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ADSL deficiency is a secondary mitochondrial disease affecting organelle homeostasis and ERK2/AKT signaling in a linear genotype-phenotype relation

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1. scibot 06 Sep 2025
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.celrep.2025.116230
  
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sciencedirect.com/science/article/pii/S2211124725010010
Jun 2025
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Derivation of induced pluripotent stem cell TUSMi012-A from a 54-year-old Chinese Han with gliocytoma

1
1. scibot 13 Jun 2025
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2025.103753
  
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sciencedirect.com/science/article/pii/S1873506125001035
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Generation of an iPSC line (DPNJMUi002-A) from a progressive familial intrahepatic cholestasis 3 (PFIC3) patient with a heterozygous mutation in the ABCB4 gene

1
1. scibot 13 Jun 2025
  
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  AB_2650582
  
  DOI: 10.1016/j.scr.2025.103745
  
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sciencedirect.com/science/article/pii/S1873506125000959
May 2025
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Post-gastrulation amnioids as a stem cell-derived model of human extra-embryonic development

1
1. scibot 17 May 2025
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.cell.2025.04.025
  
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sciencedirect.com/science/article/pii/S0092867425004581
Apr 2025
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Generation of an induced pluripotent stem cell line (PNUYHi003-A) from peripheral blood mononuclear cells of a patient with neuronal intranuclear inclusion disease

1
1. scibot 19 Apr 2025
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2025.103717
  
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sciencedirect.com/science/article/pii/S1873506125000674
Feb 2025
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Enhanced viability and functional maturity of iPSC-derived islet organoids by collagen-VI-enriched ECM scaffolds

1
1. scibot 25 Feb 2025
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.stem.2025.02.001
  
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sciencedirect.com/science/article/pii/S1934590925000402
Jan 2025
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Generation of an isogenic CRISPR/Cas9-corrected control induced pluripotent stem cell line from a patient with autosomal dominant catecholaminergic polymorphic ventricular tachycardia with a heterozygous variant in cardiac calsequestrin-2

1
1. scibot 03 Jan 2025
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2024.103650
  
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sciencedirect.com/science/article/pii/S1873506124003489
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Generation of a human induced pluripotent stem cell line (CRICKi021-A) from a patient with Ullrich congenital muscular dystrophy carrying a pathogenic mutation in the COL6A1 gene

1
1. scibot 03 Jan 2025
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2024.103648
  
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sciencedirect.com/science/article/pii/S1873506124003465
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Human induced pluripotent stem cell line (PNUSCRi005-A) generated from severe type of Hunter syndrome patient carrying exonic deletion (exon 4–7 del) in in human iduronate 2-sulfatase gene

1
1. scibot 03 Jan 2025
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2024.103639
  
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sciencedirect.com/science/article/pii/S1873506124003374
Mar 2024
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Generation of an induced pluripotent stem cell line (PNUYHi002-A) from a patient with Alzheimer’s disease carrying PRNP M232R variant

2
1. scibot 05 Mar 2024
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2024.103361
  
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2. scibot 05 Mar 2024
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2024.103361
  
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sciencedirect.com/science/article/pii/S187350612400059X
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Generation of an induced pluripotent stem cell line GWCMCi006-A from a patient with autosomal dominant neurodevelopmental disorder with or without hyperkinetic movements and seizures harboring GRIN1 c.389A > G mutation

2
1. scibot 05 Mar 2024
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2024.103371
  
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2. scibot 05 Mar 2024
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2024.103371
  
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sciencedirect.com/science/article/pii/S1873506124000692
Jul 2023
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Generation and characterization of induced pluripotent stem cell line IITGi001-A derived from adult human primary dermal fibroblasts

1
1. scibot 05 Jul 2023
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2023.103159
  
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sciencedirect.com/science/article/pii/S1873506123001459
Jun 2023
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Generation of an induced pluripotent stem cell line from a patient with conduction disease and recurrent ventricular fibrillation with a sodium voltage-gated channel alpha subunit 5 (SCN5A) gene c.392+3A>G splice-site variant

1
1. scibot 27 Jun 2023
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2023.103153
  
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sciencedirect.com/science/article/pii/S1873506123001393
Jan 2023
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Generation of four human induced pluripotent stem cell lines from COVID-19 hospitalized patients with increased levels of cardiac Troponin in the acute infection phase developing or not myocarditis

