Generation of heterozygous and homozygous hESC H9 sublines carrying inactivating mutations in RB1
Inactivation of the tumor suppressor gene RB1 is causal for development of retinoblastoma, a tumor of the neural retina arising in children under the age of five. In addition, secondary RB1 mutations are found in many other tumor types. To investigate retinoblastoma formation in vitro, stem cells wi...
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| Autores principales: | , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Elsevier
2018-12-01
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| Colección: | Stem Cell Research |
| Acceso en línea: | http://www.sciencedirect.com/science/article/pii/S187350611830237X |
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