Publications and ressources

Disruption of pathways regulated by Integrator complex in Galloway-Mowat syndrome due to WDR73 mutations.

Frances Tilley

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Generation of an iPSC line (IMAGINi022-A) from a patient carrying a SOX10 missense mutation and presenting with deafness, depigmentation and progressive neurological impairment.

Céline BANAL, Eddy Quelennec, Jeanne Amiel, Sandrine Marlin, Véronique Pingault, Nathalie Lefort, Nadège Bondurand

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Generation of two induced pluripotent stem cell lines IMAGINi004-A and IMAGINi005-A from healthy donors.

Eddy Quelennec, Céline BANAL, Marie MICHAEL, Nathalie Lefort

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Generation of an induced pluripotent stem cell (iPSC) line (IMAGINi007) from a patient with steroid-resistant nephrotic syndrome carrying the homozygous p.R138Q mutation in the podocin-encoding NPHS2 gene.

Giulia Menara, Nathalie Lefort, Corinne Antignac, Géraldine Mollet

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Urine-derived cells provide a readily accessible cell type for feeder-free mRNA reprogramming.

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High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defect.

Vincent Cantagrel, Nathalie Lefort

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Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells.

Nathalie Lefort

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Recurrent genomic instability of chromosome 1q in neural derivatives of human embryonic stem cells.

Nathalie Lefort

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Human embryonic stem cells and genomic instability.

Nathalie Lefort

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Human embryonic stem cells reveal recurrent genomic instability at 20q11.21.

Nathalie Lefort

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Striatal progenitors derived from human ES cells mature into DARPP32 neurons in vitro and in quinolinic acid-lesioned rats.

Nathalie Lefort

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