1. A novel c.287G>T NDP missense mutation in a Chinese family with Norrie disease. (3rd July 2020) Authors: Lin, Meina; Lu, Yongping; Sui, Yu; Ni, Xiang; Li, Huan; Chen, Xinren; Zhao, Ning; Jiang, Miao Journal: Ophthalmic genetics Issue: Volume 41:Number 4(2020) Page Start: 338 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel c.287G>T NDP missense mutation in a Chinese family with Norrie disease. (3rd July 2020) Authors: Lin, Meina; Lu, Yongping; Sui, Yu; Ni, Xiang; Li, Huan; Chen, Xinren; Zhao, Ning; Jiang, Miao Journal: Ophthalmic genetics Issue: Volume 41:Number 4(2020) Page Start: 338 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association between FOXE1 and non-syndromic orofacial clefts in a northeastern Chinese population. Issue 8 (October 2015) Authors: Liu, Kun; Lu, Yongping; Ai, Lisi; Jiao, Boqiang; Yu, Jiantao; Zhang, Bin; Liu, Qiang Journal: British journal of oral and maxillofacial surgery Issue: Volume 53:Issue 8(2015) Page Start: 705 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Association between FOXE1 and non-syndromic orofacial clefts in a northeastern Chinese population. Issue 8 (October 2015) Authors: Liu, Kun; Lu, Yongping; Ai, Lisi; Jiao, Boqiang; Yu, Jiantao; Zhang, Bin; Liu, Qiang Journal: British journal of oral and maxillofacial surgery Issue: Volume 53:Issue 8(2015) Page Start: 705 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. ChemInform Abstract: MgI2 Etherate‐Catalyzed Strecker Reaction: A Facile and Efficient Synthesis of α‐Aminonitriles from Aldimines and Trimethylsilyl Cyanide. Issue 24 (2nd June 2014) Authors: Lu, Yongping; Wang, Yanping; Zhang, Xingxian Journal: ChemInform Issue: Volume 45:Issue 24(2014) Page Start: no Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Deep learning Radiomics of shear wave elastography significantly improved diagnostic performance for assessing liver fibrosis in chronic hepatitis B: a prospective multicentre study. Issue 4 (5th May 2018) Authors: Wang, Kun; Lu, Xue; Zhou, Hui; Gao, Yongyan; Zheng, Jian; Tong, Minghui; Wu, Changjun; Liu, Changzhu; Huang, Liping; Jiang, Tian'an; Meng, Fankun; Lu, Yongping; Ai, Hong; Xie, Xiao-Yan; Yin, Li-ping; Liang, Ping; Tian, Jie; Zheng, Rongqin Journal: Gut Issue: Volume 68:Issue 4(2019) Page Start: 729 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Discovery and optimization of a potent and selective indazolamine series of IRAK4 inhibitors. (1st January 2021) Authors: Zhai, Wenqiang; Lu, Yongping; Zhu, Yabo; Zhou, Mengguang; Ye, Cheng; Shi, Zheng-Zheng; Qian, Wenjian; Hu, Taishan; Chen, Lei Journal: Bioorganic & medicinal chemistry letters Issue: Volume 31(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Efficient discovery of novel antimicrobials through integration of synthesis and testing in crude ribosome extract. Issue 42 (1st May 2019) Authors: Sang, Zitai; Lu, Yongping; Zhou, Yuanzheng; Ju, Yuan; An, Qi; Shen, Silan; Shi, Jianyou; He, Jun; Yang, Tao; Luo, Youfu Journal: Chemical communications Issue: Volume 55:Issue 42(2019) Page Start: 5886 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Elevated mRNA expression of PGF2α receptor splice variant 2(FP-V2) in human decidua is associated with incomplete mifepristone–misoprostol-induced early medical abortion by regulation of interleukin-8. (1st November 2016) Authors: Ma, Chao; Feng, Wenhua; Han, Weitian; Lu, Yongping; Liu, Wei; Sui, Yu; Zhao, Ning; Lye, Stephen J.; Li, Jianxin Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 29:Number 21(2016) Page Start: 3472 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Extremely severe scoliosis, heterotopic ossification, and osteoarthritis in a three‐generation family with Crouzon syndrome carrying a mutant c.799T>C FGFR2. Issue 9 (18th July 2019) Authors: Lin, Meina; Lu, Yongping; Sui, Yu; Zhao, Ning; Jin, Ying; Yi, Dongxu; Jiang, Miao Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 9(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