166 results on '"Kahr, Walter H.A."'
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2. Acidification of α-granules in megakaryocytes by vacuolar-type adenosine triphosphatase is essential for organelle biogenesis
3. Constitutive hypercoagulability in pediatric sickle cell disease patients with hemoglobin SS genotype
4. Human platelets contain a pool of free zinc in dense granules
5. PACSIN2 regulates platelet integrin β1 hemostatic function
6. The Sec1–Munc18 protein VPS33B forms a uniquely bidirectional complex with VPS16B
7. Moderate-intensity aerobic exercise vs desmopressin in adolescent males with mild hemophilia A: a randomized trial
8. Thromboelastography and thrombin generation assessments for pediatric severe hemophilia A patients are highly variable and not predictive of clinical phenotypes
9. Immune cells surveil aberrantly sialylated O-glycans on megakaryocytes to regulate platelet count
10. Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel
11. The endoplasmic reticulum protein SEC22B interacts with NBEAL2 and is required for megakaryocyte α-granule biogenesis
12. Vascular endothelial cells evade complement‐mediated membrane injury via Weibel‐Palade body mobilization
13. Human ITGAV variants are associated with immune dysregulation, brain abnormalities, and colitis
14. Human platelets contain a pool of free zinc in dense granules
15. Relative antibacterial functions of complement and NETs: NETs trap and complement effectively kills bacteria
16. Erratum to ‘Illustrated State-of-the-Art Capsules of the ISTH 2024 Congress’ [Research and Practice in Thrombosis and Haemostasis Volume 8, Issue 4, May 2024, 102432]
17. Illustrated State-of-the-Art Capsules of the ISTH 2024 Congress
18. Complement Activation Induces Neutrophil Adhesion and Neutrophil-Platelet Aggregate Formation on Vascular Endothelial Cells
19. Von Willebrand factor regulates complement on endothelial cells
20. Recent advances in inherited platelet disorders
21. FlnA binding to PACSIN2 F-BAR domain regulates membrane tubulation in megakaryocytes and platelets
22. Postthrombotic syndrome following upper extremity deep vein thrombosis in children
23. NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes
24. Pediatric Sickle Cell Disease: A Potential Role for the Complement System
25. The Complement System Mediates COVID-19 Endothelial Cell Injury, Modifying Cell Permeability
26. Abnormal megakaryocyte development and platelet function in Nbeal2−/− mice
27. Loss of the F-BAR protein CIP4 reduces platelet production by impairing membrane-cytoskeleton remodeling
28. Congenital Thrombocytopenia: Clinical Manifestations, Laboratory Abnormalities, and Molecular Defects of a Heterogeneous Group of Conditions
29. The VPS33B-binding protein VPS16B is required in megakaryocyte and platelet α-granule biogenesis
30. Bacteria differentially induce degradation of Bcl-xL, a survival protein, by human platelets
31. Platelet VPS16B is dependent on VPS33B expression, as determined in two siblings with arthrogryposis, renal dysfunction, and cholestasis syndrome
32. The role of prothrombotic factors in the ocular manifestations of abusive and non-abusive head trauma: A feasibility study
33. Platelet Disorders in Children
34. Quantitative Platelet Disorders
35. Proteasome function is required for platelet production
36. Anucleate platelets generate progeny
37. Mutations in TTC37 Cause Trichohepatoenteric Syndrome (Phenotypic Diarrhea of Infancy)
38. Platelet-associated complement factor H in healthy persons and patients with atypical HUS
39. Fibrinogen is required for maintenance of platelet intracellular and cell-surface P-selectin expression
40. MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype–Phenotype Correlations
41. Extracellular Matrix and Platelet Function in Patients With Musculocontractural Ehlers–Danlos Syndrome Caused by Mutations in the CHST14 Gene†‡
42. Cerebral sinus venous thrombosis in a child with hyperthyroidism
43. Gray platelet syndrome: NBEAL2 mutations are associated with pathology beyond megakaryocyte and platelet function defects
44. Platelet disorders in children: A diagnostic approach‡†
45. Decreased in vitro thrombin generation and clot stability in human FXII-null blood and plasma
46. Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet α-granule biogenesis
47. The Use of Elastic Compression Stockings for Post-Thrombotic Syndrome in A Child
48. Liver biopsy complicated by hemorrhage in a patient with ARC syndrome
49. Plasmacytoid Dendritic Cells Surveil Megakaryocyte Sialic Acid to Regulate Thrombopoiesis
50. A Hypoxia-Inducible HIF1–GAL3ST1-Sulfatide Axis Enhances ccRCC Immune Evasion via Increased Tumor Cell–Platelet Binding
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