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Publications by Ludwig LEHLE
Deficiency of Dolichyl-P-Man:Man7GlcNAc2-Pp-Dolichyl Mannosyltransferase Causes Congenital Disorder of Glycosylation Type Ig
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Related publications
Congenital Disorder of Glycosylation
Recycling of Dolichyl Monophosphate to the Cytoplasmic Leaflet of the Endoplasmic Reticulum After the Cleavage of Dolichyl Pyrophosphate on the Lumenal Monolayer
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Synthesis of an UnnaturalN-Glycan-linked Dolichyl Pyrophosphate Precursor
Bioscience, Biotechnology and Biochemistry
Organic Chemistry
Applied Microbiology
Molecular Biology
Biochemistry
Analytical Chemistry
Medicine
Biotechnology
MPDU1 Mutations Underlie a Novel Human Congenital Disorder of Glycosylation, Designated Type If
Journal of Clinical Investigation
Medicine
Congenital Disorder of Glycosylation Type Ia (CDG-Ia): Phenotypic Spectrum of the R141h/F119l Genotype
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
PO-0827 Conotruncal Heart Defect in a Patient With Congenital Disorder of Glycosylation Type I
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Elevated Activity of Dolichyl Phosphate Mannose Synthase Enhances Biocontrol Abilities ofTrichoderma Atroviride
Molecular Plant-Microbe Interactions
Medicine
Agronomy
Crop Science
Physiology
Pathogenic Variants in Fucokinase Cause a Congenital Disorder of Glycosylation
American Journal of Human Genetics
Genetics
Characterization of Dolichol and Dolichyl Phosphate Phosphatase From Soya Beans (Glycine Max)
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
