Biblio

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Kuwar R, Zhang N, McQuiston A, Wen X, Sun D. Generation of induced pluripotent stem cells from rat fibroblasts and optimization of its differentiation into mature functional neurons. J Neurosci Methods. 2024:110114.

Miller DC, Lisowski P, Lickfett S, Mlody B, Bünning M, Genehr C, Ulrich C, Wanker EE, Diecke S, Priller J, et al. Generation of induced pluripotent stem cells from three individuals with Huntington's disease. Stem Cell Res. 2022;65:102976.

Ohki CMarie Yde, Walter NMonet, Rickli M, Van Puyenbroeck P, Döring C, Hoffmann P, Herms S, Werling AMaria, Walitza S, Grünblatt E. Generation of induced pluripotent stem cells from two ADHD patients and two healthy controls. Stem Cell Res. 2023;69:103084.

Lin H-I, Cheng Y-C, Ko H-W, Wen C-H, Lu H-E, Huang C-Y, Hsieh PCH, Lin C-H. Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation. Stem Cell Res. 2019;37:101447.

Chan Y-H, Tsai C-Y, Ho C-H, Lu Y-C, Lin P-H, Chen T-C, Chen Y-T, Huang C-Y, Liu T-C, Hsu C-J, et al. Generation of induced pluripotent stem cells (IBMSi027-A) from a patient with hearing loss carrying WFS1 c.2051C > T (p.Ala684Val) variant. Stem Cell Res. 2023;69:103068.

Wang T, Zhou Y, Zhou R, Huang W, Wang J, Li H, Lei M, Tan X, Zhang Y. Generation of induced pluripotent stem cells (iPSCs) from a Chinese infant (XACHi015-A) with type 2 Long QT syndrome carrying the heterozygous mutation c.1814C>T(p.P605L) in KCNH2. Stem Cell Res. 2021;56:102509.

Zhang Y, Li A, Huang CL-H, Wang G, Wang D. Generation of induced pluripotent stem cells (iPSCs) from an infant with catecholaminergic polymorphic ventricular tachycardia carrying the double heterozygous mutations A1855D in RyR2 and Q1362H in SCN10A. Stem Cell Res. 2019;39:101509.

Zhang Y, Li A, Wang J, Wang G, Wang D. Generation of induced pluripotent stem cells (iPSCs) from an infant with Pompe disease carrying with compound mutations of R608X and E888X in GAA gene. Stem Cell Res. 2019;41:101621.

Erdlenbruch F, Rohwedel J, Ralfs P, Thomitzek A, Kramer J, Cakiroglu F. Generation of induced pluripotent stem cells (iPSCs) from human foreskin fibroblasts. Stem Cell Res. 2018;33:79-82.

Piovani G, Lanzi G, Ferraro RMonica, Masneri S, Barisani C, Savio G, Giliani SClara. Generation of induced pluripotent stem cells (iPSCs) from patient with Cri du Chat Syndrome. Stem Cell Res. 2019;35:101393.

Auboyer L, Monzo C, Wallon D, Rovelet-Lecrux A, Gabelle A, Gazagne I, Cacheux V, Lehmann S, Crozet C. Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene. Stem Cell Res. 2019;37:101438.

Auboyer L, Monzo C, Wallon D, Rovelet-Lecrux A, Gabelle A, Gazagne I, Cacheux V, Lehmann S, Crozet C. Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 gene. Stem Cell Res. 2019;34:101381.

Hey CAmalie Bru, Saltõkowa KBeata, Larsen LJonsgaard, Tümer Z, Brøndum-Nielsen K, Grønskov K, Hjortshøj TDuelund, Møller LBirk. Generation of induced pluripotent stem cells, KCi001-A derived from a Bardet-Biedl syndrome patient compound heterozygous for the BBS1 variants c.1169T>G/c.1135G>C. Stem Cell Res. 2018;31:235-239.

Hey CAmalie Bru, Saltõkowa KBeata, Larsen LJonsgaard, Tümer Z, Brøndum-Nielsen K, Grønskov K, Hjortshøj TDuelund, Møller LBirk. Generation of induced pluripotent stem cells, KCi002-A derived from a patient with Bardet-Biedl syndrome homozygous for the BBS10 variant c.271insT. Stem Cell Res. 2018;33:46-50.

Larsen LJonsgaard, Møller LBirk. Generation of induced pluripotent stem cells, KCi004-A derived from a male with Parkinsońs disease and homozygous for the PINK1 variant c.1366C > T, p.Gln456. Stem Cell Res. 2023;71:103175.

Datta I, Datta I, Jagtap S, Potdar C, Yadav R, Pal P. Generation of induced pluripotent stem cells (NIMHi001-A) from a Parkinson's disease patient of East Indian ethnicity carrying LRRK2 I1371V variant. Stem Cell Res. 2020;44:101768.

Datta I, Jagtap S, Yadav R, Pal PKumar. Generation of induced pluripotent stem cells (NIMHi002-A and NIMHi003-A) from two sporadic Parkinson's disease patient of East Indian ethnicity. Stem Cell Res. 2020;49:101995.

Banerjee R, Ghanty R, Jagtap S, Holla V, Kamble N, Yadav R, Pal PKumar, Datta I. Generation of induced pluripotent stem cells (NIMHi015-A) from a Parkinson's Disease patient harbouring a homozygous Exon 3 deletion in the PRKN gene. Stem Cell Res. 2024;77:103440.

Zhu X, Wang J, Chong H, Wang J, Wang D. Generation of induced pluripotent stem cells (NJDTHi001-A) from a Danon disease child with mutation of c.467 T > G in LAMP2 gene. Stem Cell Res. 2020;49:101994.

Duff C, Islam M, Gagliano O, Pramod H, Rashidi H, Kurian M, Gissen P, Baruteau J. Generation of induced pluripotent stem cells (UCLi024-A) from a patient with argininosuccinate lyase deficiency carrying a homozygous c.437G > A (p.Arg146Gln) mutation. Stem Cell Res. 2024;76:103365.

Lee CHyun, Ingrole RSJ, Gill HSingh. Generation of induced pluripotent stem cells using elastin like polypeptides as a non-viral gene delivery system. Biochim Biophys Acta Mol Basis Dis. 2019.

Estève J, Blouin J-M, Lalanne M, Azzi-Martin L, Dubus P, Bidet A, Harambat J, Llanas B, Moranvillier I, Bedel A, et al. Generation of induced pluripotent stem cells-derived hepatocyte-like cells for ex vivo gene therapy of primary hyperoxaluria type 1. Stem Cell Res. 2019;38:101467.

Gornostal E, Alsalloum A, Mityaeva O, Volchkov P. Generation of induced pluripotent stem line (MIPTi001-A) derived from patient with X-linked adrenoleukodystrophy (X-ALD). Stem Cell Res. 2023;74:103298.

Kim O-H, Hong H-E, Seo H, Kwak BJun, Choi HJoong, Kim K-H, Ahn J, Lee SChul, Kim S-J. Generation of induced secretome from adipose-derived stem cells specialized for disease-specific treatment: An experimental mouse model. World J Stem Cells. 2020;12(1):70-86.

Rim YAlice, Park N, Nam Y, Ju JHyeon. Generation of Induced-pluripotent Stem Cells Using Fibroblast-like Synoviocytes Isolated from Joints of Rheumatoid Arthritis Patients. J Vis Exp. 2016;(116).

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