49 results on '"Beuzard Y"'
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2. Mouse models of sickle cell disease
3. Improvement of mouse β-thalassemia upon erythropoietin delivery by encapsulated myoblasts
4. The Effect of Hemoglobin A and S on the Volume- and pH-Dependence of K-Cl Cotransport in Human Erythrocyte Ghosts
5. Continuous delivery of human and mouse erythropoietin in mice by genetically engineered polymer encapsulated myoblasts
6. Gène de l’érythropoïétine : régulation et intérêt thérapeutique
7. Effect of mutated TP53 on response of advanced breast cancers to high-dose chemotherapy
8. Modification of the Electronic Structure of Ferrous Iron in Hemoglobin by Ligandation and by Alterations of the Protein Structure Inferred from Mössbauer Measurements.
9. Genetic regulation of γ gene expression: Study of the interaction of β-thalassemia with heterocellular HPFH
10. Early diagnosis of renal function recovery by cystatin C in renal allograft recipients
11. Decrease in lung nitric oxide production after peritonitis in mice with sickle cell disease.
12. Oxygen tension and a pharmacological switch in the regulation of transgene expression for gene therapy.
13. Red Blood Cell Indices, Cation Content, and Membrane Cation Transports.
14. Ultrasonic interferometry: study of particle sedimentation in liquid.
15. Transgenic mouse models of sickle cell disease.
16. Lasting Hb F Reactivation and Hb A2 Reduction Induced by the Treatment of Hodgkin's Disease in a Woman Heterozygous for Beta-Thalassemia and the Swiss Type of the Heterocellular Hereditary Persistence of Hb F.
17. Beta°-Thalassemia/Hb E Association.
18. Antenatal diagnosis of haemoglobinopathies by Biorex chromatography of haemoglobin.
19. Clinical manifestations and erythrocyte adhesion to endothelium in sickle cell syndrome.
20. Prenatal diagnosis of haemoglobinopathies by ion exchange HPLC of haemoglobins.
21. Prenatal diagnosis of beta thalassaemia by reverse phase HPLC.
22. Prenatal diagnosis of β thalassaemia by reverse phase HPLC.
23. Frequency of human γ globin chain in a population from Tunisia.
24. Ultrasonic Interferometry Application To Study Of Blood.
25. Individual red blood cell (RBC) transit analysis through sized micropores of oligopore filters : Application to RBC subpopulations
26. Mesure de l'agglutination immunologique des globules rouges par interférométrie ultrasonore
27. Contact inhibition within hemoglobin S polymer by thiol reagents
28. Compartmentalization of Ca 2+ in sickle cells
29. Improvement of Microcirculation Abnormalities in Sickle Cell Patients upon Buflomedil Treatment
30. Study of protein reactivity with thiol reagents by anion-exchange high-performance liquid chromatography
31. A study of membrane protein defects and α hemoglobin chains of red blood cells in human β thalassemia
32. A high resolution NMR study of localized dynamic and structural perturbations in human hemoglobin modified with thiol reagents.
33. Polymorphism of human fetal haemoglobin studied by isoelectric focusing
34. Improvement of Mouse β-Thalassemia by Recombinant Human Erythropoietin
35. Ca2+ Permeability in Deoxygenated Sickle Cells
36. Phenotype of Early Erythroblastic Leukemias
37. Prenatal Diagnosis of Hemoglobinopathies: Comparison of the Results Obtained by Isoelectric Focusing of Hemoglobins and by Chromatography of Radioactive Globin Chains
38. Ca2+ Permeability and Cytosolic Ca2+ Concentration Are Not Impaired in β-Thalassemic and Hemoglobin C Erythrocytes
39. Elevated HbF Associated With an Unstable Hemoglobin, Hemoglobin Saint Etienne: Hb Synthesis in Blood BFUe in Culture
40. Acceleration of the Hemoglobin Switch in Cultures of Neonate Erythroid Precursors by Adult Cells
41. Isoelectric Focusing of Human Hemoglobin: Its Application to Screening, to the Characterization of 70 Variants, and to the Study of Modified Fractions of Normal Hemoglobins
42. Functional studies of the double mutant hemoglobin Stanleyville II/S α 278 Lys β 26 Val: Identification of a site of intermolecular contact on the α chain
43. Protein-protein interactions: Possible location of hemoglobin-haptoglobin contacts
44. Structural and functional studies of hemoglobin J calabria: β64 (E8) Gly → Asp
45. Alteration in protein kinase C activity and subcellular distribution in sickle erythrocytes
46. Alterations of red cell membrane proteins and hemoglobin under natural and experimental oxidant stress
47. Hémoglobine fœtale et hémopathies acquises
48. Structural studies of hemoglobin Saint Etienne β 92 (F8) his → GLN: A new abnormal hemoglobin with loss of β proximal histidine and absence of heme on the β chains
49. Crystallization of a protein - protein complex: Hemoglobin - haptoglobin
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