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- 2009
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Mark
Systematic classification of primary immunodeficiencies based on clinical, pathological, and laboratory parameters.
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- Contribution to journal › Article
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Mark
Scabies mite inactivated serine protease paralogs inhibit the human complement system.
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- Contribution to journal › Article
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Mark
A novel mutation in the complement regulator clusterin in recurrent hemolytic uremic syndrome.
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- Contribution to journal › Article
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Mark
Clinical isolates of Streptococcus pneumoniae bind the complement inhibitor C4b-binding protein in a PspC allele-dependent fashion.
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- Contribution to journal › Article
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Mark
Complement classical pathway components are all important in clearance of apoptotic and secondary necrotic cells.
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- Contribution to journal › Article
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Mark
Genetic, molecular and functional analyses of complement factor I deficiency.
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- Contribution to journal › Article
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Mark
Immunome knowledge base (IKB): an integrated service for immunome research.
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- Contribution to journal › Article
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Mark
Short leucine-rich glycoproteins of the extracellular matrix display diverse patterns of complement interaction and activation.
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- Contribution to journal › Article
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Mark
Bruton's tyrosine kinase (Btk): function, regulation, and transformation with special emphasis on the PH domain.
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- Contribution to journal › Scientific review
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Mark
Type I interferon signaling in dendritic cells stimulates the development of lymph-node-resident T follicular helper cells.
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- Contribution to journal › Article