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Urine-derived cells provide a readily accessible cell type for feeder-free mRNA reprogramming.
Gaignerie A, Lefort N, Rousselle M, Forest-Choquet V, Flippe L, Francois-Campion V, Girardeau A, Caillaud A, Chariau C, Francheteau Q, Derevier A, Chaubron F, Knöbel S, Gaborit N, Si-Tayeb K, David L. Gaignerie A, et al. Among authors: david l. Sci Rep. 2018 Sep 25;8(1):14363. doi: 10.1038/s41598-018-32645-2. Sci Rep. 2018. PMID: 30254308 Free PMC article.
[Reprogramming equals gambling?].
David L, De Vos J. David L, et al. Med Sci (Paris). 2013 Apr;29(4):405-10. doi: 10.1051/medsci/2013294014. Epub 2013 Apr 26. Med Sci (Paris). 2013. PMID: 23621936 Free article. Review. French.
Phases of reprogramming.
David L, Polo JM. David L, et al. Stem Cell Res. 2014 May;12(3):754-61. doi: 10.1016/j.scr.2014.03.007. Epub 2014 Apr 1. Stem Cell Res. 2014. PMID: 24735951 Free article. Review.
Parallel derivation of isogenic human primed and naive induced pluripotent stem cells.
Kilens S, Meistermann D, Moreno D, Chariau C, Gaignerie A, Reignier A, Lelièvre Y, Casanova M, Vallot C, Nedellec S, Flippe L, Firmin J, Song J, Charpentier E, Lammers J, Donnart A, Marec N, Deb W, Bihouée A, Le Caignec C, Pecqueur C, Redon R, Barrière P, Bourdon J, Pasque V, Soumillon M, Mikkelsen TS, Rougeulle C, Fréour T, David L; Milieu Intérieur Consortium. Kilens S, et al. Among authors: david l. Nat Commun. 2018 Jan 24;9(1):360. doi: 10.1038/s41467-017-02107-w. Nat Commun. 2018. PMID: 29367672 Free PMC article.
Cell competition during reprogramming gives rise to dominant clones.
Shakiba N, Fahmy A, Jayakumaran G, McGibbon S, David L, Trcka D, Elbaz J, Puri MC, Nagy A, van der Kooy D, Goyal S, Wrana JL, Zandstra PW. Shakiba N, et al. Among authors: david l. Science. 2019 Apr 26;364(6438):eaan0925. doi: 10.1126/science.aan0925. Epub 2019 Mar 21. Science. 2019. PMID: 30898844
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.
Belbachir N, Portero V, Al Sayed ZR, Gourraud JB, Dilasser F, Jesel L, Guo H, Wu H, Gaborit N, Guilluy C, Girardeau A, Bonnaud S, Simonet F, Karakachoff M, Pattier S, Scott C, Burel S, Marionneau C, Chariau C, Gaignerie A, David L, Genin E, Deleuze JF, Dina C, Sauzeau V, Loirand G, Baró I, Schott JJ, Probst V, Wu JC, Redon R, Charpentier F, Le Scouarnec S. Belbachir N, et al. Among authors: david l. Eur Heart J. 2019 Oct 1;40(37):3081-3094. doi: 10.1093/eurheartj/ehz308. Eur Heart J. 2019. PMID: 31114854 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: david l. 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.
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: david l. Cardiovasc Res. 2021 Jul 27;117(9):2092-2107. doi: 10.1093/cvr/cvaa259. Cardiovasc Res. 2021. PMID: 32898233 Free article.
1,565 results