HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5
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Introduction: Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease affecting the cytotoxic pathway… Expand Familial hemophagocytic lymphohistiocytosis (F‐HLH or FHL) is a potentially fatal immune dysregulation syndrome with a… Expand Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous hyperinflammatory syndrome, caused by an… Expand Familial hemophagocytic lymphohistiocytosis (FHL) is a rare primary immune disorder defined by mutations in the syntaxin binding… Expand OBJECTIVE
Intimal hyperplasia (IH) is the main cause of vein graft stenosis or failure after bypass surgery. Basic investigations… Expand OF DISSERTATION REGULATION OF PLATELET EXOCTOSIS AND ITS ROLE IN DISEASES In addition to their role in hemostasis, platelets… Expand Background Familial haemophagocytic lymphohistiocytosis (FHL) is a rare immune deficiency with uncontrolled inflammation; the… Expand Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous autosomal recessive immune disorder… Expand BackgroundThe LIM domain protein Fhl5 was previously found to interact with CREM, a DNA binding transcriptional regulator… Expand Supporting evidence for the contractile nature of fish branchial pillar cells was provided by demonstrating the presence of actin… Expand