20 results on '"Puzone, Stella"'
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2. Prenatal diagnosis of haemoglobinopathies: our experience of 523 cases
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3. Role of the cold shock domain protein A in the transcriptional regulation of HBG expression
4. Identification and molecular characterization of the —Campania deletion, a novel α°-thalassemic defect, in two unrelated Italian families
5. Identification of molecular interactors of the Cold Shock Domain Protein A (CSDA), a repressor factor of gamma globin gene expression
6. Individuazione di un repressore trascrizionale dei geni globinici fetali
7. Cold shock domain protein A (CSDA) acts as repressor factor of gamma globin gene expression in vivo
8. Knock-down of Cold shock domain protein A (CSDA) increases gamma globin gene expression in K562 cell line
9. Identification of a transcriptional factor involved in gamma globin gene expression
10. Hb Federico II, a novel haemoglobin variant (beta 106 Leu->Val) associated with a beta thalassemia phenotype
11. Structural and Functional Characterization of Csda Protein Complexes Involved In Modulation of Fetal Globin Gene Expression
12. research paper: Role of the cold shock domain protein A in the transcriptional regulation of HBG expression
13. Erratum: “Identification and molecular characterization of the-CAMPANIAdeletion, a novel α°-thalassemic defect, in two unrelated Italian families” by Sessa et al.,Am J Hematol2010, DOI number 21591
14. Identification and molecular characterization of the --CAMPANIA deletion, a novel α°-thalassemic defect, in two unrelated Italian families
15. Identification of a Transcription Factor Potentially Involved in γ-Globin Gene Expression.
16. Identification and molecular characterization of the -- CAMPANIA deletion, a novel α°-thalassemic defect, in two unrelated Italian families.
17. Identification of a Transcription Factor Potentially Involved in ?-Globin Gene Expression.
18. Molecular Basis of Thalassemia
19. Identification and molecular characterization of the --CAMPANIA deletion, a novel alpha (0) -thalassemic defect, in two unrelated Italian families [corrected].
20. Defective mRNA levels are responsible for a beta-thalassemia phenotype associated with Hb Federico II, a novel hemoglobin variant [beta-106 (G8) Leu->Val].
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