377 results on '"El Nemer, Wassim"'
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2. Combination of lentiviral and genome editing technologies for the treatment of sickle cell disease
3. Base-editing-mediated dissection of a γ-globin cis-regulatory element for the therapeutic reactivation of fetal hemoglobin expression
4. Long-term outcomes of lentiviral gene therapy for the β-hemoglobinopathies: the HGB-205 trial
5. Plasma microparticles of sickle patients during crisis or taking hydroxyurea modify endothelium inflammatory properties
6. Translatable tool to quantitatively assess the quality of red blood cell units and tailored cultured red blood cells for transfusion
7. Dimerization and phosphorylation of Lutheran/basal cell adhesion molecule are critical for its function in cell migration on laminin
8. Reticulocyte and red blood cell deformation triggers specific phosphorylation events
9. Insights into determinants of spleen injury in sickle cell anemia
10. Red Blood Cell Contribution to Thrombosis in Polycythemia Vera and Essential Thrombocythemia
11. Resolution of sickle cell disease–associated inflammation and tissue damage with 17R-resolvin D1
12. Le panorama du Paléolithique supérieur vu par les groupes sanguins
13. Absolute proteome quantification of highly purified populations of circulating reticulocytes and mature erythrocytes
14. An Optimized Lentiviral Vector Efficiently Corrects the Human Sickle Cell Disease Phenotype
15. Induction of fetal hemoglobin synthesis by CRISPR/Cas9-mediated editing of the human β-globin locus
16. L26-3 Mimer la niche érythroïde avec un modèle 3D multicellulaire
17. P-227 ERMAP dans l[StQuote]érythropoïèse humaine
18. L26-2 Génération d’un modèle 3D fonctionnel mimant la niche hématopoïétique médullaire
19. Age-related morphofunctional changes in sickle cell mice bone marrow mesenchymal stromal cells
20. Characterization of red blood cell microcirculatory parameters using a bioimpedance microfluidic device
21. Erythroid Adhesion Molecules in Sickle Cell Anaemia Infants: Insights Into Early Pathophysiology
22. In Humanized Sickle Cell Mice, Imatinib Protects Against Sickle Cell–Related Injury
23. Relevance of Howell‐Jolly body counts for measuring spleen function in sickle cell disease
24. Red blood cell proteomics reveal remnant protein biosynthesis and folding pathways in PIEZO1-related hereditary xerocytosis
25. Hydroxycarbamide Decreases Sickle Reticulocyte Adhesion to Resting Endothelium by Inhibiting Endothelial Lutheran/Basal Cell Adhesion Molecule (Lu/BCAM) through Phosphodiesterase 4A Activation
26. Supplement to: Gene thereapy in a patient with sickle cell disease.
27. A Functional in Vitro 3D Model of Human Hematopoietic Niches
28. JAK2V617F activates Lu/BCAM-mediated red cell adhesion in polycythemia vera through an EpoR-independent Rap1/Akt pathway
29. Gene Therapy in a Patient with Sickle Cell Disease: Brief Report
30. Precision Medicine and Sickle Cell Disease
31. An inherited gain‐of‐function risk allele in EPOR predisposes to familial JAK2 V617F myeloproliferative neoplasms
32. Bioimpedance single cell sensing of low and high density sickle erythrocytes using microfluidics
33. Activation State of α4β1 Integrin on Sickle Red Blood Cells Is Linked to the Duffy Antigen Receptor for Chemokines (DARC) Expression
34. An inherited gain‐of‐function risk allele in EPOR predisposes to familial JAK2V617F myeloproliferative neoplasms
35. Applying successive mechanical stresses on circulating cells using microfluidic vascular network to assess sickled red blood cells rigidity
36. Effects of Poloxamer 188 on red blood cell membrane properties in sickle cell anaemia
37. Decreased sickle red blood cell adhesion to laminin by hydroxyurea is associated with inhibition of Lu/BCAM protein phosphorylation
38. Spherocytes flow behaviours in microrestriction, compared by normal red blood cells of different heat treatment levels
39. Altered Ca2+ Homeostasis in Red Blood Cells of Polycythemia Vera Patients Following Disturbed Organelle Sorting during Terminal Erythropoiesis
40. Lu/BCAM-mediated cell adhesion as biological marker of JAK2V617F activity in erythrocytes of polycythemia vera patients
41. A biomimetic microfluidic chip to study the circulation and mechanical retention of red blood cells in the spleen
42. Revisiting Spleen Function and Pneumococcal Risk in Children with Hemoglobin SC Disease
43. Clinical Results of the Drepaglobe Trial for Sickle Cell Disease Patients
44. Base Editing-Mediated Dissection of the -200 Region of the γ-Globin Promoters to Induce Fetal Hemoglobin and Rescue Sickle Cell Disease and β-Thalassemia
45. Dysérythropoïèse dans la drépanocytose : une contribution d’origine centrale à l’anémie ?
46. Rapid change in red cell blood group systems after the main Out of Africa of Homo sapiens
47. Lysophosphatidic acid-activated calcium signaling is elevated in red cells from sickle cell disease patients
48. Different miniaturization systems of electrical biosensing and data acquisition during biological cell transiting within vessel size microchannel
49. Genetic inactivation of the laminin [[alpha].sub.5] chain receptor Lu/BCAM leads to kidney and intestinal abnormalities in the mouse
50. Ineffective Erythropoiesis Negatively Impacts the Erythroblastic Island in Sickle Cell Disease
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