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Publications

Efficient Synthesis of 2'-O-Methoxyethyl Oligonucleotide-Cationic Peptide Conjugates.

Halloy F. et al, (2021), ChemMedChem, 16, 3391 - 3395

Repurposing of glycine transport inhibitors for the treatment of erythropoietic protoporphyria.

Halloy F. et al, (2021), Cell Chem Biol, 28, 1221 - 1234.e6

RNA-PROTACs: Degraders of RNA-Binding Proteins.

Ghidini A. et al, (2021), Angew Chem Int Ed Engl, 60, 3163 - 3169

Delivery of oligonucleotides to bone marrow to modulate ferrochelatase splicing in a mouse model of erythropoietic protoporphyria

Halloy F. et al, (2020), Nucleic Acids Research, 48, 4658 - 4671

Delivery of oligonucleotides to bone marrow to modulate ferrochelatase splicing in a mouse model of Erythropoietic Protoporphyria

Halloy F. et al, (2020)

Increased Affinity of 2′-O-(2-Methoxyethyl)-Modified Oligonucleotides to RNA through Conjugation of Spermine at Cytidines

Decuypere E. et al, (2019), Helvetica Chimica Acta, 102

Delta-aminolevulinic acid synthase 2 expression in combination with iron as modifiers of disease severity in erythropoietic protoporphyria

Barman-Aksözen J. et al, (2019), Molecular Genetics and Metabolism, 128, 304 - 308

Chemical synthesis of long RNAs with terminal 5′-phosphate groups

Pradère U. et al, (2017), Chemistry - A European Journal, 23, 5210 - 5213

Synthesis and cellular activity of stereochemically-pure 2'-O-(2-methoxyethyl)-phosphorothioate oligonucleotides.

Li M. et al, (2017), Chem Commun (Camb), 53, 541 - 544

WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity.

Grenier J. et al, (2016), Ophthalmology, 123, 1989 - 1998

Carrier-free Gene Silencing by Amphiphilic Nucleic Acid Conjugates in Differentiated Intestinal Cells

Moroz E. et al, (2016), Molecular Therapy - Nucleic Acids, 5

Erratum: Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies (The American Journal of Human Genetics (2015) 97 (754-6760))

Angebault C. et al, (2015), American Journal of Human Genetics, 97

Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies

Angebault C. et al, (2015), American Journal of Human Genetics, 97, 754 - 760

Include forthcoming?