Hereditary Angioedema Type I

Known as: Angioedema, Hereditary, Type I, HAE1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2007-2016
0120072016

Papers overview

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2016
2016
Hereditary angioedema is a rare disease with great heterogeneity of symptoms such as edema of the skin, gastro-intestinal mucosa… (More)
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2012
2012
Modulating the binding affinities to IgE or changing the FcγR binding properties of anti-IgE antibodies offers an opportunity to… (More)
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Review
2009
Review
2009
The abundant membrane protein AE1 normally functions as an obligate anion exchanger, with classical carrier properties, in human… (More)
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2008
2008
The SLC4A1/AE1 gene encodes the electroneutral Cl(-)/HCO(3)(-) exchanger of erythrocytes and renal type A intercalated cells. AE1… (More)
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Review
2008
Review
2008
HAE1, a high-affinity anti-IgE monoclonal antibody, is discussed here as a case study in the use of quantitative pharmacology in… (More)
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2007
2007
The anion exchanger 1 (AE1) is encoded by the SLC4A1 gene and catalyzes the electroneutral anion exchange across cell plasma… (More)
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