Hypothesis

14 Matching Annotations

Aug 2025
www.sciencedirect.com www.sciencedirect.com

Generation of a human iPSC line, INMi007-A, carrying compound heterozygous DCT variants associated with oculocutaneous albinism type 8

1
1. scibot 26 Aug 2025
  
  in Public
  
  RRID:AB_1
  
  DOI: 10.1016/j.scr.2025.103810
  
  Resource: None
  
  Curator: @areedewitt04
  
  SciCrunch record: RRID:AB_1839587
  
  What is this?
  
  RRID:AB_1839587 RRIDCUR:Unresolved
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RRID:AB_1839587

RRIDCUR:Unresolved

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scibot

URL

sciencedirect.com/science/article/pii/S1873506125001606
Nov 2023
www.sciencedirect.com www.sciencedirect.com

Human pluripotent stem cell fate trajectories toward lung and hepatocyte progenitors

1
1. scibot 29 Nov 2023
  
  in Public
  
  RRID:AB_1839587
  
  DOI: 10.1016/j.isci.2023.108205
  
  Resource: (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1839587
  
  What is this?
  
  RRID:AB_1839587
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RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S2589004223022824
Sep 2022
www.sciencedirect.com www.sciencedirect.com

RNA-based generation of iPSCs from a boy carrying the mutation m.9185T>C in the mitochondrial gene MT-ATP6 and from his healthy mother

1
1. scibot 16 Sep 2022
  
  in Public
  
  RRID:AB_1839587
  
  DOI: 10.1016/j.scr.2022.102920
  
  Resource: (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1839587
  
  What is this?
  
  RRID:AB_1839587
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RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506122002690
Mar 2022
www.sciencedirect.com www.sciencedirect.com

Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T>G or m.8993T>C in the mitochondrial gene MT-ATP6

1
1. scibot 09 Mar 2022
  
  in Public
  
  Sigma Cat# WH0000174M1
  
  DOI: 10.1016/j.scr.2022.102742
  
  Resource: (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  Curator: @sophiastull
  
  SciCrunch record: RRID:AB_1839587
  
  What is this?
  
  RRID:AB_1839587
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RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506122000915
www.sciencedirect.com www.sciencedirect.com

Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa

1
1. scibot 02 Mar 2022
  
  in Public
  
  RRID:AB_1839587
  
  DOI: 10.1016/j.scr.2022.102738
  
  Resource: (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1839587
  
  What is this?
  
  RRID:AB_1839587
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RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506122000873
Aug 2021
www.sciencedirect.com www.sciencedirect.com

Untitled document

1
1. scibot 04 Aug 2021
  
  in Public
  
  RRID:AB_1839587
  
  DOI: 10.1016/j.scr.2018.11.007
  
  Resource: (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1839587
  
  What is this?
  
  RRID:AB_1839587
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RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506118302769
Jul 2021
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Untitled document

1
1. scibot 30 Jul 2021
  
  in Public
  
  RRID:AB_1839587
  
  DOI: 10.1016/j.scr.2018.11.004
  
  Resource: (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_1839587
  
  What is this?
  
  RRID:AB_1839587
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RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506118302721
Dec 2020
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Generation of the iPSC line IISHDOi007-A from peripheral blood mononuclear cells from a patient with McArdle disease harbouring the mutation c.2392T>C; p.Trp798Arg

1
1. scibot 08 Dec 2020
  
  in Public
  
  RRID:AB_1839587
  
  DOI: 10.1016/j.scr.2020.102108
  
  Resource: (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:AB_1839587
  
  What is this?
  
  RRIDCUR:Validated RRID:AB_1839587
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RRIDCUR:Validated

RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506120304098
Jan 2020
www.sciencedirect.com www.sciencedirect.com

Derivation of a human DOA iPSC line, IISHDOi006-A, with a mutation in the ACO2 gene: c.1999G>A; p.Glu667Lys

1
1. scibot 13 Jan 2020
  
  in Public
  
  RRID:AB_1839587
  
  DOI: 10.1016/j.scr.2019.101566
  
  Resource: (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:AB_1839587
  
  What is this?
  
  RRID:AB_1839587 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506119301965
Nov 2018
www.sciencedirect.com www.sciencedirect.com

Untitled document

1
1. scibot 05 Nov 2018
  
  in Public
  
  RRID:AB_1839587
  
  Resource used:
  
  (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  SciCrunch record: RRID:AB_1839587
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:AB_1839587
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RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506118302368
www.sciencedirect.com www.sciencedirect.com

Untitled document

1
1. scibot 05 Nov 2018
  
  in Public
  
  RRID:AB_1839587
  
  Resource used:
  
  (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  SciCrunch record: RRID:AB_1839587
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:AB_1839587
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RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506118301946
www.sciencedirect.com www.sciencedirect.com

Generation of a human iPSC line, IISHDOi002-A, with a 46, XY/47, XYY mosaicism and belonging to an African mitochondrial haplogroup

1
1. scibot 05 Nov 2018
  
  in Public
  
  RRID:AB_1839587
  
  Curator: @evieth
  
  Resource used:
  
  (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  SciCrunch record: RRID:AB_1839587
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:AB_1839587 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506118300539
Nov 2017
www.sciencedirect.com www.sciencedirect.com

Establishment of a human DOA 'plus' iPSC line, IISHDOi003-A, with the mutation in the OPA1 gene: c.1635C>A; p.Ser545Arg

1
1. scibot 08 Nov 2017
  
  in Public
  
  RRID:AB_1839587
  
  Curator: @Jmenke
  
  Resource used:
  
  (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  SciCrunch record: RRID:AB_1839587
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:AB_1839587 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:AB_1839587

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scibot

URL

sciencedirect.com/science/article/pii/S1873506117301794
www.sciencedirect.com www.sciencedirect.com

Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle disease

1
1. scibot 08 Nov 2017
  
  in Public
  
  RRID:AB_1839587
  
  Curator: @chewbeccax
  
  Resource used:
  
  (Sigma-Aldrich Cat# WH0000174M1, RRID:AB_1839587)
  
  SciCrunch record: RRID:AB_1839587
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:AB_1839587 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:AB_1839587

Annotators

scibot

URL

sciencedirect.com/science/article/pii/S1873506117301447