Tao Cai

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 8

Top Topics

Ankylosing Spondylitis

Mesenchymal Stem Cells

Intellectual Disability

Top Venues

BMC medical genetics

Science translational medicine

American journal of hematology

This page only lists publications with an associated author ORCID identifier.

Publications

Xiaoxing Kou, Jin Liu, Dandan Wang, Ming Yu, Can Li, Lu Lu, Chider Chen, Dawei Liu, Wenjing Yu, Tingting Yu, Yao Liu, Xueli Mao, Ali Naji, Tao Cai, Lingyun Sun, Songtao Shi
Exocrine pancreas regeneration modifies original pancreas to alleviate diabetes in mouse models. Science translational medicine 14 (656) (2022)
Yuan Li, Guozhu Ning, Baoling Kang, Jinwen Zhu, Xiao-Yang Wang, Qiang Wang, Tao Cai
A novel recessive mutation in OXR1 is identified in patient with hearing loss recapitulated by the knockdown zebrafish. Human molecular genetics (2022)
Jianjun Xiong, Xi Wang, Chunxin Fan, Jizhou Yan, Jinwen Zhu, Tao Cai
Hemifacial microsomia is linked to a rare homozygous variant V162I in FRK and validated in zebrafish. Oral diseases (2022)
Yi Gu, Bingwu Xiang, Lina Zhu, Xiuwei Ma, Xiang Chen, Tao Cai
Three intellectual disability-associated de novo mutations in MECP2 identified by trio-WES analysis. BMC medical genetics 21 (1) (2020)
Xiaoxing Kou, Xingtian Xu, Chider Chen, Maria Laura Sanmillan, Tao Cai, Yanheng Zhou, Claudio Giraudo, Anh D Le, Songtao Shi
The Fas/Fap-1/Cav-1 complex regulates IL-1RA secretion in mesenchymal stem cells to accelerate wound healing. Science translational medicine 10 (432) (2019)
Haixia Zhang, Bingwu Xiang, Hui Chen, Xiang Chen, Tao Cai
A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia. BMC medical genetics 20 (1) (2019)
Miao Yu, Sing-Wai Wong, Dong Han, Tao Cai
Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis. Oral diseases 25 (3) (2018)
Tao Cai, Xiang Chen, Jinchen Li, Bingwu Xiang, Liu Yang, Yidian Liu, Qiuli Chen, Zhouwen He, Kevin Sun, P Paul Liu
Identification of novel mutations in the HbF repressor gene BCL11A in patients with autism and intelligence disabilities. American journal of hematology 92 (12) (2017)