CAG-Cas9-T2A-EGFP-ires-puro Citations (8)

Originally described in: An Activating STAT3 Mutation Causes Neonatal Diabetes through Premature Induction of Pancreatic Differentiation.
Saarimaki-Vire J, Balboa D, Russell MA, Saarikettu J, Kinnunen M, Keskitalo S, Malhi A, Valensisi C, Andrus C, Eurola S, Grym H, Ustinov J, Wartiovaara K, Hawkins RD, Silvennoinen O, Varjosalo M, Morgan NG, Otonkoski T Cell Rep. 2017 Apr 11;19(2):281-294. doi: 10.1016/j.celrep.2017.03.055. PubMed Journal

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Articles Citing CAG-Cas9-T2A-EGFP-ires-puro

Articles
Transcription Factor PROX1 Suppresses Notch Pathway Activation via the Nucleosome Remodeling and Deacetylase Complex in Colorectal Cancer Stem-like Cells. Hogstrom J, Heino S, Kallio P, Lahde M, Leppanen VM, Balboa D, Wiener Z, Alitalo K. Cancer Res. 2018 Oct 15;78(20):5820-5832. doi: 10.1158/0008-5472.CAN-18-0451. Epub 2018 Aug 28. PubMed
Insulin mutations impair beta-cell development in a patient-derived iPSC model of neonatal diabetes. Balboa D, Saarimaki-Vire J, Borshagovski D, Survila M, Lindholm P, Galli E, Eurola S, Ustinov J, Grym H, Huopio H, Partanen J, Wartiovaara K, Otonkoski T. Elife. 2018 Nov 9;7. pii: 38519. doi: 10.7554/eLife.38519. PubMed
Tyrosine phosphorylation directs TACE into extracellular vesicles via unconventional secretion. Zhao Z, Kesti T, Ugurlu H, Baur AS, Fagerlund R, Saksela K. Traffic. 2019 Mar;20(3):202-212. doi: 10.1111/tra.12630. Epub 2019 Jan 21. PubMed
ALS and Parkinson's disease genes CHCHD10 and CHCHD2 modify synaptic transcriptomes in human iPSC-derived motor neurons. Harjuhaahto S, Rasila TS, Molchanova SM, Woldegebriel R, Kvist J, Konovalova S, Sainio MT, Pennonen J, Torregrosa-Munumer R, Ibrahim H, Otonkoski T, Taira T, Ylikallio E, Tyynismaa H. Neurobiol Dis. 2020 Jul;141:104940. doi: 10.1016/j.nbd.2020.104940. Epub 2020 May 11. PubMed
Neurofilament Light Regulates Axon Caliber, Synaptic Activity, and Organelle Trafficking in Cultured Human Motor Neurons. Sainio MT, Rasila T, Molchanova SM, Jarvilehto J, Torregrosa-Munumer R, Harjuhaahto S, Pennonen J, Huber N, Herukka SK, Haapasalo A, Zetterberg H, Taira T, Palmio J, Ylikallio E, Tyynismaa H. Front Cell Dev Biol. 2022 Feb 14;9:820105. doi: 10.3389/fcell.2021.820105. eCollection 2021. PubMed
De-erosion of X chromosome dosage compensation by the editing of XIST regulatory regions restores the differentiation potential in hPSCs. Motosugi N, Sugiyama A, Okada C, Otomo A, Umezawa A, Akutsu H, Hadano S, Fukuda A. Cell Rep Methods. 2022 Nov 29;2(12):100352. doi: 10.1016/j.crmeth.2022.100352. eCollection 2022 Dec 19. PubMed
Fendrr synergizes with Wnt signalling to regulate fibrosis related genes during lung development via its RNA:dsDNA triplex element. Ali T, Rogala S, Krause NM, Bains JK, Melissari MT, Wahrisch S, Schwalbe H, Herrmann BG, Grote P. Nucleic Acids Res. 2023 Jul 7;51(12):6227-6237. doi: 10.1093/nar/gkad395. PubMed
Linear DNA-driven recombination in mammalian mitochondria. Fragkoulis G, Hangas A, Fekete Z, Michell C, Moraes CT, Willcox S, Griffith JD, Goffart S, Pohjoismaki JLO. Nucleic Acids Res. 2024 Apr 12;52(6):3088-3105. doi: 10.1093/nar/gkae040. PubMed

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