Compounds > arginine

arginine and Antibody Deficiency Syndrome

arginine has been researched along with Antibody Deficiency Syndrome in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19901 (12.50)18.7374
1990's3 (37.50)18.2507
2000's4 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gauthier, S; Gros, P; Malo, D; Mullick, A; Tuite, A; Turcotte, K1
Borges, L; Derry, JM; Jain, A; Kubin, M; Liu, S; Ma, CA; Temmerman, ST1
Battaglia, M; Bosticardo, M; Casati, A; Cavazzana-Calvo, M; Facchetti, F; Frascoli, L; Gougeon, ML; Grassi, F; Lemercier, B; Marrella, V; Notarangelo, LD; Poliani, PL; Ravanini, M; Roncarolo, MG; Rucci, F; Vezzoni, P; Villa, A1
Cheng, JY; Wallis, R1
Babst, R1
Cerra, FB1
Cornaglia-Ferraris, P; Perezzani, L; Rossi, E; Stradi, R1
Berkvens, TM; Dekker, BM; Duyvesteyn, MG; Valerio, D; van der Eb, AJ; van der Voorn, L; van Ormondt, H1

Reviews

1 review(s) available for arginine and Antibody Deficiency Syndrome

ArticleYear
Role of nutrition in the management of malnutrition and immune dysfunction of trauma.
    Journal of the American College of Nutrition, 1992, Volume: 11, Issue:5

    Topics: Animals; Arginine; Fatty Acids, Omega-3; Humans; Immunologic Deficiency Syndromes; Nutrition Disorders; Uracil; Wounds and Injuries

1992

Other Studies

7 other study(ies) available for arginine and Antibody Deficiency Syndrome

ArticleYear
A mutation in the Icsbp1 gene causes susceptibility to infection and a chronic myeloid leukemia-like syndrome in BXH-2 mice.
    The Journal of experimental medicine, 2005, Mar-21, Volume: 201, Issue:6

    Topics: Amino Acid Substitution; Animals; Arginine; Chromosomes, Mammalian; Cysteine; Genetic Predisposition to Disease; Immunologic Deficiency Syndromes; Interferon Regulatory Factors; Interferon-gamma; Interleukin-12; Leukemia, Myeloid; Mice; Mutagenesis, Insertional; Mycobacterium bovis; Point Mutation; Quantitative Trait Loci; Repressor Proteins; Retroviridae; RNA, Messenger; Spleen; Tuberculosis; Virus Replication

2005
Impaired dendritic-cell function in ectodermal dysplasia with immune deficiency is linked to defective NEMO ubiquitination.
    Blood, 2006, Oct-01, Volume: 108, Issue:7

    Topics: Arginine; CD3 Complex; CD40 Antigens; Cell Proliferation; Cysteine; Dendritic Cells; Ectodermal Dysplasia; Exons; Humans; I-kappa B Kinase; Immunologic Deficiency Syndromes; Mutation; Protein Structure, Tertiary; Ubiquitin; Zinc Fingers

2006
A hypomorphic R229Q Rag2 mouse mutant recapitulates human Omenn syndrome.
    The Journal of clinical investigation, 2007, Volume: 117, Issue:5

    Topics: Amino Acid Substitution; Animals; Arginine; Cells, Cultured; Disease Models, Animal; DNA-Binding Proteins; Genetic Diseases, Inborn; Glutamine; Humans; Immune Tolerance; Immunologic Deficiency Syndromes; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mice, Transgenic; Mutagenesis, Site-Directed

2007
Molecular defects in variant forms of mannose-binding protein associated with immunodeficiency.
    Journal of immunology (Baltimore, Md. : 1950), 1999, Nov-01, Volume: 163, Issue:9

    Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; Aspartic Acid; Carrier Proteins; Collectins; Complement Fixation Tests; Cysteine; Disulfides; Glutamic Acid; Glycine; Humans; Immunologic Deficiency Syndromes; Mannans; Molecular Sequence Data; Point Mutation; Protein Processing, Post-Translational; Rats

1999
[Immunomodulation by nutritional therapy--wish or reality?].
    Praxis, 2001, Apr-26, Volume: 90, Issue:17

    Topics: Arginine; Fatty Acids, Omega-3; Glutamine; Humans; Immunologic Deficiency Syndromes; Multiple Trauma; Nucleotides; Nutritional Requirements; Nutritive Value; Randomized Controlled Trials as Topic

2001
Retention of amphotericin-B therapeutic efficacy at half doses by synergistic activation of phagocytes.
    Cancer detection and prevention, 1991, Volume: 15, Issue:4

    Topics: Adjuvants, Immunologic; Amphotericin B; Animals; Arginine; Candidiasis; Cyclophosphamide; Drug Synergism; Drug Therapy, Combination; Female; Hypoxanthines; Immunocompromised Host; Immunologic Deficiency Syndromes; Mice; Mice, Inbred BALB C; Neutrophils; Phagocytosis

1991
One adenosine deaminase allele in a patient with severe combined immunodeficiency contains a point mutation abolishing enzyme activity.
    The EMBO journal, 1986, Volume: 5, Issue:1

    Topics: Adenosine Deaminase; Alleles; Amino Acid Sequence; Animals; Arginine; Base Sequence; Cell Line; Cloning, Molecular; DNA Restriction Enzymes; Genes; Humans; Immunologic Deficiency Syndromes; Leucine; Lysine; Mice; Mutation; Nucleoside Deaminases; Plasmids; Species Specificity

1986