Hypothesis

17 Matching Annotations

Jun 2024
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Generation of an Alagille Syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi036-A) carrying a heterozygous mutation (p.Cys693*) in the JAG1 gene

1
1. scibot 07 Jun 2024
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2024.103429
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030
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scibot

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ncbi.nlm.nih.gov/pmc/articles/PMC11144073/
Oct 2023
www.sciencedirect.com www.sciencedirect.com

Generation of an Alagille syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi032-A) carrying a heterozygous mutation (p.Cys682Leufs*7) in the JAG1 gene

1
1. scibot 27 Oct 2023
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2023.103231
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030
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scibot

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sciencedirect.com/science/article/pii/S1873506123002179
Dec 2022
www.sciencedirect.com www.sciencedirect.com

Generation of three induced pluripotent stem cell lines carrying different variants of the BDNF (Val66Met) polymorphism

1
1. scibot 06 Dec 2022
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2022.102989
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030
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scibot

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sciencedirect.com/science/article/pii/S1873506122003385
Nov 2022
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Generation of one human induced pluripotent stem cell line (XACHi004-A) with heterozygous mutation of RYR2 gene from an atrial fibrillation patient

1
1. scibot 03 Nov 2022
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2022.102955
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030
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scibot

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sciencedirect.com/science/article/pii/S187350612200304X
Oct 2022
www.sciencedirect.com www.sciencedirect.com

Generation of two heterozygous GAA mutation-carrying human induced pluripotent stem cell lines (XACHi005-A, XACHi006-A) from parents of an infant with Pompe disease

1
1. scibot 04 Oct 2022
  
  in Public
  
  AB_2034030
  
  DOI: 10.1016/j.scr.2022.102934
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @a5munoz
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030
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scibot

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sciencedirect.com/science/article/pii/S1873506122002835
Aug 2021
www.sciencedirect.com www.sciencedirect.com

Generation of induced pluripotent stem cells(iPSCs) from an Chinese infant(XACHi015-A) with a Type 2 Long QT syndrome carrying the heterozygous mutation c.1814C>T(p.P605L) in KCNH2

1
1. scibot 20 Aug 2021
  
  in Public
  
  AB_2034030
  
  DOI: 10.1016/j.scr.2021.102509
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030
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sciencedirect.com/science/article/pii/S1873506121003561
www.sciencedirect.com www.sciencedirect.com

Untitled document

1
1. scibot 13 Aug 2021
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2019.101454
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030
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sciencedirect.com/science/article/pii/S1873506119300844
Jul 2021
www.sciencedirect.com www.sciencedirect.com

Untitled document

1
1. scibot 31 Jul 2021
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2018.10.019
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030
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sciencedirect.com/science/article/pii/S1873506118302642
Apr 2021
www.sciencedirect.com www.sciencedirect.com

Generation of a heterozygous GAPDH-Luciferase human ESC line (HVRDe008-A-1) for in vivo monitoring of stem cells and their differentiated progeny

1
1. scibot 28 Apr 2021
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2021.102371
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030
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sciencedirect.com/science/article/pii/S1873506121002178
Feb 2021
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Generation of one iPSC line (IMEDEAi007-A) by Sendai Virus transduction of PBMCs from a Psoriasis donor

1
1. scibot 24 Feb 2021
  
  in Public
  
  RRID:AB_2034030BD
  
  DOI: 10.1016/j.scr.2020.101917
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:AB_2034030
  
  Curator comments: Mouse IgM, k Isotype Control, Alexa Fluor 647 Conjugated, Clone G155-228 antibody BD Biosciences Cat# 560806
  
  What is this?
  
