arginine has been researched along with Bare Lymphocyte Syndrome in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (10.00) | 18.7374 |
| 1990's | 4 (40.00) | 18.2507 |
| 2000's | 4 (40.00) | 29.6817 |
| 2010's | 1 (10.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lu, CP; Roth, DB; Wong, SY | 1 |
| Ebell, W; Kühl, JS; Meisel, C; Münch, A; Pekrun, A; Schmugge, M; Schwarz, K; von Bernuth, H; Wahn, V | 1 |
| Eibl, MM; Geyer, M; Jabrane-Ferrat, N; Nekrep, N; Peterlin, BM; Wolf, HM | 1 |
| OSSERMAN, EF; WEINSTEIN, IB | 1 |
| Chung, HY; Jo, EK; Kanegane, H; Kim, SY; Kim, YH; Kim, YO; Kook, H; Kumaki, S; Noh, HY; Song, CH; Tsuchiya, S; Wei, D | 1 |
| Barker, GC; Butcher, GA; Fleck, SL; Janse, CJ; Paton, MJ; Rodriguez, MH; Sinden, RE; Waters, A | 1 |
| Hirschhorn, R; Huie, ML; Israni, A; Ownby, DR; Yang, DR | 1 |
| Iseki, M; Kenri, T; Kurosawa, Y; Moriwaki, Y; Sasaki, T; Sasaki, Y; Yamaguchi, S; Yamamoto, T; Yamashita, R | 1 |
| Arrendondo-Vega, FX; Buckley, R; Conley, ME; El Dahr, J; Hershfield, MS; Notarangelo, LD; Roifman, C; Santisteban, I | 1 |
| Elder, ME; Kadlecek, TA; Skoda-Smith, S; Wang, F; Weiss, A; Wu, J | 1 |
10 other study(ies) available for arginine and Bare Lymphocyte Syndrome
| Article | Year |
|---|---|
A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction.
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 |
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 |
Mutation in a winged-helix DNA-binding motif causes atypical bare lymphocyte syndrome.
Topics: Amino Acid Motifs; Amino Acid Sequence; Arginine; Binding Sites; Burkitt Lymphoma; Cell Line, Transformed; DNA; DNA-Binding Proteins; Genes, MHC Class II; Genetic Complementation Test; HLA-D Antigens; Humans; Models, Molecular; Molecular Sequence Data; Protein Binding; Protein Conformation; Regulatory Factor X Transcription Factors; Sequence Alignment; Sequence Homology, Amino Acid; Severe Combined Immunodeficiency; Transcription, Genetic; Tumor Cells, Cultured | 2002 |
AMINO ACID INCORPORATION INTO PROTEIN BY A CELL FREE SYSTEM FROM PLASMA CELL TUMORS.
Topics: Adenosine Triphosphate; Amino Acids; Arginine; Carbon Isotopes; Cell-Free System; Electrophoresis; gamma-Globulins; Genetic Diseases, X-Linked; Histocytochemistry; Leukemia, Hairy Cell; Liver; Lymphatic Diseases; Mice; Neoplasms, Experimental; Nucleotidyltransferases; Pharmacology; Plasmacytoma; Proteins; Puromycin; Rabbits; Rats; Research; Ribonucleases; Severe Combined Immunodeficiency | 1964 |
X-linked severe combined immunodeficiency syndrome: the first Korean case with gamma c chain gene mutation and subsequent genetic counseling.
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 |
Factors regulating natural transmission of Plasmodium berghei to the mosquito vector, and the cloning of a transmission-blocking immunogen.
Topics: Amino Acid Oxidoreductases; Amino Acid Sequence; Animals; Anopheles; Antigens, Protozoan; Arginine; Base Sequence; Cloning, Molecular; Consensus Sequence; DNA, Complementary; DNA, Protozoan; Female; Host-Parasite Interactions; Insect Vectors; Lipopolysaccharides; Malaria; Male; Mice; Mice, Inbred BALB C; Mice, SCID; Molecular Sequence Data; Nitric Oxide Synthase; omega-N-Methylarginine; Open Reading Frames; Plasmodium; Plasmodium berghei; Protozoan Proteins; Reproduction; Severe Combined Immunodeficiency; Species Specificity | 1993 |
Somatic mosaicism for a newly identified splice-site mutation in a patient with adenosine deaminase-deficient immunodeficiency and spontaneous clinical recovery.
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 |
Direct evidence of autosomal recessive inheritance of Arg24 to termination codon in purine nucleoside phosphorylase gene in a family with a severe combined immunodeficiency patient.
Topics: Amino Acid Sequence; Arginine; Base Sequence; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 14; Codon, Terminator; Consanguinity; DNA Primers; Erythrocytes; Exons; Female; Genes, Recessive; Genetic Carrier Screening; Glycine; Histidine; Humans; Male; Nuclear Family; Pedigree; Point Mutation; Polymerase Chain Reaction; Purine-Nucleoside Phosphorylase; Serine; Severe Combined Immunodeficiency | 1998 |
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.
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.
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 |