arginine has been researched along with Agammaglobulinemia in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 2 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Abinun, M; Cassani, B; Clayton-Smith, J; Coxon, FP; Crockett, JC; Frattini, A; Guerrini, MM; Helfrich, MH; Kilic, SS; Mazzolari, E; Mellis, D; Moratto, D; Notarangelo, LD; Orchard, P; Pangrazio, A; Rogers, MJ; Sobacchi, C; Tezcan, I; Vellodi, A; Vezzoni, P; Villa, A | 1 |
Ebell, W; Kühl, JS; Meisel, C; Münch, A; Pekrun, A; Schmugge, M; Schwarz, K; von Bernuth, H; Wahn, V | 1 |
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, Y | 1 |
Bossemeyer, D | 1 |
Bäckesjö, CM; Brockmann, E; Lappalainen, I; Laurén, S; Mattsson, PT; Smith, CI; Vihinen, M | 1 |
Ammann, AJ; Duquesnoy, RJ; Good, RA | 1 |
6 other study(ies) available for arginine and Agammaglobulinemia
Article | Year |
---|---|
Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations.
Topics: Acid Phosphatase; Actins; Agammaglobulinemia; Amino Acid Sequence; Amino Acid Substitution; Argentina; Arginine; Biopsy; Case-Control Studies; Cell Line, Transformed; Cell Proliferation; Cell Transformation, Viral; Cells, Cultured; Cohort Studies; Consanguinity; Cysteine; Dendrites; DNA Mutational Analysis; Female; Genes, Recessive; Herpesvirus 4, Human; Heterozygote; Homozygote; Humans; Ilium; Isoenzymes; Leukocyte Common Antigens; Leukocytes, Mononuclear; Lipopolysaccharides; Macrophage Colony-Stimulating Factor; Male; Models, Immunological; Molecular Sequence Data; Mutation, Missense; Osteoclasts; Osteopetrosis; Osteoprotegerin; Pakistan; Pedigree; Polymorphism, Genetic; Protein Structure, Tertiary; Radiography, Thoracic; RANK Ligand; Receptor Activator of Nuclear Factor-kappa B; Receptors, Vitronectin; Sequence Homology, Amino Acid; Tartrate-Resistant Acid Phosphatase; Turkey | 2008 |
Hyperbilirubinemia and rapid fatal hepatic failure in severe combined immunodeficiency caused by adenosine deaminase deficiency (ADA-SCID).
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.
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 |
Loss of kinase activity.
Topics: Adenosine Triphosphate; Agammaglobulinemia; Amino Acid Sequence; Arginine; Lysine; Molecular Sequence Data; Point Mutation; Protein Kinases | 1993 |
Six X-linked agammaglobulinemia-causing missense mutations in the Src homology 2 domain of Bruton's tyrosine kinase: phosphotyrosine-binding and circular dichroism analysis.
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 |
Endocrinological studies in ataxiatelangiectasia and other immunological deficiency diseases.
Topics: Adolescent; Adrenal Cortex Hormones; Agammaglobulinemia; Arginine; Ataxia Telangiectasia; Child; Child, Preschool; Dwarfism, Pituitary; Endocrine Glands; Female; Genes; Gonadotropins, Pituitary; Growth Hormone; Humans; Immunity, Cellular; Immunoglobulins; Insulin; Male; Pituitary-Adrenal Function Tests; Puberty; Secretory Rate; Sex Chromosomes; Thyroid Function Tests; Thyroid Hormones | 1970 |