207 results on '"Matteucci, Caterina"'
Search Results
2. Correction to: One disease, two faces: clonally-related AML and MPDCP with skin involvement
3. Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults
4. Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement
5. 14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T-lymphoid and myeloid immature acute leukemia
6. Epigenetic Modeling of Jumping Translocations of 1q Heterochromatin in Acute Myeloid Leukemia After 5'‐Azacytidine Treatment.
7. A novel mutation of indoleamine 2,3-dioxygenase 1 causes a rapid proteasomal degradation and compromises protein function
8. Design of a Comprehensive Fluorescence in Situ Hybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia
9. A case of familial donor-derived acute myeloid leukemia with underlying pre-leukemic mutations
10. Screening for gene variants causing inherited platelet disorders: are the cons always cons?
11. Activating somatic and germline TERT promoter variants in myeloid malignancies
12. A novel t(X;21)(p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in myelodysplastic syndromes and acute myeloid leukemias.
13. The EMT transcription factor Zeb2 controls adult murine hematopoietic differentiation by regulating cytokine signaling
14. High PIM1 expression is a biomarker of T-cell acute lymphoblastic leukemia with JAK/STAT activation or t(6;7)(p21;q34)/TRB@-PIM1 rearrangement
15. NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias
16. Chromosome Abnormalities in HCV-Related Lymphoproliferation
17. Comparison between Sickle Cell Disease Patients and Healthy Donors: Untargeted Lipidomic Study of Erythrocytes
18. The GNAS1 gene in myelodysplastic syndromes (MDS)
19. A Novel t(5;7)(q31;q21)/CDK6::IL3 in Immature T-cell Acute Lymphoblastic Leukemia With IL3 Expression and Eosinophilia
20. FISH analysis reveals frequent co-occurrence of 4q24/ TET2 and 5q and/or 7q deletions
21. Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement
22. Germline GATA2 variant disrupting endothelial eNOS cell function and angiogenesis can be restored by c-Jun/AP-1 upregulation
23. Germline GATA2 variant disrupting endothelial eNOS function and angiogenesis can be restored by c-Jun/AP-1 upregulation
24. 14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T and myeloid immature acute leukemia
25. New dead/H-box helicase gene (ddx41) mutation in an Italian family with recurrent leukemia
26. Chromosome Abnormalities in HCV-Related Lymphoproliferation
27. Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study
28. Activating somatic and germline TERT promoter variants in myeloid malignancies
29. Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study
30. Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome
31. Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia
32. Interpretation of the complex karyotype and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization on the U937-I cell line
33. 14q32 rearrangements deregulating BCL11Bmark a distinct subgroup of T-lymphoid and myeloid immature acute leukemia
34. Interphase FISH for Y Chromosome, VNTR Polymorphisms, and RT-PCR for BCR-ABL in the Monitoring of HLA-Matched and Mismatched Transplants
35. Microdissection and FISH Investigations in Acute Myeloid Leukemia: A Step Forward to Full Identification of Complex Karyotypic Changes
36. Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study
37. Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin
38. Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment
39. Activating somatic and germline TERTpromoter variants in myeloid malignancies
40. Design of a Comprehensive Fluorescence in SituHybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia
41. Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations
42. Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor
43. Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia
44. MN1-ETV6 fusion gene arising from MDS With 5q−
45. Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia
46. Comparative genomic hybridization identifies 17q11.2 approximately q12 duplication as an early event in cutaneous T-cell lymphomas
47. Chronic lymphocytic leukaemia Is terminal del(14)(q24) a new marker for prognostic stratification?
48. Submicroscopic deletions in 5q- associated malignancies
49. Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations
50. High PIM1expression is a biomarker of T-cell acute lymphoblastic leukemia with JAK/STAT activation or t(6;7)(p21;q34)/TRB@-PIM1rearrangement
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