42 results on '"Zachariadis, Vasilios"'
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2. Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
3. Stem cell-derived brainstem mouse astrocytes obtain a neurotoxic phenotype in vitro upon neuroinflammation
4. A somatic UBA2 variant preceded ETV6-RUNX1 in the concordant BCP-ALL of monozygotic twins
5. Predisposition to childhood acute lymphoblastic leukemia caused by a constitutional translocation disrupting ETV6
6. Silencing of CEBPB-AS1 modulates CEBPB expression and resensitizes BRAF-inhibitor resistant melanoma cells to vemurafenib
7. Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
8. Mesenchymal stem cells transplanted into spinal cord injury adopt immune cell-like characteristics
9. Metabolic reprogramming of acute lymphoblastic leukemia cells in response to glucocorticoid treatment
10. Whole‐Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation
11. The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013
12. Spinal Cord Injury Induces Permanent Reprogramming of Microglia into a Disease-Associated State Which Contributes to Functional Recovery
13. Homozygous deletions of CDKN2A are present in all dic(9;20)(p13·2;q11·2)-positive B-cell precursor acute lymphoblastic leukaemias and may be important for leukaemic transformation
14. A Highly Scalable Method for Joint Whole-Genome Sequencing and Gene-Expression Profiling of Single Cells
15. Direct nuclear tagmentation and RNA-sequencing (DNTR-seq) v1
16. Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth
17. Microdeletion of 7p12.1p13, including IKZF1, causes intellectual impairment, overgrowth, and susceptibility to leukaemia
18. A somatic UBA2variant preceded ETV6-RUNX1in the concordant BCP-ALL of monozygotic twins
19. Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia
20. Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth
21. Syngeneic, in contrast to allogeneic, mesenchymal stem cells have superior therapeutic potential following spinal cord injury
22. Somatic Structural Alterations in Childhood Leukemia Can Be Backtracked in Neonatal Dried Blood Spots by Use of Whole-Genome Sequencing and Digital PCR
23. High-resolution detection of chromosomal rearrangements in leukemias through mate pair whole genome sequencing
24. Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia.
25. Microdeletion of 7p12.1p13, including IKZF 1 , causes intellectual impairment, overgrowth, and susceptibility to leukaemia
26. High-resolution detection of chromosomal rearrangements in leukemias through mate pair whole genome sequencing
27. Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation
28. PAX5-ESRRB is a recurrent fusion gene in B-cell precursor pediatric acute lymphoblastic leukemia
29. Transcription-coupled genetic instability marks acute lymphoblastic leukemia structural variation hotspots
30. Author response: Transcription-coupled genetic instability marks acute lymphoblastic leukemia structural variation hotspots
31. Detailed gene dose analysis reveals recurrent focal gene deletions in pediatric B-cell precursor acute lymphoblastic leukemia
32. De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations
33. DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia
34. DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia
35. DNA Methylation-Based Subtype Prediction for Pediatric Acute Lymphoblastic Leukemia (ALL)
36. Novel Focal Gene Deletions in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia Detected By Array Comparative Genomic Hybridization
37. DNA Methylation-Based Subtype Prediction for Pediatric Acute Lymphoblastic Leukemia (ALL)
38. Homozygous deletions ofCDKN2Aare present in all dic(9;20)(p13·2;q11·2)-positive B-cell precursor acute lymphoblastic leukaemias and may be important for leukaemic transformation
39. Silencing of CEBPB-AS1 modulates CEBPB expression and resensitizes BRAF-inhibitor resistant melanoma cells to vemurafenib
40. Microdeletion of 7p12.1p13, including IKZF1, causes intellectual impairment, overgrowth, and susceptibility to leukaemia.
41. PAX5-ESRRB is a recurrent fusion gene in B-cell precursor pediatric acute lymphoblastic leukemia.
42. Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells.
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