1
1. scibot 06 Jan 2023
  
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  RRID:AB_2650582RRID
  
  DOI: 10.1016/j.scr.2023.103018
  
  Resource: (Cell Signaling Technology Cat# 81778, RRID:AB_2650582)
  
  Curator: @a5munoz
  
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  RRID:AB_2650582 RRIDCUR:Unresolved
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sciencedirect.com/science/article/pii/S1873506123000041
Dec 2022
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Generation and Characterization of Three Induced Pluripotent Stem Cells Lines from an 86-Year Old Female Individual Diagnosed with an Invasive Lobular Mammary Carcinoma

1
1. scibot 04 Dec 2022
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2022.102988
  
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sciencedirect.com/science/article/pii/S1873506122003373
Oct 2022
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Differentiation of human induced pluripotent stem cells into hypothalamic vasopressin neurons with minimal exogenous signals and partial conversion to the naive state

1
1. scibot 18 Oct 2022
  
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  RRID:AB_2650582
  
  DOI: 10.1038/s41598-022-22405-8
  
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nature.com/articles/s41598-022-22405-8
Sep 2022
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Generation of two induced pluripotent stem cell lines (TMOi001-A-5, TMOi001-A-6) carrying variants in DISC1 exon 2 using CRISPR/Cas9 gene editing

1
1. scibot 22 Sep 2022
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2022.102925
  
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sciencedirect.com/science/article/pii/S1873506122002744
Aug 2022
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Establishment of Four Induced Pluripotent Stem Cell Lines from CD34+ Hematopoietic Stem and Progenitor Cells from a Patient Diagnosed with an Invasive Lobular Mammary Carcinoma

1
1. scibot 27 Aug 2022
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2022.102902
  
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sciencedirect.com/science/article/pii/S1873506122002513
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Reprogramming of dermal fibroblasts from a Duchenne muscular dystrophy patient carrying a deletion of exons 45-50 into an induced pluripotent stem cell line (CCMi005-A)

1
1. scibot 06 Aug 2022
  
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  RRID:AB_2650582RRID
  
  DOI: 10.1016/j.scr.2022.102889
  
  Resource: (Cell Signaling Technology Cat# 81778, RRID:AB_2650582)
  
  Curator: @sophiastull
  
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  RRIDCUR:Unresolved RRID:AB_2650582
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sciencedirect.com/science/article/pii/S1873506122002380
Jul 2022
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Establishment of SIAISi021-A, an induced pluripotent stem cell (iPSC) line from a 71-year-old Chinese Han male with Alzheimer's disease (AD) having two copies of APOE4/4 allele

1
1. scibot 15 Jul 2022
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2022.102866
  
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sciencedirect.com/science/article/pii/S187350612200215X
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Generation of two iPSC cell lines (SIAISi020-A and SIAISi019-A) from an 82-year-old mild cognitive impairment (MCI) and her unaffected child from Chinese Han population

1
1. scibot 14 Jul 2022
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2022.102869
  
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sciencedirect.com/science/article/pii/S1873506122002185
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In vitro modeling of amyotrophic lateral sclerosis with induced pluripotent stem cell technology-derived cell line ORIONi002-A

1
1. scibot 14 Jul 2022
  
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  RRID:AB_2650582Cell
  
  DOI: 10.1016/j.scr.2022.102870
  
  Resource: (Cell Signaling Technology Cat# 81778, RRID:AB_2650582)
  
  Curator: @sophiastull
  
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  RRIDCUR:Unresolved RRID:AB_2650582
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sciencedirect.com/science/article/pii/S1873506122002197
Jun 2022
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Stub1 maintains proteostasis of master transcription factors in embryonic stem cells

1
1. scibot 09 Jun 2022
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.celrep.2022.110919
  
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sciencedirect.com/science/article/pii/S2211124722006969
Sep 2021
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Generation of a CRISPR/Cas9-corrected-hiPSC (NCCDFWi001-A-1) from a Marfan syndrome patient hiPSC with a heterozygous c.2613A > C variant in the fibrillin 1 (FBN1) gene

1
1. scibot 21 Sep 2021
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2021.102543
  
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sciencedirect.com/science/article/pii/S1873506121003901
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Modeling of dilated cardiomyopathy by establishment of isogenic human iPSC lines carrying phospholamban C25T (R9C) mutation (UPITTi002-A-1) using CRISPR/Cas9 editing

1
1. scibot 21 Sep 2021
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2021.102544
  
  Resource: (Cell Signaling Technology Cat# 81778, RRID:AB_2650582)
  
