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10 Matching Annotations

Apr 2025
link.springer.com link.springer.com

Generation of iPSC Lines from Family with Glycogen Storage Disease Type Ia

1
1. scibot 24 Apr 2025
  
  in Public
  
  RRID:AB_10863255
  
  DOI: 10.1134/S1062360425700067
  
  Resource: (Abcam Cat# ab108396, RRID:AB_10863255)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_10863255
  
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  RRID:AB_10863255
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RRID:AB_10863255

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scibot

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link.springer.com/article/10.1134/S1062360425700067
Feb 2024
www.sciencedirect.com www.sciencedirect.com

Generation of an induced pluripotent stem cell line (UMi043-A) from an African American patient with Alzheimer’s disease carrying an ABCA7 deletion (p.Arg578Alafs)

1
1. scibot 29 Feb 2024
  
  in Public
  
  RRID:AB_10863255
  
  DOI: 10.1016/j.scr.2024.103364
  
  Resource: (Abcam Cat# ab108396, RRID:AB_10863255)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_10863255
  
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  RRID:AB_10863255
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sciencedirect.com/science/article/pii/S187350612400062X
Nov 2023
www.sciencedirect.com www.sciencedirect.com

Generation of induced pluripotent stem cell line (RCMGi012-A) from fibroblasts of patient with mucopolysaccharidosis type VI

1
1. scibot 28 Nov 2023
  
  in Public
  
  RRID:AB_10863255
  
  DOI: 10.1016/j.scr.2023.103259
  
  Resource: (Abcam Cat# ab108396, RRID:AB_10863255)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_10863255
  
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  RRID:AB_10863255
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RRID:AB_10863255

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scibot

URL

sciencedirect.com/science/article/pii/S1873506123002453
Aug 2023
www.sciencedirect.com www.sciencedirect.com

Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12

1
1. scibot 17 Aug 2023
  
  in Public
  
  RRID:AB_10863255
  
  DOI: 10.1016/j.scr.2023.103183
  
  Resource: (Abcam Cat# ab108396, RRID:AB_10863255)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_10863255
  
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  RRID:AB_10863255
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RRID:AB_10863255

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sciencedirect.com/science/article/pii/S1873506123001691
Jan 2023
www.sciencedirect.com www.sciencedirect.com

Generation of OCIAD2 homozygous knockout (BJNhem20-OCIAD2-CRISPR-33) and heterozygous knockout (BJNhem20-OCIAD2-CRISPR-40) human embryonic stem cell lines using CRISPR-Cas9 mediated targeting

1
1. scibot 11 Jan 2023
  
  in Public
  
  RRID:AB_10863255
  
  DOI: 10.1016/j.scr.2023.103026
  
  Resource: (Abcam Cat# ab108396, RRID:AB_10863255)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_10863255
  
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  RRID:AB_10863255
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RRID:AB_10863255

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URL

sciencedirect.com/science/article/pii/S1873506123000120
Aug 2022
www.sciencedirect.com www.sciencedirect.com

Generation of two induced pluripotent stem cell lines (RCMGi005-A/B) from human skin fibroblasts of a cystic fibrosis patient with homozygous F508del mutation in CFTR gene

1
1. scibot 22 Aug 2022
  
  in Public
  
  RRID:AB_10863255
  
  DOI: 10.1016/j.scr.2022.102896
  
  Resource: (Abcam Cat# ab108396, RRID:AB_10863255)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_10863255
  
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  RRID:AB_10863255
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RRID:AB_10863255

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scibot

URL

sciencedirect.com/science/article/pii/S1873506122002458
Jun 2022
www.sciencedirect.com www.sciencedirect.com

Generation of two iPSC lines (UMi038-A & UMi039-A) from siblings bearing an Alzheimer’s disease-associated variant in SORL1

1
1. scibot 03 Jun 2022
  
  in Public
  
  RRID:AB_10863255
  
  DOI: 10.1016/j.scr.2022.102823
  
  Resource: (Abcam Cat# ab108396, RRID:AB_10863255)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_10863255
  
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  RRID:AB_10863255
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RRID:AB_10863255

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URL

sciencedirect.com/science/article/pii/S1873506122001726
Jul 2021
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Untitled document

1
1. scibot 29 Jul 2021
  
  in Public
  
  AB_10863255
  
  DOI: 10.1210/en.2017-00361
  
  Resource: (Abcam Cat# ab108396, RRID:AB_10863255)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_10863255
  
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  RRID:AB_10863255
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RRID:AB_10863255

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URL

ncbi.nlm.nih.gov/pmc/articles/PMC5695839/
Feb 2021
www.sciencedirect.com www.sciencedirect.com

Generation of two induced pluripotent stem cell lines (RCMGi004-A and -B) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/W1282X mutations in CFTR gene

1
1. scibot 12 Feb 2021
  
  in Public
  
  RRID:AB_10863255
  
  DOI: 10.1016/j.scr.2021.102232
  
  Resource: (Abcam Cat# ab108396, RRID:AB_10863255)
  
  Curator: @evieth
  
  SciCrunch record: RRID:AB_10863255
  
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  RRID:AB_10863255 RRIDCUR:Validated
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RRID:AB_10863255

RRIDCUR:Validated

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scibot

URL

sciencedirect.com/science/article/pii/S1873506121000787
Nov 2018
academic.oup.com academic.oup.com

Pioneer Factors FOXA1 and FOXA2 Assist Selective Glucocorticoid Receptor Signaling in Human Endometrial Cells

1
1. scibot 05 Nov 2018
  
  in Public
  
  AB_10863255
  
  Resource used:
  
  (Abcam Cat# ab108396, RRID:AB_10863255)
  
  SciCrunch record: RRID:AB_10863255
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:AB_10863255
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RRID:AB_10863255

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scibot

URL

academic.oup.com/endo/article/158/11/4076/4096797