Compounds > arginine

arginine and Wiskott-Aldrich Syndrome

arginine has been researched along with Wiskott-Aldrich Syndrome in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Anderson, KC; Antón, IM; Calamito, M; de la Fuente, MA; Elkhal, A; Gallego, MD; Geha, RS; Ochs, HD; Ramesh, N; Rosen, FS; Sasahara, Y; Siminovitch, K; Suresh, K1
Kolluri, R; Lamhonwah, AM; Peacocke, M; Shehabeldin, A; Siminovitch, KA; Teichert-Kuliszewska, K; Weissman, SM1
Blaese, RM; Hagemann, TL; Knutsen, A; Kwan, SP; Rosen, FS1
Cavieres, M; dal Borgo, P; Español, T; Estivill, X; Fillat, C; Oset, M; Volpini, V1

Other Studies

4 other study(ies) available for arginine and Wiskott-Aldrich Syndrome

ArticleYear
WIP is a chaperone for Wiskott-Aldrich syndrome protein (WASP).
    Proceedings of the National Academy of Sciences of the United States of America, 2007, Jan-16, Volume: 104, Issue:3

    Topics: Actins; Animals; Arginine; Boronic Acids; Bortezomib; Calpain; Carrier Proteins; Cytoskeletal Proteins; Enzyme Inhibitors; Humans; Interleukin-2; Intracellular Signaling Peptides and Proteins; Jurkat Cells; Lymphocytes; Mice; Mice, Knockout; Molecular Chaperones; Mutation, Missense; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Protein Binding; Pyrazines; Wiskott-Aldrich Syndrome; Wiskott-Aldrich Syndrome Protein

2007
Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus.
    Human molecular genetics, 1995, Volume: 4, Issue:7

    Topics: Adolescent; Adult; Alleles; Arginine; Base Sequence; Child; Child, Preschool; Exons; Female; Gene Expression; Humans; Infant; Male; Molecular Sequence Data; Mutation; Phenotype; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Proteins; Thrombocytopenia; Wiskott-Aldrich Syndrome; Wiskott-Aldrich Syndrome Protein

1995
Scanning of the Wiskott-Aldrich syndrome (WAS) gene: identification of 18 novel alterations including a possible mutation hotspot at Arg86 resulting in thrombocytopenia, a mild WAS phenotype.
    Human molecular genetics, 1995, Volume: 4, Issue:10

    Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Child; Child, Preschool; Chromosome Mapping; Codon; Frameshift Mutation; Humans; Introns; Phenotype; Point Mutation; Polymorphism, Single-Stranded Conformational; Proteins; Sequence Deletion; Thrombocytopenia; Wiskott-Aldrich Syndrome; Wiskott-Aldrich Syndrome Protein; X Chromosome

1995
Two novel mutations in the WASP gene in Wiskott-Aldrich patients of Chile origin: W64R and A124E.
    Human mutation, 2000, Volume: 15, Issue:5

    Topics: Alanine; Amino Acid Substitution; Arginine; Chile; Glutamic Acid; Humans; Infant; Male; Point Mutation; Proteins; Tryptophan; Wiskott-Aldrich Syndrome; Wiskott-Aldrich Syndrome Protein

2000