n-acetylglucosaminylasparagine and Chromosome Deletion

n-acetylglucosaminylasparagine has been researched along with Chromosome Deletion in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Aula, P; Grön, K; Halila, R; Ikonen, E; Manninen, T; Peltonen, L; Syvänen, AC; Tollersrud, O	1
Aronson, NN; Fisher, KJ	1

Other Studies

2 other study(ies) available for n-acetylglucosaminylasparagine and Chromosome Deletion

Article	Year
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

Article

Year

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