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Generation of KCL035 research grade human embryonic stem cell line carrying a mutation in HBB gene
The KCL035 human embryonic stem cell line was derived from an embryo donated for research that carried a mutation in the HBB gene, which is linked to the β-thalassemia syndrome. The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation a...
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| Publicat a: | Stem Cell Res |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4823668/ https://ncbi.nlm.nih.gov/pubmed/27345970 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.scr.2016.01.007 |
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