메뉴 건너뛰기




Volumn 133, Issue 5, 1998, Pages 593-600

Disorders in protein glycosylation and potential therapy: Tip of an iceberg?

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATE; MANNOSE; PROTEIN; TRANSFERRIN;

EID: 0031744335     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(98)70096-4     Document Type: Article
Times cited : (69)

References (56)
  • 2
    • 0000984470 scopus 로고
    • Disorders of glycoprotein degradation and structure: α-mannosidosis, β-mannosidosis, fucosidosis, sialidosis, aspartylglucosaminuria, and carbohydrate-deficient glycoprotein syndrome
    • GH Thomas AL Beaudet Disorders of glycoprotein degradation and structure: α-mannosidosis, β-mannosidosis, fucosidosis, sialidosis, aspartylglucosaminuria, and carbohydrate-deficient glycoprotein syndrome 7th ed CR Scriver AL Beaudet WS Sly MD Valle The metabolic and molecular bases of inherited diseases 1995 : McGraw-Hill, Inc New York 2529 2562
    • (1995) , pp. 2529-2562
    • Thomas, GH1    Beaudet, AL2
  • 3
    • 0000869162 scopus 로고
    • The mucopolysaccharidoses
    • EF Neufeld J Muenzer The mucopolysaccharidoses 7th ed CR Scriver AL Beaudet WS Sly MD Valle The metabolic and molecular bases of inherited diseases 1995 : McGraw-Hill, Inc New York 2465 2494
    • (1995) , pp. 2465-2494
    • Neufeld, EF1    Muenzer, J2
  • 4
    • 0000070998 scopus 로고    scopus 로고
    • Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy
    • R Niehues M Hasilik G Alton C Korner M Schiebe-Sukumar HG Koch Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy J Clin Invest 101 1998 1414 1420
    • (1998) J Clin Invest , vol.101 , pp. 1414-1420
    • Niehues, R1    Hasilik, M2    Alton, G3    Korner, C4    Schiebe-Sukumar, M5    Koch, HG6
  • 6
    • 17444448342 scopus 로고    scopus 로고
    • Phosphomannose isomerase deficiency—A carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation
    • J Jaeken G Matthijs JM Saudubray C Dionisivici E Bertini P Delonlay Phosphomannose isomerase deficiency—A carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation Am J Hum Genet 62 1998 1535 1539
    • (1998) Am J Hum Genet , vol.62 , pp. 1535-1539
    • Jaeken, J1    Matthijs, G2    Saudubray, JM3    Dionisivici, C4    Bertini, E5    Delonlay, P6
  • 7
    • 0000249979 scopus 로고
    • Familial psychomotor retardation with markedly fluctuative serum prolactin, FSH and GH levels, partial TBG deficiency, increased serum arylsulfatase A and increased CSF protein: A new syndrome? [abstract]
    • J Jaeken M Vanderschueren-Lodewyckx P Caeaer Familial psychomotor retardation with markedly fluctuative serum prolactin, FSH and GH levels, partial TBG deficiency, increased serum arylsulfatase A and increased CSF protein: A new syndrome? [abstract] Pediatr Res 14 1980 179
    • (1980) Pediatr Res , vol.14 , pp. 179
    • Jaeken, J1    Vanderschueren-Lodewyckx, M2    Caeaer, P3
  • 8
    • 0030977458 scopus 로고    scopus 로고
    • Inherited disorders of glycoprotein synthesis: cell biological insights
    • G McDowell WA Gahl Inherited disorders of glycoprotein synthesis: cell biological insights Proc Soc Exp Biol Med 215 1997 145 157
    • (1997) Proc Soc Exp Biol Med , vol.215 , pp. 145-157
    • McDowell, G1    Gahl, WA2
  • 9
    • 0030630528 scopus 로고    scopus 로고
    • Carbohydrate-deficient glycoprotein syndrome
    • D Krasnewich WA Gahl Carbohydrate-deficient glycoprotein syndrome Adv Pediatr 44 1997 109 140
    • (1997) Adv Pediatr , vol.44 , pp. 109-140
    • Krasnewich, D1    Gahl, WA2
  • 10
    • 0027440619 scopus 로고
    • The carbohydrate-deficient glycoprotein syndromes: Pre-Golgi and Golgi disorders?
