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Page 1
Generation of a patient-specific induced pluripotent stem cell line carrying the DES p.R406W mutation, an isogenic control and a DES p.R406W knock-in line.
Geryk M, Canac R, Forest V, Lindenbaum P, Girardeau A, Baudic M, Baron E, Bibonne A, Chariau C, Kyndt F, Redon R, Schott JJ, Gourraud JB, Barc J, Charpentier F. Geryk M, et al. Among authors: chariau c. Stem Cell Res. 2024 Jun;77:103396. doi: 10.1016/j.scr.2024.103396. Epub 2024 Mar 21. Stem Cell Res. 2024. PMID: 38522388 Free article.
In vitro and in vivo models define a molecular signature reference for human embryonic notochordal cells.
Warin J, Vedrenne N, Tam V, Zhu M, Yin D, Lin X, Guidoux-D'halluin B, Humeau A, Roseiro L, Paillat L, Chédeville C, Chariau C, Riemers F, Templin M, Guicheux J, Tryfonidou MA, Ho JWK, David L, Chan D, Camus A. Warin J, et al. Among authors: chariau c. iScience. 2024 Jan 26;27(2):109018. doi: 10.1016/j.isci.2024.109018. eCollection 2024 Feb 16. iScience. 2024. PMID: 38357665 Free PMC article.
Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis.
Delamare M, Le Roy A, Pacault M, Schmitt L, Garrec C, Maaziz N, Myllykoski M, Rimbert A, Karaghiannis V, Aral B, Catherwood M, Airaud F, Mansour-Hendili L, Hoogewijs D, Peroni E, Idriss S, Lesieur V, Caillaud A, Si-Tayeb K, Chariau C, Gaignerie A, Rab M, Haferlach T, Meggendorfer M, Bézieau S, Benetti A, Casadevall N, Hirsch P, Rose C, Wemeau M, Galacteros F, Cassinat B, Bellosillo B, Bento C, Van Wijk R, Petrides PE, Randi ML, McMullin MF, Koivunen P, Girodon F, Gardie B; ECYT-3 consortium. Delamare M, et al. Among authors: chariau c. Haematologica. 2023 Nov 1;108(11):3068-3085. doi: 10.3324/haematol.2023.282913. Haematologica. 2023. PMID: 37317877 Free PMC article.
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic background.
Girardeau A, Atticus D, Canac R, Cimarosti B, Caillaud A, Chariau C, Simonet F, Cariou B, Charpentier F, Gourraud JB, Probst V, Belbachir N, Jesel L, Lemarchand P, Barc J, Redon R, Gaborit N, Lamirault G. Girardeau A, et al. Among authors: chariau c. Stem Cell Res. 2022 Mar;59:102647. doi: 10.1016/j.scr.2021.102647. Epub 2021 Dec 28. Stem Cell Res. 2022. PMID: 34999420 Free article.
A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype.
Al Sayed ZR, Jouni M, Gourraud JB, Belbachir N, Barc J, Girardeau A, Forest V, Derevier A, Gaignerie A, Chariau C, Cimarosti B, Canac R, Olchesqui P, Charpentier E, Schott JJ, Redon R, Baró I, Probst V, Charpentier F, Loussouarn G, Zibara K, Lamirault G, Lemarchand P, Gaborit N. Al Sayed ZR, et al. Among authors: chariau c. Clin Transl Med. 2021 Jun;11(6):e413. doi: 10.1002/ctm2.413. Clin Transl Med. 2021. PMID: 34185406 Free PMC article. No abstract available.
Induction of Human Trophoblast Stem Cells from Somatic Cells and Pluripotent Stem Cells.
Castel G, Meistermann D, Bretin B, Firmin J, Blin J, Loubersac S, Bruneau A, Chevolleau S, Kilens S, Chariau C, Gaignerie A, Francheteau Q, Kagawa H, Charpentier E, Flippe L, François-Campion V, Haider S, Dietrich B, Knöfler M, Arima T, Bourdon J, Rivron N, Masson D, Fournier T, Okae H, Fréour T, David L. Castel G, et al. Among authors: chariau c. Cell Rep. 2020 Nov 24;33(8):108419. doi: 10.1016/j.celrep.2020.108419. Cell Rep. 2020. PMID: 33238118 Free article.
Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction.
Al Sayed ZR, Canac R, Cimarosti B, Bonnard C, Gourraud JB, Hamamy H, Kayserili H, Girardeau A, Jouni M, Jacob N, Gaignerie A, Chariau C, David L, Forest V, Marionneau C, Charpentier F, Loussouarn G, Lamirault G, Reversade B, Zibara K, Lemarchand P, Gaborit N. Al Sayed ZR, et al. Among authors: chariau c. Cardiovasc Res. 2021 Jul 27;117(9):2092-2107. doi: 10.1093/cvr/cvaa259. Cardiovasc Res. 2021. PMID: 32898233 Free article.
TET3 controls the expression of the H3K27me3 demethylase Kdm6b during neural commitment.
Montibus B, Cercy J, Bouschet T, Charras A, Maupetit-Méhouas S, Nury D, Gonthier-Guéret C, Chauveau S, Allegre N, Chariau C, Hong CC, Vaillant I, Marques CJ, Court F, Arnaud P. Montibus B, et al. Among authors: chariau c. Cell Mol Life Sci. 2021 Jan;78(2):757-768. doi: 10.1007/s00018-020-03541-8. Epub 2020 May 14. Cell Mol Life Sci. 2021. PMID: 32405722 Free PMC article.
A dominant vimentin variant causes a rare syndrome with premature aging.
Cogné B, Bouameur JE, Hayot G, Latypova X, Pattabiraman S, Caillaud A, Si-Tayeb K, Besnard T, Küry S, Chariau C, Gaignerie A, David L, Bordure P, Kaganovich D, Bézieau S, Golzio C, Magin TM, Isidor B. Cogné B, et al. Among authors: chariau c. Eur J Hum Genet. 2020 Sep;28(9):1218-1230. doi: 10.1038/s41431-020-0583-2. Epub 2020 Feb 17. Eur J Hum Genet. 2020. PMID: 32066935 Free PMC article.
13 results