23 results on '"De Gobbi, Marco"'
Search Results
2. GITMO Registry Study on Allogeneic Transplantation in Patients Aged ≥60 Years from 2000 to 2017: Improvements and Criticisms
3. Efficacy and Safety of Luspatercept in Adult Patients with Transfusion-Dependent Anemia Due to Very Low, Low and Intermediate Risk Myelodysplastic Syndromes (MDS) with Ring Sideroblasts, Who Had an Unsatisfactory Response to or Are Ineligible for Erythropoietin-Based Therapy: A Retrospective Multicenter Study By Fondazione Italiana Sindromi Mielodisplastiche (FiSiM ETS)
4. Intragenic Enhancers Act as Alternative Promoters
5. Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1α localization in erythroblasts
6. ATR-X Syndrome Protein Targets Tandem Repeats and Influences Allele-Specific Expression in a Size-Dependent Manner
7. The role of the polycomb complex in silencing α-globin gene expression in nonerythroid cells
8. Tissue-specific histone modification and transcription factor binding in α globin gene expression
9. Juvenile hemochromatosis
10. Genetic haemochromatosis: genes and mutations associated with iron loading
11. Hemochromatosis Due to Mutations in Transferrin Receptor 2
12. Enhancer deletion generates cellular phenotypic diversity due to bimodal gene expression
13. Overall Survival Improvement Following ALLO-SCT in Patients Older THAN 60 YEARS: A Gruppo Italiano Trapianto DI Midollo Osseo (GITMO) Registry Study
14. New mutations inactivating transferrin receptor 2 in hemochromatosis type 3
15. Transferrin Saturation and Its Association with Platelet Reactivity
16. Identification of New BMP6 Pro-Peptide Mutations in Patients with Unexplained Iron-Overload
17. Discovering Regulatory SNPs by Genome-Wide Analysis of Differential Scl/TAL-1 Occupancy in Human Primary Erythroid Cells,
18. Codanin-1 Mutations In Congenital Dyserythropoietic Anemia Type 1 Affect HP1α Localization In Erythroblasts
19. Long-range chromosomal interactions regulate the timing of the transition between poised and active gene expression
20. The mechanism of alpha-globin activation during erythropoiesis
21. An Entirely Novel Form of α Thalassemia in Patients from the South Pacific Linked to Chromosome 16.
22. Identification of a Gain-of-Function SNP Causing a New Model of α-Thalassaemia.
23. Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.