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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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Modulation of in vitro proliferation kinetics and primitive hematopoietic potential of individual human CD34+CD38-/lo cells in G0.

TL;DR: Results suggest that although exit from quiescence and commitment to proliferation might be stochastic, kinetics of proliferation, and possibly fate of primitive HPCs, might be modulated by extrinsic factors.
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Delayed Targeting of Cytokine-Nonresponsive Human Bone Marrow CD34+ Cells With Retrovirus-Mediated Gene Transfer Enhances Transduction Efficiency and Long-Term Expression of Transduced Genes

TL;DR: It is demonstrated that prolonged stimulation of primitive HPCs is essential for achieving efficient RMGT into cells capable of sustaining long-term in vitro hematopoiesis and may have significant implications for the development of clinical gene therapy protocols.
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Muscle-derived CD45-SCA-1+c-kit- progenitor cells give rise to skeletal muscle myotubes in vitro.

TL;DR: It is concluded that murine skeletal muscle possesses two populations of progenitor cells that can be directly isolated and one population expressing the phenotype S+CD34− may contain satellite cells, whereas the S+ CD34+ population is devoid of satellite cell markers.
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Skeletal muscle-derived progenitor cells exhibit neural competence.

TL;DR: It is demonstrated that phenotypically homogenous skeletal muscle progenitor cells defined as Lin−CD45−CD117−CD90+ cells express neural stem cell markers and are responsive to neural induction signals.
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Nonmarrow hematopoiesis occurs in a hyaluronic-acid-rich node and duct system in mice.

TL;DR: A hyaluronic acid-rich node and duct system (HAR-NDS) was found on the surface of internal organs of mice, and inside their blood and lymph vessels as mentioned in this paper.