16 results on '"Jarolim, Petr"'
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2. Modulation of Gardos channel activity by cytokines in sickle erythrocytes
3. miR-15a/16-1deletion in activated B cells promotes plasma cell and mature B-cell neoplasms
4. Germinal Center-Derived Lymphomas and Plasmacytomas in Mice with Targeted Deletion of MiR-15a/16-1 in Activated B Cells
5. Modeling Lymphoplasmacytic Lymphoma/Waldenström Macroglobulinemia in Transgenic Mice Using Human MYD88L256P Mutated Protein
6. Markedly Reduced Overall Survival of CYP2C19 *2/*2 Homozygotes After Myeloablative Hematopoietic Stem Cell Transplantation
7. Genetic Variations in CYP2B6 and Risk of Cyclophosphamide Toxicity in Patients Undergoing Myeloablative Stem Cell Transplantation.
8. Structural and Functional Heterogeneity of α Spectrin Mutations Involving the Spectrin Heterodimer Self-Association Site: Relationships to Hematologic Expression of Homozygous Hereditary Elliptocytosis and Hereditary Pyropoikilocytosis
9. Effect of Hemoglobin Oxidation Products on the Stability of Red Cell Membrane Skeletons and the Associations of Skeletal Proteins: Correlation With a Release of Hemin
10. Mutations of Conserved Arginines in the Membrane Domain of Erythroid Band 3 Lead to a Decrease in Membrane-Associated Band 3 and to the Phenotype of Hereditary Spherocytosis
11. Band 3 Tuscaloosa: Pro327→ Arg327Substitution in the Cytoplasmic Domain of Erythrocyte Band 3 Protein Associated With Spherocytic Hemolytic Anemia and Partial Deficiency of Protein 4.2
12. Modeling Lymphoplasmacytic Lymphoma/Waldenström Macroglobulinemia in Transgenic Mice Using Human MYD88L256PMutated Protein
13. The Homozygous State for the Band 3 Protein Mutation in Southeast Asian Ovalocytosis May Be Lethal
14. Characterization of 13 Novel Band 3 Gene Defects in Hereditary Spherocytosis With Band 3 Deficiency
15. Band 3 Tuscaloosa: Pro327 → Arg327 Substitution in the Cytoplasmic Domain of Erythrocyte Band 3 Protein Associated With Spherocytic Hemolytic Anemia and Partial Deficiency of Protein 4.2
16. Band 3 Memphis: A Widespread Polymorphism With Abnormal Electrophoretic Mobility of Erythrocyte Band 3 Protein Caused by Substitution AAG → GAG (Lys → Glu) in Codon 56
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