28 results on '"Beuzard Y"'
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2. Effect of mutated TP53 on response of advanced breast cancers to high-dose chemotherapy
3. Early diagnosis of renal function recovery by cystatin C in renal allograft recipients
4. R475 Cinetique de la troponine Ic (Tn Ic) au cours du choc septique
5. S5.6. Study of erythrocytes by ultrasonic interferometry: Effect of deoxygenation on aggregation, agglutination and packing of sickle cells
6. S5.5. Characterization of red blood cell mechanical properties and interactions by ultrasonic interferometry
7. F40. Determination of blood group by ultrasonic interferometry
8. The involvement of the Ca-dependent K channel and of the KCl co-transport in sickle cell dehydration during cyclic deoxygenation
9. Mesure de l'agglutination immunologique des globules rouges par interférométrie ultrasonore
10. Improvement of Microcirculation Abnormalities in Sickle Cell Patients upon Buflomedil Treatment
11. Individual red blood cell (RBC) transit analysis through sized micropores of oligopore filters : Application to RBC subpopulations
12. Mouse beta thalassemia, a model for the membrane defects of erythrocytes in the human disease
13. Entrapment of purified alpha-hemoglobin chains in normal erythrocytes. A model for beta thalassemia.
14. Association of hemoglobin Saint Etienne (alpha2beta295F8 His replaced by G1n) with hemoglobins A and F. Synthesis and subunit exchange in vitro.
15. Study of protein reactivity with thiol reagents by anion-exchange high-performance liquid chromatography
16. Contact inhibition within hemoglobin S polymer by thiol reagents
17. Alterations of red cell membrane proteins and hemoglobin under natural and experimental oxidant stress
18. A study of membrane protein defects and α hemoglobin chains of red blood cells in human β thalassemia
19. Modification of human hemoglobin by glutathione. III. Perturbations of hemoglobin conformation analyzed by computer modeling.
20. A high resolution NMR study of localized dynamic and structural perturbations in human hemoglobin modified with thiol reagents.
21. Protein-protein interactions: Possible location of hemoglobin-haptoglobin contacts
22. Alteration in protein kinase C activity and subcellular distribution in sickle erythrocytes
23. Structural and functional studies of hemoglobin J calabria: β64 (E8) Gly → Asp
24. Functional studies of the double mutant hemoglobin Stanleyville II/S α278 Lys β26 Val: Identification of a site of intermolecular contact on the α chain
25. Covalent binding of glutathione to hemoglobin. II. Functional consequences and structural changes reflected in NMR spectra.
26. Covalent binding of glutathione to hemoglobin. I. Inhibition of hemoglobin S polymerization.
27. Compartmentalization of Ca2+ in sickle cells
28. Hémoglobine fœtale et hémopathies acquises
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