55 results on '"Hammarstrom, Lennart"'
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2. Helicobacter pylori attachment-blocking antibodies protect against duodenal ulcer disease
3. Conversion of monoclonal IgG to dimeric and secretory IgA restores neutralizing ability and prevents infection of Omicron lineages
4. Heterologous inactivated virus/mRNA vaccination response to BF.7, BQ.1.1, and XBB.1
5. CVID-Associated B Cell Activating Factor Receptor Variants Change Receptor Oligomerization, Ligand Binding, and Signaling Responses
6. Design, structure and plasma binding of ancestral β-CoV scaffold antigens
7. Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency
8. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies
9. CVID-Associated B Cell Activating Factor Receptor Variants Change Receptor Oligomerization, Ligand Binding and Signaling Responses
10. Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits
11. Known and potential molecules associated with altered B cell development leading to predominantly antibody deficiencies
12. A Heterodimeric Antibody Fragment for Passive Immunotherapy Against Norovirus Infection
13. Monozygotic Twins Concordant for Common Variable Immunodeficiency: Strikingly Similar Clinical and Immune Profile Associated With a Polygenic Burden
14. Defective TLR9-driven STAT3 activation in B cells of patients with CVID
15. Heterozygosity for transmembrane activator and calcium modulator ligand interactor A144E causes haploinsufficiency and pneumococcal susceptibility in mice
16. Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects
17. OR13 Human leukocyte antigen analysis using high resolution SNP data: Imputation, association and amino acid binding pocket residues investigation in IgAD patients
18. Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
19. Different brands of intravenous immunoglobulin for primary immunodeficiencies: how to choose the best option for the patient?
20. Important differences in the diagnostic spectrum of primary immunodeficiency in adults versus children
21. Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations
22. A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency
23. Ribosomal Protein SA Haploinsufficiency in Humans with Isolated Congenital Asplenia
24. Risk for myasthenia gravis maps to a151Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08
25. Analysis of Immunoglobulin Transcripts in the Ostrich Struthio camelus, a Primitive Avian Species
26. The immunoglobulin δ gene in jawed vertebrates: A comparative overview
27. Passive oral rice-based antibody prophylaxis and therapy against rotavirus infection (106.19)
28. Familial aggregation of IgAD and autoimmunity
29. F.112. Human BAFF-R Deficiency is Associated with Primary Antibody Deficiency Syndrome
30. Common variable immunodeficiency disorders: division into distinct clinical phenotypes
31. Severe Congenital Neutropenia or Hyper-IgM Syndrome? A Novel Mutation of CD40 Ligand in a Patient with Severe Neutropenia
32. Progression of Selective IgA Deficiency to Common Variable Immunodeficiency
33. Genomic organization of the immunoglobulin light chain gene loci in Xenopus tropicalis: Evolutionary implications
34. Effective prophylaxis against rotavirus diarrhea using a combination of Lactobacillus rhamnosus GG and antibodies
35. AID from bony fish catalyzes class switch recombination
36. ICOS deficiency in patients with common variable immunodeficiency
37. Cloning of the complete rat immunoglobulin delta gene: evolutionary implications
38. Artiodactyl IgD: The Missing Link
39. Clinical and molecular analysis of patients with defects in μ heavy chain gene
40. Faculty Opinions recommendation of Rapid detection of antibodies to immunoglobulin A molecules by using the particle gel immunoassay.
41. Faculty Opinions recommendation of Analysis of Ig subclass deficiency: First reported case of IgG2, IgG4, and IgA deficiency caused by deletion of C alpha 1, psi C gamma, C gamma 2, C gamma 4, and C epsilon in a Mongoloid patient.
42. Autologous T lymphocytes recognize the tumour-derived immunoglobulin VH-CDR3 region in patients with B-cell chronic lymphocytic leukaemia
43. Clinical spectrum of X-linked hyper-IgM syndrome
44. CD40Lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome
45. Semiquantitative estimation ofShigellaantigen-specific antibodies: correlation with disease severity during shigellosis
46. Lifelong treatment with gammaglobulin for primary antibody deficiencies: the patients' experiences of subcutaneous self-infusions and home therapy
47. Systemic and Topical Immunoglobulin Treatment in Immunocompromised Patients
48. Hepatitis C virus transmission by intravenous immunoglobulin
49. Specificity and levels of oral and systemic antibodies to Actinobacillus actinomycetemcomitans
50. Molecular basis for human immunodeficiencies
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