Page last updated: 2024-08-17

histidine and Agammaglobulinemia

histidine has been researched along with Agammaglobulinemia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ebell, W; Kühl, JS; Meisel, C; Münch, A; Pekrun, A; Schmugge, M; Schwarz, K; von Bernuth, H; Wahn, V1
Andersen, JT; Bjarnarson, SP; de Haas, M; Gerritsen, J; Jonsdottir, I; Kleijer, M; Sandlie, I; Stapleton, NM; Stemerding, AM; van der Schoot, CE; Verheul, RC; Vidarsson, G; Zhao, Y1
Bäckesjö, CM; Brockmann, E; Lappalainen, I; Laurén, S; Mattsson, PT; Smith, CI; Vihinen, M1
Rostenberg, A; Solomon, LM1

Other Studies

4 other study(ies) available for histidine and Agammaglobulinemia

ArticleYear
Hyperbilirubinemia and rapid fatal hepatic failure in severe combined immunodeficiency caused by adenosine deaminase deficiency (ADA-SCID).
    Klinische Padiatrie, 2011, Volume: 223, Issue:2

    Topics: Adenosine Deaminase; Agammaglobulinemia; Amino Acid Substitution; Arginine; Bone Marrow Transplantation; Consanguinity; Exons; Fatal Outcome; Female; Hepatorenal Syndrome; Histidine; Humans; Hyperbilirubinemia, Neonatal; Infant; Infant, Newborn; Leukocyte Count; Liver Failure; Liver Function Tests; Lymphocyte Activation; Mutation, Missense; Neutrophils; Severe Combined Immunodeficiency

2011
Competition for FcRn-mediated transport gives rise to short half-life of human IgG3 and offers therapeutic potential.
    Nature communications, 2011, Dec-20, Volume: 2

    Topics: Agammaglobulinemia; Amino Acid Substitution; Animals; Antibodies, Monoclonal; Arginine; Binding, Competitive; Cell Line, Tumor; Disease Models, Animal; Half-Life; Histidine; Histocompatibility Antigens Class I; Humans; Hydrogen-Ion Concentration; Immunoglobulin G; Mice; Molecular Targeted Therapy; Pneumococcal Infections; Protein Binding; Protein Transport; Receptors, Fc; Streptococcus pneumoniae

2011
Six X-linked agammaglobulinemia-causing missense mutations in the Src homology 2 domain of Bruton's tyrosine kinase: phosphotyrosine-binding and circular dichroism analysis.
    Journal of immunology (Baltimore, Md. : 1950), 2000, Apr-15, Volume: 164, Issue:8

    Topics: Agammaglobulinaemia Tyrosine Kinase; Agammaglobulinemia; Amino Acid Substitution; Arginine; Circular Dichroism; Genetic Linkage; Glycine; Histidine; Humans; Mutation, Missense; Peptide Fragments; Phosphotyrosine; Protein Binding; Protein Conformation; Protein-Tyrosine Kinases; Solubility; src Homology Domains; Structure-Activity Relationship; X Chromosome

2000
Infantile eczema and systemic disease.
    Archives of dermatology, 1968, Volume: 98, Issue:1

    Topics: Acrodermatitis; Agammaglobulinemia; Ataxia Telangiectasia; Child; Dermatitis, Atopic; Eczema; Gastrointestinal Diseases; Glutens; Hartnup Disease; Histidine; Humans; Infant; Lymphatic Diseases; Mucopolysaccharidoses; Phenylketonurias; Wiskott-Aldrich Syndrome

1968