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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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The in vitro and in vivo effects of stem cell factor on human hematopoiesis.

TL;DR: In vivo administration of SCF led to an increase in both differentiated and primitive hematopoietic progenitor cells within the marrow, suggesting that in vivo SCF administration may be useful for improving the quality of bone marrow grafts to be used either for autologous or allogeneic bone marrow transplantation.
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CD166 regulates human and murine hematopoietic stem cells and the hematopoietic niche

TL;DR: In this article, the authors demonstrate that CD166 is a functional hematopoietic stem cell (HSC) marker that identifies both murine and human long-term repopulating cells.
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Adult Bone Marrow–derived Cells Do Not Acquire Functional Attributes of Cardiomyocytes When Transplanted into Peri-infarct Myocardium

TL;DR: Investigation of the ability of transplanted BM cells to develop intracellular calcium transients in response to membrane depolarization in situ concludes that engrafted BM-derived cells lack attributes of functioning cardiomyocytes, calling into question the concept that adult BM cells can give rise to substantiveCardiomyocyte regeneration within the infarcted heart.
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Homing, cell cycle kinetics and fate of transplanted hematopoietic stem cells.

TL;DR: Homing of transplanted hematopoietic stem cells to recipient bone marrow is a critical step in engraftment and initiation of marrow reconstitution and the fate of marrow-homed cells shortly after transplantation and the rapidity at which they begin to proliferate in their new marrow microenvironment is confused.
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Differential staining of DNA and RNA.

TL;DR: This unit presents two protocols for differential staining, one using the metachromatic dye acridine orange (AO) and the other a combination of pyronin Y (PY) and Hoechst 33342, which has its advantages and limitations.