433 results on '"Seo, Eul-Ju"'
Search Results
2. P-434 A patient with CD20-positive small cell variant plasma cell myeloma misdiagnosed as lymphoplasmacytic lymphoma
3. P404: IMMUNOGLOBULIN GENE REARRANGEMENT IN KOREAN PATIENTS WITH B-LYMPHOBLASTIC LEUKEMIA – AN IMMUNOPHENOTYPE AND REPERTOIRE ANALYSIS
4. Clinical characteristics and disease progression of retinitis pigmentosa associated with PDE6B mutations in Korean patients
5. Prognostic significance of recurrent additional chromosomal abnormalities in adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia
6. Data from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
7. Supplementary Figure Legends 1-5 from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
8. Supplementary Table 1 from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
9. Supplementary Figure 3 from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
10. Supplementary Table 2 from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
11. Supplementary Methods and Materials from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
12. Supplementary Figure 4 from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
13. Supplementary Figure 1 from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
14. Supplementary Table 3 from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
15. Supplementary Figure 5 from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
16. Supplementary Figure 2 from Mammalian Sterile 20–like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation
17. Novel Compound Heterozygote Mutation in IL10RA in a Patient With Very Early-Onset Inflammatory Bowel Disease
18. A Patient With CD20-positive T-cell Lymphoma Concurrently Exhibiting B-cell Neoplasm-related Genetic Abnormalities Shows Clonal Escape Post CD20-targeting Treatment
19. Emergence of a BCR::ABL1 rearrangement following a uniquely complex clonal evolution pattern in a patient undergoing Fms‐like tyrosine kinase 3 inhibitor therapy for acute myeloid leukemia
20. High CXCR4 and low VLA-4 expression predicts poor survival in adults with acute lymphoblastic leukemia
21. Patient-derived multicellular tumor spheroids towards optimized treatment for patients with hepatocellular carcinoma
22. Clinical implications and genetic features of clonal cytopenia of undetermined significance compared to lower‐risk myelodysplastic syndrome
23. Emergence of a BCR::ABL1 rearrangement following a uniquely complex clonal evolution pattern in a patient undergoing Fms‐like tyrosine kinase 3 inhibitor therapy for acute myeloid leukemia.
24. VLA-4 and CXCR4 expression levels show contrasting prognostic impact (favorable and unfavorable, respectively) in acute myeloid leukemia
25. Monosomal karyotype in acute myeloid leukemia and the role of allogeneic hematopoietic cell transplantation
26. Rare Case of Accelerated-Phase Chronic Myeloid Leukemia Diagnosed During Treatment for JAK2 V617F–Positive Primary Myelofibrosis
27. Comparison of clinical and laboratory characteristics of nonsecretory multiple myeloma and secretory multiple myeloma in a tertiary care hospital
28. Response to “Familial Intracranial Aneurysm Requires Not Only Whole-Exome Sequencing, But Also Mitochondrial DNA Sequencing”
29. Whole Exome Sequencing in Patients with Phenotypically Associated Familial Intracranial Aneurysm
30. Genetic Profile and Associated Characteristics of 150 Korean Patients with Retinitis Pigmentosa
31. Bone Marrow Findings in Patients With Ewing Sarcoma/Primitive Neuroectodermal Tumor
32. A case of ALK negative anaplastic large cell lymphoma with leukaemic manifestation, transformed from CD4 positive T-cell large granular lymphocytic leukaemia
33. Clinical significance of GSTM1 and GSTT1 polymorphisms in younger patients with acute myeloid leukemia of intermediate-risk cytogenetics
34. T-cell Large Granular Lymphocytic Leukemia Presenting as Post-transplant Lymphoproliferative Disorder: A Report of Two Cases and Literature Review
35. Immune Checkpoint Programmed Cell Death Protein-1 (PD-1) Expression on Bone Marrow T Cell Subsets in Patients With Plasma Cell Myeloma
36. An illustrative case of t(14;19)/BCL3 rearrangement as a karyotypic evolution of chronic lymphocytic leukemia
37. Cytogenetic classification in Korean multiple myeloma patients: prognostic significance of hyperdiploidy with 47–50 chromosomes and the number of structural abnormalities
38. Comparison of clinicopathologic findings according to JAK2 V617F mutation in patients with essential thrombocythemia
39. The CCR5 (−2135C/T) Polymorphism may be Associated with the Development of Kawasaki Disease in Korean Children
40. Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort
41. Revised World Health Organization Criteria-Defined Acute Myeloid Leukemia in a Large Cohort: Highlighting the Frequency and Characterization of Recategorized Cases
42. Unique ethnic features of DDX41 mutations in patients with idiopathic cytopenia of undetermined significance, myelodysplastic syndrome, or acute myeloid leukemia
43. Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: A Korean multicenter study
44. Interpretation of XIAP Variants of Uncertain Significance in Paediatric Patients with Refractory Crohn’s Disease
45. Rare Neurovascular Diseases in Korea: Classification and Related Genetic Variants
46. Double-hit myeloma with IGH/MYC and IGH/CCND1 translocations
47. THE PRACTICAL UTILITY OF RISK STRATIFICATION WITH A USE OF MOLECULAR TESTING IN PATIENTS WITH ACUTE LEUKEMIA: 401
48. Identification of 13q deletion, trisomy 1q, and IgH rearrangement as the most frequent chromosomal changes found in Korean patients with multiple myeloma
49. Identification of the mechanism underlying a human chimera by SNP array analysis
50. A Combination of CD15/CD10, CD64/CD33, CD16/CD13 or CD11b Flow Cytometric Granulocyte Panels is Sensitive and Specific for Diagnosis of Myelodysplastic Syndrome
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