16 results on '"Hammarstrom, Lennart"'
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2. Heterozygosity for transmembrane activator and calcium modulator ligand interactor A144E causes haploinsufficiency and pneumococcal susceptibility in mice
3. Structural Insights into Polymorphic ABO Glycan Binding by Helicobacter pylori
4. OR13 Human leukocyte antigen analysis using high resolution SNP data: Imputation, association and amino acid binding pocket residues investigation in IgAD patients
5. A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency
6. The immunoglobulin δ gene in jawed vertebrates: A comparative overview
7. Familial aggregation of IgAD and autoimmunity
8. F.112. Human BAFF-R Deficiency is Associated with Primary Antibody Deficiency Syndrome
9. Genomic organization of the immunoglobulin light chain gene loci in Xenopus tropicalis: Evolutionary implications
10. ICOS deficiency in patients with common variable immunodeficiency
11. Clinical spectrum of X-linked hyper-IgM syndrome
12. CD40Lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome
13. Hepatitis C virus transmission by intravenous immunoglobulin
14. Molecular basis for human immunodeficiencies
15. Captopril-induced IgA deficiency
16. SELECTION OF AUTOANTIBODIES
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