373 results on '"Davi, Frédéric"'
Search Results
2. Updates of the ERIC recommendations on how to report the results from immunoglobulin heavy variable gene analysis in chronic lymphocytic leukemia
3. Molecular characterization of Richter syndrome identifies de novo diffuse large B-cell lymphomas with poor prognosis
4. Detecting measurable residual disease beyond 10−4 by an IGHV leader-based NGS approach improves prognostic stratification in CLL
5. EuroClonality-NGS recommendations for evaluation of B cell clonality analysis by next-generation sequencing – a structured approach with the DEPART algorithm
6. Immunoglobulin gene sequence analysis in chronic lymphocytic leukemia: the 2022 update of the recommendations by ERIC, the European Research Initiative on CLL
7. Epstein-Barr Virus and immune status imprint the immunogenomics of non-Hodgkin lymphomas occurring in immune-suppressed environments
8. The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants
9. Validation of the EuroClonality-NGS DNA capture panel as an integrated genomic tool for lymphoproliferative disorders
10. Higher-order connections between stereotyped subsets: implications for improved patient classification in CLL
11. Artificial intelligence classifies and predicts the outcome of primary CNS and nodal large B-cell lymphomas
12. Genetic characterization of B-cell prolymphocytic leukemia: a prognostic model involving MYC and TP53
13. Targeting chronic lymphocytic leukemia with N-methylated thrombospondin-1–derived peptides overcomes drug resistance
14. Primary CNS lymphoma patient-derived orthotopic xenograft model capture the biological and molecular characteristics of the disease
15. Next-generation sequencing of immunoglobulin gene rearrangements for clonality assessment: a technical feasibility study by EuroClonality-NGS
16. Quality control and quantification in IG/TR next-generation sequencing marker identification: protocols and bioinformatic functionalities by EuroClonality-NGS
17. Standardized next-generation sequencing of immunoglobulin and T-cell receptor gene recombinations for MRD marker identification in acute lymphoblastic leukaemia; a EuroClonality-NGS validation study
18. The Mutator Pathway Is a Feature of Immunodeficiency-Related Lymphomas
19. Hepatitis C virus – Associated marginal zone lymphoma
20. ViCloD, an interactive web tool for visualizing B cell repertoires and analyzing intraclonal diversities: application to human B-cell tumors
21. CombiningMYD88 L265Pmutation detection and clonality determination on CSF cellular and cell‐free DNA improves diagnosis of primary CNS lymphoma
22. Exploring the genetic landscape of HCV-related B-cell lymphomas using whole exome sequencing
23. Optimizing therapy for nodal marginal zone lymphoma
24. Whole-exome sequencing in relapsing chronic lymphocytic leukemia: clinical impact of recurrent RPS15 mutations
25. The Broad Spectrum of TP53 Mutations in CLL: Evidence of Multiclonality and Novel Mutation Hotspots
26. Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL
27. Targeted High-throughput Sequencing for Hematological Malignancies: A GBMHM Survey of Practice and Cost Evaluation in France.
28. Molecular Evidence for Antigen Drive in the Natural History of Mantle Cell Lymphoma
29. ViCloD, an interactive web tool for visualizing B cell repertoires and analyzing intraclonal diversities: application to human B-cell tumors
30. Mass cytometry analysis reveals attrition of naïve and anergized self-reactive non-malignant B cells in chronic lymphocytic leukemia patients
31. Splenic Marginal Zone Lymphoma
32. Clinical effect of stereotyped B-cell receptor immunoglobulins in chronic lymphocytic leukaemia: a retrospective multicentre study
33. Studies of Rearrangements and Somatic Hypermutation of IGHV Genes in Chronic Lymphocytic Leukemia
34. A multi-objective based clustering for inferring BCR clonal lineages from high-throughput B cell repertoire data
35. Combining MYD88 L265P mutation detection and clonality determination on CSF cellular and cell‐free DNA improves diagnosis of primary CNS lymphoma.
36. A Comprehensive DNA Methylome Analysis of Stereotyped and Non-Stereotyped CLL Reveals an Epigenetic Signature with Strong Clinical Impact Encompassing IGHV Status, Stereotypes and IGLV3-21R110
37. A Mendelian predisposition to B-cell lymphoma caused by IL-10R deficiency
38. Immunoglobulin gene sequence analysis in chronic lymphocytic leukemia:the 2022 update of the recommendations by ERIC, the European Research Initiative on CLL
39. Therapy-related Myeloid Neoplasms in Patients With Chronic Lymphocytic Leukemia Who Received FCR/FC as Frontline Therapy
40. La maladie de Waldenström ou macroglobulinémie
41. Identification of Prognostic Factors in Post-Transplant Lymphoproliferative Disorders
42. Prevalence of IGLV3-21R110 among familial CLL: a retrospective study of 45 cases
43. TP53 mutations at codon 234 are associated with chlorambucil treatment in chronic lymphocytic leukemia
44. Stereotyped B-cell receptors in one-third of chronic lymphocytic leukemia: a molecular classification with implications for targeted therapies
45. Molecular and clinical diversity in primary central nervous system lymphoma: a LOC Network study
46. Reconstructing the evolutionary history of a B cell lineage with minimum spanning tree and genotype abundances
47. Mast cell density and its clinical relevance in Waldenström's macroglobulinemia
48. Types of lymphomas in transplant and other immunosuppressed patients
49. A unique proteomic profile on surface IgM ligation in unmutated chronic lymphocytic leukemia
50. Autologous stem cell transplantation as a first-line treatment strategy for chronic lymphocytic leukemia: a multicenter, randomized, controlled trial from the SFGM-TC and GFLLC
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