S. Moore

发表

Processing of N-linked glycans during endoplasmic-reticulum-associated degradation of a short-lived variant of ribophorin I.

M. Ermonval, O. Kellermann, N. Ivessa, 2003, The Biochemical journal.

Endoplasmic Reticulum-associated Degradation (ERAD) and Free Oligosaccharide Generation in Saccharomyces cerevisiae*

D. Harvey, I. Chantret, S. Moore, 2011, The Journal of Biological Chemistry.

The Compartmentalisation of Phosphorylated Free Oligosaccharides in Cells from a CDG Ig Patient Reveals a Novel ER-to-Cytosol Translocation Process

O. Danos, B. Bader-Meunier, P. de Lonlay, 2010, PloS one.

Mono, di and tri-mannopyranosyl phosphates as mannose-1-phosphate prodrugs for potential CDG-Ia therapy.

C. Gravier-Pelletier, Y. Le Merrer, T. Dupré, 2007, Bioorganic & medicinal chemistry letters.

A Deficiency in Dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl α3-Glucosyltransferase Defines a New Subtype of Congenital Disorders of Glycosylation*

P. Codogno, O. Danos, R. Oriol, 2003, The Journal of Biological Chemistry.

Bacterial Lipid II Analogs: Novel In Vitro Substrates for Mammalian Oligosaccharyl Diphosphodolichol Diphosphatase (DLODP) Activities

C. Dowson, D. Roper, A. Bouhss, 2019, Molecules.

A New Intronic Mutation in the DPM1 Gene Is Associated With a Milder Form of CDG Ie in Two French Siblings

I. Sfaello, T. Dupré, G. Durand, 2006, Pediatric Research.

A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity

N. Dorison, D. Heron, C. Mignot, 2016, Orphanet Journal of Rare Diseases.

Synthetic Route to Glycosyl β-1C-(phosphino)-phosphonates as Unprecedented Stable Glycosyl Diphosphate Analogs and Their Preliminary Biological Evaluation

Susan J Paik, C. Gravier-Pelletier, S. Moore, 2020, Molecules.

Synthesis and biological evaluation of chemical tools for the study of Dolichol Linked Oligosaccharide Diphosphatase (DLODP).

A. Bouhss, C. Gravier-Pelletier, I. Chantret, 2017, European journal of medicinal chemistry.

Free-oligosaccharide control in the yeast Saccharomyces cerevisiae: roles for peptide:N-glycanase (Png1p) and vacuolar mannosidase (Ams1p).

I. Chantret, S. Moore, J. Frénoy, 2003, The Biochemical journal.

Perturbation of free oligosaccharide trafficking in endoplasmic reticulum glucosidase I-deficient and castanospermine-treated cells.

S. Moore, C. Durrant, 2002, The Biochemical journal.

Cytosol-to-lysosome Transport of Free Polymannose-type Oligosaccharides

P. Codogno, A. Saint-Pol, S. Moore, 1999, The Journal of Biological Chemistry.

Transport of free polymannose-type oligosaccharides from the endoplasmic reticulum into the cytosol is inhibited by mannosides and requires a thapsigargin-sensitive calcium store.

S. Moore, 1998, Glycobiology.

Transfer of Free Polymannose-type Oligosaccharides from the Cytosol to Lysosomes in Cultured Human Hepatocellular Carcinoma HEPG2 Cells

C. Bauvy, P. Codogno, A. Saint-Pol, 1997, The Journal of cell biology.

Defects in Galactose Metabolism and Glycoconjugate Biosynthesis in a UDP-Glucose Pyrophosphorylase-Deficient Cell Line Are Reversed by Adding Galactose to the Growth Medium

A. Rötig, A. Katz, M. Ermonval, 2020, International journal of molecular sciences.

Brefeldin A promotes the appearance of oligosaccharyl phosphates derived from Glc3Man9GlcNAc2-PP-dolichol within the endomembrane system of HepG2 cells

C. Gravier-Pelletier, I. Chantret, S. Moore, 2016, Journal of Lipid Research.

Demonstration of an oligosaccharide-diphosphodolichol diphosphatase activity whose subcellular localization is different than those of dolichyl-phosphate-dependent enzymes of the dolichol cycle

C. Gravier-Pelletier, I. Chantret, N. Auberger, 2016, Journal of Lipid Research.

Two Proteins Homologous to the N- and C-terminal Domains of the Bacterial Glycosyltransferase Murg Are Required for the Second Step of Dolichyl-linked Oligosaccharide Synthesis in Saccharomyces cerevisiae*

A. Barbat, I. Chantret, Julia Dancourt, 2005, Journal of Biological Chemistry.

Novel variants and clinical symptoms in four new ALG3‐CDG patients, review of the literature, and identification of AAGRP‐ALG3 as a novel ALG3 variant with alanine and glycine‐rich N‐terminus

A. Ziegler, J. Denecke, I. Sinning, 2019, Human mutation.

Activity, Splice Variants, Conserved Peptide Motifs, and Phylogeny of Two New α1,3-Fucosyltransferase Families (FUT10 and FUT11)*

R. Oriol, R. Mollicone, I. Martínez-Duncker, 2009, Journal of Biological Chemistry.

Wide clinical spectrum in ALG8-CDG: clues from molecular findings suggest an explanation for a milder phenotype in the first-described patient

A. Couvineau, F. Mattioli, M. Schiff, 2018, Pediatric Research.

Congenital Disorders of Glycosylation Type Ig Is Defined by a Deficiency in Dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl Mannosyltransferase*

P. Codogno, O. Danos, R. Oriol, 2002, The Journal of Biological Chemistry.

Cardiomyopathy in the congenital disorders of glycosylation (CDG): a case of late presentation and literature review

M. Burch, M. Burch, I. Chantret, 2009, Journal of Inherited Metabolic Disease.

Free oligosaccharide regulation during mammalian protein N-glycosylation.

I. Chantret, S. Moore, 2007, Glycobiology.

Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle Variants.

L. Servais, A. Slama, M. Schiff, 2016, JIMD reports.

Identification of Roles for Peptide: N-Glycanase and Endo-β-N-Acetylglucosaminidase (Engase1p) during Protein N-Glycosylation in Human HepG2 Cells

H. Sadou Yayé, I. Chantret, M. Fasseu, 2010, PloS one.

Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations

A. Afenjar, C. Barnérias, P. de Lonlay, 2010, Journal of Medical Genetics.

Alteration of mannose transport in fibroblasts from type I carbohydrate deficient glycoprotein syndrome patients.

P. Codogno, E. Ogier-Denis, V. Cormier-Daire, 1999, Biochimica et biophysica acta.

Brefeldin A promotes the appearance of oligosaccharyl phosphates derived from Glc3Man9GlcNAc2-PP-dolichol within the endomembrane system of HepG2 cells

C. Gravier-Pelletier, I. Chantret, S. Moore, 2016, Journal of Lipid Research.

Activity, Splice Variants, Conserved Peptide Motifs, and Phylogeny of Two New α1,3-Fucosyltransferase Families (FUT10 and FUT11)*

R. Oriol, R. Mollicone, I. Martínez-Duncker, 2009, Journal of Biological Chemistry.