50 results on '"Guinta, Kathryn"'
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2. Microbiomic profiles of bile in patients with benign and malignant pancreaticobiliary disease
3. Patterns of missplicing due to somatic U2AF1 mutations in myeloid neoplasms
4. STAT3 mutations unify the pathogenesis of chronic lymphoproliferative disorders of NK cells and T-cell large granular lymphocyte leukemia
5. Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
6. Somatic STAT3 Mutations in Large Granular Lymphocytic Leukemia
7. Microbiomic profiles of bile in patients with benign and malignant pancreaticobiliary disease.
8. Cytogenetic and molecular predictors of response in patients with myeloid malignancies without del[5q] treated with lenalidomide
9. Integrated Analysis of Copy-Number Alterations and Gene Mutations in 2,000 Patients with Myeloid Neoplasms
10. Microbiome signature of bile from pancreatic and biliary tract cancer patients: A pilot study.
11. Dynamics of clonal evolution in myelodysplastic syndromes
12. the Impact of Clonal Dynamics on Prognosis and Outcome in Myelodysplastic Syndromes
13. NGS-Based Copy Number Analysis in 1,185 Patients with Myeloid Neoplasms
14. Serial Sequencing in Myelodysplastic Syndromes Reveals Dynamic Changes in Clonal Architecture and Allows for a New Prognostic Assessment of Mutations Detected in Cross-Sectional Testing
15. In Analogy to AML, MDS Can be Sub-Classified By Ancestral Mutations
16. Germline Events In GFI1 In Myelodysplastic Syndrome
17. Clinical “MUTATOME” Of Myelodysplastic Syndrome; Comparison To Primary Acute Myelogenous Leukemia
18. Clinical and Molecular Features Of Young Patients With Myelodisplastic Syndromes (MDS)
19. Molecular Defects In BRCC3 Complex, a Novel Pathogenic Pathway In MDS
20. Single nucleotide polymorphism array karyotyping: A diagnostic and prognostic tool in myelodysplastic syndromes with unsuccessful conventional cytogenetic testing
21. Somatic SETBP1 mutations in myeloid malignancies
22. Various Germline Congenital Disorder Genes Are Somatically Mutated in Myeloid Malignancies
23. Somatic Mutations in Schinzel-Giedion Syndrome Gene SETBP1 Determine Progression in Myeloid Malignancies
24. Mutational Spectrum of Myelodysplastic Syndrome Malignancies Revealed by Whole Exome Sequencing
25. Molecular Diversity Detected by Whole Exome Sequencing in Chronic Myelomonocytic Leukemia
26. Novel Recurrent Mutations in the Ras-Like GTP-Binding Gene Rit1 in Myeloid Malignancies
27. SomaticSTAT3Mutations in Large Granular Lymphocytic Leukemia
28. The Impact of Molecular Lesions in Post-Transplant Acute Myeloid Leukemia (AML) in Correlation with Cytogenetic Abnormalities,
29. Spliceosome GENE MUTATIONS ARE Also PRESENT In the Diverse Mutational Spectrum of CHRONIC Myelomonocytic LEUKEMIA
30. Association of SF3B1 with Ring Sideroblasts in patients, In Vivo, and In Vitro models of Spliceosomal Dysfunction
31. Pathogenesis of MONOSOMY 7 In BONE MARROW FAILURE SYNDROMES
32. Distinction of Early and Late Molecular Events In Patients with Myelodysplastic Syndromes (MDS) Who Progressed to Acute Myeloid Leukemia (AML),
33. Mass Screening for Non-Synonymous SNPs Using Custom Cancer Microarrays Directly Reveals Possible Pathogenic Predisposition Factors in AA
34. Acquired Molecular Defects in Spliceosome Machinery: Novel Pathogenetic Pathways in Myeloid Leukemogenesis
35. *401 Distribution and Significance of EZH2 Mutations in MDS and Related Myeloid Malignancies
36. Cytogenetic Predictors of Response to Lenalidomide In Myeloid Malignancies without Del(5q)
37. New TET2, ASXL1 and CBL Mutations Have Poor Prognostic Impact In Systemic Mastocytosis and Related Disorders
38. SNP-A Karyotyping Provides Clinically Relevant Results In Myeloid Hematologic Disorders with Unsuccessful Routine Cytogenetic Testing.
39. Next Generation Exome Sequencing for Identification of the Gene Mutations Associated with Loss of Heterozygozity on Chromosome 7 In Myeloid Malignancies
40. Identification of Oncogenic EZH2 Mutations In Myelodysplastic Syndromes and Related Myeloid Malignancies
41. Predisposition to Myelodysplastic Syndrome with Deletion 5q Is Associated with TP53 Codon 72 Genotype
42. Dynamics of clonal evolution in myelodysplastic syndromes
43. Somatic Mutational Screen For Improved Prediction Of The Outcomes Of Epigenetic Therapy In MDS
44. Somatic Mutations in Schinzel-Giedion Syndrome Gene SETBP1Determine Progression in Myeloid Malignancies
45. Novel Recurrent Mutations in the Ras-Like GTP-Binding Gene Rit1in Myeloid Malignancies
46. Association of SF3B1with Ring Sideroblasts in patients, In Vivo,and In Vitromodels of Spliceosomal Dysfunction
47. Predisposition to Myelodysplastic Syndrome with Deletion 5q Is Associated with TP53Codon 72 Genotype
48. Identification of Oncogenic EZH2Mutations In Myelodysplastic Syndromes and Related Myeloid Malignancies
49. New TET2, ASXL1and CBLMutations Have Poor Prognostic Impact In Systemic Mastocytosis and Related Disorders
50. Spliceosomal gene mutations are frequent events in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemia.
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