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Perforin gene defects in familial hemophagocytic lymphohistiocytosis
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Dive into the research topics of 'Perforin gene defects in familial hemophagocytic lymphohistiocytosis'. Together they form a unique fingerprint.
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Keyphrases
Hemophagocytic Lymphohistiocytosis
100%
Perforin Gene
100%
Gene Defects
100%
Perforin
60%
Coding Region
20%
Abnormal Cells
20%
T Cell Activation
20%
Macrophages
20%
Effector Mechanisms
20%
Missense mutation
20%
Autosomal Recessive
20%
Inflammatory Cytokines
20%
Immunostaining
20%
Immune Activation
20%
Homozygous Nonsense mutation
20%
Patient mutations
20%
Lymphocytes
20%
Cytotoxic Activity
20%
Linkage Analysis
20%
Lysis
20%
Immune Disorders
20%
Granules
20%
Overproduction
20%
Cellular Immune Response
20%
Immunology and Microbiology
Perforin
100%
Hemophagocytic Lymphohistiocytosis
100%
Cytotoxicity
20%
T Cell
20%
Autosomal Recessive Inheritance
20%
Immunostaining
20%
Lymphocyte Culture
20%
Macrophage
20%
Inflammatory Cytokine
20%
Downregulation
20%
Missense Mutation
20%
Nonsense Mutation
20%
Immunity
20%
Immune System Disorders
20%