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sciencedirect.com/science/article/pii/S1873506121003913
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Generation of a laminopathies-specific iPSC line EHTJUi005-A-3 with homozygous knockout of the LMNA gene by CRISPR/Cas9 technology

1
1. scibot 04 Sep 2021
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2021.102530
  
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sciencedirect.com/science/article/pii/S1873506121003779
Aug 2021
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CRISPR/Cas9 mediated generation of a iPSC line EHTJUi005-A-1 with homozygous knockout of the SUV39H1 gene

1
1. scibot 27 Aug 2021
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2021.102519
  
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sciencedirect.com/science/article/pii/S1873506121003664
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Untitled document

1
1. scibot 02 Aug 2021
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2018.11.011
  
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sciencedirect.com/science/article/pii/S1873506118302800
Jun 2021
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Generation and characterization of the human induced pluripotent stem cell line NMIi010-A from peripheral blood mononuclear cells of a healthy 49–year old male individual

1
1. scibot 12 Jun 2021
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2021.102427
  
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sciencedirect.com/science/article/pii/S1873506121002749
May 2021
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An induced pluripotent stem cell line (EHTJUi004-A) generated from a neonate with c.4683_4684delCT:p.Leu1563fs mutation in the gene DSP causing Familial Arrhythmogenic Right Ventricular Dysplasia (ARVD)

1
1. scibot 12 May 2021
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2021.102369
  
  Resource: (Cell Signaling Technology Cat# 81778, RRID:AB_2650582)
  
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sciencedirect.com/science/article/pii/S1873506121002154
Apr 2021
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An induced pluripotent stem cell line (EHTJUi003-A) generated from a neonate with c.1377delC mutation in the gene MYBPC3 causing hypertrophic cardiomyopathy

1
1. scibot 13 Apr 2021
  
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  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2021.102328
  
  Resource: (Cell Signaling Technology Cat# 81778, RRID:AB_2650582)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:AB_2650582
  
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  RRIDCUR:Validated RRID:AB_2650582
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sciencedirect.com/science/article/pii/S1873506121001744
Jan 2021
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Generation of an induced pluripotent stem cell line (SIAISi009-A) from a 60-year-old Chinese Han female with mild cognitive impairment (MCI) having two copies of APOE4/4 allele

1
1. scibot 28 Jan 2021
  
  in Public
  
  RRID:AB_2650582
  
  DOI: 10.1016/j.scr.2021.102198
  
  Resource: (Cell Signaling Technology Cat# 81778, RRID:AB_2650582)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:AB_2650582
  
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Generation of a human-derived induced pluripotent stem cell line (SIAISi012-A) from an 82-year-old healthy Chinese Han male

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  DOI: 10.1016/j.scr.2021.102186
  
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An induced pluripotent stem cell line (EHTJUi002-A) derived from a neonate with c.678G>A mutation in the gene FZD4 causing exudative vitreoretinopathy

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Generation of the Becker muscular dystrophy patient derived induced pluripotent stem cell line carrying the DMD splicing mutation c.1705-8 T>C.

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Generation and characterization of human induced pluripotent stem cells lines from four patients diagnosed with schizophrenia and one healthy control

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  DOI: 10.1016/j.scr.2020.101961
  
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GATA3 Mediates a Fast, Irreversible Commitment to BMP4-Driven Differentiation in Human Embryonic Stem Cells

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Generation of an induced pluripotent stem cell line (SIAISi003-A) from a 79-year-old patient with Alzheimer's disease having APOE3/4 genetic background

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Establishment of a Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line carrying a deletion of exons 51–53 of the dystrophin gene (CCMi003-A)

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Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c.4435G>T, p.(Gly1479*) and c.3474G>A, p.(Trp1158*) and missense c.4627G>T, p.(Asp1543Tyr) mutations

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Untitled document

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Untitled document

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Generation of the Rubinstein-Taybi syndrome type 2 patient-derived induced pluripotent stem cell line (IAIi001-A) carrying the EP300 exon 23 stop mutation c.3829A > T, p.(Lys1277*)

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Generation of an integration-free iPSC line (CSCRi005-A) from erythroid progenitor cells of a healthy Indian male individual

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Generation of induced pluripotent stem cells from a Becker muscular dystrophy patient carrying a deletion of exons 45-55 of the dystrophin gene (CCMi002BMD-A-9 ∆45-55)

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Derivation of the Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line lacking DMD exons 49 and 50 (CCMi001DMD-A-3, ∆ 49, ∆ 50)

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