V. Piller

发表

Transfection efficiency and uptake process of polyplexes in human lung endothelial cells: a comparative study in non‐polarized and polarized cells

C. Kieda, C. Pichon, P. Midoux, 2005, The journal of gene medicine.

The sugar binding activity of MR60, a mannose-specific shuttling lectin, requires a dimeric state.

M. Monsigny, A. Roche, A. Legrand, 1999, Glycobiology.

Glycophorins C and D are generated by the use of alternative translation initiation sites.

V. Piller, J. Cartron, Y. Colin, 1996, Blood.

Comparison of the carbohydrate-binding specificities of seven N-acetyl-D-galactosamine-recognizing lectins.

V. Piller, J. Cartron, F. Piller, 1990, European journal of biochemistry.

Fold recognition and molecular modeling of a lectin-like domain in UDP-GalNac:polypeptide N-acetylgalactosaminyltransferases.

A. Imberty, C. Breton, V. Piller, 1997, Protein engineering.

Coupling of Immunostimulants to Live Cells through Metabolic Glycoengineering and Bioorthogonal Click Chemistry.

V. Piller, F. Piller, Aline Mongis, 2017, Bioconjugate chemistry.

Two-step enzymatic synthesis of UDP-N-acetylgalactosamine.

V. Piller, Vanessa Bourgeaux, F. Piller, 2005, Bioorganic & medicinal chemistry letters.

Metabolic Glyco-Engineering in Eukaryotic Cells and Selected Applications.

V. Piller, F. Piller, Aline Mongis, 2015, Methods in molecular biology.

Evaluation of analogues of GalNAc as substrates for enzymes of the mammalian GalNAc salvage pathway.

V. Piller, Vanessa Bourgeaux, F. Piller, 2012, ACS chemical biology.

Increased alpha2,6 sialylation of N-glycans in a transgenic mouse model of hepatocellular carcinoma.

M. Monsigny, V. Piller, F. Piller, 1997, Cancer research.

High levels of ceruloplasmin in the serum of transgenic mice developing hepatocellular carcinoma.

V. Piller, F. Piller, D. Pousset, 2001, European journal of biochemistry.

Synthesis of branched oxime-linked peptide mimetics of the MUC1 containing a universal T-helper epitope.

A. Delmas, V. Piller, D. Lelièvre, 2004, Chemistry.

O-glycosylation of leukosialin in K562 cells. Evidence for initiation and elongation in early Golgi compartments.

M. Fukuda, V. Piller, F. Klier, 1989, European journal of biochemistry.

Combining triazole ligation and enzymatic glycosylation on solid phase simplifies the synthesis of very long glycoprotein analogues† †Electronic supplementary information (ESI) available: Detailed synthetic procedures, characterization and optimization. See DOI: 10.1039/c5sc00773a

A. Delmas, V. Piller, M. Galibert, 2015, Chemical science.

Human T-lymphocyte activation is associated with changes in O-glycan biosynthesis.

M. Fukuda, V. Piller, R. Fox, 1988, The Journal of biological chemistry.

Synthesis of aryl-thioglycopeptides through chemoselective Pd-mediated conjugation† †Electronic supplementary information (ESI) available: General, experimental procedures, and characterization of all new compounds. See DOI: 10.1039/c8sc02370k

V. Piller, M. Amoura, M. Beltramo, 2018, Chemical science.

Changes in Metabolic Chemical Reporter Structure Yield a Selective Probe of O-GlcNAc Modification

V. Piller, F. Piller, M. Pratt, 2014, Journal of the American Chemical Society.

Biosynthesis of truncated O-glycans in the T cell line Jurkat. Localization of O-glycan initiation.

M. Fukuda, V. Piller, F. Piller, 1990, The Journal of biological chemistry.

Enzymatic large-scale synthesis of MUC6-Tn glycoconjugates for antitumor vaccination.

C. Leclerc, S. Bay, V. Piller, 2006, Glycobiology.

Ras oncogene induces β‐galactoside α2,6‐sialyltransferase (ST6Gal I) via a RalGEF‐mediated signal to its housekeeping promoter

M. Dalziel, V. Piller, F. dall’Olio, 2004 .

Phosphorylation of the major leukocyte surface sialoglycoprotein, leukosialin, is increased by phorbol 12-myristate 13-acetate.

M. Fukuda, V. Piller, F. Piller, 1989, The Journal of biological chemistry.

Ras oncogene induces beta-galactoside alpha2,6-sialyltransferase (ST6Gal I) via a RalGEF-mediated signal to its housekeeping promoter.

M. Dalziel, V. Piller, F. dall’Olio, 2004, European journal of biochemistry.

MUC1 in human and murine mammary carcinoma cells decreases the expression of core 2 β1,6-N-acetylglucosaminyltransferase and β-galactoside α2,3-sialyltransferase.

T. Owczarek, V. Piller, P. Dzięgiel, 2012, Glycobiology.

of core 2 6-N-acetylglucosaminyltransferase and -galactoside 2,3-sialyltransferase

T. Owczarek, V. Piller, B. Puła, 2012 .

Synthesis and biological evaluation of new UDP-GalNAc analogues for the study of polypeptide-α-GalNAc-transferases

V. Piller, O. Martin, F. Piller, 2003 .

Metabolic glycoengineering through the mammalian GalNAc salvage pathway

V. Piller, Sabrina Pouilly, Véronique Piller, 2012, The FEBS journal.

Synthesis and Biological Evaluation of a Multiantigenic Tn/TF‐Containing Glycopeptide Mimic of the Tumor‐Related MUC1 Glycoprotein

A. Delmas, V. Piller, H. Kunz, 2006, ChemMedChem.

Increased α2,6 Sialylation of N-Glycans in a Transgenic Mouse Model of Hepatocellular Carcinoma

M. Monsigny, V. Piller, F. Piller, 1997 .

Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter.

R. Oriol, V. Piller, G. Tchernia, 2005, Blood.

Efficient Enzymatic Glycosylation of Peptides and Oligosaccharides from GalNAc and UTP

M. Cadene, V. Piller, Vanessa Bourgeaux, 2007, Chembiochem : a European journal of chemical biology.

Enzyme‐Cleavable Linkers for Protein Chemical Synthesis through Solid‐Phase Ligations

V. Piller, M. Amoura, J. Madinier, 2021, Angewandte Chemie.

Enzyme-cleavable linkers for protein chemical synthesis through solid-phase ligations.

V. Piller, M. Amoura, J. Madinier, 2021, Angewandte Chemie.

Isolation and characterization of an N-acetylgalactosamine specific lectin from Salvia sclarea seeds.

V. Piller, J. Cartron, F. Piller, 1986, The Journal of biological chemistry.

Changes in Metabolic Chemical Reporter Structure Yield a Selective Probe of O-GlcNAc Modification

V. Piller, Matthew R. Pratt, F. Piller, 2014, Journal of the American Chemical Society.