Cargando…
Monosomy X in isogenic human iPSC-derived trophoblast model impacts expression modules preserved in human placenta
Mammalian sex chromosomes encode homologous X/Y gene pairs that were retained on the Y chromosome in males and escape X chromosome inactivation (XCI) in females. Inferred to reflect X/Y pair dosage sensitivity, monosomy X is a leading cause of miscarriage in humans with near full penetrance. This ph...
Autores principales: | Ahern, Darcy T., Bansal, Prakhar, Armillei, Maria K., Faustino, Isaac V., Kondaveeti, Yuvabharath, Glatt-Deeley, Heather R., Banda, Erin C., Pinter, Stefan F. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546589/ https://www.ncbi.nlm.nih.gov/pubmed/36161909 http://dx.doi.org/10.1073/pnas.2211073119 |
Ejemplares similares
-
Isogenic hiPSC models of Turner syndrome reveal shared roles of inactive X and Y in the human cranial neural crest network
por: Ahern, Darcy T., et al.
Publicado: (2023) -
Contiguous erosion of the inactive X in human pluripotency concludes with global DNA hypomethylation
por: Bansal, Prakhar, et al.
Publicado: (2021) -
Forged by DXZ4, FIRRE, and ICCE: How Tandem Repeats Shape the Active and Inactive X Chromosome
por: Bansal, Prakhar, et al.
Publicado: (2020) -
Generation of a CHIP isogenic human iPSC-derived cortical neuron model for functional proteomics
por: Dias, Catarina, et al.
Publicado: (2022) -
Generation of a gene-corrected human isogenic iPSC line from an Alzheimer’s disease iPSC line carrying the London mutation in APP (V717I)
por: Hernández, Damián, et al.
Publicado: (2021)