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Generation of 5 hiPSC lines from pediatric patients with Heritable pulmonary arterial hypertension (HPAH) caused by heterozygous mutations in the TBX4 gene

1
1. scibot 16 Dec 2025
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2025.103886
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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  RRID:AB_2653527
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sciencedirect.com:5037/science/article/pii/S1873506125002363
Aug 2025
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Generation of human induced pluripotent stem cell line from an obesity patient with POMC deficiency due to POMC:W84X mutation

1
1. scibot 26 Aug 2025
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2025.103814
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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sciencedirect.com/science/article/pii/S1873506125001643
Jul 2025
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Generation of an isogenic iPSC line via CRISPR correction of the POMC:W84X mutation for monogenic obesity modeling

1
1. scibot 29 Jul 2025
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2025.103786
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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  RRID:AB_2653527
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sciencedirect.com/science/article/pii/S1873506125001369
May 2025
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Generation of two human induced pluripotent stem cell lines from Allan-Herndon-Dudley syndrome (AHDS) patients with SLC16A2:G401R or SLC16A2: H192R mutation

1
1. scibot 18 May 2025
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2025.103725
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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sciencedirect.com/science/article/pii/S1873506125000753
Apr 2025
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Generation of hiPSC lines with fusion tagged thyroid hormone receptor α isoforms to study isoform-specific actions of TRα1 and TRα2

1
1. scibot 24 Apr 2025
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2025.103720
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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sciencedirect.com/science/article/pii/S1873506125000704
Mar 2025
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Correction iPSC line of the Allan-Herndon-Dudley syndrome-causing SLC16A2 mutation: G401R

1
1. scibot 20 Mar 2025
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2025.103698
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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  RRID:AB_2653527
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sciencedirect.com/science/article/pii/S1873506125000480
Mar 2024
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Generation of two human induced pluripotent stem cell lines with BAX and BAK1 double knock-out using CRISPR/Cas9

2
1. scibot 14 Mar 2024
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2024.103377
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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  RRID:AB_2653527
2. scibot 14 Mar 2024
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2024.103377
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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  RRID:AB_2653527
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sciencedirect.com/science/article/pii/S1873506124000758
Dec 2023
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Generation of THRB-GS(E125G_G126S) and THRB-KO human iPSC lines to study noncanonical thyroid hormone signalling

1
1. scibot 14 Dec 2023
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2023.103275
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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  RRID:AB_2653527
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RRID:AB_2653527

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sciencedirect.com/science/article/pii/S1873506123002611
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Generation of iPSC lines with SLC16A2:G401R or SLC16A2 knock out

1
1. scibot 01 Dec 2023
  
  in Public
  
  AB_2653527
  
  DOI: 10.1016/j.scr.2023.103256
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653527
  
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  RRID:AB_2653527
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RRID:AB_2653527

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sciencedirect.com/science/article/pii/S1873506123002428
Apr 2022
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Generation of the human induced pluripotent stem cell line (IBKMOLi002-A) from PBMCs of a patient carrying the heterozygous L271H mutation of the voltage-gated calcium channel subunit Cav1.3-encoding CACNA1D gene

1
1. scibot 13 Apr 2022
  
  in Public
  
  RRID:AB_2653527
  
  DOI: 10.1016/j.scr.2022.102784
  
  Resource: (Miltenyi Biotec Cat# 130-105-053, RRID:AB_2653527)
  
  Curator: @sophiastull
  
  SciCrunch record: RRID:AB_2653527
  
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  RRID:AB_2653527
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RRID:AB_2653527

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sciencedirect.com/science/article/pii/S1873506122001337