    • J Jaeken H Carchon H Stibler The carbohydrate-deficient glycoprotein syndromes: Pre-Golgi and Golgi disorders? Glycobiology 3 1993 423 428
    • (1993) Glycobiology , vol.3 , pp. 423-428
    • Jaeken, J1    Carchon, H2    Stibler, H3
  • 12
    • 0025775842 scopus 로고
    • The carbohydrate-deficient glycoprotein syndrome. A new inherited multisystemic disease with severe nervous system involvement
    • J Jaeken H Stibler B Hagberg The carbohydrate-deficient glycoprotein syndrome. A new inherited multisystemic disease with severe nervous system involvement Acta Paediatr Scand Suppl 375 1991 1 71
    • (1991) Acta Paediatr Scand Suppl , vol.375 , pp. 1-71
    • Jaeken, J1    Stibler, H2    Hagberg, B3
  • 13
    • 0026731777 scopus 로고
    • Multiple serum protein abnormalities in carbohydrate-deficient glycoprotein syndrome: Pathognomonic finding of two-dimensional electrophoresis?
    • HH Harrison KL Miller MD Harbison AE Slonim Multiple serum protein abnormalities in carbohydrate-deficient glycoprotein syndrome: Pathognomonic finding of two-dimensional electrophoresis? Clin Chem 38 1992 1390 1392
    • (1992) Clin Chem , vol.38 , pp. 1390-1392
    • Harrison, HH1    Miller, KL2    Harbison, MD3    Slonim, AE4
  • 14
    • 12644271204 scopus 로고    scopus 로고
    • Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: apparent deficiencies in clusterin and serum amyloid P
    • H Henry JD Tissot B Messerli M Markert A Muntau D Skladal Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: apparent deficiencies in clusterin and serum amyloid P J Lab Clin Med 129 1997 412 421
    • (1997) J Lab Clin Med , vol.129 , pp. 412-421
    • Henry, H1    Tissot, JD2    Messerli, B3    Markert, M4    Muntau, A5    Skladal, D6
  • 15
    • 0031909015 scopus 로고    scopus 로고
    • Isoforms and levels of transferrin, antithrombin, alpha(1)-antitrypsin and thyroxine-binding globulin in 48 patients with carbohydrate-deficient glycoprotein syndrome type I
    • H Stibler U Holzbach B Kristiansson Isoforms and levels of transferrin, antithrombin, alpha(1)-antitrypsin and thyroxine-binding globulin in 48 patients with carbohydrate-deficient glycoprotein syndrome type I Scand J Clin Lab Invest 58 1998 55 61
    • (1998) Scand J Clin Lab Invest , vol.58 , pp. 55-61
    • Stibler, H1    Holzbach, U2    Kristiansson, B3
  • 16
    • 0027177255 scopus 로고
    • Carbohydrate-deficient glycoprotein (CDG) syndrome—a new variant, type III
    • H Stibler B Westerberg F Hanefeld B Hagberg Carbohydrate-deficient glycoprotein (CDG) syndrome—a new variant, type III Neuropediatrics 24 1993 51 52
    • (1993) Neuropediatrics , vol.24 , pp. 51-52
    • Stibler, H1    Westerberg, B2    Hanefeld, F3    Hagberg, B4
  • 17
    • 0028851977 scopus 로고
    • Carbohydrate-deficient glycoprotein syndrome—a fourth subtype
    • H Stibler U Stephani U Kutsch Carbohydrate-deficient glycoprotein syndrome—a fourth subtype Neuropediatrics 26 1995 235 237
    • (1995) Neuropediatrics , vol.26 , pp. 235-237
    • Stibler, H1    Stephani, U2    Kutsch, U3
  • 19
    • 0021891884 scopus 로고
    • Assembly of asparagine-linked oligosaccharides
    • R Kornfeld S Kornfeld Assembly of asparagine-linked oligosaccharides Annu Rev Biochem 54 1985 631 664
    • (1985) Annu Rev Biochem , vol.54 , pp. 631-664
    • Kornfeld, R1    Kornfeld, S2
  • 20
    • 0028185911 scopus 로고
    • The major glycosylation pathways of mammalian membranes. A summary
    • A Varki HH Freeze The major glycosylation pathways of mammalian membranes. A summary Subcell Biochem 22 1994 71 100
    • (1994) Subcell Biochem , vol.22 , pp. 71-100
    • Varki, A1    Freeze, HH2
  • 22
    • 0029957579 scopus 로고    scopus 로고
    • Inhibition of phosphomannose isomerase by fructose 1-phosphate: an explanation for defective N-glycosylation in hereditary fructose intolerance
