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12 Matching Annotations

Jul 2026
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Establishment of CRISPR/Cas9-edited LEMD2 knock-in (UKWCHFi001-B-1) and knock-out (UKWCHFi001-B-2) iPSC lines to investigate the mechanisms of LEMD2-associated cardiomyopathy

1
1. scibot 03 Jul 2026
  
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  RRID:AB_2653520
  
  DOI: 10.1016/j.scr.2026.104049
  
  Resource: (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653520
  
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  RRID:AB_2653520
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scibot

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sciencedirect.com/science/article/pii/S1873506126001455
Jan 2026
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Generation of the human induced pluripotent stem cell line UKWNLi010 derived from a patient carrying two homozygous single nucleotide polymorphisms (rs2839629 and rs915854) associated with an increased risk of painful bortezomib-induced peripheral neuropathy

1
1. scibot 13 Jan 2026
  
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  AB_2653520
  
  DOI: 10.1016/j.scr.2025.103898
  
  Resource: (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653520
  
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  RRID:AB_2653520
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scibot

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sciencedirect.com/science/article/pii/S187350612500248X
Apr 2025
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Generation of a gene-corrected human isogenic iPSC line from a patient with Fabry disease carrying the GLA variant c.1069C>T using CRISPR/Cas9-mediated homology directed repair

1
1. scibot 17 Apr 2025
  
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  AB_2653520
  
  DOI: 10.1016/j.scr.2025.103711
  
  Resource: (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653520
  
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  RRID:AB_2653520
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scibot

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sciencedirect.com/science/article/pii/S1873506125000613
Apr 2023
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Generation of induced pluripotent stem cell line (UKWNLi008) derived from a patient carrying a c.1678C>G variant in the transient receptor potential cation channel subfamily A member (TRPA1) gene potentially associated with small fiber neuropathy

1
1. scibot 13 Apr 2023
  
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  AB_2653520
  
  DOI: 10.1016/j.scr.2023.103094
  
  Resource: (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653520
  
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  RRID:AB_2653520
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scibot

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sciencedirect.com/science/article/pii/S1873506123000806
Jan 2023
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Generation of two induced pluripotent stem cell lines UKWNLi006 and UKWNLi007 derived from two patients with an active site GLA mutation leading to a painful and painless phenotype in Fabry disease

1
1. scibot 11 Jan 2023
  
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  AB_2653520
  
  DOI: 10.1016/j.scr.2023.103025
  
  Resource: (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653520
  
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  RRID:AB_2653520
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scibot

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sciencedirect.com/science/article/pii/S1873506123000119
Mar 2022
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Generation of the induced pluripotent stem cell line UKWNLi005-A derived from a patient with the GLA mutation c.376A>G of unknown pathogenicity in Fabry disease

1
1. scibot 18 Mar 2022
  
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  AB_2653520
  
  DOI: 10.1016/j.scr.2022.102747
  
  Resource: (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2653520
  
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  RRID:AB_2653520
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scibot

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sciencedirect.com/science/article/pii/S1873506122000964
Feb 2021
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CRISPR/Cas9-edited PKP2 knock-out (JMUi001-A-2) and DSG2 knock-out (JMUi001-A-3) iPSC lines as an isogenic human model system for arrhythmogenic cardiomyopathy (ACM)

1
1. scibot 24 Feb 2021
  
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  RRID:AB_2653520
  
  DOI: 10.1016/j.scr.2021.102256
  
  Resource: (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:AB_2653520
  
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  RRIDCUR:Validated RRID:AB_2653520
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RRID:AB_2653520

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scibot

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sciencedirect.com/science/article/pii/S1873506121001021
Sep 2020
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Generation of two patient-derived iPSC lines from siblings (LIBUCi001-A and LIBUCi002-A) and a genetically modified iPSC line (JMUi001-A-1) to mimic dilated cardiomyopathy with ataxia (DCMA) caused by a homozygous DNAJC19 mutation

1
1. scibot 23 Sep 2020
  
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  RRID:AB_2653520
  
  DOI: 10.1016/j.scr.2020.101856
  
  Resource: (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:AB_2653520
  
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  RRIDCUR:Validated RRID:AB_2653520
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RRIDCUR:Validated

RRID:AB_2653520

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scibot

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sciencedirect.com/science/article/pii/S1873506120301574
Jan 2020
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Untitled document

1
1. scibot 13 Jan 2020
  
  in Public
  
  RRID:AB_2653520
  
  DOI: 10.1016/j.scr.2019.101396
  
  Resource: (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  Curator: @evieth
  
  SciCrunch record: RRID:AB_2653520
  
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  RRID:AB_2653520 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:AB_2653520

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scibot

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sciencedirect.com/science/article/pii/S1873506119300261
Nov 2018
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Untitled document

1
1. scibot 05 Nov 2018
  
  in Public
  
  RRID:AB_2653520
  
  Resource used:
  
  (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  SciCrunch record: RRID:AB_2653520
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
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  RRID:AB_2653520
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RRID:AB_2653520

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scibot

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sciencedirect.com/science/article/pii/S1873506118302629
www.sciencedirect.com www.sciencedirect.com

Untitled document

1
1. scibot 05 Nov 2018
  
  in Public
  
  RRID:AB_2653520
  
  Resource used:
  
  (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  SciCrunch record: RRID:AB_2653520
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:AB_2653520
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RRID:AB_2653520

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scibot

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sciencedirect.com/science/article/pii/S1873506118302010
www.sciencedirect.com www.sciencedirect.com

Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3

1
1. scibot 05 Nov 2018
  
  in Public
  
  RRID:AB_2653520
  
  Curator: @evieth
  
  Resource used:
  
  (Miltenyi Biotec Cat# 130-098-347, RRID:AB_2653520)
  
  SciCrunch record: RRID:AB_2653520
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:AB_2653520 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:AB_2653520

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scibot

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sciencedirect.com/science/article/pii/S1873506118300497