HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5

Known as: Fhl5, HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL 5 
 
National Institutes of Health

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2018
2018
INTRODUCTION Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease affecting the cytotoxic pathway… (More)
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2016
2016
Familial hemophagocytic lymphohistiocytosis (F-HLH or FHL) is a potentially fatal immune dysregulation syndrome with a… (More)
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2014
2014
Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous hyperinflammatory syndrome, caused by an… (More)
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2013
2013
BACKGROUND Familial hemophagocytic lymphohistiocytosis (FHL) is a rare primary immune disorder defined by mutations in the… (More)
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2013
2013
OBJECTIVE Intimal hyperplasia (IH) is the main cause of vein graft stenosis or failure after bypass surgery. Basic investigations… (More)
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2012
2012
Hemophagocytic lymphohistocytosis (HLH) is a life-threatening hyperinflammatory condition characterized by fever, cytopenia… (More)
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2012
2012
OF DISSERTATION REGULATION OF PLATELET EXOCTOSIS AND ITS ROLE IN DISEASES In addition to their role in hemostasis, platelets… (More)
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2010
2010
BACKGROUND Familial haemophagocytic lymphohistiocytosis (FHL) is a rare immune deficiency with uncontrolled inflammation; the… (More)
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2009
2009
BACKGROUND The LIM domain protein Fhl5 was previously found to interact with CREM, a DNA binding transcriptional regulator… (More)
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2004
2004
Supporting evidence for the contractile nature of fish branchial pillar cells was provided by demonstrating the presence of actin… (More)
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