Compounds > acetylglucosamine
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acetylglucosamine and Chromosome Deletion

acetylglucosamine has been researched along with Chromosome Deletion in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's4 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Balaji, PV; Boeggeman, EE; Qasba, PK1
Berger-Bächi, B; Jenni, R1
Aula, P; Grön, K; Halila, R; Ikonen, E; Manninen, T; Peltonen, L; Syvänen, AC; Tollersrud, O1
Aronson, NN; Fisher, KJ1

Other Studies

4 other study(ies) available for acetylglucosamine and Chromosome Deletion

ArticleYear
Functional domains of bovine beta-1,4 galactosyltransferase.
    Glycoconjugate journal, 1995, Volume: 12, Issue:6

    Topics: Acetylglucosamine; Animals; Base Sequence; Binding Sites; Cattle; Chromosome Deletion; Escherichia coli; Genetic Vectors; Kinetics; Molecular Sequence Data; Mutagenesis, Site-Directed; N-Acetyllactosamine Synthase; Protein Structure, Tertiary; Recombinant Fusion Proteins; Recombinant Proteins; Solubility; Uridine Diphosphate Galactose

1995
Teichoic acid content in different lineages of Staphylococcus aureus NCTC8325.
    Archives of microbiology, 1998, Volume: 170, Issue:3

    Topics: Acetylglucosamine; Alanine; Attachment Sites, Microbiological; Bacteriolysis; Cell Wall; Chromosome Deletion; Deoxyribonucleases, Type II Site-Specific; Glycerol; Lipopolysaccharides; Lysogeny; Methicillin Resistance; Phosphates; Ribitol; Staphylococcus aureus; Staphylococcus Phages; Teichoic Acids; Transduction, Genetic; Transformation, Bacterial

1998
Spectrum of mutations in aspartylglucosaminuria.
    Proceedings of the National Academy of Sciences of the United States of America, 1991, Dec-15, Volume: 88, Issue:24

    Topics: Acetylglucosamine; Adolescent; Adult; Alleles; Aspartylglucosaminuria; Aspartylglucosylaminase; Base Sequence; Cell Line; Child; Child, Preschool; Chromosome Deletion; Codon; DNA; DNA Transposable Elements; Fibroblasts; Humans; Infant; Leukocytes; Molecular Sequence Data; Mutation; Oligodeoxyribonucleotides; Polymerase Chain Reaction; Polymorphism, Genetic; RNA; RNA Splicing

1991
Deletion of exon 8 causes glycosylasparaginase deficiency in an African American aspartylglucosaminuria (AGU) patient.
    FEBS letters, 1991, Aug-19, Volume: 288, Issue:1-2

    Topics: Acetylglucosamine; Amino Acid Sequence; Aspartylglucosaminuria; Aspartylglucosylaminase; Base Sequence; Black People; Child; Chromosome Deletion; Exons; Fluorescent Antibody Technique; Glycosuria; Humans; Male; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Protein Conformation; RNA Splicing

1991