesis directed by 'Supernatant' 10S RNA from Rabbit Reticulocytes

37. Sardinian delta beta zero-thalassemia: a further example of a C to T substitution at position -196 of the A gamma globin gene promoter

38. Bromodeoxyuridine treatment of normal adult erythroid colonies: an in vitro model for reactivation of human fetal globin genes

39. Increased erythroid-specific expression of a mutated HPFH gamma-globin promoter requires the erythroid factor NFE-1

40. Delta thalassemia: a non-deletion defect

41. An erythroid specific nuclear factor binding to the proximal CACCC box of the beta-globin gene promoter

42. Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?

44. The effects of HPFH mutations in the human gamma-globin promoter on binding of ubiquitous and erythroid specific nuclear factors

45. A direct estimate of the number of human gamma-globin genes

46. Human globin chain separation by isoelectric focusing

47. Human T gamma globin chain is a variant of A gamma chain (A gamma Sardinia)

48. Italian type of deletional hereditary persistence of fetal hemoglobin

49. Presence of gene for beta globin in homozygous beta0 thalassaemia

50. A protein factor binding to an octamer motif in the gamma-globin promoter disappears upon induction of differentiation and hemoglobin synthesis in K562 cells

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