    • J Jaeken M Pirard M Adamowicz E Pronicka E Van Schaftingen Inhibition of phosphomannose isomerase by fructose 1-phosphate: an explanation for defective N-glycosylation in hereditary fructose intolerance Pediatr Res 40 1996 764 766
    • (1996) Pediatr Res , vol.40 , pp. 764-766
    • Jaeken, J1    Pirard, M2    Adamowicz, M3    Pronicka, E4    Van Schaftingen, E5
  • 23
    • 0031981557 scopus 로고    scopus 로고
    • Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A
    • G Matthijs E Schollen E Van Schaftingen JJ Cassiman J Jaeken Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A Am J Hum Genet 62 1998 542 550
    • (1998) Am J Hum Genet , vol.62 , pp. 542-550
    • Matthijs, G1    Schollen, E2    Van Schaftingen, E3    Cassiman, JJ4    Jaeken, J5
  • 24
    • 8544228332 scopus 로고    scopus 로고
    • Phosphomannomutase deficiency is the main cause of carbohydrate-deficient glycoprotein syndrome with type I isoelectrofocusing pattern of serum sialotransferrins
    • J Jaeken J Artigas R Barone A Fiumara TJ de Koning BT Poll-The Phosphomannomutase deficiency is the main cause of carbohydrate-deficient glycoprotein syndrome with type I isoelectrofocusing pattern of serum sialotransferrins J Inherit Metab Dis 20 1997 447 449
    • (1997) J Inherit Metab Dis , vol.20 , pp. 447-449
    • Jaeken, J1    Artigas, J2    Barone, R3    Fiumara, A4    de Koning, TJ5    Poll-The, BT6
  • 25
    • 0029585865 scopus 로고
    • Phosphomannomutase deficiency is a cause of carbohydrate-deficient glycoprotein syndrome type I
    • E Van Schaftingen J Jaeken Phosphomannomutase deficiency is a cause of carbohydrate-deficient glycoprotein syndrome type I FEBS Lett 377 1995 318 320
    • (1995) FEBS Lett , vol.377 , pp. 318-320
    • Van Schaftingen, E1    Jaeken, J2
  • 26
    • 0031005847 scopus 로고    scopus 로고
    • Mutations in PMM2, a phosphomannomutase gene on chromosome 16p 13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)
    • G Matthijs E Schollen E Pardon M Veiga-Da-Cunha J Jaeken J-J Cassiman Mutations in PMM2, a phosphomannomutase gene on chromosome 16p 13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome) Nat Genet 16 1997 88 92
    • (1997) Nat Genet , vol.16 , pp. 88-92
    • Matthijs, G1    Schollen, E2    Pardon, E3    Veiga-Da-Cunha, M4    Jaeken, J5    Cassiman, J-J6
  • 27
    • 0031568887 scopus 로고    scopus 로고
    • PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13
    • G Matthijs E Schollen M Pirard ML Budarf E Van Schaftingen JJ Cassiman PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13 Genomics 40 1997 41 47
    • (1997) Genomics , vol.40 , pp. 41-47
    • Matthijs, G1    Schollen, E2    Pirard, M3    Budarf, ML4    Van Schaftingen, E5    Cassiman, JJ6
  • 28
    • 0031004767 scopus 로고    scopus 로고
    • Brain contains HNK-1 immunoreactive O-glycans of the sulfoglucuronyl lactosamine series that terminate in 2-1inked or 2,6-1inked hexose (mannose)
    • CT Yuen W Chai RW Loveless AM Lawson RU Margolis T Feizi Brain contains HNK-1 immunoreactive O-glycans of the sulfoglucuronyl lactosamine series that terminate in 2-1inked or 2,6-1inked hexose (mannose) J Biol Chem 272 1997 8924 8931
    • (1997) J Biol Chem , vol.272 , pp. 8924-8931
    • Yuen, CT1    Chai, W2    Loveless, RW3    Lawson, AM4    Margolis, RU5    Feizi, T6
  • 29
    • 0031026624 scopus 로고    scopus 로고
    • Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin
    • A Chiba K Matsumura H Yamada T Inazu T Shimizu S Kusunoki Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin J Biol Chem 272 1997 2156 2162
    • (1997) J Biol Chem , vol.272 , pp. 2156-2162
    • Chiba, A1    Matsumura, K2    Yamada, H3    Inazu, T4    Shimizu, T5    Kusunoki, S6
  • 30
    • 0027970923 scopus 로고
    • Carbohydrate-deficient glycoprotein syndrome: Not an N-linked oligosaccharide processing defect, but an abnormality in lipid-linked oligosaccharide biosynthesis?
