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Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene

The KCL018 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation affecting one allele of the DMPK gene encoding the dystrophia myotonica protein kinase (2200 trinucleotide repeats; 14 for the normal allele). The ICM was isolated us...

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Autores principales: Miere, Cristian, Hewitson, Heema, Devito, Liani, Wood, Victoria, Kadeva, Neli, Cornwell, Glenda, Codognotto, Stefano, Stephenson, Emma, Ilic, Dusko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823665/
https://www.ncbi.nlm.nih.gov/pubmed/27346000
http://dx.doi.org/10.1016/j.scr.2016.01.004
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author Miere, Cristian
Hewitson, Heema
Devito, Liani
Wood, Victoria
Kadeva, Neli
Cornwell, Glenda
Codognotto, Stefano
Stephenson, Emma
Ilic, Dusko
author_facet Miere, Cristian
Hewitson, Heema
Devito, Liani
Wood, Victoria
Kadeva, Neli
Cornwell, Glenda
Codognotto, Stefano
Stephenson, Emma
Ilic, Dusko
author_sort Miere, Cristian
collection PubMed
description The KCL018 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation affecting one allele of the DMPK gene encoding the dystrophia myotonica protein kinase (2200 trinucleotide repeats; 14 for the normal allele). The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation and cell line propagation were performed in an animal product-free environment. Pluripotent state and differentiation potential were confirmed by in vitro assays.
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spelling pubmed-48236652016-04-15 Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene Miere, Cristian Hewitson, Heema Devito, Liani Wood, Victoria Kadeva, Neli Cornwell, Glenda Codognotto, Stefano Stephenson, Emma Ilic, Dusko Stem Cell Res Lab Resource: Stem Cell Line The KCL018 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation affecting one allele of the DMPK gene encoding the dystrophia myotonica protein kinase (2200 trinucleotide repeats; 14 for the normal allele). The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation and cell line propagation were performed in an animal product-free environment. Pluripotent state and differentiation potential were confirmed by in vitro assays. Elsevier 2016-03 /pmc/articles/PMC4823665/ /pubmed/27346000 http://dx.doi.org/10.1016/j.scr.2016.01.004 Text en © 2016 University of Texas at Austin Dell Medical School http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Lab Resource: Stem Cell Line
Miere, Cristian
Hewitson, Heema
Devito, Liani
Wood, Victoria
Kadeva, Neli
Cornwell, Glenda
Codognotto, Stefano
Stephenson, Emma
Ilic, Dusko
Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene
title Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene
title_full Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene
title_fullStr Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene
title_full_unstemmed Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene
title_short Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene
title_sort generation of kcl018 research grade human embryonic stem cell line carrying a mutation in the dmpk gene
topic Lab Resource: Stem Cell Line
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823665/
https://www.ncbi.nlm.nih.gov/pubmed/27346000
http://dx.doi.org/10.1016/j.scr.2016.01.004
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