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Edward F. Srour

Researcher at Indiana University

Publications -  204
Citations -  10614

Edward F. Srour is an academic researcher from Indiana University. The author has contributed to research in topics: Stem cell & Haematopoiesis. The author has an hindex of 51, co-authored 202 publications receiving 9991 citations. Previous affiliations of Edward F. Srour include Indiana University – Purdue University Indianapolis & University of New Mexico.

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Individualized Breast Cancer Characterization through Single-Cell Analysis of Tumor and Adjacent Normal Cells.

TL;DR: In this article, a single-cell genomics of breast tumors and adjacent normal cells propagated for a short duration under growth conditions that enable epithelial reprogramming was performed, where cells analyzed were either unselected for a specific subpopulation or phenotypically defined as undifferentiated and highly clonogenic ALDH+/CD49f+/EpCAM+ luminal progenitors.
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Animal models for human hematopoiesis.

TL;DR: The development, peculiarities, shortcomings, and applications of human-animal models as well as their potential use in exploring the field of human lymphohematopoiesis are the focus of this review.
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Megakaryocyte and Osteoblast Interactions Modulate Bone Mass and Hematopoiesis.

TL;DR: In this article, the loss of megakaryocytes (MK) negatively impacts osteoblastogenesis and hematopoiesis, and a significant 20-fold increase in femoral midshaft bone volume.
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Expansion of prostate epithelial progenitor cells after inflammation of the mouse prostate.

TL;DR: In this paper, a novel epithelial progenitor cell population is induced to expand during inflammation, and this population is increased in bacterially induced inflamed mouse prostates relative to naive control prostates.
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Aging negatively impacts the ability of megakaryocytes to stimulate osteoblast proliferation and bone mass.

TL;DR: In this paper, the ability of megakaryocytes (MKs) to support osteoblast proliferation was attenuated during aging as transplantation of GATA1low/low hematopoietic donor cells from young mice resulted in an increase in bone mass of recipient mice compared to transplanting of young wild-type donor cells.