    • LD Powell K Paneerselvam R Vij S Diaz A Manzi N Buist Carbohydrate-deficient glycoprotein syndrome: Not an N-linked oligosaccharide processing defect, but an abnormality in lipid-linked oligosaccharide biosynthesis? J Clin Invest 94 1994 1901 1909
    • (1994) J Clin Invest , vol.94 , pp. 1901-1909
    • Powell, LD1    Paneerselvam, K2    Vij, R3    Diaz, S4    Manzi, A5    Buist, N6
  • 31
    • 0029984537 scopus 로고    scopus 로고
    • Mannose corrects altered N-glycosylation in carbohydrate-deficient glycoprotein syndrome fibroblasts
    • K Panneerselvam HH Freeze Mannose corrects altered N-glycosylation in carbohydrate-deficient glycoprotein syndrome fibroblasts J Clin Invest 97 1996 1478 1487
    • (1996) J Clin Invest , vol.97 , pp. 1478-1487
    • Panneerselvam, K1    Freeze, HH2
  • 32
    • 0029095453 scopus 로고
    • Abnormal synthesis of dolichol-linked oligosaccharides in carbohydrate-deficient glycoprotein syndrome
    • DM Krasnewich GD Holt M Brantly F Skovby J Redwine WA Gahl Abnormal synthesis of dolichol-linked oligosaccharides in carbohydrate-deficient glycoprotein syndrome Glycobiology 5 1995 503 510
    • (1995) Glycobiology , vol.5 , pp. 503-510
    • Krasnewich, DM1    Holt, GD2    Brantly, M3    Skovby, F4    Redwine, J5    Gahl, WA6
  • 33
    • 0038599459 scopus 로고    scopus 로고
    • Abnormal synthesis of mannose 1-phosphate derived carbohydrates in carbohydrate-deficient glycoprotein syndrome type I fibroblasts with phosphomannomutase deficiency
    • C Korner L Lehle K Von Figura Abnormal synthesis of mannose 1-phosphate derived carbohydrates in carbohydrate-deficient glycoprotein syndrome type I fibroblasts with phosphomannomutase deficiency Glycobiology 8 1998 165 171
    • (1998) Glycobiology , vol.8 , pp. 165-171
    • Korner, C1    Lehle, L2    Von Figura, K3
  • 34
    • 0032528886 scopus 로고    scopus 로고
    • A novel carbohydrate-deficient glycoprotein syndrome characterized by a deficiency in glucosylation of the dolichol-linked oligosaccharide
    • P Burda L Borsig J de Rijk-van Andel R Wevers J Jaeken H Carchon A novel carbohydrate-deficient glycoprotein syndrome characterized by a deficiency in glucosylation of the dolichol-linked oligosaccharide J Clin Invest 102 1998 647 652
    • (1998) J Clin Invest , vol.102 , pp. 647-652
    • Burda, P1    Borsig, L2    de Rijk-van Andel, J3    Wevers, R4    Jaeken, J5    Carchon, H6
  • 35
    • 0030957595 scopus 로고    scopus 로고
    • A partial deficiency of dehydrodolichol reduction is a cause of carbohydrate-deficient glycoprotein syndrome type I
    • T Ohkura K Fukushima A Kurisaki H Sagami K Ogura K Ohno A partial deficiency of dehydrodolichol reduction is a cause of carbohydrate-deficient glycoprotein syndrome type I J Biol Chem 272 1997 6868 6875
    • (1997) J Biol Chem , vol.272 , pp. 6868-6875
    • Ohkura, T1    Fukushima, K2    Kurisaki, A3    Sagami, H4    Ogura, K5    Ohno, K6
  • 36
    • 0029820486 scopus 로고    scopus 로고
    • Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development
    • J Tan J Dunn J Jaeken H Schachter Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development Am J Hum Genet 59 1996 810 817
    • (1996) Am J Hum Genet , vol.59 , pp. 810-817
    • Tan, J1    Dunn, J2    Jaeken, J3    Schachter, H4
  • 37
    • 0029986487 scopus 로고    scopus 로고
    • Mannose enters mammalian cells using a specific transporter that is insensitive to glucose
    • K Panneerselvam HH Freeze Mannose enters mammalian cells using a specific transporter that is insensitive to glucose J Biol Chem 19 271 1996 9417 9421
    • (1996) J Biol Chem , vol.19 , Issue.271 , pp. 9417-9421
