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1.
Witthoff, F.* et al.: Generation of human induced pluripotent stem cell lines carrying a heterozygous and homozygous PRKD1 c.1774G > A genetic variant causing syndromic congenital defects. Stem Cell Res. 92:103937 (2026)
2.
Gasparini, G. et al.: Generation of two human iPSC lines from fibroblasts of BPAN patients carrying pathogenic variants in the WDR45 gene. Stem Cell Res. 90:103892 (2025)
3.
Greisle, T. et al.: Generation of a Flattop-T2A-H2B-Venus x C-peptide-mCherry double reporter human iPSC line to monitor WNT/Planar cell polarity pathway activity. Stem Cell Res. 88:103838 (2025)
4.
Setyono, E.S.A. ; Rogers, N.K. ; Hofmann, A. ; Lickert, H. & Burtscher, I.: Generation of ARX-T2A-H2B-CFP x C-PEP-mCherry-hiPSC double reporter line for monitoring of pancreatic differentiation. Stem Cell Res. 84:103685 (2025)
5.
Zanuttigh, E. et al.: Generation of two human iPSC lines, HMGUi004-A and FINCBi004-A, from fibroblasts of MPAN patients carrying pathogenic recessive mutations in the gene C19orf12. Stem Cell Res. 72:103197 (2023)
6.
Iuso, A. et al.: Generation of two human iPSC lines, HMGUi003-A and MRIi028-A, carrying pathogenic biallelic variants in the PPCS gene. Stem Cell Res. 61:102773 (2022)
7.
Siehler, J. et al.: Generation of a heterozygous C-peptide-mCherry reporter human iPSC line (HMGUi001-A-8). Stem Cell Res. 50:102126 (2021)
8.
Blöchinger, A. et al.: Generation of an INSULIN-H2B-Cherry reporter human iPSC line. Stem Cell Res. 45:101797 (2020)
9.
Moya, N. et al.: Generation of a homozygous ARX nuclear CFP (ARX(nCFP/nCFP)) reporter human iPSC line (HMGUi001-A-4). Stem Cell Res. 46:101874 (2020)
10.
Shahryaria, A. et al.: Generation of a human iPSC line harboring a biallelic large deletion at the INK4 locus (HMGUi001-A-5). Stem Cell Res. 47:101927 (2020)
11.
Wang, X. et al.: Generation of a human induced pluripotent stem cell line (HMGUi002-A) from a healthy male individual. Stem Cell Res. 39:101531 (2019)
12.
Wang, X. et al.: Generation of a human induced pluripotent stem cell (iPSC) line from a patient with family history of diabetes carrying a C18R mutation in the PDX1 gene. Stem Cell Res. 17, 292-295 (2016)
13.
Wang, X. et al.: Generation of a human induced pluripotent stem cell (iPSC) line from a patient carrying a P33T mutation in the PDX1 gene. Stem Cell Res. 17, 273-276 (2016)
14.
Tonge, P.D.* ; Shigeta, M. ; Schroeder, T. & Andrews, P.W.*: Functionally defined substates within the human embryonic stem cell compartment. Stem Cell Res. 7, 145-153 (2011)
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