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Protein Glycosylation, Conserved from Yeast to Man: A Model Organism Helps Elucidate Congenital Human Diseases

Angewandte Chemie International Edition, 2006-10, Vol.45 (41), p.6802-6818

2006

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Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing

Human molecular genetics, 2012-10, Vol.21 (19), p.4151-4161

2012

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Kex1 Protease Is Involved in Yeast Cell Death Induced by Defective N-Glycosylation, Acetic Acid, and Chronological Aging

The Journal of biological chemistry, 2008-07, Vol.283 (27), p.19151-19163

2008

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Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation

PLoS genetics, 2011-12, Vol.7 (12), p.e1002427-e1002427

2011

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Biochemical Characterization and Membrane Topology of Alg2 from Saccharomyces cerevisiae as a Bifunctional α1,3- and 1,6-Mannosyltransferase Involved in Lipid-linked Oligosaccharide Biosynthesis

The Journal of biological chemistry, 2009-05, Vol.284 (18), p.11900-11912

2009

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The Auxin-induced Maize Gene ZmSAUR2 Encodes a Short-lived Nuclear Protein Expressed in Elongating Tissues

The Journal of biological chemistry, 2003-06, Vol.278 (26), p.23936-23943

2003

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The oligosaccharyltransferase complex from yeast

BBA - General Subjects, 1999-01, Vol.1426 (2), p.259-273

1999

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Yeast oligosaccharyltransferase consists of two functionally distinct sub-complexes, specified by either the Ost3p or Ost6p subunit

FEBS letters, 2005-12, Vol.579 (29), p.6564-6568

2005

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A New Type of Congenital Disorders of Glycosylation (CDG-Ii) Provides New Insights into the Early Steps of Dolichol-linked Oligosaccharide Biosynthesis

The Journal of biological chemistry, 2003-06, Vol.278 (25), p.22498-22505

2003

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Deficiency of GDP-Man:GlcNAc2-PP-Dolichol mannosyltransferase causes congenital disorder of glycosylation type iK

American journal of human genetics, 2004-03, Vol.74 (3), p.472-481

2004

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Carbohydrate-Deficient Glycoprotein Syndrome Type V: Deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl Glucosyltransferase

Proceedings of the National Academy of Sciences - PNAS, 1998-10, Vol.95 (22), p.13200-13205

1998

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More than 40 years of glycobiology in Regensburg

Biochemical and biophysical research communications, 2012-08, Vol.425 (3), p.578-582

2012

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C. elegans DPY-19 Is a C-Mannosyltransferase Glycosylating Thrombospondin Repeats

Molecular cell, 2013-04, Vol.50 (2), p.295-302

2013

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Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig

Biochemical journal, 2002-10, Vol.367 (Pt 1), p.195-201

2002

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Deletion of New Covalently Linked Cell Wall Glycoproteins Alters the Electrophoretic Mobility of Phosphorylated Wall Components of Saccharomyces cerevisiae

Journal of Bacteriology, 1999-05, Vol.181 (10), p.3076-3086

1999

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Pir Proteins of Saccharomyces cerevisiae Are Attached to β-1,3-Glucan by a New Protein-Carbohydrate Linkage

The Journal of biological chemistry, 2006-04, Vol.281 (17), p.11523-11529

2006

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Biochemical characterization, membrane association and identification of amino acids essential for the function of Alg11 from Saccharomyces cerevisiae , an α1,2-mannosyltransferase catalysing two sequential glycosylation steps in the formation of the lipid-linked core oligosaccharide

Biochemical journal, 2010-03, Vol.426 (2), p.205-217

2010

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Biosynthesis of Lipid-Linked Oligosaccharides in Yeast: the ALG3 Gene Encodes the Dol-P-Man:Man5GlcNAc2-PP-Dol Mannosyltransferase

Biological chemistry, 2001-02, Vol.382 (2), p.321-328

2001

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Biosynthesis of Lipid-linked Oligosaccharides in Saccharomyces cerevisiae

