47 results on '"Broccardo, Cyril"'
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2. GATA2 mutated allele specific expression is associated with a hyporesponsive state of HSC in GATA2 deficiency syndrome.
3. The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11
4. PAX5-ELN oncoprotein promotes multistep B-cell acute lymphoblastic leukemia in mice
5. LOSS OF HSC STEMNESS IDENTITY IS ASSOCIATED WITH EXHAUSTION AND HYPORESPONSIVENESS IN GATA2 DEFICIENCY SYNDROME
6. Stem cell–like reprogramming is required for leukemia-initiating activity in B-ALL
7. High Density Lipoprotein Deficiency and Foam Cell Accumulation in Mice with Targeted Disruption of ATP-Binding Cassette Transporter-1
8. Human ATP-Binding Cassette Transporter 1 (ABC1): Genomic Organization and Identification of the Genetic Defect in the Original Tangier Disease Kindred
9. OC 21 - LOSS OF HSC STEMNESS IDENTITY IS ASSOCIATED WITH EXHAUSTION AND HYPORESPONSIVENESS IN GATA2 DEFICIENCY SYNDROME
10. From normal hematopoiesis to malignancies: Highlights from the 2021 Meeting of the Club Hematopoiesis and Oncogenesis
11. Retroviral transduction of lineage antigen-negative (Lin−) cells: A valuable alternative for the generation of T cell receptor (TCR) retrogenic mice
12. Deletion of the Scl +19 enhancer increases the blood stem cell compartment without affecting the formation of mature blood lineages
13. CELL QUIESCENCE AND REPROGRAMMING ARE DISTINCTIVE FEATURES OF PRE- LEUKEMIC STEM CELLS IN BACUTE LYMPHOBLASTIC LEUKEMIA
14. Wide diversity of PAX5 alterations in B-ALL: a Groupe Francophone de Cytogénétique Hématologique study
15. 3084 – CELL QUIESCENCE AND REPROGRAMMING ARE DISTINCTIVE FEATURES OF PRE-LEUKEMIC STEM CELLS IN B-ACUTE LYMPHOBLASTIC LEUKEMIA
16. Germline PAX5 mutation predisposes to familial B-cell precursor acute lymphoblastic leukemia
17. New Approach to Decipher GATA2 Deficiency Syndrome: Focus on the Recurrent GATA2 R396Q Mutation
18. Germline PAX5 mutation predisposes to familial B acute lymphoblastic leukemia
19. A novel PAX5-ELN fusion protein identified in B-cell acute lymphoblastic leukemia acts as a dominant negative on wild-type PAX5
20. Identification of novel, clonally stable, somatic mutations targeting transcription factors PAX5 and NKX2-3, the epigenetic regulator LRIF1, and BRAF in a case of atypical B-cell chronic lymphocytic leukemia harboring a t(14;18)(q32;q21)
21. ABCA2 is a marker of neural progenitors and neuronal subsets in the adult rodent brain
22. The CADM1tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11
23. PAX5AandPAX5Bisoforms are both efficient to drive B cell differentiation
24. The ABCA subclass of mammalian transporters
25. Germline PAX5mutation predisposes to familial B-cell precursor acute lymphoblastic leukemia
26. Homeobox NKX2-3 promotes marginal-zone lymphomagenesis by activating B-cell receptor signalling and shaping lymphocyte dynamics
27. Stem cell–like reprogramming is required for leukemia-initiating activity in B-ALL
28. Identification of a transforming MYB-GATA1 fusion gene in acute basophilic leukemia: a new entity in male infants
29. GATA2, a new oncogene of sporadic and familial acute myeloid leukemias
30. Wide diversity of PAX5 alterations in B-ALL: a Groupe Francophone de Cytogenetique Hematologique study
31. PAX5 mutations occur frequently in adult B-Cell acute lymphoblastic leukemia (B-ALL) and is significantly associated with BCR-ABL1 fusion gene
32. The scl +18/19 Stem Cell Enhancer Is Not Required for Hematopoiesis: Identification of a 5' Bifunctional Hematopoietic-Endothelial Enhancer Bound by Fli-1 and Elf-1
33. Homeobox NKX2-3 Is Over-Expressed in Human B-Cell Lymphomas and Drives Marginal Zone B-Cell Lymphomagenesis in Mice
34. ATP-binding cassette transporter hallmarks tissue macrophages and modulates cytokine-triggered polarization programs
35. PAX5 Mutations Occur Frequently in Adult B-Cell Acute Lymphoblastic Leukemia (B-ALL) and Is Significantly Associated with BCR-ABL1 Fusion Gene.
36. A novel PAX5-ELN fusion protein identified in B-cell acute lymphoblastic leukemia acts as a dominant negative on wild-type PAX5
37. The scl +18/19 Stem Cell Enhancer Is Not Required for Hematopoiesis: Identification of a 5′ Bifunctional Hematopoietic-Endothelial Enhancer Bound by Fli-1 and Elf-1
38. ABC1 promotes engulfment of apoptotic cells and transbilayer redistribution of phosphatidylserine.
39. Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice
40. Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)
41. Identification of a transforming MYB-GATA1fusion gene in acute basophilic leukemia: a new entity in male infants
42. Wide diversity of PAX5alterations in B-ALL: a Groupe Francophone de Cytogénétique Hématologique study
43. New Approach to Decipher GATA2 Deficiency Syndrome: Focus on the Recurrent GATA2R396Q Mutation
44. The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11
45. The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11
46. Identification of novel, clonally stable, somatic mutations targeting transcription factors PAX5 and NKX2-3, the epigenetic regulator LRIF1, and BRAF in a case of atypical B-cell chronic lymphocytic leukemia harboring a t(14;18)(q32;q21).
47. PAX5A and PAX5B isoforms are both efficient to drive B cell differentiation.
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