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141 results on '"Pounds, Stanley B."'

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1. The genomic basis of childhood T-lineage acute lymphoblastic leukaemia

3. The St. Jude STEM Clubs: An Afterschool STEM Club for Upper Elementary School Students in Memphis, TN

5. Genome-wide CRISPR/Cas9 screen identifies etoposide response modulators associated with clinical outcomes in pediatric AML

7. Genomic Determinants of Outcome in Acute Lymphoblastic Leukemia.

8. Venetoclax in combination with cytarabine with or without idarubicin in children with relapsed or refractory acute myeloid leukaemia: a phase 1, dose-escalation study

9. Computing Power and Sample Size for the False Discovery Rate in Multiple Applications.

10. Genomic subtyping and therapeutic targeting of acute erythroleukemia

11. H3.3 K27M depletion increases differentiation and extends latency of diffuse intrinsic pontine glioma growth in vivo

12. Forty-five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor

13. Clinical characteristics and outcomes of children with newly diagnosed acute myeloid leukemia and hyperleukocytosis managed with different cytoreductive methods.

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

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

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

17. Correction to: H3.3 K27M depletion increases differentiation and extends latency of diffuse intrinsic pontine glioma growth in vivo

18. Genomic Analysis Reveals Few Genetic Alterations in Pediatrie Acute Myeloid Leukemia

21. Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia

22. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

23. The genetic basis of early T-cell precursor acute lymphoblastic leukaemia

25. Cross-species genomics matches driver mutations and cell compartments to model ependymoma

32. A Transcriptional Classifier Identifies Pediatric T-Cell Acute Lymphoblastic Leukemias at High Risk for End of Induction Minimal Residual Disease

33. Single-Cell Pan-Cancer Analysis Reveals Treatment Resistance Stem/Progenitor-like Subpopulation in the High-Risk Pediatric Leukemia

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

38. DNA Methylation‐Based Epigenetic Repression of SLC22A4 Promotes Resistance to Cytarabine in Acute Myeloid Leukemia.

39. SVSI: Fast and Powerful Set-Valued System Identification Approach to Identifying Rare Variants in Sequencing Studies for Ordered Categorical Traits: SVSIfor Genetic Association Studies

40. DNA Methylation Profiling Reveals Prognostically Significant Groups in Pediatric Adrenocortical Tumors: A Report From the International Pediatric Adrenocortical Tumor Registry.

41. Uncovering the Genomic Landscape in Newly Diagnosed and Relapsed Pediatric Cytogenetically Normal FLT3‐ITD AML.

42. Identification of Clinical and Biologic Correlates Associated With Outcome in Children With Adrenocortical Tumors Without Germline TP53 Mutations: A St Jude Adrenocortical Tumor Registry and Children's Oncology Group Study.

43. Genomic determinants of outcome in acute lymphoblastic leukemia: A Children's Oncology Group study.

44. Contribution of the TP53 R337H mutation to the cancer burden in southern Brazil: Insights from the study of 55 families of children with adrenocortical tumors.

46. Transcriptome profiling of patient derived xenograft models established from pediatric acute myeloid leukemia patients confirm maintenance of FLT3-ITD mutation.

47. CC-PROMISE effectively integrates two forms of molecular data with multiple biologically related endpoints.

49. Empirical Bayesian Selection of Hypothesis Testing Procedures for Analysis of Sequence Count Expression Data.

50. Estimation and control of multiple testing error rates for microarray studies.

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