212 results on '"Joiner, Clinton H."'
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2. Extracellular fluid tonicity impacts sickle red blood cell deformability and adhesion
3. Complement Drives Acute Chest Syndrome in a Model of Sickle Cell Disease
4. Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease
5. Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell trait
6. Complement Activation during Vaso-Occlusive Pain Crisis in Pediatric Sickle Cell Disease
7. Red cell life span heterogeneity in hematologically normal people is sufficient to alter HbA1c
8. Assessment of Cerebral Blood Flow and Oxygen Extraction in Pediatric Sickle Cell Disease with Non-Invasive Diffuse Optical Spectroscopies
9. KCl cotransport mediates abnormal sulfhydryl-dependent volume regulation in sickle reticulocytes
10. Stiff Erythrocyte Subpopulations Biomechanically Induce Endothelial Inflammation in Sickle Cell Disease
11. Rehydration of high-density sickle erythrocytes in vitro
12. Dipyridamole inhibits sickling-induced cation fluxes in sickle red blood cells
13. The survival characteristics of dense sickle cells
14. Effect of Acute Transfusion on Cerebral Oxygenation in Patients with Sickle Cell Disease
15. Cellular Hydration and Oxidation As Phenotype Modifiers in Sickle Cell Anemia
16. Biochemical Surrogate Markers of Hemolysis Do Not Correlate with Directly Measured Erythrocyte Survival in Sickle Cell Anemia
17. Engineering a "Self-Healing" Hydrogel-Based Microvasculature-on-a-Chip for Investigating the Effects of Cellular and Biomolecular Interactions on Endothelial Permeability in Sickle Cell Disease
18. Hydroxyurea Effectiveness in Children and Adolescents with Sickle Cell Anemia: A Large Retrospective, Population-Based Cohort Study
19. Vessel Geometry Interacts with Red Blood Cell Stiffness to Promote Endothelial Dysfunction in Sickle Cell Disease
20. The Novel PIEZO1 Mutation p.L2023V Is Causal for Hereditary Xerocytosis Resulting in Delayed Channel Inactivation and a Dehydrated Red Blood Cell Phenotype
21. Measurement Of Erythrocyte Survival In Vivo using a Stable Isotope Label In Sickle Cell Anemia
22. Development Of a Comprehensive Rapid Next-Generation Sequencing Assay For The Diagnosis Of Inherited Hemolytic Anemia
23. Impact Of Use Of a Disease-Specific Patient Portal On Transition Readiness and Quality Of Life In Adolescents With Sickle Cell Disease
24. A Phase I Trial Of Zileuton In Sickle Cell Disease
25. Six-Month Data From a Pilot Self-Management Intervention ForAdolescents With Sickle Cell Disease
26. Next Generation Sequencing for Diagnostic Testing of Erythrocyte Cytoskeleton Disorders
27. VEGF Mediated Regulation of KCl Cotransporters Gene Expression in Erythroid Cells,
28. Elevated Reactive Oxygen Species Production In Sickle Erythrocytes Is Modulated by a Pathway Involving Endothelin-1, TGFβ1, PKC, and Rac GTPases
29. Vascular Endothelial Growth Factor (VEGF) Increases KCC4 Expression In Erythroid Cells Via Signaling Pathways Involving HIF-1α
30. Effects of Hydroxyurea (HU) and Magnesium Pidolate (Mg) in Hemoglobin SC Disease (HbSC): the “CHAMPS” Trial.
31. Sickle Erythrocytes Have Increased Adducin Phosphorylation and Increased ROS Production Mediated by Signaling Pathways Involving Protein Kinase C and Rac GTPases.
32. Structural and Functional Interactions of KCl Cotransport Proteins KCC1 and KCC3 in Sickle and Normal Erythrocyte Membranes
33. Red Blood Cell Scramblase Activation Is Induced by Phorbol Ester and Prevented by Inhibition of Protein Kinase C
34. Cyclical Changes in Erythrocyte Characteristics during Chronic Transfusion Therapy in Pediatric Sickle Cell Patients
35. Correction of Sickle Cell Anemia with γ-Globin Gene Delivered by Lentivirus Vector in the Setting of Myeloablative or Reduced Intensity Conditioning, and Establishing Critical Determinants for Successful Gene Therapy for Sickle Cell Disease.
36. Gardos pathway to sickle cell therapies?
37. Change in Expressional Profile of KCl Cotransporter Genes during Human Erythroid Differentiation.
38. External PS in Sickle RBC: Relationships among Aminophospholipid Translocase (APLT), Phospholipid Scramblase (PLSCR), Cell Maturity, and Cell Density.
39. A GC Box Element Is Critical for Transcriptional Regulation of the K-Cl Cotransporter Isoform KCC3a in Hematopoetic Cells.
40. Rac GTPases regulate the morphology and deformability of the erythrocyte cytoskeleton
41. Aminophospholipid Translocase Activity and Phosphatidylserine Externalization in Sickle Red Blood Cell Subpopulations.
42. Functional Comparison of Red Cell KCl Cotransporter Isoforms, KCC1, KCC3, and KCC4.
43. Alternative Splicing within Exon 1 of the KCl Cotransporter-3 (KCC3) Gene Results in Novel Transcripts in Erythroid Cells.
44. Urea stimulation of KCl cotransport induces abnormal volume reduction in sickle reticulocytes
45. The effect of fetal hemoglobin on the survival characteristics of sickle cells
46. Expression of a KCC1 Splice Variant Is Suppressed by NF-ΚB in Erythroid Cells.
47. Mature Sickle and Normal Red Cells Exhibit Regulatory Volume Decrease Activated by Urea and Mediated by KCl Cotransport.
48. A Second Promoter for the Human KCl Cotransporter 1 (KCC1) Gene Drives Differential Expression of a Variant Isoform in Sickle Versus Normal Reticulocytes.
49. Sickle Cell Patietns with a High Percentage of HBF-Containing RBC (F Cells) Have Shorter Survival of RBC that Lack HBF.
50. Activation of KCI Cotransport by Urea Induces Dehydration in Both Sickle and Normal Reticulocytes.
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