acetylcysteine and Deficiency, Glucosephosphatase

acetylcysteine has been researched along with Deficiency, Glucosephosphatase in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Chen, LY; Chou, JY; Pan, CJ; Shieh, JJ	1
Chen, LY; Chou, JY; Hiraiwa, H; Marsh, J; Pan, CJ; Shieh, JJ; Terzioglu, M	1

Other Studies

2 other study(ies) available for acetylcysteine and Deficiency, Glucosephosphatase

Article	Year
Structure-function analysis of the glucose-6-phosphate transporter deficient in glycogen storage disease type Ib. Human molecular genetics, 2002, Dec-01, Volume: 11, Issue:25 Topics: Acetylcysteine; Adenoviridae; Amino Acid Sequence; Animals; Antiporters; Cell Line; Chlorocebus aethiops; COS Cells; Cysteine Endopeptidases; Cysteine Proteinase Inhibitors; Endoplasmic Reticulum; Genetic Vectors; Glucose-6-Phosphatase; Glucose-6-Phosphate; Glycogen Storage Disease Type I; Humans; Intracellular Membranes; Microsomes; Molecular Sequence Data; Monosaccharide Transport Proteins; Multienzyme Complexes; Mutation, Missense; Peptides; Proteasome Endopeptidase Complex; Protein Structure, Tertiary; Sequence Deletion; Structure-Activity Relationship; Viral Proteins	2002
The molecular basis of glycogen storage disease type 1a: structure and function analysis of mutations in glucose-6-phosphatase. The Journal of biological chemistry, 2002, Feb-15, Volume: 277, Issue:7 Topics: Acetylcysteine; Amino Acid Sequence; Animals; beta-Galactosidase; Binding Sites; Blotting, Western; Cell Membrane; Codon; COS Cells; Cysteine Proteinase Inhibitors; Cytoplasm; DNA, Complementary; Endoplasmic Reticulum; Exons; Gene Deletion; Genotype; Glucose; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Heterozygote; Homeostasis; Homozygote; Humans; Immunoblotting; Molecular Sequence Data; Mutation; Mutation, Missense; Phenotype; Phosphoric Monoester Hydrolases; Polymorphism, Single-Stranded Conformational; Protein Biosynthesis; Protein Structure, Tertiary; Structure-Activity Relationship; Time Factors; Transcription, Genetic; Transfection	2002

Article

Year

Structure-function analysis of the glucose-6-phosphate transporter deficient in glycogen storage disease type Ib.

Human molecular genetics, 2002, Dec-01, Volume: 11, Issue:25

Topics: Acetylcysteine; Adenoviridae; Amino Acid Sequence; Animals; Antiporters; Cell Line; Chlorocebus aethiops; COS Cells; Cysteine Endopeptidases; Cysteine Proteinase Inhibitors; Endoplasmic Reticulum; Genetic Vectors; Glucose-6-Phosphatase; Glucose-6-Phosphate; Glycogen Storage Disease Type I; Humans; Intracellular Membranes; Microsomes; Molecular Sequence Data; Monosaccharide Transport Proteins; Multienzyme Complexes; Mutation, Missense; Peptides; Proteasome Endopeptidase Complex; Protein Structure, Tertiary; Sequence Deletion; Structure-Activity Relationship; Viral Proteins

2002

The molecular basis of glycogen storage disease type 1a: structure and function analysis of mutations in glucose-6-phosphatase.

The Journal of biological chemistry, 2002, Feb-15, Volume: 277, Issue:7

Topics: Acetylcysteine; Amino Acid Sequence; Animals; beta-Galactosidase; Binding Sites; Blotting, Western; Cell Membrane; Codon; COS Cells; Cysteine Proteinase Inhibitors; Cytoplasm; DNA, Complementary; Endoplasmic Reticulum; Exons; Gene Deletion; Genotype; Glucose; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Heterozygote; Homeostasis; Homozygote; Humans; Immunoblotting; Molecular Sequence Data; Mutation; Mutation, Missense; Phenotype; Phosphoric Monoester Hydrolases; Polymorphism, Single-Stranded Conformational; Protein Biosynthesis; Protein Structure, Tertiary; Structure-Activity Relationship; Time Factors; Transcription, Genetic; Transfection

2002