    • Panneerselvam, K1    Freeze, HH2
  • 38
    • 0030760044 scopus 로고    scopus 로고
    • Human fibroblasts prefer mannose over glucose as a source of mannose for N-glycosylation. Evidence for the functional importance of transported mannose
    • K Panneerselvam JR Etchison HH Freeze Human fibroblasts prefer mannose over glucose as a source of mannose for N-glycosylation. Evidence for the functional importance of transported mannose J Biol Chem 272 1997 23123 23129
    • (1997) J Biol Chem , vol.272 , pp. 23123-23129
    • Panneerselvam, K1    Etchison, JR2    Freeze, HH3
  • 39
    • 17744411208 scopus 로고    scopus 로고
    • Oral ingestion of mannose elevates blood mannose levels: a first step toward a potential therapy for carbohydrate-deficient glycoprotein syndrome type I
    • G Alton S Kjaergaard JR Etchison F Skovby HH Freeze Oral ingestion of mannose elevates blood mannose levels: a first step toward a potential therapy for carbohydrate-deficient glycoprotein syndrome type I Biochem Mol Med 60 1997 127 133
    • (1997) Biochem Mol Med , vol.60 , pp. 127-133
    • Alton, G1    Kjaergaard, S2    Etchison, JR3    Skovby, F4    Freeze, HH5
  • 41
    • 0028136581 scopus 로고
    • The emergence of a basolateral 1-deoxymannojirimycin-sensitive mannose carrier is a function of intestinal epithelial cell differentiation. Evidence for a new inhibitory effect of 1-deoxymannojirimycin on facilitative mannose transport
    • E Ogier-Denis A Blais JJ Houri T Voisin G Trugnan P Codogno The emergence of a basolateral 1-deoxymannojirimycin-sensitive mannose carrier is a function of intestinal epithelial cell differentiation. Evidence for a new inhibitory effect of 1-deoxymannojirimycin on facilitative mannose transport J Biol Chem 269 1994 4285 4290
    • (1994) J Biol Chem , vol.269 , pp. 4285-4290
    • Ogier-Denis, E1    Blais, A2    Houri, JJ3    Voisin, T4    Trugnan, G5    Codogno, P6
  • 42
    • 0014753459 scopus 로고
    • Specificity of monosaccharide transport in dog kidney
    • M Silverman MA Aganon FP Chinard Specificity of monosaccharide transport in dog kidney Am J Physiol 218 1970 743 750
    • (1970) Am J Physiol , vol.218 , pp. 743-750
    • Silverman, M1    Aganon, MA2    Chinard, FP3
  • 43
    • 0019796775 scopus 로고
    • Reaction of monosaccharides with proteins: possible evolutionary significance
    • HF Bunn PJ Higgins Reaction of monosaccharides with proteins: possible evolutionary significance Science 213 1981 222 224
    • (1981) Science , vol.213 , pp. 222-224
    • Bunn, HF1    Higgins, PJ2
  • 44
    • 0027174523 scopus 로고
    • Cell type-dependent variations in the subcellular distribution of alpha-mannosidase I and II
    • A Velasco L Hendricks KW Moremen DR Tulsiani O Touster MG Farquhar Cell type-dependent variations in the subcellular distribution of alpha-mannosidase I and II J Cell Biol 122 1993 39 51
    • (1993) J Cell Biol , vol.122 , pp. 39-51
    • Velasco, A1    Hendricks, L2    Moremen, KW3    Tulsiani, DR4    Touster, O5    Farquhar, MG6
  • 45
    • 0030809002 scopus 로고    scopus 로고
    • Continuous mannose infusion in carbohydrate-deficient glycoprotein syndrome type I
    • E Mayatepek M Schroder D Kohlmuller WP Bieger W Nutzenadel Continuous mannose infusion in carbohydrate-deficient glycoprotein syndrome type I Acta Paediatr 86 1997 1138 1140
    • (1997) Acta Paediatr , vol.86 , pp. 1138-1140
    • Mayatepek, E1    Schroder, M2    Kohlmuller, D3    Bieger, WP4    Nutzenadel, W5
  • 46
    • 0001276826 scopus 로고    scopus 로고
    • Mannose therapy in carbohydrate-deficient glycoprotein syndrome type 1: first results from the German multicenter study [abstract]
