F
Feng Zhang
Researcher at Fudan University
Publications - 2715
Citations - 225233
Feng Zhang is an academic researcher from Fudan University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 172, co-authored 1278 publications receiving 181865 citations. Previous affiliations of Feng Zhang include Cincinnati Children's Hospital Medical Center & Nanjing Medical University.
Papers
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Journal ArticleDOI
Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice.
Chunyu Liu,Xiaojin He,Wangjie Liu,Wangjie Liu,Shenmin Yang,Lingbo Wang,Weiyu Li,Weiyu Li,Huan Wu,Shuyan Tang,Xiaoqing Ni,Jiaxiong Wang,Yang Gao,Shixiong Tian,Shixiong Tian,Lin Zhang,Jiangshan Cong,Z. Zhang,Qing Tan,Jingjing Zhang,Hong Li,Yading Zhong,Mingrong Lv,Jinsong Li,Li Jin,Yunxia Cao,Feng Zhang,Feng Zhang +27 more
TL;DR: Bi-allelic mutations in TTC29, as an important genetic pathogeny, can induce MMAF-related asthenoteratospermia and provide effective guidance for clinical diagnosis and assisted reproduction treatments.
Journal ArticleDOI
Cancer-derived exosomal HSPC111 promotes colorectal cancer liver metastasis by reprogramming lipid metabolism in cancer-associated fibroblasts
Chong Zhang,Xiang-Yu Wang,Feng Zhang,Taotao He,Jia-Hao Han,Rui Zhang,Jing Lin,Jie Fan,Lu Lu,Hu-Liang Jia,Ju-Bo Zhang,Jinhong Chen +11 more
TL;DR: Zhang et al. as mentioned in this paper identified HSPC111 was the leading upregulated gene in hepatic stellate cells (HSCs) incubated with CRC cell-derived exosomes.
Journal ArticleDOI
Compact RNA editors with small Cas13 proteins.
Soumya Kannan,Han Altae-Tran,Xin Jin,Victoria J Madigan,Rachel Oshiro,Kira S. Makarova,Eugene V. Koonin,Feng Zhang +7 more
Abstract: CRISPR-Cas13 systems have been developed for precise RNA editing, and can potentially be used therapeutically when temporary changes are desirable or when DNA editing is challenging. We have identified and characterized an ultrasmall family of Cas13b proteins-Cas13bt-that can mediate mammalian transcript knockdown. We have engineered compact variants of REPAIR and RESCUE RNA editors by functionalizing Cas13bt with adenosine and cytosine deaminase domains, and demonstrated packaging of the editors within a single adeno-associated virus.
Journal ArticleDOI
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
Jiaqi Liu,Jiaqi Liu,Yangzhong Zhou,Sen Liu,Sen Liu,Xiaofei Song,Xinzhuang Yang,Yanhui Fan,Weisheng Chen,Weisheng Chen,Zeynep Coban Akdemir,Zihui Yan,Zihui Yan,Yuzhi Zuo,Yuzhi Zuo,Renqian Du,Zhenlei Liu,Bo Yuan,Sen Zhao,Sen Zhao,Gang Liu,Gang Liu,Yixin Chen,Yixin Chen,Yanxue Zhao,Yanxue Zhao,Mao Lin,Mao Lin,Qiankun Zhu,Qiankun Zhu,Yuchen Niu,Yuchen Niu,Pengfei Liu,Shiro Ikegawa,You-Qiang Song,Jennifer E. Posey,Guixing Qiu,Guixing Qiu,Disco,COmorbidities (Disco) study,Feng Zhang,Feng Zhang,Zhihong Wu,Zhihong Wu,James R. Lupski,James R. Lupski,Nan Wu,Nan Wu +47 more
TL;DR: It is proposed that detecting co-existent CNVs when evaluating the association signals between SNPs and disease traits could improve genetic model analyses and better integrate GWAS with robust Mendelian principles.
Patent
Protected guide rnas (pgrnas)
TL;DR: In this article, structural information on the Cas protein of the CRISPR-Cas system, use of this information in generating modified components of the Cas complex, vectors and vector systems which encode one or more components or modified components, as well as methods for the design and use of such vectors and components.