Compounds > cysteine

cysteine and Severe Combined Immunodeficiency

cysteine has been researched along with Severe Combined Immunodeficiency in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's3 (75.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chung, HY; Jo, EK; Kanegane, H; Kim, SY; Kim, YH; Kim, YO; Kook, H; Kumaki, S; Noh, HY; Song, CH; Tsuchiya, S; Wei, D1
Arrendondo-Vega, FX; Buckley, R; Conley, ME; El Dahr, J; Hershfield, MS; Notarangelo, LD; Roifman, C; Santisteban, I1
Elder, ME; Kadlecek, TA; Skoda-Smith, S; Wang, F; Weiss, A; Wu, J1
Horinouchi, K; Owada, M; Sakiyama, T; Tsuda, M1

Other Studies

4 other study(ies) available for cysteine and Severe Combined Immunodeficiency

ArticleYear
X-linked severe combined immunodeficiency syndrome: the first Korean case with gamma c chain gene mutation and subsequent genetic counseling.
    Journal of Korean medical science, 2004, Volume: 19, Issue:1

    Topics: Arginine; Chromosomes, Human, X; Cysteine; DNA; DNA Mutational Analysis; Female; Flow Cytometry; Genetic Counseling; Genetic Linkage; Heterozygote; Humans; Immunoglobulins; Immunophenotyping; Korea; Male; Mutation; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Receptors, Immunologic; Sequence Analysis, DNA; Severe Combined Immunodeficiency; Time Factors

2004
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
Distinct T cell developmental consequences in humans and mice expressing identical mutations in the DLAARN motif of ZAP-70.
    Journal of immunology (Baltimore, Md. : 1950), 2001, Jan-01, Volume: 166, Issue:1

    Topics: Amino Acid Motifs; Animals; Arginine; Catalysis; CD4-Positive T-Lymphocytes; CD8-Positive T-Lymphocytes; Cell Differentiation; Cell Survival; Cells, Cultured; Cysteine; Enzyme Activation; Enzyme Precursors; Humans; Infant; Intracellular Signaling Peptides and Proteins; Lymphocyte Activation; Male; Mice; Mutation, Missense; Phosphorylation; Phosphotyrosine; Protein-Tyrosine Kinases; Receptors, Antigen, T-Cell; Severe Combined Immunodeficiency; Syk Kinase; T-Lymphocyte Subsets; Up-Regulation; ZAP-70 Protein-Tyrosine Kinase

2001
Novel missense mutation in the purine nucleoside phosphorylase gene in a Japanese patient with purine nucleoside phosphorylase deficiency.
    Pediatrics international : official journal of the Japan Pediatric Society, 2002, Volume: 44, Issue:3

    Topics: Child; Cysteine; DNA Mutational Analysis; Female; Humans; Metabolism, Inborn Errors; Mutation, Missense; Purine-Nucleoside Phosphorylase; Severe Combined Immunodeficiency; Tyrosine

2002