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Identification and functional analysis of a defect in the human ALG9 gene: Definition of congenital disorder of glycosylation type IL

American journal of human genetics, 2004-07, Vol.75 (1), p.146-150

2004

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Golgi enzymes are enriched in perforated zones of golgi cisternae but are depleted in COPI vesicles

Molecular biology of the cell, 2004-10, Vol.15 (10), p.4710-4724

2004

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Genome-wide analysis of the unfolded protein response in fibroblasts from congenital disorders of glycosylation type-I patients

The FASEB journal, 2005-02, Vol.19 (2), p.240-242

2005

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GTP-Bound Forms of rab6 Induce the Redistribution of Golgi Proteins into the Endoplasmic Reticulum

Proceedings of the National Academy of Sciences - PNAS, 1997-03, Vol.94 (5), p.1828-1833

1997

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Transition of galactosyltransferase 1 from trans-Golgi cisterna to the trans-Golgi network is signal mediated

Molecular biology of the cell, 2006-12, Vol.17 (12), p.5153-5162

2006

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Fibrotic response in fibroblasts from congenital disorders of glycosylation

Journal of cellular and molecular medicine, 2011-08, Vol.15 (8), p.1788-1796

2011

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Tn-syndrome

BBA - Molecular Basis of Disease, 1999-10, Vol.1455 (2), p.255-268

Berger, Eric G

1999

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Small Cargo Proteins and Large Aggregates Can Traverse the Golgi by a Common Mechanism without Leaving the Lumen of Cisternae

The Journal of cell biology, 2001-12, Vol.155 (7), p.1225-1238

2001

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Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik

Human molecular genetics, 2004-03, Vol.13 (5), p.535-542

2004

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MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If

The Journal of clinical investigation, 2001-12, Vol.108 (11), p.1687-1695

2001

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Localization of three human polypeptide GalNAc-transferases in HeLa cells suggests initiation of O-linked glycosylation throughout the Golgi apparatus

Journal of cell science, 1998-01, Vol.111 ( Pt 1) (1), p.45-60

1998

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ALG12 mannosyltransferase defect in congenital disorder of glycosylation type Ig

Human molecular genetics, 2002-09, Vol.11 (19), p.2331-2339

2002

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Mapping the distribution of Golgi enzymes involved in the construction of complex oligosaccharides

Journal of cell science, 1995-04, Vol.108 ( Pt 4) (4), p.1617-1627

1995

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Ectopic localizations of Golgi glycosyltransferases

Glycobiology (Oxford), 2002-02, Vol.12 (2), p.29R-36R

Berger, Eric G

2002

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A Mutation in the Human Ortholog of the Saccharomyces cerevisiae ALG6 Gene Causes Carbohydrate-Deficient Glycoprotein Syndrome Type-Ic

Proceedings of the National Academy of Sciences - PNAS, 1999-06, Vol.96 (12), p.6982-6987

1999

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The β1,3-Galactosyltransferase β3GalT-V Is a Stage-specific Embryonic Antigen-3 (SSEA-3) Synthase

The Journal of biological chemistry, 2000-07, Vol.275 (30), p.22631-22634

2000

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The C-Disaccharide α-C(1→3)-Mannopyranoside of N-Acetylgalactosamine Is an Inhibitor of Glycohydrolases and of Human α-1,3-Fucosyltransferase VI. Its Epimer α-(1→3)-Mannopyranoside of N-Acetyltalosamine Is Not

Journal of organic chemistry, 2000-07, Vol.65 (14), p.4251-4260

2000

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A β -1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine Synthase Activity Is Structurally Related to β -1,3-galactosyltransferases

Proceedings of the National Academy of Sciences - PNAS, 1999-01, Vol.96 (2), p.406-411

1999

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Localization of α1,3-fucosyltransferase VI in Weibel–Palade bodies of human endothelial cells

Proceedings of the National Academy of Sciences - PNAS, 2000-07, Vol.97 (15), p.8369-8374

2000

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Chemo-Enzymatic synthesis of the galili epitope Galα(1→3)Galβ(1→4)GlcNAc on a homogeneously soluble PEG polymer by a multi-Enzyme system

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (18), p.2503-2506

2001

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Colocalization of β1,4galactosyltransferase with mannose 6-phosphate receptor in monensin-induced TGN-derived structures

Histochemistry and cell biology, 2001-02, Vol.115 (2), p.157-168

2001

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Golgi-disturbing agents

Histochemistry and cell biology, 1998-05, Vol.109 (5-6), p.571-590

1998

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The yeast expression system for recombinant glycosyltransferases

Glycoconjugate journal, 1999-02, Vol.16 (2), p.125-139

1999

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Molecular cloning of a human UDP‐galactose:GlcNAcβ1,3GalNAc β1,3 galactosyltransferase gene encoding an O‐linked core3‐elongation enzyme

European journal of biochemistry, 1999-07, Vol.263 (2), p.571-576

1999

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ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg

Human molecular genetics, 2002-09, Vol.11 (19), p.2331-2339

2002

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Identification and functional analysis of a defect in the human ALG9 gene: Definition of congenital disorder of glycosylation type IL

Golgi enzymes are enriched in perforated zones of golgi cisternae but are depleted in COPI vesicles

Genome-wide analysis of the unfolded protein response in fibroblasts from congenital disorders of glycosylation type-I patients

GTP-Bound Forms of rab6 Induce the Redistribution of Golgi Proteins into the Endoplasmic Reticulum

Transition of galactosyltransferase 1 from trans-Golgi cisterna to the trans-Golgi network is signal mediated

Fibrotic response in fibroblasts from congenital disorders of glycosylation

Tn-syndrome

Small Cargo Proteins and Large Aggregates Can Traverse the Golgi by a Common Mechanism without Leaving the Lumen of Cisternae

Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik

MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If

Localization of three human polypeptide GalNAc-transferases in HeLa cells suggests initiation of O-linked glycosylation throughout the Golgi apparatus

ALG12 mannosyltransferase defect in congenital disorder of glycosylation type Ig

Mapping the distribution of Golgi enzymes involved in the construction of complex oligosaccharides

Ectopic localizations of Golgi glycosyltransferases

A Mutation in the Human Ortholog of the Saccharomyces cerevisiae ALG6 Gene Causes Carbohydrate-Deficient Glycoprotein Syndrome Type-Ic

The β1,3-Galactosyltransferase β3GalT-V Is a Stage-specific Embryonic Antigen-3 (SSEA-3) Synthase

The C-Disaccharide α-C(1→3)-Mannopyranoside of N-Acetylgalactosamine Is an Inhibitor of Glycohydrolases and of Human α-1,3-Fucosyltransferase VI. Its Epimer α-(1→3)-Mannopyranoside of N-Acetyltalosamine Is Not

A β -1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine Synthase Activity Is Structurally Related to β -1,3-galactosyltransferases

Localization of α1,3-fucosyltransferase VI in Weibel–Palade bodies of human endothelial cells

Chemo-Enzymatic synthesis of the galili epitope Galα(1→3)Galβ(1→4)GlcNAc on a homogeneously soluble PEG polymer by a multi-Enzyme system

Colocalization of β1,4galactosyltransferase with mannose 6-phosphate receptor in monensin-induced TGN-derived structures

Golgi-disturbing agents

The yeast expression system for recombinant glycosyltransferases

Molecular cloning of a human UDP‐galactose:GlcNAcβ1,3GalNAc β1,3 galactosyltransferase gene encoding an O‐linked core3‐elongation enzyme

ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg

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