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Cheng Zhang

Researcher at The Chinese University of Hong Kong

Publications -  11
Citations -  208

Cheng Zhang is an academic researcher from The Chinese University of Hong Kong. The author has contributed to research in topics: Angiogenesis & In vivo. The author has an hindex of 7, co-authored 11 publications receiving 161 citations. Previous affiliations of Cheng Zhang include Capital Normal University.

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The roles of endoplasmic reticulum stress response in female mammalian reproduction.

TL;DR: The study of the functions of the ERS response in mammalian reproduction might provide novel insights into and an understanding of reproductive cell survival and apoptosis under physiological and pathological conditions.
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Cocoa tea (Camellia ptilophylla) water extract inhibits adipocyte differentiation in mouse 3T3-L1 preadipocytes.

TL;DR: This is the first study that demonstrates cocoa tea has the capacity to suppress adipogenesis in pre-adipocyte 3T3-L1 similar to traditional green tea.
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Melatonin as Potential Targets for Delaying Ovarian Aging.

TL;DR: The mechanism of ovarian aging and the extensive role of melatonin in the ovarian aging process are described herein, and new insights into ovarian aging are supply and a novel drug ofmelatonin for ovarian aging treatment is supply.
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Pro-angiogenic effects of Carthami Flos whole extract in human microvascular endothelial cells in vitro and in zebrafish in vivo.

TL;DR: Investigation of the angiogenic potential of CF whole extract and the underlying mechanisms in human microvascular endothelial cells (HMEC-1) in vitro and in transgenic TG(fli1:EGFP)(y1)/+(AB) zebrafish with transgenic endothelium cells expressing EGFP (Enhanced Green Fluorescent Protein) in vivo found increased angiogenesis in HMEC- 1 cells with multiple mechanisms.
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Characteristics of stem cells derived from rat fascia: In vitro proliferative and multilineage potential assessment

TL;DR: FDSCs possessed high chondrogenic potential, low osteogenic and adipogenic differentiation potential and were responsive to the induction signals for collagen‑rich fascial structure regeneration, suggesting that FDSCs may represent an improved alternative cell source to conventional ADSCs and BMSCs for musculoskeletal tissue repair and tissue engineering.