Lefort N - Search Results

1

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

Duclaux-Loras R, Lebreton C, Berthelet J, Charbit-Henrion F, Nicolle O, Revenu des Courtils C, Waich S, Valovka T, Khiat A, Rabant M, Racine C, Guerrera IC, Baptista J, Mahe MM, Hess MW, Durel B, Lefort N, Banal C, Parisot M, Talbotec C, Lacaille F, Ecochard-Dugelay E, Demir AM, Vogel GF, Faivre L, Rodrigues A, Fowler D, Janecke AR, Müller T, Huber LA, Rodrigues-Lima F, Ruemmele FM, Uhlig HH, Del Bene F, Michaux G, Cerf-Bensussan N, Parlato M. Duclaux-Loras R, et al. Among authors: lefort n. J Clin Invest. 2022 May 16;132(10):e154997. doi: 10.1172/JCI154997. J Clin Invest. 2022. PMID: 35575086 Free PMC article.

2

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

Medina-Cano D, Ucuncu E, Nguyen LS, Nicouleau M, Lipecka J, Bizot JC, Thiel C, Foulquier F, Lefort N, Faivre-Sarrailh C, Colleaux L, Guerrera IC, Cantagrel V. Medina-Cano D, et al. Among authors: lefort n. Elife. 2018 Oct 12;7:e38309. doi: 10.7554/eLife.38309. Elife. 2018. PMID: 30311906 Free PMC article.

3

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

Banal C, Quelennec E, Bertani-Torres W, Gacem N, Amiel J, Marlin S, Petit F, Pingault V, Lefort N, Bondurand N. Banal C, et al. Among authors: lefort n. Stem Cell Res. 2020 Oct;48:101936. doi: 10.1016/j.scr.2020.101936. Epub 2020 Aug 2. Stem Cell Res. 2020. PMID: 32795927 Free article.

4

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

Quelennec E, Banal C, Hamlin M, Clémantine D, Michael M, Lefort N. Quelennec E, et al. Among authors: lefort n. Stem Cell Res. 2020 Oct;48:101959. doi: 10.1016/j.scr.2020.101959. Epub 2020 Aug 20. Stem Cell Res. 2020. PMID: 32866896 Free article.

5

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

Barnabei L, Castela M, Banal C, Lefort N, Rieux-Laucat F. Barnabei L, et al. Among authors: lefort n. Stem Cell Res. 2020 Dec 2;50:102107. doi: 10.1016/j.scr.2020.102107. Online ahead of print. Stem Cell Res. 2020. PMID: 33340797 Free article.

6

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

Tilley FC, Arrondel C, Chhuon C, Boisson M, Cagnard N, Parisot M, Menara G, Lefort N, Guerrera IC, Bole-Feysot C, Benmerah A, Antignac C, Mollet G. Tilley FC, et al. Among authors: lefort n. Sci Rep. 2021 Mar 8;11(1):5388. doi: 10.1038/s41598-021-84472-7. Sci Rep. 2021. PMID: 33686175 Free PMC article.

7

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

Banal C, Lefort N. Banal C, et al. Among authors: lefort n. Stem Cell Res. 2022 May;61:102755. doi: 10.1016/j.scr.2022.102755. Epub 2022 Mar 21. Stem Cell Res. 2022. PMID: 35334405 Free article.

8

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

Boutaud L, Michael M, Banal C, Calderon D, Farcy S, Pernelle J, Goudin N, Maillard C, Dimartino C, Deleschaux C, Dupichaud S, Lebreton C, Saunier S, Attié-Bitach T, Bahi-Buisson N, Lefort N, Thomas S. Boutaud L, et al. Among authors: lefort n. J Vis Exp. 2022 Mar 25;(181). doi: 10.3791/62667. J Vis Exp. 2022. PMID: 35389978

9

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

Banal C, Quelennec E, Talbotec C, Khiat A, Charbit-Henrion F, Cerf-Bensussan N, Lefort N, Lebreton C. Banal C, et al. Among authors: lefort n. Stem Cell Res. 2023 Apr;68:103057. doi: 10.1016/j.scr.2023.103057. Epub 2023 Feb 26. Stem Cell Res. 2023. PMID: 36868038 Free article.

10

Generation and characterization of induced pluripotent stem cell lines from two patients with recessive dystrophic epidermolysis Bullosa.

Vincent C, Lefort N, Hamlin M, Banal C, Hovnanian A, Izmiryan A. Vincent C, et al. Among authors: lefort n. Stem Cell Res. 2023 Jun;69:103104. doi: 10.1016/j.scr.2023.103104. Epub 2023 Apr 24. Stem Cell Res. 2023. PMID: 37148821 Free article.

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