glutamine and ARSB Deficiency

glutamine has been researched along with ARSB Deficiency in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Arlt, G; Bielicki, J; Bindloss-Petherbridge, CA; Bradford, TM; Brooks, DA; Hopwood, JJ; Isbrandt, D; Peters, C; von Figura, K	1
Chang, JG; Lee, CC; Tsai, FJ; Wu, JY; Yang, CF	1

Other Studies

2 other study(ies) available for glutamine and ARSB Deficiency

Article	Year
Juvenile form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). A C-terminal extension causes instability but increases catalytic efficiency of arylsulfatase B. The Journal of biological chemistry, 1994, Apr-01, Volume: 269, Issue:13 Topics: Alleles; Amino Acid Sequence; Base Sequence; Cell Line; Child; Chondro-4-Sulfatase; Cloning, Molecular; Codon; DNA; DNA Primers; Frameshift Mutation; Glutamine; Humans; Molecular Sequence Data; Mucopolysaccharidosis VI; Open Reading Frames; Polymerase Chain Reaction; RNA, Messenger; Sequence Deletion; Transcription, Genetic	1994
A novel mutation (Q239R) identified in a Taiwan Chinese patient with type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome). Human mutation, 2000, Volume: 15, Issue:4 Topics: Alleles; Amino Acid Substitution; Arginine; Asian People; China; Genes, Recessive; Germ-Line Mutation; Glutamine; Humans; Mucopolysaccharidosis VI; Mutation, Missense; N-Acetylgalactosamine-4-Sulfatase; Syndrome; Taiwan	2000

Article

Year

Juvenile form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). A C-terminal extension causes instability but increases catalytic efficiency of arylsulfatase B.

The Journal of biological chemistry, 1994, Apr-01, Volume: 269, Issue:13

Topics: Alleles; Amino Acid Sequence; Base Sequence; Cell Line; Child; Chondro-4-Sulfatase; Cloning, Molecular; Codon; DNA; DNA Primers; Frameshift Mutation; Glutamine; Humans; Molecular Sequence Data; Mucopolysaccharidosis VI; Open Reading Frames; Polymerase Chain Reaction; RNA, Messenger; Sequence Deletion; Transcription, Genetic

1994

A novel mutation (Q239R) identified in a Taiwan Chinese patient with type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome).

Human mutation, 2000, Volume: 15, Issue:4

Topics: Alleles; Amino Acid Substitution; Arginine; Asian People; China; Genes, Recessive; Germ-Line Mutation; Glutamine; Humans; Mucopolysaccharidosis VI; Mutation, Missense; N-Acetylgalactosamine-4-Sulfatase; Syndrome; Taiwan

2000