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Suo-Feng Ma

Researcher at Shandong Agricultural University

Publications -  11
Citations -  358

Suo-Feng Ma is an academic researcher from Shandong Agricultural University. The author has contributed to research in topics: In vitro maturation & Oocyte. The author has an hindex of 10, co-authored 11 publications receiving 335 citations.

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Parthenogenetic activation of mouse oocytes by strontium chloride: a search for the best conditions.

TL;DR: The concentration and duration of SrCl(2) treatment and the presence or absence of CB in activating medium and cumulus cells had marked effects on mouse oocyte activation and development.
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Changes in germinal vesicle (GV) chromatin configurations during growth and maturation of porcine oocytes.

TL;DR: The results suggested that the GV0 configuration in porcine oocytes corresponded to the “nonsurrounded nucleolus” pattern in mice and other species, and the in vitro systems currently used were not favorable for oocytes to switch toward ovulation (or final maturation) or atresia.
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Production of cloned goats by nuclear transfer of cumulus cells and long-term cultured fetal fibroblast cells into abattoir-derived oocytes.

TL;DR: Cloned goats were produced by NT from cumulus cells and long‐term cultured fetal fibroblast cells to abattoir‐derived oocytes and microsatellite analysis of 10 markers confirmed that all cloned offspring were derived from corresponding donor cells.
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Fate of the first polar bodies in mouse oocytes.

TL;DR: The results were consistent with the possibility that the displacement of the FPB was a time‐ and PVS‐dependent process, indicating that PVS would increase with time and its formation and enlargement would facilitate the lateral displacement ofThe degenerating FPB.
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Hypoxanthine (HX) inhibition of in vitro meiotic resumption in goat oocytes

TL;DR: Goat oocytes were capable of normal nuclear maturation and activation after temporal arrest by HX, but prolonged exposure to HX induced spontaneous activation, consistent with the possibility that the decline of HX inhibitory effect was not due to Hx depletion but rather due to the negative feedback of the metabolites on its further uptake by oocytes.