Sandrine Duvet

Centre National de la Recherche Scientifique — France

Biochemistry, Genetics and Molecular Biology · Life Sciences

23h-index1.5kcitations44works0.02yr avg
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Research Topics

Glycosylation and Glycoproteins Research(28), Carbohydrate Chemistry and Synthesis(13), Cellular transport and secretion(11), Endoplasmic Reticulum Stress and Disease(11), Galectins and Cancer Biology(9)

Publications44 total

Variation of the serum <i>N</i>‐glycosylation during the pregnancy of a <scp>MPI‐CDG</scp> patient
JIMD Reports·2021· 4 citedOpen Access
Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylation
The American Journal of Human Genetics·2021· 19 citedOpen Access
New insights into the ORF2 capsid protein, a key player of the hepatitis E virus lifecycle
Scientific Reports·2019· 63 citedOpen Access
Involvement of thapsigargin– and cyclopiazonic acid–sensitive pumps in the rescue of TMEM165‐associated glycosylation defects by Mn <sup>2+</sup>
The FASEB Journal·2018· 30 citedOpen Access
New insights into the ORF2 capsid protein, a key player of the hepatitis E virus lifecycle
2018· 5 citedOpen Access
Use of Endoglycosidase H as a diagnostic tool for MAN1B1‐CDG patients
Electrophoresis·2018· 13 cited
Mutations in the X-linked <i>ATP6AP2</i> cause a glycosylation disorder with autophagic defects
The Journal of Experimental Medicine·2017· 84 citedOpen Access
Investigating the function of Gdt1p in yeast Golgi glycosylation
Biochimica et Biophysica Acta (BBA) - General Subjects·2017· 30 citedOpen Access
Manganese-induced turnover of TMEM165
Biochemical Journal·2017· 50 citedOpen Access
Evidence for splice transcript variants of TMEM165, a gene involved in CDG
Biochimica et Biophysica Acta (BBA) - General Subjects·2017· 8 citedOpen Access
Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasis
Human Molecular Genetics·2016· 105 citedOpen Access
Accumulation of Free Oligosaccharides and Tissue Damage in Cytosolic α-Mannosidase (Man2c1)-deficient Mice
Journal of Biological Chemistry·2014· 20 citedOpen Access
Cohen syndrome is associated with major glycosylation defects
Human Molecular Genetics·2013· 96 citedOpen Access
Free oligosaccharides accumulation and tissue damages in Ma2c1 deficient mice
Current Opinion in Biotechnology·2013
Impact of disease-causing mutations on TMEM165 subcellular localization, a recently identified protein involved in CDG-II
Human Molecular Genetics·2013· 44 citedOpen Access
Lysosomal di-N-acetylchitobiase-deficient mouse tissues accumulate Man2GlcNAc2 and Man3GlcNAc2
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease·2012· 15 citedOpen Access
PUGNAc treatment leads to an unusual accumulation of free oligosaccharides in CHO cells
The Journal of Biochemistry·2012· 22 cited
Identification of phosphorylated oligosaccharides in cells of patients with a congenital disorders of glycosylation (CDG-I)
Biochimie·2011· 26 cited
Differential effects of lobe A and lobe B of the Conserved Oligomeric Golgi complex on the stability of β1,4-galactosyltransferase 1 and α2,6-sialyltransferase 1
Glycobiology·2010· 35 citedOpen Access
Overexpression of Man2C1 leads to protein underglycosylation and upregulation of endoplasmic reticulum-associated degradation pathway
Glycobiology·2010· 26 citedOpen Access
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Frequent Co-authors

René Cacan(19), Jean Dubuisson(13), François Foulquier(11), Laurence Cocquerel(10), Gert Matthijs(8), Anne‐Marie Mir(8), Czeslaw Wychowski(7), André Verbert(7), Anne Op De Beeck(6), François Foulquier(6), André Klein(6), Sven Potelle(5), Willy Morelle(5), Geoffroy de Bettignies(5), Romain Péanne(5), Frédéric Chirat(5), Tommaso Beccari(5), Eudoxie Dulary(4), Marie‐Ange Krzewinski‐Recchi(4), Dominique Legrand(4)