  RRID:AB_2034030 RRIDCUR:Unresolved RRIDCUR:SyntaxError
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RRID:AB_2034030

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scibot

URL

sciencedirect.com/science/article/pii/S187350612030218X
Sep 2020
www.sciencedirect.com www.sciencedirect.com

Generation of a human iPSC line (IMEDEAi008-A) derived from natural homozygous CCR5-Δ32 PBMCs enriched in the pro-erythroblast population

1
1. scibot 23 Sep 2020
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2020.101918
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030 RRIDCUR:Validated
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RRIDCUR:Validated

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scibot

URL

sciencedirect.com/science/article/pii/S1873506120302191
www.sciencedirect.com www.sciencedirect.com

Generation of three iPSC lines (XACHi007-A, XACHi008-A, XACHi009-A) from a Chinese family with long QT syndrome type 5 with heterozygous c.226G>A (p.D76N) mutation in KCNE1gene

1
1. scibot 04 Sep 2020
  
  in Public
  
  Alexa Fluor 647 Mouse IgM, κ Isotype Control)TRA-1-60(
  
  DOI: 10.1016/j.scr.2020.101798
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:AB_2034030
  
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  RRID:AB_2034030 RRIDCUR:Missing
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RRID:AB_2034030

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scibot

URL

sciencedirect.com/science/article/pii/S187350612030101X
Jan 2020
www.sciencedirect.com www.sciencedirect.com

Generation of an induced pluripotent stem cell line from a patient with autism spectrum disorder and SCN2A haploinsufficiency

1
1. scibot 13 Jan 2020
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2019.101488
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:AB_2034030
  
  What is this?
  
  RRID:AB_2034030 RRIDCUR:Validated
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RRID:AB_2034030

RRIDCUR:Validated

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scibot

URL

sciencedirect.com/science/article/pii/S1873506119301187
www.sciencedirect.com www.sciencedirect.com

Untitled document

1
1. scibot 13 Jan 2020
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.scr.2019.101440
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:AB_2034030
  
  What is this?
  
  RRID:AB_2034030 RRIDCUR:Validated
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RRID:AB_2034030

RRIDCUR:Validated

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scibot

URL

sciencedirect.com/science/article/pii/S1873506119300704
www.sciencedirect.com www.sciencedirect.com

Human Pluripotency Is Initiated and Preserved by a Unique Subset of Founder Cells

1
1. scibot 12 Jan 2020
  
  in Public
  
  RRID:AB_2034030
  
  DOI: 10.1016/j.cell.2019.03.013
  
  Resource: (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:AB_2034030
  
  What is this?
  
  RRID:AB_2034030 RRIDCUR:Validated
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RRID:AB_2034030

RRIDCUR:Validated

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scibot

URL

sciencedirect.com/science/article/pii/S0092867419302752
Nov 2018
www.sciencedirect.com www.sciencedirect.com

Generation of two induced pluripotent stem cells lines from Mucopolysaccharydosis IIIA patient: IMEDEAi004-A and IMEDEAi004-B

1
1. scibot 05 Nov 2018
  
  in Public
  
  RRID:AB_2034030
  
  Resource used:
  
  (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  SciCrunch record: RRID:AB_2034030
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
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  RRID:AB_2034030
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RRID:AB_2034030

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scibot

URL

sciencedirect.com/science/article/pii/S1873506118302290
www.sciencedirect.com www.sciencedirect.com

Generation of an induced pluripotent stem cell (iPSC) line from a patient with maturity-onset diabetes of the young type 3 (MODY3) carrying a hepatocyte nuclear factor 1-alpha (HNF1A) mutation

1
1. scibot 05 Nov 2018
  
  in Public
  
  BD Biosciences Cat# 560806
  
  Curator: @evieth
  
  Curator note: Alexa Fluor 647 Mouse IgM
  
  Resource used:
  
  (BD Biosciences Cat# 560806, RRID:AB_2034030)
  
  SciCrunch record: RRID:AB_2034030
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:AB_2034030 RRIDCUR:Missing
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RRIDCUR:Missing

RRID:AB_2034030

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scibot

URL

sciencedirect.com/science/article/pii/S1873506118300709