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Fatih Arslan

Researcher at Utrecht University

Publications -  58
Citations -  7936

Fatih Arslan is an academic researcher from Utrecht University. The author has contributed to research in topics: Myocardial infarction & Reperfusion injury. The author has an hindex of 28, co-authored 52 publications receiving 6747 citations. Previous affiliations of Fatih Arslan include University Medical Center Utrecht & University of Nevada, Reno.

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Exosome secreted by MSC reduces myocardial ischemia/reperfusion injury.

TL;DR: The novel role of exosomes highlights a new perspective into intercellular mediation of tissue injury and repair, and engenders novel approaches to the development of biologics for tissue repair.
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Mesenchymal stem cell-derived exosomes increase ATP levels, decrease oxidative stress and activate PI3K/Akt pathway to enhance myocardial viability and prevent adverse remodeling after myocardial ischemia/reperfusion injury

TL;DR: This study shows that intact exosomes restore bioenergetics, reduce oxidative stress and activate pro-survival signaling, thereby enhancing cardiac function and geometry after myocardial I/R injury, and Hence, mesenchymal stem cell-derived exosome are a potential adjuvant to reperfusion therapy for my cardiac infarction.
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Reduction of myocardial infarct size by human mesenchymal stem cell conditioned medium.

TL;DR: The data identify human MSC-CM as a promising therapeutic option to reduce myocardial infarct size in patients with acute MI and suggest that the use of stem cell secretions could extend the applicability of stem cells for therapeutic purposes.
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Prognostic value of fractional flow reserve: linking physiologic severity to clinical outcomes.

TL;DR: FFR demonstrates a continuous and independent relationship with subsequent outcomes, modulated by medical therapy versus revascularization, such that lower FFR values confer a higher risk and therefore receive larger absolute benefits fromRevascularization.
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Proteolytic Potential of the MSC Exosome Proteome: Implications for an Exosome-Mediated Delivery of Therapeutic Proteasome

TL;DR: 20S proteasome is a candidate exosome protein that could synergize with other constituents to ameliorate tissue damage and be correlated with a modest but significant reduction in oligomerized protein in a mouse model of myocardial infarction.