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Exome sequencing‐aided precise diagnosis of four families with type I Stickler syndrome.
Published in:
Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2331
By:
- Tian, Runyi;
- Tong, Ping;
- He, Yuhong;
- Zang, Liyu;
- Zhou, Shimin;
- Tian, Qi
Publication type:
Article
A novel NHS mutation causes Nance-Horan Syndrome in a Chinese family.
Published in:
BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-016-0360-9
By:
- Qi Tian;
- Yunping Li;
- Rizwana Kousar;
- Hui Guo;
- Fenglan Peng;
- Yu Zheng;
- Xiaohua Yang;
- Zhigao Long;
- Runyi Tian;
- Kun Xia;
- Haiying Lin;
- Qian Pan
Publication type:
Article
PINK1 phosphorylates Drp1S616 to regulate mitophagy‐independent mitochondrial dynamics.
Published in:
EMBO Reports, 2020, v. 21, n. 8, p. 1, doi. 10.15252/embr.201948686
By:
- Han, Hailong;
- Tan, Jieqiong;
- Wang, Ruoxi;
- Wan, Huida;
- He, Yaohui;
- Yan, Xinxiang;
- Guo, Jifeng;
- Gao, Qingtao;
- Li, Jie;
- Shang, Shuai;
- Chen, Fang;
- Tian, Runyi;
- Liu, Wen;
- Liao, Lujian;
- Tang, Beisha;
- Zhang, Zhuohua
Publication type:
Article
PINK1-mediated Drp1S616 phosphorylation modulates synaptic development and plasticity via promoting mitochondrial fission.
Published in:
Signal Transduction & Targeted Therapy, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41392-022-00933-z
By:
- Gao, Qingtao;
- Tian, Runyi;
- Han, Hailong;
- Slone, Jesse;
- Wang, Caifang;
- Ke, Xiao;
- Zhang, Tongmei;
- Li, Xiangyu;
- He, Yuhong;
- Liao, Panlin;
- Wang, Fang;
- Chen, Ye;
- Fu, Shiqing;
- Zhang, Kexuan;
- Zeng, Fangfang;
- Yang, Yingxuan;
- Li, Zhuo;
- Tan, Jieqiong;
- Li, Jiada;
- Lu, Youming
Publication type:
Article
PINK1-mediated Drp1S616 phosphorylation modulates synaptic development and plasticity via promoting mitochondrial fission.
Published in:
Signal Transduction & Targeted Therapy, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41392-022-00933-z
By:
- Qingtao Gao;
- Runyi Tian;
- Hailong Han;
- Slone, Jesse;
- Caifang Wang;
- Xiao Ke;
- Tongmei Zhang;
- Xiangyu Li;
- Yuhong He;
- Panlin Liao;
- Fang Wang;
- Ye Chen;
- Shiqing Fu;
- Kexuan Zhang;
- Fangfang Zeng;
- Yingxuan Yang;
- Zhuo Li;
- Jieqiong Tan;
- Jiada Li;
- Youming Lu
Publication type:
Article

Found: 5

Exome sequencing‐aided precise diagnosis of four families with type I Stickler syndrome.

A novel NHS mutation causes Nance-Horan Syndrome in a Chinese family.

PINK1 phosphorylates Drp1<sup>S616</sup> to regulate mitophagy‐independent mitochondrial dynamics.

PINK1-mediated Drp1<sup>S616</sup> phosphorylation modulates synaptic development and plasticity via promoting mitochondrial fission.

PINK1-mediated Drp1<sup>S616</sup> phosphorylation modulates synaptic development and plasticity via promoting mitochondrial fission.