glutamine and Severe Combined Immunodeficiency

glutamine has been researched along with Severe Combined Immunodeficiency in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lu, CP; Roth, DB; Wong, SY1
Hirschhorn, R; Huie, ML; Israni, A; Ownby, DR; Yang, DR1
Arrendondo-Vega, FX; Buckley, R; Conley, ME; El Dahr, J; Hershfield, MS; Notarangelo, LD; Roifman, C; Santisteban, I1

Other Studies

3 other study(ies) available for glutamine and Severe Combined Immunodeficiency

ArticleYear
A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction.
    Journal of immunology (Baltimore, Md. : 1950), 2008, Sep-15, Volume: 181, Issue:6

    Topics: Amino Acid Motifs; Amino Acid Substitution; Animals; Arginine; Catalytic Domain; CHO Cells; Cricetinae; Cricetulus; Gene Rearrangement, beta-Chain T-Cell Antigen Receptor; Genes, T-Cell Receptor beta; Glutamine; Homeodomain Proteins; Humans; Mice; Mutagenesis, Site-Directed; Severe Combined Immunodeficiency; VDJ Recombinases

2008
Somatic mosaicism for a newly identified splice-site mutation in a patient with adenosine deaminase-deficient immunodeficiency and spontaneous clinical recovery.
    American journal of human genetics, 1994, Volume: 55, Issue:1

    Topics: Adenosine Deaminase; Alleles; Arginine; B-Lymphocytes; Base Sequence; Cell Line; Child, Preschool; Chromosomes, Human, Pair 16; Chromosomes, Human, Pair 20; Deoxyadenine Nucleotides; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Glutamine; Humans; Male; Molecular Sequence Data; Mosaicism; Point Mutation; Remission, Spontaneous; Repetitive Sequences, Nucleic Acid; RNA Splicing; RNA, Messenger; Severe Combined Immunodeficiency; Y Chromosome

1994
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. Online.
    Human mutation, 1998, Volume: 11, Issue:6

    Topics: Adenosine Deaminase; Adolescent; Adult; Age of Onset; Arginine; Cysteine; Glutamic Acid; Glutamine; Glycine; Humans; Methionine; Mutation; Proline; Sequence Deletion; Severe Combined Immunodeficiency; Tryptophan; Valine

1998