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3. PD-1H/VISTA mediates immune evasion in acute myeloid leukemia

4. LAIR-1 agonism as a therapy for acute myeloid leukemia

6. Clinical, immunophenotypic and genomic findings of NK lymphoblastic leukemia: a study from the Bone Marrow Pathology Group

7. Cell-programmed nutrient partitioning in the tumour microenvironment

9. PD-1H/VISTA mediates immune evasion in acute myeloid leukemia

15. Supplementary File 1 from PI3K Inhibition Restores and Amplifies Response to Ruxolitinib in Patients with Myelofibrosis

16. Data from PI3K Inhibition Restores and Amplifies Response to Ruxolitinib in Patients with Myelofibrosis

17. PI3K Inhibition Restores and Amplifies Response to Ruxolitinib in patients with Myelofibrosis

21. Contributing Authors

23. Extranodal Marginal Zone Lymphomas Show Recurrent Mutations in DNA Repair Genes, Cancer-Associated Proliferative Signaling and NOTCH1 Signaling Pathways, Regardless of Anatomic Site

24. TP53 Mutations Are Associated with Increased Infections and Reduced Hematopoietic Cell Transplantation Rates in Myelodysplastic Syndrome and Acute Myeloid Leukemia

25. Secondary‐type mutations do not impact prognosis in acute myelogenous leukemia AML with mutated NPM1

28. Myeloid sarcoma with NPM1 mutation may be clinically and genetically distinct from AML with NPM1 mutation: a study from the Bone Marrow Pathology Group.

31. Impact of Molecular Features of Diffuse Large B-Cell Lymphoma on Treatment Outcomes with Anti-CD19 Chimeric Antigen Receptor (CAR) T-Cell Therapy

40. Chronic myeloid leukemia with pure erythroid leukemia blast crisis.

42. Whole Exome and Transcriptome Sequencing in 1042 Cases Reveals Distinct Clinically Relevant Genetic Subgroups of Follicular Lymphoma

44. Bone Marrow Morphologic Findings in Patients Receiving IDH Inhibitor Therapy in Combination with Intensive Induction Chemotherapy: Challenges with Interpretation of the Day 14 Bone Marrow Biopsy

47. Clinicopathologic and genetic characterization of nonacute NPM1-mutated myeloid neoplasms

48. 52. A rare (7;12) translocation resulting in a rearrangement of the IKZF1 locus with concurrent deletion of CDKN2A, CDKN2B and PAX5 loci: an unannotated genetic abnormality in pediatric B-lymphoblastic leukemia/lymphoma

49. Case 3: Priapism in a 13-year-old Boy

50. Hematopoietic Neoplasms of the Sinonasal Tract

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