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- 2022
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Mark
Alternative splicing encodes functional intracellular CD59 isoforms that mediate insulin secretion and are down-regulated in diabetic islets
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- Contribution to journal › Article
- 2015
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Mark
Therapeutic Targeting of Nuclear Gamma-Tubulin in RB1-negative Tumors.
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- Contribution to journal › Article
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Mark
Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patients.
(
- Contribution to journal › Article
- 2013
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Mark
Molecular basis of coagulation factor V deficiency caused by the R1698W inter-domain mutation
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- Contribution to journal › Article
- 2012
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Mark
Analysis of binding sites on complement factor I using artificial N-linked glycosylation.
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- Contribution to journal › Article
- 2010
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Mark
Analysis of binding sites on complement Factor I that are required for its activity
(
- Contribution to journal › Published meeting abstract
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Mark
Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I
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- Contribution to journal › Article
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Mark
Analysis of binding sites on complement factor I that are required for its activity.
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- Contribution to journal › Article
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Mark
Tensin2 reduces intracellular phosphatidylinositol 3,4,5-trisphosphate levels at the plasma membrane.
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- Contribution to journal › Article
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Mark
Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
(
- Contribution to journal › Article
- 2009
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Mark
Characterization of the complement inhibitory function of Rhesus rhadinovirus complement control protein (RCP).
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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
- 2008
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Mark
Molecular and functional analysis of complement factor I mutations in atypical haemolytic uraemic syndrome patients
(
- Contribution to journal › Published meeting abstract
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Mark
Mapping of the factor Xa-binding site on factor Va by site-directed mutagenesis.
(
- Contribution to journal › Article
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Mark
A Novel Non-Synonymous Polymorphism (p.Arg240His) in C4b-Binding Protein Is Associated with Atypical Hemolytic Uremic Syndrome and Leads to Impaired Alternative Pathway Cofactor Activity.
(
- Contribution to journal › Article