Cargando…
The isochromosome 20q abnormality of pluripotent cells interrupts germ layer differentiation
Chromosome 20 abnormalities are some of the most frequent genomic changes acquired by human pluripotent stem cell (hPSC) cultures worldwide. Yet their effects on differentiation remain largely unexplored. We investigated a recurrent abnormality also found on amniocentesis, the isochromosome 20q (iso...
Autores principales: | Vitillo, Loriana, Anjum, Fabiha, Hewitt, Zoe, Stavish, Dylan, Laing, Owen, Baker, Duncan, Barbaric, Ivana, Coffey, Pete |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031278/ https://www.ncbi.nlm.nih.gov/pubmed/36801002 http://dx.doi.org/10.1016/j.stemcr.2023.01.007 |
Ejemplares similares
-
Nucleosides Rescue Replication-Mediated Genome Instability of Human Pluripotent Stem Cells
por: Halliwell, Jason A., et al.
Publicado: (2020) -
Integrin and FAK Regulation of Human Pluripotent Stem Cells
por: Vitillo, Loriana, et al.
Publicado: (2017) -
Turner Syndrome With Isochromosome Structural Abnormalities: A Case Report
por: Ferdousi, Tahmina, et al.
Publicado: (2023) -
Genetically variant human pluripotent stem cells selectively eliminate wild-type counterparts through YAP-mediated cell competition
por: Price, Christopher J., et al.
Publicado: (2021) -
GMP-grade neural progenitor derivation and differentiation from clinical-grade human embryonic stem cells
por: Vitillo, Loriana, et al.
Publicado: (2020)