483 results on '"Skokowa, Julia"'
Search Results
2. CD19-immunoPET for noninvasive visualization of CD19 expression in B-cell lymphoma patients
3. Functionally-instructed modifiers of response to ATR inhibition in experimental glioma
4. A JAGN1-associated severe congenital neutropenia zebrafish model revealed an altered G-CSFR signaling and UPR activation
5. Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients
6. Correction: NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells
7. The design of functional proteins using tensorized energy calculations
8. A topological refactoring design strategy yields highly stable granulopoietic proteins
9. Case report: Granulocyte-macrophage colony-stimulating factor sargramostim did not rescue the neutrophil phenotype in two patients with JAGN1-mutant severe congenital neutropenia.
10. SRP54 mutations induce congenital neutropenia via dominant-negative effects on XBP1 splicing
11. NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells
12. LMO2 activation by deacetylation is indispensable for hematopoiesis and T-ALL leukemogenesis
13. Human iPSC-based model of severe congenital neutropenia reveals elevated UPR and DNA damage in CD34+ cells preceding leukemic transformation
14. P779: LONG-TERM COURSE OF HAX1-RELATED CONGENITAL NEUTROPENIA: AN ANALYSIS OF THE EUROPEAN SEVERE CHRONIC NEUTROPENIA INTERNATIONAL REGISTRY (SCNIR)
15. P780: G-CSF THERAPY IN EUROPEAN PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME
16. S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION
17. P751: UNRAVELING THE DIFFERENT PATHOMECHANISMS OF CONGENITAL AND CYCLIC NEUTROPENIAS: CYCLIC EXPRESSION OF HEMATOPOIETIC STEM-CELL-SPECIFIC TRANSCRIPTION FACTORS IN CYCLIC NEUTROPENIA
18. P1357: MILESTONE (MODIFYING ELANE GOLDBERG–HOGNES BOX TO INHIBIT EXPRESSION), A UNIVERSAL, SAFE AND EFFECTIVE CRISPR/CAS9N-MEDIATED GENOME EDITING STRATEGY FOR ELANE RELATED SEVERE CONGENITAL NEUTROPENIA
19. P458: HIPSC DISEASE MODELING TO STUDY LEUKEMIA DEVELOPMENT IN HAX1 VS ELANE ASSOCIATED CONGENITAL NEUTROPENIA
20. PB1703: MODELING T-CELL DEVELOPMENT AND T-ALL INITIATION
21. The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action
22. The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children:A Consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action
23. HAX1-related congenital neutropenia: Long-term observation in paediatric and adult patients enrolled in the European branch of the Severe Chronic Neutropenia International Registry (SCNIR)
24. Differential Expression of C/Ebpa and Its Stem Cell-Specific Targets in Congenital Neutropenias and Cyclic Neutropenias
25. Accumulation of Specific Somatic Leukemia-Associated Mutations in Congenital Neutropenia Precedes Malignant Transformation - New Preconditions for Treatment Decisions
26. Corrigendum to ‘Human iPSC-based model of severe congenital neutropenia reveals elevated UPR and DNA damage in CD34+ cells preceding leukemic transformation’ <[Experimental Hematology, Volume 71, 2019;71:51−60]>
27. Regenerative medicine meets translational oncology: Modeling leukemic bone marrow niche
28. Bortezomib inhibits STAT5-dependent degradation of LEF-1, inducing granulocytic differentiation in congenital neutropenia CD34+ cells
29. Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis
30. A lack of secretory leukocyte protease inhibitor (SLPI) causes defects in granulocytic differentiation
31. Generation, expansion, and drug treatment of hematopoietic progenitor cells derived from human iPSCs
32. Development of a First-in-Class Small-Molecule Inhibitor of the C-Terminal Hsp90 Dimerization
33. CLPB in neutropenia: 1 gene with many faces
34. Old drug revisited: disulfiram, NETs, and sepsis
35. miR-155 Is Associated with the Leukemogenic Potential of the Class IV Granulocyte Colony-Stimulating Factor Receptor in CD34+ Progenitor Cells
36. Neutrophil elastase is severely down-regulated in severe congenital neutropenia independent of ELA2 or HAX1 mutations but dependent on LEF-1
37. iPSC modeling of stage-specific leukemogenesis reveals BAALC as a key oncogene in severe congenital neutropenia
38. Additional file 1 of NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells
39. Additional file 3 of NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells
40. Interactions among HCLS1, HAX1 and LEF-1 proteins are essential for G-CSF triggered granulopoiesis
41. NAMPT is essential for the G-CSF-induced myeloid differentiation via a [NAD.sup.+]-sirtuin-1--dependent pathway
42. SRP54mutations induce congenital neutropenia via dominant-negative effects onXBP1splicing
43. LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia
44. Design of novel granulopoietic proteins by topological rescaffolding
45. Efficient Correction of HAX1 Mutations in Primary HSPCs of Severe Congenital Neutropenia Patients Using CRISPR/CAS9 GENE-Editing
46. A Zebrafish Model for Severe Congenital Neutropenia with Jagn1b-Deficiency
47. Transcriptome Analysis of Severe Congenital Neutropenia Associated Leukemia with Different Types of RUNX1 Mutations in an iPSC-Based Model
48. De Novo Design of Granulopoietic Proteins
49. Nicotinamide (NA) Treatment Improves Response to G-CSF in Severe Congenital Neutropenia (SCN) Patients
50. Congenital and Acquired Chronic Neutropenias: Challenges, Perspectives and Implementation of the EuNet-INNOCHRON Action
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