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2. The genomic landscape of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21

3. Genomic landscape of Down syndrome–associated acute lymphoblastic leukemia

4. Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma

5. Molecular basis of ETV6-mediated predisposition to childhood acute lymphoblastic leukemia

6. Germ line genetic NBNvariation and predisposition to B-cell acute lymphoblastic leukemia in children

8. The Influence of Genetic Ancestry on Disease Biology in Pediatric T-Cell Acute Lymphoblastic Leukemia

9. Comprehensive Genome Characterization of Childhood T-ALL Links Oncogene Activation Mechanism and Subtypes to Prognosis

10. Progenitor Sub-Populations in Treatment Resistant T-ALL

11. Rare Deleterious TCF3 Germline Variants and Predisposition to Acute Lymphoblastic Leukemia in Children

12. Integrated Genomic Analysis Identifies UBTF Tandem Duplications As a Subtype-Defining Lesion in Pediatric Acute Myeloid Leukemia

13. Assessment of Outcomes of Consolidation Therapy By Number of Cycles of Blinatumomab Received in Newly Diagnosed Measurable Residual Disease Negative Patients with B-Lineage Acute Lymphoblastic Leukemia: In the ECOG-ACRIN E1910 Randomized Phase III National Clinical Trials Network Trial

16. Molecular classification improves risk assessment in adult BCR-ABL1–negative B-ALL

17. Enhancer Hijacking of BCL11B Defines a Subtype of Lineage Ambiguous Acute Leukemia

19. Regulation of gene expression by miR-144/451 during mouse erythropoiesis

21. Data Access and Interactive Visualization of Whole Genome Sequence of Sickle Cell Patients within the St. Jude Cloud

23. Precision Medicine for Sickle Cell Disease through Whole Genome Sequencing

24. Insulin-like Growth Factor Binding Protein-3 (IGFBP3) Induces Fetal Hemoglobin in Hematopoietic Stem and Progenitor Cells from Patients with Sickle Cell Anemia

26. Comprehensive Functional Characterization of Germline ETV6 Variants Associated with Inherited Predisposition to Acute Lymphoblastic Leukemia in Children

28. Tyrosine kinome sequencing of pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group TARGET Project

29. Expression of an Oncogenic ERG isoform Characterizes a Distinct Subtype of B-Progenitor Acute Lymphoblastic Leukemia

30. Genomic Landscape of Relapsed Acute Lymphoblastic Leukemia

31. Germline Genetic Variation in ETV6 and Predisposition to Childhood Acute Lymphoblastic Leukemia

33. Incidence of Germline Mutations in Cancer-Predisposition Genes in Children with Hematologic Malignancies: a Report from the Pediatric Cancer Genome Project

34. a Proposal for a New Staging System of Extranodal Natural Killer T-cell Lymphoma, Nasal-Type: a Multicenter Study of Chinese Southwest Oncology Group (CSWOG)

36. Comparison Of Mutational Profiles Of Diagnosis and Relapsed Pediatric B-Acute Lymphoblastic Leukemia: A Report From The COG ALL Target Project

37. Discovery of Novel Recurrent Mutations in Childhood Early T-Cell Precursor Acute Lymphoblastic Leukemia by Whole Genome Sequencing - a Report From the St Jude Children's Research Hospital - Washington University Pediatric Cancer Genome Project

38. Whole Genome Sequence Analysis of 22 MLL Rearranged Infant Acute Lymphoblastic Leukemias Reveals Remarkably Few Somatic Mutations: A Report From the St Jude Children‘s Research Hospital - Washington University Pediatric Cancer Genome Project

39. Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group

40. Enhancer Hijacking of BCL11BDefines a Subtype of Lineage Ambiguous Acute Leukemia

42. Comprehensive Functional Characterization of Germline ETV6Variants Associated with Inherited Predisposition to Acute Lymphoblastic Leukemia in Children

43. Germline Genetic Variation in ETV6and Predisposition to Childhood Acute Lymphoblastic Leukemia

44. Expression of an Oncogenic ERGisoform Characterizes a Distinct Subtype of B-Progenitor Acute Lymphoblastic Leukemia

45. Whole Genome Sequence Analysis of 22 MLLRearranged Infant Acute Lymphoblastic Leukemias Reveals Remarkably Few Somatic Mutations: A Report From the St Jude Children‘s Research Hospital - Washington University Pediatric Cancer Genome Project

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