Alteration of mannose transport in fibroblasts from type I carbohydrate deficient glycoprotein syndrome patients

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1453, Issue 3, 1999, Pages 369-377

  Dupre, T ^a   Ogier Denis, E ^b   Moore, S E H ^b   Cormier Daire, V ^c   Dehoux, M ^a   Durand, G ^a,d   Seta, N ^a,e   Codogno, P ^b  

^a BICHAT HOSPITAL   (France)

^b INSERM   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d UNIVERSITÉ PARIS SACLAY   (France)

^e UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Carbohydrate deficient glycoprotein syndrome; Mannose uptake; Phosphomannomutase; Phosphomannose isomerase

Indexed keywords

MANNOSE; MANNOSE PHOSPHATE ISOMERASE; PHOSPHOMANNOMUTASE;

ARTICLE; CARBOHYDRATE TRANSPORT; CHILD; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; HUMAN; HUMAN CELL; KINETICS; PRIORITY JOURNAL; SKIN FIBROBLAST;

BIOLOGICAL TRANSPORT; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; CELLS, CULTURED; FIBROBLASTS; GLYCOPROTEINS; HUMANS; MANNOSE; SKIN;

EID: 0033010082     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4439(99)00009-5     Document Type: Article

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