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Generation of KCL017 research grade human embryonic stem cell line carrying a mutation in VHL gene
The KCL017 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation affecting splicing site of the VHL gene encoding von Hippel–Lindau tumor suppressor E3 ubiquitin protein ligase (676 + 3 A > T). The ICM was isolated using laser m...
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| Publicado no: | Stem Cell Res |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4823763/ https://ncbi.nlm.nih.gov/pubmed/27345980 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.scr.2016.01.013 |
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