The Journal of biological chemistry, 2005-10, Vol.280 (41), p.34500-34506

2005

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Deficiency of Dol-P-Man Synthase Subunit DPM3 Bridges the Congenital Disorders of Glycosylation with the Dystroglycanopathies

American journal of human genetics, 2009-07, Vol.85 (1), p.76-86

2009

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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip

Human molecular genetics, 2010-04, Vol.19 (8), p.1413-1424

2010

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Identification of the Gene Encoding the α1,3-Mannosyltransferase (ALG3) in Arabidopsis and Characterization of Downstream N-Glycan Processing

The Plant cell, 2008-06, Vol.20 (6), p.1652-1664

2008

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The essential endoplasmic reticulum chaperone Rot1 is required for protein N- and O-glycosylation in yeast

Glycobiology (Oxford), 2012-07, Vol.22 (7), p.939-947

2012

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yeast oligosaccharyltransferase complex can be replaced by STT3 from Leishmania major

Glycobiology (Oxford), 2009-02, Vol.19 (2), p.160-171

2009

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Protein Glycosylation, Conserved from Yeast to Man: A Model Organism Helps Elucidate Congenital Human Diseases

Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing

SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder

Kex1 Protease Is Involved in Yeast Cell Death Induced by Defective N-Glycosylation, Acetic Acid, and Chronological Aging

Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation

Biochemical Characterization and Membrane Topology of Alg2 from Saccharomyces cerevisiae as a Bifunctional α1,3- and 1,6-Mannosyltransferase Involved in Lipid-linked Oligosaccharide Biosynthesis

The Auxin-induced Maize Gene ZmSAUR2 Encodes a Short-lived Nuclear Protein Expressed in Elongating Tissues

The oligosaccharyltransferase complex from yeast

Yeast oligosaccharyltransferase consists of two functionally distinct sub-complexes, specified by either the Ost3p or Ost6p subunit

A New Type of Congenital Disorders of Glycosylation (CDG-Ii) Provides New Insights into the Early Steps of Dolichol-linked Oligosaccharide Biosynthesis

Deficiency of GDP-Man:GlcNAc2-PP-Dolichol mannosyltransferase causes congenital disorder of glycosylation type iK

Carbohydrate-Deficient Glycoprotein Syndrome Type V: Deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl Glucosyltransferase

More than 40 years of glycobiology in Regensburg

C. elegans DPY-19 Is a C-Mannosyltransferase Glycosylating Thrombospondin Repeats

Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig

Deletion of New Covalently Linked Cell Wall Glycoproteins Alters the Electrophoretic Mobility of Phosphorylated Wall Components of Saccharomyces cerevisiae

Pir Proteins of Saccharomyces cerevisiae Are Attached to β-1,3-Glucan by a New Protein-Carbohydrate Linkage

Biochemical characterization, membrane association and identification of amino acids essential for the function of Alg11 from Saccharomyces cerevisiae , an α1,2-mannosyltransferase catalysing two sequential glycosylation steps in the formation of the lipid-linked core oligosaccharide

Biosynthesis of Lipid-Linked Oligosaccharides in Yeast: the ALG3 Gene Encodes the Dol-P-Man:Man5GlcNAc2-PP-Dol Mannosyltransferase

Biosynthesis of Lipid-linked Oligosaccharides in Saccharomyces cerevisiae

Deficiency of Dol-P-Man Synthase Subunit DPM3 Bridges the Congenital Disorders of Glycosylation with the Dystroglycanopathies

A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip

Identification of the Gene Encoding the α1,3-Mannosyltransferase (ALG3) in Arabidopsis and Characterization of Downstream N-Glycan Processing

The essential endoplasmic reticulum chaperone Rot1 is required for protein N- and O-glycosylation in yeast

yeast oligosaccharyltransferase complex can be replaced by STT3 from Leishmania major

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