122 results on '"Kahr, Walter H.A."'
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2. Human platelets contain a pool of free zinc in dense granules
3. PACSIN2 regulates platelet integrin β1 hemostatic function
4. The Sec1–Munc18 protein VPS33B forms a uniquely bidirectional complex with VPS16B
5. Moderate-intensity aerobic exercise vs desmopressin in adolescent males with mild hemophilia A: a randomized trial
6. Thromboelastography and thrombin generation assessments for pediatric severe hemophilia A patients are highly variable and not predictive of clinical phenotypes
7. Immune cells surveil aberrantly sialylated O-glycans on megakaryocytes to regulate platelet count
8. Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel
9. The endoplasmic reticulum protein SEC22B interacts with NBEAL2 and is required for megakaryocyte α-granule biogenesis
10. Vascular endothelial cells evade complement‐mediated membrane injury via Weibel‐Palade body mobilization
11. Human ITGAV variants are associated with immune dysregulation, brain abnormalities, and colitis
12. Human platelets contain a pool of free zinc in dense granules
13. 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]
14. Illustrated State-of-the-Art Capsules of the ISTH 2024 Congress
15. Complement Activation Induces Neutrophil Adhesion and Neutrophil-Platelet Aggregate Formation on Vascular Endothelial Cells
16. Von Willebrand factor regulates complement on endothelial cells
17. FlnA binding to PACSIN2 F-BAR domain regulates membrane tubulation in megakaryocytes and platelets
18. Postthrombotic syndrome following upper extremity deep vein thrombosis in children
19. NBEAL2 (Neurobeachin-Like 2) Is Required for Retention of Cargo Proteins by α-Granules During Their Production by Megakaryocytes
20. Pediatric Sickle Cell Disease: A Potential Role for the Complement System
21. The Complement System Mediates COVID-19 Endothelial Cell Injury, Modifying Cell Permeability
22. Abnormal megakaryocyte development and platelet function in Nbeal2−/− mice
23. Loss of the F-BAR protein CIP4 reduces platelet production by impairing membrane-cytoskeleton remodeling
24. The VPS33B-binding protein VPS16B is required in megakaryocyte and platelet α-granule biogenesis
25. Bacteria differentially induce degradation of Bcl-xL, a survival protein, by human platelets
26. Platelet VPS16B is dependent on VPS33B expression, as determined in two siblings with arthrogryposis, renal dysfunction, and cholestasis syndrome
27. Proteasome function is required for platelet production
28. Anucleate platelets generate progeny
29. Mutations in TTC37 Cause Trichohepatoenteric Syndrome (Phenotypic Diarrhea of Infancy)
30. Platelet-associated complement factor H in healthy persons and patients with atypical HUS
31. Fibrinogen is required for maintenance of platelet intracellular and cell-surface P-selectin expression
32. Gray platelet syndrome: NBEAL2 mutations are associated with pathology beyond megakaryocyte and platelet function defects
33. Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet α-granule biogenesis
34. A Hypoxia-Inducible HIF1–GAL3ST1-Sulfatide Axis Enhances ccRCC Immune Evasion via Increased Tumor Cell–Platelet Binding
35. Platelets from patients with the Quebec platelet disorder contain and secrete abnormal amounts of urokinase-type plasminogen activator
36. Decreased numbers of dense granules in fetal and neonatal platelets
37. Intracellular Trafficking, Localization, and Mobilization of Platelet-Borne Thiol Isomerases
38. Molecular basis of platelet granule defects
39. Dynamin 2 (DNM2) and PACSIN2 Regulate Megakaryocyte Demarcation Membrane System Formation and Platelet Production in Concert
40. Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly
41. MYH9-related disease: A novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations
42. Impact of Exercise on Hemostasis in Boys with Hemophilia a (HA) and B (HB): Principal Findings of the Sickkids Hemophilia Exercise Study
43. Platelet production: new players in the field
44. The Cell Motility Modulator Slit2 Is a Potent Inhibitor of Platelet Function
45. The full-of-bacteria gene is required for phagosome maturation during immune defense in Drosophila
46. Type 3 Von Willebrand Disease: Plasma Versus Platelets.
47. Engagement of Fibrinogen and β3 Integrin Is Required for Maintenance of Platelet Intracellular and Cell Surface P-Selectin Expression
48. Complement Factor H in Human Platelets: Implications for Atypical HUS.
49. Insights into Disturbed Hemostasis in the Quebec Platelet Disorder Using Thromboelastography, Blood Clots Formed at Low Shear, and Perfusion Studies of Fibrinolysis.
50. Inherited macrothrombocytopenias on the rise
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