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Generation of induced pluripotent stem cell lines TRNDi037-A and TRNDi038-A from two patients with Alagille syndrome carrying heterozygous JAG1 mutations.
Evans EF, Chen G, Pavlinov I, Huang X, Linask K, Liu C, Lopez AR, Gilbert MA, Spinner NB, Rodemse S, Baumgärtele K, Chen CZ, Zou J, Zheng W. Evans EF, et al. Among authors: pavlinov i. Stem Cell Res. 2024 Dec 17;82:103634. doi: 10.1016/j.scr.2024.103634. Online ahead of print. Stem Cell Res. 2024. PMID: 39719802 Free article.
Generation of two gene corrected human isogenic iPSC lines (NCATS-CL6104 and NCATS-CL6105) from a patient line (NCATS-CL6103) carrying a homozygous p.R401X mutation in the NGLY1 gene using CRISPR/Cas9.
Pavlinov I, Farkhondeh A, Yang S, Xu M, Cheng YS, Beers J, Zou J, Liu C, Might M, Rodems S, Baumgärtel K, Zheng W. Pavlinov I, et al. Stem Cell Res. 2021 Oct;56:102554. doi: 10.1016/j.scr.2021.102554. Epub 2021 Sep 30. Stem Cell Res. 2021. PMID: 34619643 Free PMC article.
Generation of an Alagille syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi032-A) carrying a heterozygous mutation (p.Cys682Leufs*7) in the JAG1 gene.
Hatim O, Pavlinov I, Xu M, Linask K, Beers J, Liu C, Baumgärtel K, Gilbert M, Spinner N, Chen C, Zou J, Zheng W. Hatim O, et al. Among authors: pavlinov i. Stem Cell Res. 2023 Dec;73:103231. doi: 10.1016/j.scr.2023.103231. Epub 2023 Oct 18. Stem Cell Res. 2023. PMID: 37890331 Free PMC article.
Generation of an Alagille Syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi036-A) carrying a heterozygous mutation (p.Cys693*) in the JAG1 gene.
Hatim O, Xu M, Pavlinov I, Linask K, Beers J, Zou J, Liu C, Rodems S, Baumgärtel K, Gilbert MA, Spinner NB, Chen C, Zheng W. Hatim O, et al. Among authors: pavlinov i. Stem Cell Res. 2024 Jun;77:103429. doi: 10.1016/j.scr.2024.103429. Epub 2024 Apr 29. Stem Cell Res. 2024. PMID: 38703666 Free PMC article.
Corrigendum to "Generation of two gene corrected human isogenic iPSC lines (NCATS-CL6104 and NCATS-CL6105) from a patient line (NCATS-CL6103) carrying a homozygous p.R401X mutation in the NGLY1 gene using CRISPR/Cas9" [Stem Cell Res. 56 (2021) 102554].
Pavlinov I, Farkhondeh A, Yang S, Xu M, Cheng YS, Beers J, Zou J, Liu C, Might M, Rodems S, Baumgärtel K, Zheng W. Pavlinov I, et al. Stem Cell Res. 2021 Dec;57:102602. doi: 10.1016/j.scr.2021.102602. Epub 2021 Nov 17. Stem Cell Res. 2021. PMID: 34801429 Free PMC article. No abstract available.
Therapeutics Development for Alagille Syndrome.
Sanchez P, Farkhondeh A, Pavlinov I, Baumgaertel K, Rodems S, Zheng W. Sanchez P, et al. Among authors: pavlinov i. Front Pharmacol. 2021 Aug 23;12:704586. doi: 10.3389/fphar.2021.704586. eCollection 2021. Front Pharmacol. 2021. PMID: 34497511 Free PMC article. Review.
Generation and characterization of NGLY1 patient-derived midbrain organoids.
Abbott J, Tambe M, Pavlinov I, Farkhondeh A, Nguyen HN, Xu M, Pradhan M, York T, Might M, Baumgärtel K, Rodems S, Zheng W. Abbott J, et al. Among authors: pavlinov i. Front Cell Dev Biol. 2023 Feb 16;11:1039182. doi: 10.3389/fcell.2023.1039182. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 36875753 Free PMC article.
43 results