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Emily M. Holloway

Researcher at University of Michigan

Publications -  22
Citations -  558

Emily M. Holloway is an academic researcher from University of Michigan. The author has contributed to research in topics: Biology & Organoid. The author has an hindex of 7, co-authored 13 publications receiving 224 citations.

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In Vitro and In Vivo Development of the Human Airway at Single-Cell Resolution.

TL;DR: This work used homogeneous human bud tip organoid cultures and identified SMAD signaling as a key regulator of the bud tip-to-airway transition and shed light on human airway differentiation in vitro and provides a single-cell atlas of the developing human lung.
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Mapping Development of the Human Intestinal Niche at Single-Cell Resolution.

TL;DR: This work uses single-cell mRNA sequencing with in situ validation approaches to interrogate human intestinal development from 7-21 weeks post conception, assigning molecular identities and spatial locations to cells and factors that comprise the niche.
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Differentiation of Human Intestinal Organoids with Endogenous Vascular Endothelial Cells

TL;DR: HIOs can co-differentiate a native EC population that is properly patterned with an intestine-specific EC transcriptional signature in vitro, and it is found that HIO ECs grown in vitro share the highest similarity with native intestinal ECs relative to kidney and lung.
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Biologically inspired approaches to enhance human organoid complexity

TL;DR: Efforts to characterize human organ cellular complexity and attempts to make organoid models more realistic through co-culture, transplantation and bioengineering approaches are discussed.
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Plasticity of distal nephron epithelia from human kidney organoids enables the induction of ureteric tip and stalk.

TL;DR: In this article, the authors re-analyzed the transcriptional distinction between distal nephron and ureteric epithelium in human fetal kidney, and showed that the distal kidney segment alone displays significant in vitro plasticity and can adopt a uteric tip identity when isolated and cultured in defined conditions.