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HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5

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

Papers overview

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