Phytoextraction of uranium from contaminated soil by Macleaya cordata before and after application of EDDS and CA
In: Environmental science and pollution research: ESPR, Band 22, Heft 8, S. 6155-6163
ISSN: 1614-7499
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In: Environmental science and pollution research: ESPR, Band 22, Heft 8, S. 6155-6163
ISSN: 1614-7499
In: Journal of vocational behavior, Band 136, S. 103741
ISSN: 1095-9084
In: Environmental science and pollution research: ESPR, Band 24, Heft 6, S. 5134-5143
ISSN: 1614-7499
In: Environmental science and pollution research: ESPR, Band 26, Heft 36, S. 37125-37136
ISSN: 1614-7499
In: Environmental science and pollution research: ESPR, Band 22, Heft 23, S. 18918-18926
ISSN: 1614-7499
In: Child abuse & neglect: the international journal ; official journal of the International Society for the Prevention of Child Abuse and Neglect, Band 149, S. 106196
ISSN: 1873-7757
In: PNAS nexus, Band 1, Heft 5
ISSN: 2752-6542
Abstract
The cornea is a protective and refractive barrier in the eye crucial for vision. Understanding the human cornea in health, disease, and cell-based treatments can be greatly advanced with cornea organoids developed in culture from induced pluripotent stem cells. While a limited number of studies have investigated the single-cell transcriptomic composition of the human cornea, its organoids have not been examined similarly. Here, we elucidated the transcriptomic cell fate map of 4-month-old human cornea organoids and human donor corneas. The organoids harbor cell clusters that resemble cells of the corneal epithelium, stroma, and endothelium, with subpopulations that capture signatures of early developmental states. Unlike the adult cornea where the largest cell population is stromal, the organoids contain large proportions of epithelial and endothelial-like cells. These corneal organoids offer a 3D model to study corneal diseases and integrated responses of different cell types.