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1. Cover Image, Volume 232, Number 9, September 2017

3. Alterations of negative regulators of cytokine signalling in immunodeficiency-related non-Hodgkin lymphoma

4. Analysis ofSF3B1mutations in monoclonal B-cell lymphocytosis

5. Integrated DNA copy number and methylation profiling of lymphoid neoplasms using a single array

6. Molecular history of Richter syndrome: origin from a cell already present at the time of chronic lymphocytic leukemia diagnosis

7. B-cell receptor, clinical course and prognosis in chronic lymphocytic leukaemia: the growing saga of the IGHV3 subgroup gene usage

8. Mutations of CD79A, CD79B and EZH2 genes in immunodeficiency-related non-Hodgkin lymphomas

9. IGHD3-3fails to behave as unfavourable prognostic marker in chronic lymphocytic leukaemia

10. Single nucleotide polymorphism-arrays provide new insights in the pathogenesis of post-transplant diffuse large B-cell lymphoma

11. Genome wide DNA-profiling of HIV-related B-cell lymphomas

13. Molecular characterization of post‐transplant lymphoproliferative disorders of donor origin occurring in liver transplant recipients

14. Molecular and clinical features of chronic lymphocytic leukaemia with stereotyped B cell receptors: results from an Italian multicentre study

15. Genome‐wide DNA analysis identifies recurrent imbalances predicting outcome in chronic lymphocytic leukaemia with 17p deletion

16. Biological and clinical risk factors of chronic lymphocytic leukaemia transformation to Richter syndrome

17. High density genome-wide DNA profiling reveals a remarkably stable profile in hairy cell leukaemia

20. A case of nodular sclerosis Hodgkin’s lymphoma repeatedly relapsing in the context of composite plasma cell-hyaline vascular Castleman’s disease: successful response to rituximab and radiotherapy

24. Analysis of immunoglobulin heavy and light chain variable genes in post‐transplant lymphoproliferative disorders

25. Comparative genome‐wide profiling of post‐transplant lymphoproliferative disorders and diffuse large B‐cell lymphomas

27. Downregulation of the major histocompatibility complex class I molecules by human herpesvirus type 8 and impaired natural killer cell activity in primary effusion lymphoma development

30. Aberrant somatic hypermutation in post-transplant lymphoproliferative disorders

31. Aberrant methylation in the promoter region of the reduced folate carrier gene is a potential mechanism of resistance to methotrexate in primary central nervous system lymphomas

32. Incidence of novel N-glycosylation sites in the B-cell receptor of lymphomas associated with immunodeficiency

33. Frequent aberrant promoter hypermethylation of O6‐methylguanine‐DNA methyltransferase and death‐associated protein kinase genes in immunodeficiency‐related lymphomas

36. Molecular histogenesis of plasmablastic lymphoma of the oral cavity

40. Mutation ofBAX occurs infrequently in acquired immunodeficiency syndrome-related non-Hodgkin's lymphomas

42. Genetic characterization of HHV-8/KSHV-positive primary effusion lymphoma reveals frequent mutations ofBCL6: Implications for disease pathogenesis and histogenesis

43. Patterns of cytokine expression in AIDS‐related non‐Hodgkin's lymphoma

45. Detection ofBCL-6 rearrangements andp53 mutations in malt-lymphomas

48. Genetic lesions associated with blastic transformation of polycythemia vera and essential thrombocythemia

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