Compounds > mannose 1-phosphate

mannose 1-phosphate and Carbohydrate-Deficient Glycoprotein Syndrome

mannose 1-phosphate has been researched along with Carbohydrate-Deficient Glycoprotein Syndrome in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (50.00)18.2507
2000's3 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Freeze, HH1
Clima, JM; Dorman, JA; Eklund, EA; Freeze, HH; Ichikawa, M; Merbouh, N; Nishikawa, A; Norberg, T1
Dupré, T; Gravier-Pelletier, C; Hardré, R; Khaled, A; Le Merrer, Y; Moore, S; Willemetz, A1
Jaeken, J; Van Schaftingen, E1
Körner, C; Lehle, L; von Figura, K1
Kjaergaard, S; Schwartz, M; Skovby, F1

Reviews

1 review(s) available for mannose 1-phosphate and Carbohydrate-Deficient Glycoprotein Syndrome

ArticleYear
Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients.
    Biochimica et biophysica acta, 2009, Volume: 1792, Issue:9

    Topics: Animals; Carbohydrate Metabolism, Inborn Errors; Congenital Disorders of Glycosylation; Enzyme Activation; Glycosylation; Humans; Mannosephosphates; Phosphotransferases (Phosphomutases)

2009

Other Studies

5 other study(ies) available for mannose 1-phosphate and Carbohydrate-Deficient Glycoprotein Syndrome

ArticleYear
Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts.
    Glycobiology, 2005, Volume: 15, Issue:11

    Topics: Carbohydrate Conformation; Carbohydrate Metabolism; Cell Proliferation; Congenital Disorders of Glycosylation; Culture Media; Dose-Response Relationship, Drug; Fibroblasts; Glycosylation; Humans; Mannosephosphates; Mutation; Phosphotransferases (Phosphomutases); Sugar Phosphates; Time Factors

2005
Mono, di and tri-mannopyranosyl phosphates as mannose-1-phosphate prodrugs for potential CDG-Ia therapy.
    Bioorganic & medicinal chemistry letters, 2007, Jan-01, Volume: 17, Issue:1

    Topics: Carbohydrate Sequence; Congenital Disorders of Glycosylation; Humans; Mannosephosphates; Molecular Sequence Data; Organophosphates; Prodrugs

2007
Phosphomannomutase deficiency is a cause of carbohydrate-deficient glycoprotein syndrome type I.
    FEBS letters, 1995, Dec-27, Volume: 377, Issue:3

    Topics: Adult; Child, Preschool; Congenital Disorders of Glycosylation; Female; Glucose; Glycosylation; Humans; Infant; Liver; Mannose-6-Phosphate Isomerase; Mannosephosphates; Phosphoglucomutase; Phosphotransferases (Phosphomutases); Protein Processing, Post-Translational

1995
Abnormal synthesis of mannose 1-phosphate derived carbohydrates in carbohydrate-deficient glycoprotein syndrome type I fibroblasts with phosphomannomutase deficiency.
    Glycobiology, 1998, Volume: 8, Issue:2

    Topics: Carbohydrates; Cells, Cultured; Congenital Disorders of Glycosylation; Dolichol Monophosphate Mannose; Fibroblasts; Guanosine Diphosphate Fucose; Guanosine Diphosphate Mannose; Humans; Lipopolysaccharides; Mannosephosphates; Phosphotransferases (Phosphomutases)

1998
Carbohydrate-deficient glycoprotein syndrome type 1A: expression and characterisation of wild type and mutant PMM2 in E. coli.
    European journal of human genetics : EJHG, 1999, Volume: 7, Issue:8

    Topics: Acyl Carrier Protein; Congenital Disorders of Glycosylation; Escherichia coli; Genotype; Humans; Mannosephosphates; Mutation, Missense; Phosphoglucomutase; Phosphotransferases (Phosphomutases); Temperature

1999