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24 Matching Annotations

Apr 2025
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Generation and validation of a Leber Congenital Amaurosis, Type 12 patient-specific iPSC line (LVPEIi006-B) with a splice-site mutation in RD3 and an isogenic mutation-corrected iPSC line (LVPEIi006-B-1)

1
1. scibot 05 Apr 2025
  
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  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2025.103703
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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scibot

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sciencedirect.com/science/article/pii/S1873506125000534
Jun 2024
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Generation and characterization of a Stargardt’s disease-specific induced pluripotent stem cell line (LVPEIi008-A) with a homozygous missense mutation in exon 44 of ABCA4

1
1. scibot 07 Jun 2024
  
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  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2024.103458
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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sciencedirect.com/science/article/pii/S1873506124001569
Apr 2024
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Generation of two induced pluripotent stem cell lines (LVPEIi004-A and LVPEIi005-A) from probands with Leber Congenital Amaurosis 2 (LCA2) and harboring mutations in RPE65

1
1. scibot 19 Apr 2024
  
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  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2024.103413
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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scibot

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sciencedirect.com/science/article/pii/S1873506124001119
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Generation of two induced pluripotent stem cell lines (LVPEIi007-B, LVPEIi008-B) from patients harboring homozygous mutation in ABCA4 (c.6088C>T) using non-integrative Sendai virus-based approach

1
1. scibot 12 Apr 2024
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2024.103418
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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scibot

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sciencedirect.com/science/article/pii/S1873506124001168
Mar 2024
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Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3

1
1. scibot 14 Mar 2024
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2024.103380
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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sciencedirect.com/science/article/pii/S1873506124000783
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Generation and characterization of three CRISPR/Cas9 edited RB1 null hiPSC lines for retinoblastoma disease modelling

1
1. scibot 05 Mar 2024
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2024.103373
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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sciencedirect.com/science/article/pii/S1873506124000710
Feb 2024
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Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying MYBPC3 nonsense mutations

1
1. scibot 29 Feb 2024
  
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  AB_1977399
  
  DOI: 10.1016/j.scr.2024.103362
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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sciencedirect.com/science/article/pii/S1873506124000606
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Generation of an induced pluripotent stem cell line (LVPEIi002-A) with heterozygous RB1 mutation using peri-orbital fat derived mesenchymal cells of a patient with inherited retinoblastoma

1
1. scibot 09 Feb 2024
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2024.103329
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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scibot

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sciencedirect.com/science/article/pii/S1873506124000278
Dec 2023
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Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying the MYBPC3 missense c.1484G>A mutation

1
1. scibot 29 Dec 2023
  
  in Public
  
  AB_1977399
  
  DOI: 10.1016/j.scr.2023.103282
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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sciencedirect.com/science/article/pii/S1873506123002684
Apr 2023
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Transient suppression of SUMOylation in embryonic stem cells generates embryo-like structures

1
1. scibot 20 Apr 2023
  
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  AB_1977399
  
  DOI: 10.1016/j.celrep.2023.112380
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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sciencedirect.com/science/article/pii/S2211124723003911
Jan 2023
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Generation of feeder-independent transgene-free iPSC lines from a young-onset Parkinson’s disease (YOPD) patient with a homozygous PLA2G6: c.2222G>A (p. Arg741Gln) mutation (NCBSi003-A) and unaffected heterozygous parent (NCBSi004-A)

1
1. scibot 26 Jan 2023
  
  in Public
  
  AB_1977399
  
  DOI: 10.1016/j.scr.2023.103033
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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sciencedirect.com/science/article/pii/S1873506123000193
Oct 2022
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Generation of three human iPSC lines from patients with Huntington’s Disease with different CAG lengths and human control iPSC line from a healthy donor

1
1. scibot 04 Oct 2022
  
  in Public
  
  RRID:AB_1977399RRID:AB_2536667RRID
  
  DOI: 10.1016/j.scr.2022.102931
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @a5munoz
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399 RRIDCUR:Unresolved
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RRIDCUR:Unresolved

RRID:AB_1977399

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scibot

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sciencedirect.com/science/article/pii/S187350612200280X
Sep 2022
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Generation of iPSC lines from hereditary spastic paraplegia 56 (SPG56) patients and family members carrying CYP2U1 mutations

