P
Ping Zhou
Researcher at Anhui Medical University
Publications - 118
Citations - 1558
Ping Zhou is an academic researcher from Anhui Medical University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 17, co-authored 84 publications receiving 995 citations. Previous affiliations of Ping Zhou include Chinese Ministry of Education & Fudan University.
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Comparison of survival and embryonic development in human oocytes cryopreserved by slow-freezing and vitrification
TL;DR: Vitrification is superior to the slow-freezing method, leading to improved oocyte survival rate, fertilization, and embryonic development in vitro, and these results may be related to vitrified human oocytes incurring less damage to spindle integrity and chromosome alignment.
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Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome
Fuxi Zhu,Fengsong Wang,Xiaoyu Yang,Jingjing Zhang,Huan Wu,Zhou Zhang,Zhiguo Zhang,Xiaojin He,Ping Zhou,Zhaolian Wei,Jozef Gecz,Yunxia Cao +11 more
TL;DR: It is demonstrated that biallelic SUN5 mutations cause male infertility due to autosomal-recessive acephalic spermatozoa syndrome and certain variants altered SUN5 distribution in the head-tail junction of the sperm.
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Cryopreservation of immature and in-vitro matured human oocytes by vitrification.
TL;DR: Oocyte maturation rates were significantly reduced when oocytes were vitrified at immature GV stage followed by IVM, suggesting that better results can be achieved by vitrifying mature oocytes rather than immature oocytes.
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Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome.
Fuxi Zhu,Chao Liu,Fengsong Wang,Xiaoyu Yang,Jingjing Zhang,Huan Wu,Zhiguo Zhang,Xiaojin He,Zhou Zhang,Ping Zhou,Zhaolian Wei,Yongliang Shang,Lina Wang,Ruidan Zhang,Ying-Chun Ouyang,Qing-Yuan Sun,Yunxia Cao,Wei Li +17 more
TL;DR: Mutations in PMFBP1 are an important cause of infertility in men with acephalic spermatozoa syndrome and could be successfully overcome by intracytoplasmic sperm injection (ICSI) in both mouse and human.
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Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella
Xiaojin He,Weiyu Li,Huan Wu,Mingrong Lv,Wangjie Liu,Wangjie Liu,Chunyu Liu,Chunyu Liu,Fuxi Zhu,Caihua Li,Youyan Fang,Chenyu Yang,Huiru Cheng,Junqiang Zhang,Jing Tan,Tingting Chen,Dongdong Tang,Bing Song,Xue Wang,Xiaomin Zha,Hongyan Wang,Hongyan Wang,Zhaolian Wei,Shenmin Yang,Hexige Saiyin,Ping Zhou,Li Jin,Jian Wang,Zhiguo Zhang,Feng Zhang,Yunxia Cao +30 more
TL;DR: The experimental findings elucidate that homozygous loss-of-function mutations in CFAP69 can lead to asthenoteratospermia with MMAF in humans and mice.