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Ludwig Lehle

University of Regensburg

20

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1326

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

2013 Molecular Cell
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Congenital disorder of glycosylation type Ij (CDG-Ij, DPAGT1-CDG): Extending the clinical and molecular spectrum of a rare disease

2012 Molecular Genetics and Metabolism
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Defining the Phenotype in Congenital Disorder of Glycosylation Due to ALG1 Mutations

2012 Pediatrics
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The essential endoplasmic reticulum chaperone Rot1 is required for protein N- and O-glycosylation in yeast

2012 Glycobiology
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Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation.

2011 PLOS Genetics
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SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder

2010 Cell
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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip

2010 Human Molecular Genetics
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SRD5A3 is required for the conversion of polyprenol to dolichol, essential for N-linked protein glycosylation

2010 Brain Cell Biology
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Deficiency of Dol-P-Man Synthase Subunit DPM3 Bridges the Congenital Disorders of Glycosylation with the Dystroglycanopathies

2009 American Journal of Human Genetics
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The yeast oligosaccharyltransferase complex can be replaced by STT3 from Leishmania major

2008 Glycobiology
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