1
1. scibot 16 Sep 2022
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2022.102917
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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RRID:AB_1977399

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sciencedirect.com/science/article/pii/S1873506122002665
Mar 2022
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Generation and characterization of induced pluripotent stem cell line (IBBISTi004-A) from an Angelman syndrome patient carrying a class II deletion of the maternal chromosome 15q11.2-q13

1
1. scibot 25 Mar 2022
  
  in Public
  
  AB_1977399
  
  DOI: 10.1016/j.scr.2022.102757
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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RRID:AB_1977399

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scibot

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sciencedirect.com/science/article/pii/S1873506122001064
Jan 2022
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Human induced pluripotent stem cells generated from epilepsy patients for use as in vitro models for drug screening

1
1. scibot 21 Jan 2022
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2022.102673
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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scibot

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sciencedirect.com/science/article/pii/S1873506122000228
Oct 2021
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Generation of induced pluripotent stem cell lines from peripheral blood mononuclear cells of three drug resistant and three drug responsive epilepsy patients

1
1. scibot 12 Oct 2021
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2021.102564
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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RRID:AB_1977399

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sciencedirect.com/science/article/pii/S1873506121004116
Sep 2021
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Ataxia Telangiectasia iPSC line generated from a patient olfactory biopsy identifies novel disease-causing mutations

1
1. scibot 03 Sep 2021
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2021.102528
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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RRID:AB_1977399

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scibot

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sciencedirect.com/science/article/pii/S1873506121003755
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Reprogramming of human olfactory neurosphere-derived cells from olfactory mucosal biopsies of a control cohort

1
1. scibot 03 Sep 2021
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2021.102527
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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sciencedirect.com/science/article/pii/S1873506121003743
Apr 2021
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Generation and characterization of induced pluripotent stem cells heterozygous for the Portuguese BRCA2 founder mutation

2
1. scibot 24 Apr 2021
  
  in Public
  
  AB_1977399
  
  DOI: 10.1016/j.scr.2021.102364
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:AB_1977399
  
  What is this?
  
  RRID:AB_1977399
2. scibot 24 Apr 2021
  
  in Public
  
  AB_1977399
  
  DOI: 10.1016/j.scr.2021.102364
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399
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RRID:AB_1977399

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scibot

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sciencedirect.com/science/article/pii/S1873506121002105
Feb 2021
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Generation and characterization of induced pluripotent stem cells from a family carrying the BRCA1 mutation c.3612delA

1
1. scibot 12 Feb 2021
  
  in Public
  
  AB_1977399
  
  DOI: 10.1016/j.scr.2021.102242
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @evieth
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:AB_1977399

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scibot

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sciencedirect.com/science/article/pii/S187350612100088X
www.sciencedirect.com www.sciencedirect.com

Establishment of two hiPSC lines (IIMCBi001-A and IIMCBi002-A) from dermal fibroblasts of healthy donors and characterization of their cell cycle

1
1. scibot 09 Feb 2021
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2021.102225
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @evieth
  
  SciCrunch record: RRID:AB_1977399
  
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  RRIDCUR:Validated RRID:AB_1977399
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RRIDCUR:Validated

RRID:AB_1977399

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scibot

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sciencedirect.com/science/article/pii/S1873506121000714
Sep 2020
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Induced pluripotent stem cell line (INSAi002-A) from a Fabry Disease patient hemizygote for the rare p.W287X mutation

1
1. scibot 12 Sep 2020
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2020.101794
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:AB_1977399
  
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  RRID:AB_1977399 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:AB_1977399

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scibot

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sciencedirect.com/science/article/pii/S1873506120300970
Jan 2020
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Induced pluripotent stem cell line (INSAi001-A) from a Gaucher Disease type 3 patient compound heterozygote for mutations in the GBA1 gene

1
1. scibot 13 Jan 2020
  
  in Public
  
  RRID:AB_1977399
  
  DOI: 10.1016/j.scr.2019.101595
  
  Resource: (Millipore Cat# MAB4419, RRID:AB_1977399)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:AB_1977399
  
  What is this?
  
  RRID:AB_1977399 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:AB_1977399

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scibot

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sciencedirect.com/science/article/pii/S1873506119302259