Search

Your search keyword '"Broccardo, Cyril"' showing total 47 results

Search Constraints

Start Over You searched for: Author "Broccardo, Cyril" Remove constraint Author: "Broccardo, Cyril"
47 results on '"Broccardo, Cyril"'

Search Results

1. Niche-expressed Galectin-1 is involved in pre-B acute lymphoblastic leukemia relapse through pre-B cell receptor activation

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

8. Human ATP-Binding Cassette Transporter 1 (ABC1): Genomic Organization and Identification of the Genetic Defect in the Original Tangier Disease Kindred

10. From normal hematopoiesis to malignancies: Highlights from the 2021 Meeting of the Club Hematopoiesis and Oncogenesis

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

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)

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

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

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

35. PAX5 Mutations Occur Frequently in Adult B-Cell Acute Lymphoblastic Leukemia (B-ALL) and Is Significantly Associated with BCR-ABL1 Fusion Gene.

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

39. Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice

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.

Catalog

Books, media, physical & digital resources