N. Lefort

发表

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

J. Bizot, C. Thiel, I. Guerrera, 2018, eLife.

UNC45A deficiency causes microvillus inclusion disease–like phenotype by impairing myosin VB–dependent apical trafficking

F. Del Bene, J. Baptista, H. Uhlig, 2022, The Journal of clinical investigation.

In vitro identiﬁcation of human pro-B cells that give rise to macrophages, natural killer cells, and T cells

Y. Lévy, L. Coulombel, Elodie Manié, 2003 .

In vitro identification of human pro-B cells that give rise to macrophages, natural killer cells, and T cells.

Y. Lévy, L. Coulombel, Elodie Manié, 2003, Blood.

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

M. Peschanski, A. Bennaceur-Griscelli, G. Tachdjian, 2008, Nature Biotechnology.

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

E. Quelennec, N. Lefort, Céline Banal, 2020, Stem cell research.

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

M. Peschanski, M. Feyeux, J. Denis, 2012, The Journal of clinical investigation.

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

M. Peschanski, L. Jones, N. Déglon, 2012, Human molecular genetics.

Human embryonic stem cells and genomic instability.

M. Peschanski, A. Perrier, N. Lefort, 2009, Regenerative medicine.

CYP1B1 mutations in French patients with early-onset primary open-angle glaucoma

H. Garchon, A. Brézin, R. Melki, 2004, Journal of Medical Genetics.

The Feeder layer‐mediated extended lifetime of cultured human skin keratinocytes is associated with altered levels of the transcription factors Sp1 and Sp3

C. Fugère, L. Germain, C. Paquet, 2006, Journal of cellular physiology.

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

M. Peschanski, L. Aubry, A. Perrier, 2008, Proceedings of the National Academy of Sciences.

C-STEM: ENGINEERING NICHE-LIKE MICRO-COMPARTMENTS FOR OPTIMAL AND SCALE-INDEPENDENT EXPANSION OF HUMAN PLURIPOTENT STEM CELLS IN BIOREACTORS

P. V. Liedekerke, C. Rieu, P. Nassoy, 2021, bioRxiv.

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

C. Chariau, A. Gaignerie, L. Flippe, 2018, Scientific Reports.

Genomic Integrity of Embryonic and Neural Stem Cells

M. Peschanski, N. Lefort, 2014 .

Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin.

E. Hirsch, N. Déglon, F. Saudou, 2006, Molecular biology of the cell.

Short exposure to Notch ligand Delta-4 is sufficient to induce T-cell differentiation program and to increase the T cell potential of primary human CD34+ cells.

Yves Lévy, Y. Lévy, Clarisse Benne, 2006, Experimental hematology.

MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia

A. Munnich, A. Saiardi, N. Boddaert, 2020, Nature Communications.

CYP 1 B 1 mutations in French patients with early-onset primary open-angle glaucoma

H. Garchon, A. Brézin, R. Melki, 2004 .

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

G. Mollet, C. Antignac, C. Bole-Feysot, 2021, Scientific Reports.

Association of a common coding polymorphism (N453S) of the cytochrome P450 1B1 (CYP1B1) gene with optic disc cupping and visual field alteration in French patients with primary open-angle glaucoma.

H. Garchon, A. Brézin, R. Melki, 2005, Molecular vision.

Engineering 3D micro-compartments for highly efficient and scale-independent expansion of human pluripotent stem cells in bioreactors.

P. Van Liedekerke, C. Rieu, P. Nassoy, 2023, Biomaterials.

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.

G. Mollet, C. Antignac, N. Lefort, 2020, Stem cell research.

Generation of an iPSC line (IMAGINi011-A) from a patient carrying a STING mutation.

F. Rieux-Laucat, L. Barnabei, M. Castela, 2020, Stem cell research.

Generation and characterization of IMAGINi013-A, an induced pluripotent stem cell line generated from a healthy donor.

N. Lefort, Céline Banal, 2022, Stem Cell Research.

Generation of induced pluripotent stem cells (iPSCs) from a microvillus inclusion disease patient with a homozygous missense mutation in UNC45A.

N. Cerf-Bensussan, E. Quelennec, Corinne Lebreton, 2023, Stem cell research.

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

E. Quelennec, J. Amiel, F. Petit, 2020, Stem cell research.

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

J. Bizot, C. Thiel, I. Guerrera, 2018, eLife.

2D and 3D Human Induced Pluripotent Stem Cell-Based Models to Dissect Primary Cilium Involvement during Neocortical Development.

S. Saunier, Nicolas Goudin, N. Bahi-Buisson, 2022, Journal of visualized experiments : JoVE.