    • T Marquardt M Hasilik R Niehues M Herting A Muntau U Holzbach Mannose therapy in carbohydrate-deficient glycoprotein syndrome type 1: first results from the German multicenter study [abstract] Amino Acids 12 1997 389
    • (1997) Amino Acids , vol.12 , pp. 389
    • Marquardt, T1    Hasilik, M2    Niehues, R3    Herting, M4    Muntau, A5    Holzbach, U6
  • 47
  • 48
    • 0022627651 scopus 로고
    • Relationships between glucose and mannose during late gestation in normal pregnancy and pregnancy complicated by diabetes mellitus: concurrent concentrations in maternal plasma and amniotic fluid
    • S Akazawa BE Metzger N Freinkel Relationships between glucose and mannose during late gestation in normal pregnancy and pregnancy complicated by diabetes mellitus: concurrent concentrations in maternal plasma and amniotic fluid J Clin Endocrinol Metab 62 1986 984 989
    • (1986) J Clin Endocrinol Metab , vol.62 , pp. 984-989
    • Akazawa, S1    Metzger, BE2    Freinkel, N3
  • 49
    • 0345032001 scopus 로고    scopus 로고
    • Initial trial of N-acetyl glucosamine in children with chronic inflammatory bowel disease [abstract]
    • S Salvatore R Heushkel S Davies S Walker Smith S Murch Initial trial of N-acetyl glucosamine in children with chronic inflammatory bowel disease [abstract] J Pediatr Gastroenterol Nutr 26 1998 563
    • (1998) J Pediatr Gastroenterol Nutr , vol.26 , pp. 563
    • Salvatore, S1    Heushkel, R2    Davies, S3    Walker Smith, S4    Murch, S5
  • 50
    • 0031115895 scopus 로고    scopus 로고
    • Carbohydrate-deficient glycoprotein syndrome: hidden treasures
    • WA Gahl Carbohydrate-deficient glycoprotein syndrome: hidden treasures J Lab Clin Med 129 1997 394 395
    • (1997) J Lab Clin Med , vol.129 , pp. 394-395
    • Gahl, WA1
  • 51
    • 0032037786 scopus 로고    scopus 로고
    • Diseases of abnormal protein glycosylation—an emerging area
    • S Komfeld Diseases of abnormal protein glycosylation—an emerging area J Clin Invest 101 1998 1293 1295
    • (1998) J Clin Invest , vol.101 , pp. 1293-1295
    • Komfeld, S1
  • 52
    • 0001033564 scopus 로고
    • Oligosaccharides in vertebrate development
    • A Varki J Marth Oligosaccharides in vertebrate development Dev Biol 6 1995 127 138
    • (1995) Dev Biol , vol.6 , pp. 127-138
    • Varki, A1    Marth, J2
  • 53
    • 0031455984 scopus 로고    scopus 로고
    • Alpha-mannosidase-II deficiency results in dyserythropoiesis and unveils an alternate pathway in oligosaccharide biosynthesis
    • D Chui M Oh-Eda YF Liao K Panneerselvam A Lal KW Marek Alpha-mannosidase-II deficiency results in dyserythropoiesis and unveils an alternate pathway in oligosaccharide biosynthesis Cell 90 1997 157 167
    • (1997) Cell , vol.90 , pp. 157-167
    • Chui, D1    Oh-Eda, M2    Liao, YF3    Panneerselvam, K4    Lal, A5    Marek, KW6
  • 55
    • 0032537568 scopus 로고    scopus 로고
    • Defective intracellular activity of GDP-D-mannose-4,6-dehydratase in leukocyte adhesion deficiency type II syndrome
    • L Sturla A Etzioni A Bisso D Zanardi G Deflora L Silengo Defective intracellular activity of GDP-D-mannose-4,6-dehydratase in leukocyte adhesion deficiency type II syndrome FEBS Lett 429 1998 274 278
    • (1998) FEBS Lett , vol.429 , pp. 274-278
    • Sturla, L1    Etzioni, A2    Bisso, A3    Zanardi, D4    Deflora, G5    Silengo, L6
  • 56
    • 0027318961 scopus 로고
    • Biological roles of oligosaccharides: all of the theories are correct
    • A Varki Biological roles of oligosaccharides: all of the theories are correct Glycobiology 3 1993 97 130
    • (1993) Glycobiology , vol.3 , pp. 97-130
    • Varki, A1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.