548 results on '"Sachs, Ulrich J."'
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102. The nonconservativeCD177single‐nucleotide polymorphism c.1291G>A is a genetic determinant for human neutrophil antigen‐2 atypical/low expression and deficiency
103. Diagnosing Immune Thrombocytopenia
104. Transfusion of Soluble Target Antigens to Pre-Immunized Recipients: A Previously Overlooked Mechanism in Transfusion-Related Acute Lung Injury
105. Anti-Glycoprotein V Autoantibodies in Patients with Immune Thrombocytopenia: Regularly Detectable and Functionally Relevant
106. Fcγ Receptors I and III on Splenic Macrophages Mediate GPIIb/IIIa Autoantibody-Dependent Phagocytosis of Platelets in Human Immune Thrombocytopenia
107. Molecular and Functional Characterization of Fcγ Receptor IIIb-Ligand Interaction: Implications for Neutrophil-Mediated Immune Mechanisms in Malaria
108. Hämolytische Erkrankung des Fetus und Neugeborenen
109. Unmatched Type O RhD+ Red Blood Cells in Multiple Injured Patients
110. Improvement of monoclonal antibody-immobilized granulocyte antigen assay for the detection of anti-HNA-1 alloantibodies
111. Sunitinib in the Treatment of Thymoma and Associated Autoimmune Neutropenia
112. HLA-DRB3*01:01 is a predictor of immunization against human platelet antigen-1a but not of the severity of fetal and neonatal alloimmune thrombocytopenia
113. CD16b: Primary Structure of Human Neutrophil Antigen Epitopes and Their Functional Consequences
114. Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)-associated inflammatory diseases
115. The nonconservative CD177 single-nucleotide polymorphism c.1291G>A is a genetic determinant for human neutrophil antigen-2 atypical/low expression and deficiency.
116. Antiendothelial αvβ3 Antibodies Are a Major Cause of Intracranial Bleeding in Fetal/Neonatal Alloimmune Thrombocytopenia
117. A sequence-specific polymerase chain reaction method for HNA-2 genotyping: homozygous c.843A>T mutation predicts the absence of CD177
118. Transfusion‐related lung injury
119. Update on the nomenclature of human neutrophil antigens and alleles
120. Immunisation against αIIbβ3 and αvβ3 in a type 1 variant of Glanzmann’s thrombasthenia caused by a missense mutation Gly540Asp on β3
121. Partially desulfated heparin modulates the interaction between anti-protamine/heparin antibodies and platelets
122. Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)-associated inflammatory diseases
123. HNA-1d: a new human neutrophil antigen located on Fc gamma receptor IIIb associated with neonatal immune neutropenia
124. A bead-based assay in the work-up of suspected platelet alloimmunization
125. Choline Transporter-Like Protein-2
126. Anti-Granulocyte Antibodies in Transfusion Medicine
127. Deglycosylated Human Monoclonal Antibody Against HPA-1a Prevents Anti-HPA-1a Alloantibodies Mediated Endothelial Apoptosis
128. HLA-DRB3*01:01 is a predictor of immunization against human platelet antigen-1a but not of the severity of fetal and neonatal alloimmune thrombocytopenia.
129. Transfusion-Related Acute Lung Injury
130. Multicentric validation of a rapid assay for heparin-induced thrombocytopenia with different specimen types
131. Non-transient “self-sustaining” heparin-induced thrombocytopenia: 4-year persistence of a platelet-activating PF4/heparin–antibody status without heparin exposure
132. N-Glycosylation Of Human ITP Autoantibodies Affects Complement Activation, Platelet Phagocytosis, and Platelet Survival In a Murine Model
133. Anti–Human Neutrophil Antigen-3a Induced Transfusion-Related Acute Lung Injury in Mice by Direct Disturbance of Lung Endothelial Cells
134. Prevalence of hereditary antithrombin mutations is higher than estimated in patients with thrombotic events
135. Glycosylation of autoantibodies: Insights into the mechanisms of immune thrombocytopenia
136. Partially desulfated heparin modulates the interaction between anti- protamine/ heparin antibodies and platelets.
137. The implementation of surface plasmon resonance technique in monitoring pregnancies with expected fetal and neonatal alloimmune thrombocytopenia
138. Rapid enzyme-linked immunosorbent assay for the detection of antibodies against human neutrophil antigens -1a, -1b, and -1c
139. A point mutation in the EGF-4 domain of β3 integrin is responsible for the formation of the Seca platelet alloantigen and affects receptor function
140. Autoantibody-mediated complement activation on platelets is a common finding in patients with immune thrombocytopenic purpura (ITP)
141. The Janus Face of Neutrophil Specific Antigen CD177 in Bacterial Infection: Focal Disease Versus Systemic Disease
142. Lung Endothelial Injury Induced by HNA-3a Antibodies in TRALI
143. Evaluation of a New Nanoparticle-Based Lateral-Flow Immunoassay for the Exclusion of Heparin-Induced Thrombocytopenia (HIT),
144. Recent insights into the mechanism of transfusion-related acute lung injury
145. Prediction of fetal status in fetal/neonatal alloimmune thrombocytopenia (FNAIT)?
146. Implication of transfected cell lines for the detection of alloantibodies against human neutrophil antigen-3
147. Mechanism of transfusion-related acute lung injury induced by HLA class II antibodies
148. GP IIb/Iiia-Dependent Complement Activation Is Common In Patients with Immune Thrombocytopenic Purpura.
149. Neutrophil Transmigration Mediated by the Neutrophil-Specific Antigen CD177 Is Influenced by the Endothelial S536N Dimorphism of Platelet Endothelial Cell Adhesion Molecule-1
150. IMMUNOHEMATOLOGY: Rapid screening of granulocyte antibodies with a novel assay: flow cytometric granulocyte immunofluorescence test
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