295 results on '"La Starza R"'
Search Results
2. P307: DEL(17)(Q11) IS TYPICAL MARKER OF IMMATURE T-ALL OF ADULTS, WITH NF1, UTP6, AND SUZ12 HAPLOINSUFFICIENCY, GENOME INSTABILITY, AND GENE DOWNREGULATION
3. Identification of an Epi-metabolic dependency on EHMT2/G9a in T-cell acute lymphoblastic leukemia
4. Early T-Cell Precursor ALL and Beyond: Immature and Ambiguous Lineage T-ALL Subsets
5. The Italian External Quality Assessment Scheme in Classical Cytogenetics : Four Years of Activity
6. CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12
7. A new NDE1/PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome
8. A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T-cell Acute Lymphoblastic Leukemia
9. Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia
10. Aberrant subcellular expression of nucleophosmin and NPM-MLF1 fusion protein in acute myeloid leukaemia carrying t(3;5): A comparison with NPMc+ AML
11. CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients
12. Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype
13. Structure of the (SR) Ca2+-ATPase bound to the inhibitor compound CAD204520 and TNP-ATP
14. A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene
15. Different genomic imbalances in low- and high-grade HCV-related lymphomas
16. FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells
17. TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia
18. Regions of juxtaposition in unbalanced 1q rearrangements of malignant hemopathies
19. MLL tandem duplication in two cases of acute myelocytic leukemia with unbalanced translocations : der(16)t(11;16)(q23;p13) and der(18)t(11;18)(q22;p11.2)
20. A novel germline mutation in CDK4 codon 24 associated to familial melanoma
21. Erratum: CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12
22. A novel germline mutation in CDK4 codon 24 associated to familial melanoma
23. Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia
24. Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: A GIMEMA centralized biological study
25. TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia [4]
26. Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia
27. RNA sequencing unravels the genetics of refractory/relapsed T-cell acute lymphoblastic leukemia. Prognostic and therapeutic implications
28. TP53 mutations in adult acute lymphoblastic leukemia (ALL) are relatively frequent in molecularly negative case of both B- and T-lineage and correlate with poor response to induction therapy
29. Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia
30. COMBINED INTERPHASE FLUORESCENCE IN SITU HYBRIDIZATION (CI-FISH) DELINEATES THE GENOMIC PROFILE OF T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA IN CHILDREN
31. Prognostic impact of genetic characterization in the GIMEMA LAM99P multicenter study for newly diagnosed acute myeloidleukemia
32. Genetic pathways in low-and high-grade HCV-related lymphomas are different
33. Dual-color split signal fluorescence in situ hybridization assays for the detection of CALM/AF10 in t(10;11)(p13;q14-q21)-positive acute leukemia
34. Haplo-identical haematopoietic stem cell transplantation for secondary leukaemia
35. Cytoplasmic Nucleophosmin (NPM) Identifies a Subtype of Acute Myelogenous Leukemia With A Normal Karyotype and NPM Gene Mutations
36. CIZ gene rearrangements in acute leukemia: Report of a diagnostic FISH assay and clinical features of nine patients [13]
37. DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia
38. PROSPECTIVE KARYOTYPIC ANALYSIS IN ADULT ACUTE LYMPHOBLASTIC LEUKEMIA AT RELAPSE: RESULTS OF THE MULTICENTRIC STUDY GROUP GIMEMA ALL 0496
39. Recurrent rearrangementof the Ewing's sarcoma gene, EWSRI, or its homologue, TAF15, with the transcription factor CIZ/NMP4 in acute leukemia
40. Complex variant Philadelphia translocations involving the short arm of chromosome 6 in chronic myeloid leukemia
41. t(4;11)(q21;p15) translocation involving NUP98 and RAP1GDS1 genes: characterization of a new subset of T acute lymphoblastic leukaemia
42. t(4;11)(q21;p15) translocation involving NUP98 and RAP1GDS1 genes: characterization of a new subset of T acute lymphoblastic leukaemia
43. Different boundaries characterize isolated and non-isolated 5q deletions in myelodysplastic syndromes and acute myeloid leukemias
44. A novel germline mutation in CDK4 codon 24 associated to familial melanoma.
45. CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12
46. 253 Insights on centromeric breakpoints of 5q deletions
47. 252 NPM1 haploinsufficiency in human myeloid diseases with non-isolated −5/5q-
48. 251 MN1-ETV6 fusion gene and −7: an unusual karyotypic evolution in AML after MDS with 5q-
49. t(12;22)(p13;q12)
50. ZNF384 (zinc finger protein 384)
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