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secreted by human adipose tissues, and has multi-mechanisms protective against cerebral ischemic injury, it
is of great potential in the application of clinical treatment of ischemic stroke in the future.
DECLARATIONS
Acknowledgments
The author is grateful to Prof. Mao-Tsun Lin, Prof. Chao-Ching Huang, and Prof. Chun Y. Hsu for
mentoring, and colleagues of Chi Mei Medical Center, and team members of Taiwan Stroke Biosignature for
support.
Authors’ contributions
Wu MH is responsible for design and conceptualization of the study, drafting and revising the manuscript,
and obtaining funding.
Availability of data and materials
Not applicable.
Financial support and sponsorship
This study was supported by grants from Chi Mei Medical Center (CMNCKU9908), Chi Mei Medical
Center, Liouying (CLFHR10607), and Academia Sinica Taiwan Stroke Biosignature Project (AS-BD-108-11).
Conflicts of interest
The author declared that there are no conflicts of interest.
Ethical approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Copyright
© The Author(s) 2019.
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